Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10575 |
| ensemblid | ENSG00000115484.15 |
| hgncid | 1617 |
| symbol | CCT4 |
| name | chaperonin containing TCP1 subunit 4 |
| refseq_nuc | NM_006430.4 |
| refseq_prot | NP_006421.2 |
| ensembl_nuc | ENST00000394440.8 |
| ensembl_prot | ENSP00000377958.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 61868085 |
| end | 61888656 |
| strand | - |
| ver | v1.2 |
| region | chr2:61868085-61888656 |
| region5000 | chr2:61863085-61893656 |
| regionname0 | CCT4_chr2_61868085_61888656 |
| regionname5000 | CCT4_chr2_61863085_61893656 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 539 | 409 | 88 | 75 | 182 | 18 | 44 | 138 | CCT4_chr2_61863085_61893656 | CCT4 | MPENV others(534): Show |
chr2 | 61863085 | 61893656 |
| a0002 | 0/0 | 539 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CCT4_chr2_61863085_61893656 | CCT4 | MPENV others(534): Show |
chr2 | 61863085 | 61893656 |
| a0003 | 0/0 | 539 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | MPENV others(534): Show |
chr2 | 61863085 | 61893656 |
| a0004 | 0/0 | 539 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | MPENV others(534): Show |
chr2 | 61863085 | 61893656 |
| a0005 | 0/0 | 539 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | MPENV others(534): Show |
chr2 | 61863085 | 61893656 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1617 | 352 | 63 | 67 | 174 | 14 | 33 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 | ||
| a0001c0002 | 0/1 | 1617 | 53 | 24 | 8 | 6 | 4 | 10 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 | ||
| a0001c0004 | 0/0 | 1617 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 | ||
| a0001c0006 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 | ||
| a0001c0009 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 | ||
| a0001c0010 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 | ||
| a0002c0003 | 0/0 | 1617 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 | ||
| a0003c0005 | 0/0 | 1617 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 | ||
| a0004c0007 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 | ||
| a0005c0008 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | ATGCC others(1612): Show |
chr2 | 61863085 | 61893656 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2376 | 347 | 61 | 65 | 174 | 14 | 32 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0001c0001t0003 | 0/0 | 2376 | 3 | 0 | 2 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0001c0001t0004 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2298): Show |
chr2 | 61863085 | 61893656 |
| a0001c0001t0005 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0001c0002t0002 | 0/1 | 2376 | 53 | 24 | 8 | 6 | 4 | 10 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0001c0004t0001 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0001c0006t0001 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0001c0009t0001 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0001c0010t0001 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0002c0003t0001 | 0/0 | 2376 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0003c0005t0001 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0004c0007t0001 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| a0005c0008t0001 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | CTTCT others(2371): Show |
chr2 | 61863085 | 61893656 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 0 | 2 | 14 | 3 | 2 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0002 | 0/0 | 16 | 2 | 4 | 4 | 1 | 5 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0003 | 0/0 | 15 | 0 | 3 | 9 | 1 | 2 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0004 | 0/0 | 11 | 2 | 0 | 9 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 3 | 3 | 1 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 1 | 2 | 0 | 3 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0040 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0012 | 0/0 | 6 | 0 | 0 | 3 | 2 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0053 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0238 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0006t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0009t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0001c0010t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0002c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0003c0005t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0004c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| a0005c0008t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01071 | hp1 | a0003 | c0005 | t0001 | g0170 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0227 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0229 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0237 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0012 | EUR | IBS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0012 | EUR | IBS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0254 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0250 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0246 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0225 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0224 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02683 | hp2 | a0001 | c0004 | t0001 | g0195 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0243 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0240 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0232 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02886 | hp2 | a0001 | c0006 | t0001 | g0221 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0233 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0249 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0251 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0051 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0230 | SAS | STU | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0053 | SAS | STU | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0234 | SAS | PJL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0247 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0191 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | STU | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | YRI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18963 | hp2 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18983 | hp2 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18994 | hp2 | a0004 | c0007 | t0001 | g0220 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | LWK | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0226 | AFR | LWK | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | LWK | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19062 | hp1 | a0001 | c0009 | t0001 | g0081 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19065 | hp1 | a0001 | c0010 | t0001 | g0084 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19066 | hp1 | a0005 | c0008 | t0001 | g0080 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0253 | AFR | ASW | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0236 | EUR | TSI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0248 | EUR | TSI | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | GIH | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0252 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0228 | AFR | ACB | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0238 | REF | REF | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0040 | REF | REF | CCT4_chr2_61863085_61893656 | CCT4 | chr2 | 61863085 | 61893656 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61872546 | C | A | 1 | a0004 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.1168G>T | p.Val390Phe | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 11/14 | 1317/2376 | 1168/1620 | 390/539 | chr2 | 61872546 | |||
| chr2:61873030 | T | C | 1 | a0002 | 2 | NA18963.hp2 NA18983.hp2 |
missense_variant | MODERATE | c.1097A>G | p.Asn366Ser | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 10/14 | 1246/2376 | 1097/1620 | 366/539 | chr2 | 61873030 | |||
| chr2:61876149 | T | G | 1 | a0005 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.863A>C | p.Lys288Thr | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/14 | 1012/2376 | 863/1620 | 288/539 | chr2 | 61876149 | |||
| chr2:61876999 | A | G | 1 | a0003 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.698T>C | p.Val233Ala | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/14 | 847/2376 | 698/1620 | 233/539 | chr2 | 61876999 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61872085 | T | G | 1 | a0001c0006 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1488A>C | p.Arg496Arg | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/14 | 1637/2376 | 1488/1620 | 496/539 | chr2 | 61872085 | |||
| chr2:61873245 | G | T | 1 | a0001c0002 | 52 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(49): Show |
synonymous_variant | LOW | c.966C>A | p.Ile322Ile | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 9/14 | 1115/2376 | 966/1620 | 322/539 | chr2 | 61873245 | |||
| chr2:61877434 | G | A | 1 | a0001c0009 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.603C>T | p.Thr201Thr | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 6/14 | 752/2376 | 603/1620 | 201/539 | chr2 | 61877434 | |||
| chr2:61877455 | C | T | 1 | a0001c0004 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.582G>A | p.Val194Val | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 6/14 | 731/2376 | 582/1620 | 194/539 | chr2 | 61877455 | |||
| chr2:61883492 | T | C | 1 | a0001c0010 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.237A>G | p.Lys79Lys | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/14 | 386/2376 | 237/1620 | 79/539 | chr2 | 61883492 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61868163 | C | T | 1 | a0001c0001t0005 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*529G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 14/14 | 529 | chr2 | 61868163 | ||||||
| chr2:61868290 | GTTCAGAG others(66): Show |
G | 1 | a0001c0001t0004 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*329_*401delGGCCTT others(67): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 14/14 | 329 | chr2 | 61868290 | ||||||
| chr2:61868399 | T | C | 1 | a0001c0001t0003 | 3 | HG00639.hp1 HG01255.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*293A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 14/14 | 293 | chr2 | 61868399 | ||||||
| chr2:61868436 | CTTTTATT others(3): Show |
C | 1 | a0001c0001t0001 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*246_*255delACTAAT others(4): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 14/14 | 246 | chr2 | 61868436 | ||||||
| chr2:61888641 | G | A | 1 | a0001c0002t0002 | 52 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-134C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/14 | 134 | chr2 | 61888641 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61868718 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1606-12T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61868718 | |||||||
| chr2:61868859 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.1606-153T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61868859 | |||||||
| chr2:61868933 | G | A | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1606-227C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61868933 | |||||||
| chr2:61868990 | C | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0147 a0001c0001t0004g0146 |
4 | HG02145.hp1 HG02630.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1606-284G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61868990 | |||||||
| chr2:61869062 | A | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(47): Show |
82 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1606-356T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869062 | |||||||
| chr2:61869073 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0201 |
4 | NA18973.hp1 NA18977.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1605+367G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869073 | |||||||
| chr2:61869085 | T | A | 1 | a0001c0001t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1605+355A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869085 | |||||||
| chr2:61869122 | A | G | 1 | a0001c0001t0001g0014 | 4 | HG00438.hp1 HG02056.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1605+318T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869122 | |||||||
| chr2:61869143 | GA | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(72): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1605+296delT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869143 | |||||||
| chr2:61869143 | GAA | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1605+295_1605+296d others(4): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869143 | |||||||
| chr2:61869143 | GAAA | G | 8 | a0001c0001t0001g0066 a0001c0001t0001g0070 a0001c0001t0001g0091 others(5): Show |
8 | HG00099.hp2 HG03041.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.1605+294_1605+296d others(5): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869143 | |||||||
| chr2:61869143 | GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1605+286_1605+296d others(13): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869143 | |||||||
| chr2:61869372 | C | A | 1 | a0001c0001t0001g0109 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1605+68G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869372 | |||||||
| chr2:61869373 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1605+67T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869373 | |||||||
| chr2:61869409 | C | A | 1 | a0001c0001t0001g0039 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1605+31G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 13/13 | chr2 | 61869409 | |||||||
| chr2:61869655 | TTCTG | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(19): Show |
40 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.1492-106_1492-103d others(6): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61869655 | |||||||
| chr2:61869657 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0180 a0001c0001t0001g0181 |
6 | HG00735.hp1 HG01884.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1492-104G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61869657 | |||||||
| chr2:61869864 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0180 a0001c0001t0001g0181 |
6 | HG00735.hp1 HG01884.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1492-311A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61869864 | |||||||
| chr2:61869969 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG03579.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1492-416G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61869969 | |||||||
| chr2:61870015 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1492-462G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61870015 | |||||||
| chr2:61870209 | G | A | 1 | a0001c0001t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1492-656C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61870209 | |||||||
| chr2:61870228 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1492-675A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61870228 | |||||||
| chr2:61870256 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.1492-703G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61870256 | |||||||
| chr2:61870408 | C | T | 1 | a0001c0001t0001g0034 | 2 | NA19001.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1492-855G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61870408 | |||||||
| chr2:61870489 | C | A | 2 | a0001c0002t0002g0051 a0001c0002t0002g0226 |
3 | HG02451.hp1 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1492-936G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61870489 | |||||||
| chr2:61870979 | GA | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.1491+1102delT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61870979 | |||||||
| chr2:61871029 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1491+1053A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871029 | |||||||
| chr2:61871031 | G | GT | 16 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0068 others(13): Show |
17 | HG00438.hp2 HG01928.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.1491+1050dupA | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871031 | |||||||
| chr2:61871031 | GT | G | 7 | a0001c0001t0001g0057 a0001c0001t0001g0135 a0001c0001t0001g0174 others(4): Show |
8 | HG00642.hp1 HG01175.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1491+1050delA | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871031 | |||||||
| chr2:61871033 | T | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(17): Show |
38 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.1491+1049A>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871033 | |||||||
| chr2:61871034 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1491+1048A>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871034 | |||||||
| chr2:61871114 | C | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0218 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1491+968G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871114 | |||||||
| chr2:61871176 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1491+906A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871176 | |||||||
| chr2:61871197 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1491+885T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871197 | |||||||
| chr2:61871229 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(118): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1491+853T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871229 | |||||||
| chr2:61871317 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG03579.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1491+765G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871317 | |||||||
| chr2:61871327 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1491+755G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871327 | |||||||
| chr2:61871410 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG02630.hp1 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1491+672A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871410 | |||||||
| chr2:61871469 | G | C | 1 | a0001c0001t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1491+613C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871469 | |||||||
| chr2:61871637 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(118): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1491+445A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871637 | |||||||
| chr2:61871659 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(19): Show |
40 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.1491+423G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871659 | |||||||
| chr2:61871726 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1491+356G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871726 | |||||||
| chr2:61871815 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0134 |
3 | HG02486.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1491+267G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871815 | |||||||
| chr2:61871858 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1491+224G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61871858 | |||||||
| chr2:61872000 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1491+82C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61872000 | |||||||
| chr2:61872021 | T | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1491+61A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 12/13 | chr2 | 61872021 | |||||||
| chr2:61872627 | C | CA | 5 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-40dupT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 10/13 | chr2 | 61872627 | |||||||
| chr2:61872656 | G | A | 7 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0158 others(4): Show |
7 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1126-68C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 10/13 | chr2 | 61872656 | |||||||
| chr2:61872710 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1126-122C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 10/13 | chr2 | 61872710 | |||||||
| chr2:61872825 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1125+177C>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 10/13 | chr2 | 61872825 | |||||||
| chr2:61872921 | C | T | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1125+81G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 10/13 | chr2 | 61872921 | |||||||
| chr2:61872956 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1125+46G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 10/13 | chr2 | 61872956 | |||||||
| chr2:61872990 | T | C | 1 | a0001c0002t0002g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1125+12A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 10/13 | chr2 | 61872990 | |||||||
| chr2:61873318 | G | C | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG03579.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.918-25C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873318 | |||||||
| chr2:61873365 | TTTAA | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0219 |
3 | NA18940.hp1 NA18998.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.918-76_918-73delTT others(2): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873365 | |||||||
| chr2:61873418 | A | C | 1 | a0001c0002t0002g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.918-125T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873418 | |||||||
| chr2:61873525 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.918-232G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873525 | |||||||
| chr2:61873547 | T | C | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.918-254A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873547 | |||||||
| chr2:61873555 | CATTT | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(19): Show |
40 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.918-266_918-263del others(4): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873555 | |||||||
| chr2:61873598 | C | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0164 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.918-305G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873598 | |||||||
| chr2:61873631 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.918-338A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873631 | |||||||
| chr2:61873754 | C | T | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.918-461G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873754 | |||||||
| chr2:61873755 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0214 |
3 | HG02055.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.918-462C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873755 | |||||||
| chr2:61873776 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG03579.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.918-483G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873776 | |||||||
| chr2:61873877 | T | C | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.918-584A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61873877 | |||||||
| chr2:61874107 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.918-814G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874107 | |||||||
| chr2:61874142 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.918-849T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874142 | |||||||
| chr2:61874188 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.918-895C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874188 | |||||||
| chr2:61874209 | T | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(83): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.918-916A>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874209 | |||||||
| chr2:61874292 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.918-999G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874292 | |||||||
| chr2:61874321 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.918-1028A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874321 | |||||||
| chr2:61874436 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA18967.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.918-1143A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874436 | |||||||
| chr2:61874471 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0077 |
4 | HG00423.hp1 HG00609.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.918-1178C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874471 | |||||||
| chr2:61874528 | T | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG03579.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.918-1235A>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874528 | |||||||
| chr2:61874567 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.918-1274G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874567 | |||||||
| chr2:61874611 | CA | C | 11 | a0001c0001t0001g0057 a0001c0001t0001g0099 a0001c0001t0001g0133 others(8): Show |
12 | HG01167.hp2 HG02055.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.918-1319delT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874611 | |||||||
| chr2:61874780 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.917+1315T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874780 | |||||||
| chr2:61874785 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0147 a0001c0001t0004g0146 |
4 | HG02145.hp1 HG02630.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.917+1310A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874785 | |||||||
| chr2:61874832 | T | C | 1 | a0001c0002t0002g0250 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.917+1263A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874832 | |||||||
| chr2:61874860 | T | C | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.917+1235A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874860 | |||||||
| chr2:61874878 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.917+1217G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874878 | |||||||
| chr2:61874905 | G | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.917+1190C>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874905 | |||||||
| chr2:61874970 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.917+1125G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61874970 | |||||||
| chr2:61875058 | C | T | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.917+1037G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875058 | |||||||
| chr2:61875127 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.917+968C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875127 | |||||||
| chr2:61875133 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.917+962G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875133 | |||||||
| chr2:61875141 | C | CA | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.917+953dupT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875141 | |||||||
| chr2:61875141 | C | CAA | 12 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(9): Show |
12 | HG01243.hp2 HG01496.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.917+952_917+953dup others(2): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875141 | |||||||
| chr2:61875229 | TA | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.917+865delT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875229 | |||||||
| chr2:61875303 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.917+792C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875303 | |||||||
| chr2:61875407 | T | A | 1 | a0001c0001t0001g0039 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.917+688A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875407 | |||||||
| chr2:61875420 | A | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0137 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.917+675T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875420 | |||||||
| chr2:61875429 | A | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0145 a0001c0001t0001g0147 others(1): Show |
5 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.917+666T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875429 | |||||||
| chr2:61875450 | C | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.917+645G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875450 | |||||||
| chr2:61875582 | CA | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.917+512delT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875582 | |||||||
| chr2:61875582 | CAA | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(19): Show |
40 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.917+511_917+512del others(2): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875582 | |||||||
| chr2:61875587 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.917+508T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875587 | |||||||
| chr2:61875677 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.917+418G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875677 | |||||||
| chr2:61875694 | T | C | 1 | a0001c0001t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.917+401A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875694 | |||||||
| chr2:61875789 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.917+306A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875789 | |||||||
| chr2:61875834 | A | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0055 a0001c0001t0001g0166 others(1): Show |
5 | HG01106.hp1 HG01123.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.917+261T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875834 | |||||||
| chr2:61875835 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(117): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.917+260T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875835 | |||||||
| chr2:61875879 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.917+216G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875879 | |||||||
| chr2:61875903 | A | G | 1 | a0001c0002t0002g0240 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.917+192T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875903 | |||||||
| chr2:61875907 | T | C | 1 | a0001c0002t0002g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.917+188A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 8/13 | chr2 | 61875907 | |||||||
| chr2:61876319 | G | A | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.778-85C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/13 | chr2 | 61876319 | |||||||
| chr2:61876324 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.778-90T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/13 | chr2 | 61876324 | |||||||
| chr2:61876401 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.778-167T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/13 | chr2 | 61876401 | |||||||
| chr2:61876401 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.778-167T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/13 | chr2 | 61876401 | |||||||
| chr2:61876526 | T | G | 1 | a0001c0001t0001g0036 | 2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.778-292A>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/13 | chr2 | 61876526 | |||||||
| chr2:61876589 | C | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.777+331G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/13 | chr2 | 61876589 | |||||||
| chr2:61876633 | C | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.777+287G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/13 | chr2 | 61876633 | |||||||
| chr2:61876808 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.777+112G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/13 | chr2 | 61876808 | |||||||
| chr2:61876855 | A | G | 1 | a0001c0001t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.777+65T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 7/13 | chr2 | 61876855 | |||||||
| chr2:61877173 | T | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0218 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.645-121A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 6/13 | chr2 | 61877173 | |||||||
| chr2:61877208 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(117): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.645-156G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 6/13 | chr2 | 61877208 | |||||||
| chr2:61877369 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.644+24G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 6/13 | chr2 | 61877369 | |||||||
| chr2:61877525 | T | TA | 5 | a0001c0001t0001g0217 a0001c0002t0002g0020 a0001c0002t0002g0051 others(2): Show |
8 | HG02280.hp1 HG02451.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.523-12dupT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61877525 | |||||||
| chr2:61877525 | TA | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.523-12delT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61877525 | |||||||
| chr2:61877547 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.523-33A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61877547 | |||||||
| chr2:61877691 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.523-177G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61877691 | |||||||
| chr2:61877715 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.523-201A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61877715 | |||||||
| chr2:61877779 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.523-265T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61877779 | |||||||
| chr2:61877812 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.523-298C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61877812 | |||||||
| chr2:61877999 | A | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(30): Show |
66 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.523-485T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61877999 | |||||||
| chr2:61878013 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.523-499G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878013 | |||||||
| chr2:61878208 | G | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0085 others(4): Show |
13 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.522+661C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878208 | |||||||
| chr2:61878253 | A | G | 1 | a0001c0002t0002g0239 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.522+616T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878253 | |||||||
| chr2:61878325 | A | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.522+544T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878325 | |||||||
| chr2:61878500 | A | C | 11 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
11 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.522+369T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878500 | |||||||
| chr2:61878549 | T | A | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.522+320A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878549 | |||||||
| chr2:61878591 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.522+278G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878591 | |||||||
| chr2:61878632 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.522+237A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878632 | |||||||
| chr2:61878684 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.522+185G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878684 | |||||||
| chr2:61878834 | C | G | 1 | a0001c0001t0001g0169 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.522+35G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878834 | |||||||
| chr2:61878851 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
4 | HG00738.hp2 HG01192.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+18G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 5/13 | chr2 | 61878851 | |||||||
| chr2:61879023 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.380-12C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879023 | |||||||
| chr2:61879120 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02572.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.380-109G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879120 | |||||||
| chr2:61879253 | A | G | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.380-242T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879253 | |||||||
| chr2:61879254 | T | C | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.380-243A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879254 | |||||||
| chr2:61879256 | C | CT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.380-246dupA | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879256 | |||||||
| chr2:61879256 | C | CTT | 41 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0039 others(38): Show |
63 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.380-247_380-246dup others(2): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879256 | |||||||
| chr2:61879256 | C | CTTT | 33 | a0001c0001t0001g0090 a0001c0001t0001g0163 a0001c0001t0001g0165 others(30): Show |
46 | HG00733.hp2 HG01106.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.380-248_380-246dup others(3): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879256 | |||||||
| chr2:61879276 | T | TC | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG03579.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.380-266_380-265ins others(1): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879276 | |||||||
| chr2:61879320 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.380-309C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879320 | |||||||
| chr2:61879338 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.380-327A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879338 | |||||||
| chr2:61879439 | A | AT | 95 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(92): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.380-429dupA | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879439 | |||||||
| chr2:61879486 | C | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.380-475G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879486 | |||||||
| chr2:61879575 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.380-564C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879575 | |||||||
| chr2:61879642 | A | C | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.380-631T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879642 | |||||||
| chr2:61879747 | CT | C | 36 | a0001c0001t0001g0181 a0001c0002t0002g0012 a0001c0002t0002g0021 others(33): Show |
46 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.379+538delA | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879747 | |||||||
| chr2:61879794 | C | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.379+492G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879794 | |||||||
| chr2:61879855 | G | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.379+431C>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879855 | |||||||
| chr2:61879973 | C | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
218 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.379+313G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61879973 | |||||||
| chr2:61880039 | T | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0147 a0001c0001t0004g0146 |
4 | HG02145.hp1 HG02630.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+247A>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61880039 | |||||||
| chr2:61880241 | T | TC | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.379+44_379+45insG | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 4/13 | chr2 | 61880241 | |||||||
| chr2:61880497 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.271-103C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61880497 | |||||||
| chr2:61880666 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271-272A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61880666 | |||||||
| chr2:61880711 | A | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
128 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.271-317T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61880711 | |||||||
| chr2:61880722 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.271-328A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61880722 | |||||||
| chr2:61880732 | G | A | 5 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-338C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61880732 | |||||||
| chr2:61880879 | T | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.271-485A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61880879 | |||||||
| chr2:61880914 | G | A | 1 | a0001c0001t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.271-520C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61880914 | |||||||
| chr2:61881178 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.271-784C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881178 | |||||||
| chr2:61881196 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.271-802A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881196 | |||||||
| chr2:61881200 | T | C | 1 | a0001c0001t0001g0048 | 2 | NA18973.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.271-806A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881200 | |||||||
| chr2:61881214 | CTTATT | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.271-825_271-821del others(5): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881214 | |||||||
| chr2:61881258 | C | A | 36 | a0001c0002t0002g0012 a0001c0002t0002g0021 a0001c0002t0002g0050 others(33): Show |
46 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.271-864G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881258 | |||||||
| chr2:61881295 | G | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.271-901C>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881295 | |||||||
| chr2:61881337 | CTGTCGAA others(804): Show |
C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0121 |
2 | NA19011.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.270+1311_271-944de others(1): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881337 | |||||||
| chr2:61881377 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02965.hp2 HG03579.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-983G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881377 | |||||||
| chr2:61881385 | G | A | 1 | a0001c0001t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.271-991C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881385 | |||||||
| chr2:61881564 | CAGAA | C | 5 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0245 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-1174_271-1171d others(6): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881564 | |||||||
| chr2:61881783 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG03579.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.271-1389C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881783 | |||||||
| chr2:61881861 | G | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0169 |
4 | NA18990.hp1 NA19007.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1467C>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881861 | |||||||
| chr2:61881878 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.271-1484T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881878 | |||||||
| chr2:61881881 | A | AT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.271-1488_271-1487i others(3): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881881 | |||||||
| chr2:61881882 | A | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0041 others(23): Show |
44 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.271-1488T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881882 | |||||||
| chr2:61881886 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0126 |
3 | HG01358.hp2 HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.271-1492A>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881886 | |||||||
| chr2:61881917 | A | AT | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-1524dupA | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881917 | |||||||
| chr2:61881936 | CTTT | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.270+1520_270+1522d others(5): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881936 | |||||||
| chr2:61881956 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.270+1503C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61881956 | |||||||
| chr2:61882089 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.270+1370G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882089 | |||||||
| chr2:61882143 | G | C | 36 | a0001c0002t0002g0012 a0001c0002t0002g0021 a0001c0002t0002g0050 others(33): Show |
46 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.270+1316C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882143 | |||||||
| chr2:61882145 | C | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0049 others(3): Show |
11 | HG00423.hp2 HG00673.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.270+1314G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882145 | |||||||
| chr2:61882224 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(30): Show |
62 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.270+1235G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882224 | |||||||
| chr2:61882236 | T | C | 3 | a0001c0002t0002g0052 a0001c0002t0002g0230 a0001c0002t0002g0234 |
4 | HG01175.hp1 HG03688.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+1223A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882236 | |||||||
| chr2:61882315 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.270+1144C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882315 | |||||||
| chr2:61882542 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.270+917C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882542 | |||||||
| chr2:61882687 | T | C | 1 | a0001c0001t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+772A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882687 | |||||||
| chr2:61882778 | C | T | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.270+681G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882778 | |||||||
| chr2:61882779 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.270+680C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882779 | |||||||
| chr2:61882809 | CT | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(81): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.270+649delA | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882809 | |||||||
| chr2:61882823 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.270+636A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882823 | |||||||
| chr2:61882829 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.270+630C>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882829 | |||||||
| chr2:61882893 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.270+566G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882893 | |||||||
| chr2:61882929 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.270+530T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61882929 | |||||||
| chr2:61883052 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG00738.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.270+407T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883052 | |||||||
| chr2:61883093 | T | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.270+366A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883093 | |||||||
| chr2:61883117 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.270+342G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883117 | |||||||
| chr2:61883286 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.270+173A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883286 | |||||||
| chr2:61883292 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0044 |
4 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+167C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883292 | |||||||
| chr2:61883416 | C | CA | 32 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0022 others(29): Show |
57 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.270+42dupT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883416 | |||||||
| chr2:61883416 | C | CAA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0115 others(5): Show |
16 | HG01070.hp1 HG01071.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+41_270+42dupTT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883416 | |||||||
| chr2:61883416 | CA | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.270+42delT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883416 | |||||||
| chr2:61883416 | CAA | C | 38 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0002t0002g0012 others(35): Show |
48 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.270+41_270+42delTT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883416 | |||||||
| chr2:61883436 | G | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.270+23C>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 3/13 | chr2 | 61883436 | |||||||
| chr2:61883742 | T | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
67 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.181-194A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883742 | |||||||
| chr2:61883771 | T | TAGAC | 16 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0026 others(13): Show |
27 | HG00140.hp2 HG00597.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.181-227_181-224dup others(4): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883771 | |||||||
| chr2:61883773 | G | GAC | 12 | a0001c0001t0001g0150 a0001c0001t0001g0188 a0001c0001t0001g0190 others(9): Show |
17 | HG00280.hp2 HG00639.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.181-227_181-226dup others(2): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | G | GACAC | 11 | a0001c0001t0001g0017 a0001c0001t0003g0191 a0001c0002t0002g0239 others(8): Show |
13 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.181-229_181-226dup others(4): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | G | GACACACA others(3): Show |
1 | a0001c0002t0002g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.181-235_181-226dup others(10): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | G | GACAGAC | 52 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
99 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.181-226_181-225ins others(6): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | G | GACAGACA others(1): Show |
15 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0025 others(12): Show |
28 | HG00438.hp2 HG01099.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.181-226_181-225ins others(8): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | G | GACAGACA others(3): Show |
1 | a0001c0001t0001g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.181-226_181-225ins others(10): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | G | GACAGACA others(5): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0001g0128 |
4 | HG01981.hp2 NA18951.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-226_181-225ins others(12): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | G | GACAGACA others(9): Show |
1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.181-226_181-225ins others(16): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GAC | G | 16 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0060 others(13): Show |
20 | HG01167.hp1 HG01168.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.181-227_181-226del others(2): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GACAC | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0042 others(28): Show |
61 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.181-229_181-226del others(4): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GACACAC | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0041 others(27): Show |
49 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.181-231_181-226del others(6): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GACACACA others(3): Show |
G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0162 |
2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.181-235_181-226del others(10): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GACACACA others(5): Show |
G | 2 | a0001c0001t0001g0161 a0001c0001t0005g0159 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.181-237_181-226del others(12): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GACACACA others(7): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.181-239_181-226del others(14): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GACACACA others(9): Show |
G | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.181-241_181-226del others(16): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GACACACA others(11): Show |
G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0056 a0001c0001t0001g0057 others(4): Show |
10 | HG00735.hp1 HG01884.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.181-243_181-226del others(18): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GACACACA others(17): Show |
G | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.181-249_181-226del others(24): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883773 | GACACACA others(19): Show |
G | 1 | a0001c0001t0001g0039 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.181-251_181-226del others(26): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883773 | |||||||
| chr2:61883775 | C | CAG | 12 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0076 others(9): Show |
14 | HG00558.hp2 HG01358.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.181-228_181-227ins others(2): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883775 | |||||||
| chr2:61883777 | C | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0034 others(16): Show |
36 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.181-229G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883777 | |||||||
| chr2:61883779 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.181-231G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883779 | |||||||
| chr2:61883781 | C | G | 1 | a0001c0001t0001g0063 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.181-233G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883781 | |||||||
| chr2:61883782 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0178 |
3 | HG00673.hp2 HG02132.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.181-234T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883782 | |||||||
| chr2:61883783 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.181-235G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883783 | |||||||
| chr2:61883783 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0178 |
3 | HG00673.hp2 HG02132.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.181-235G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883783 | |||||||
| chr2:61883784 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0049 others(17): Show |
37 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.181-236T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883784 | |||||||
| chr2:61883785 | C | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0178 |
3 | HG00673.hp2 HG02132.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.181-237G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883785 | |||||||
| chr2:61883785 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0049 others(17): Show |
37 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.181-237G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883785 | |||||||
| chr2:61883786 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.181-238T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883786 | |||||||
| chr2:61883787 | C | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0049 others(17): Show |
37 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.181-239G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883787 | |||||||
| chr2:61883787 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.181-239G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883787 | |||||||
| chr2:61883789 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.181-241G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883789 | |||||||
| chr2:61883795 | C | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0094 a0001c0001t0001g0180 |
6 | HG00735.hp1 HG01884.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-247G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61883795 | |||||||
| chr2:61884002 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.181-454T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884002 | |||||||
| chr2:61884024 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0145 a0001c0001t0001g0147 others(1): Show |
5 | HG01891.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-476T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884024 | |||||||
| chr2:61884030 | G | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0034 others(23): Show |
43 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.181-482C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884030 | |||||||
| chr2:61884097 | TAC | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0026 others(10): Show |
22 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.181-551_181-550del others(2): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884097 | |||||||
| chr2:61884299 | A | G | 1 | a0001c0002t0002g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.180+721T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884299 | |||||||
| chr2:61884323 | A | C | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.180+697T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884323 | |||||||
| chr2:61884364 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG03579.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.180+656G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884364 | |||||||
| chr2:61884385 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.180+635G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884385 | |||||||
| chr2:61884449 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.180+571A>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884449 | |||||||
| chr2:61884526 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.180+494C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884526 | |||||||
| chr2:61884530 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.180+490A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884530 | |||||||
| chr2:61884531 | G | C | 1 | a0001c0002t0002g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.180+489C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884531 | |||||||
| chr2:61884621 | TTTTTA | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02965.hp2 HG03579.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+394_180+398del others(5): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884621 | |||||||
| chr2:61884639 | T | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.180+381A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884639 | |||||||
| chr2:61884692 | A | C | 1 | a0001c0001t0005g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.180+328T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884692 | |||||||
| chr2:61884705 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.180+315G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884705 | |||||||
| chr2:61884895 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.180+125C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884895 | |||||||
| chr2:61884918 | G | A | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.180+102C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884918 | |||||||
| chr2:61884946 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(13): Show |
26 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.180+74G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884946 | |||||||
| chr2:61884978 | A | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0069 others(5): Show |
13 | HG00408.hp2 HG00544.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.180+42T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 2/13 | chr2 | 61884978 | |||||||
| chr2:61885086 | G | GA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(113): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.128-15_128-14insT | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885086 | |||||||
| chr2:61885087 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(116): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.128-15C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885087 | |||||||
| chr2:61885111 | C | CT | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.128-40dupA | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885111 | |||||||
| chr2:61885111 | CT | C | 6 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
6 | HG01243.hp2 HG02056.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-40delA | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885111 | |||||||
| chr2:61885218 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.128-146A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885218 | |||||||
| chr2:61885254 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.128-182A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885254 | |||||||
| chr2:61885346 | A | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0184 others(7): Show |
13 | HG00639.hp1 HG01255.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.128-274T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885346 | |||||||
| chr2:61885405 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.128-333G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885405 | |||||||
| chr2:61885409 | GTAT | G | 8 | a0001c0002t0002g0050 a0001c0002t0002g0222 a0001c0002t0002g0223 others(5): Show |
9 | HG02055.hp2 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-340_128-338del others(3): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885409 | |||||||
| chr2:61885702 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.128-630T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885702 | |||||||
| chr2:61885704 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.128-632C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885704 | |||||||
| chr2:61885763 | C | CTTCCTTC others(18): Show |
22 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(19): Show |
40 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.128-716_128-692dup others(25): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885763 | |||||||
| chr2:61885801 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.128-729C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885801 | |||||||
| chr2:61885931 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.128-859C>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885931 | |||||||
| chr2:61885986 | C | G | 1 | a0001c0002t0002g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.128-914G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61885986 | |||||||
| chr2:61886031 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.128-959A>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886031 | |||||||
| chr2:61886039 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(117): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.128-967A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886039 | |||||||
| chr2:61886092 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG00558.hp2 NA18967.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.128-1020C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886092 | |||||||
| chr2:61886099 | A | G | 1 | a0001c0001t0001g0022 | 2 | NA18944.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.128-1027T>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886099 | |||||||
| chr2:61886137 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.128-1065C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886137 | |||||||
| chr2:61886356 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-1284C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886356 | |||||||
| chr2:61886463 | A | T | 7 | a0001c0002t0002g0050 a0001c0002t0002g0222 a0001c0002t0002g0223 others(4): Show |
8 | HG02055.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-1391T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886463 | |||||||
| chr2:61886544 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(115): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.128-1472C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886544 | |||||||
| chr2:61886550 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.128-1478G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886550 | |||||||
| chr2:61886551 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.128-1479C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886551 | |||||||
| chr2:61886624 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG00323.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.128-1552C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886624 | |||||||
| chr2:61886649 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.128-1577G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886649 | |||||||
| chr2:61886656 | G | A | 1 | a0001c0002t0002g0250 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.128-1584C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886656 | |||||||
| chr2:61886749 | T | C | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127+1632A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886749 | |||||||
| chr2:61886791 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.127+1590G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886791 | |||||||
| chr2:61886817 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
8 | HG00735.hp1 HG01884.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+1564A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886817 | |||||||
| chr2:61886835 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.127+1546G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886835 | |||||||
| chr2:61886855 | G | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02965.hp2 HG03579.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+1526C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886855 | |||||||
| chr2:61886858 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127+1523G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886858 | |||||||
| chr2:61886894 | G | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
127 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.127+1487C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886894 | |||||||
| chr2:61886943 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.127+1438C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61886943 | |||||||
| chr2:61887086 | C | G | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127+1295G>C | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887086 | |||||||
| chr2:61887114 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127+1267A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887114 | |||||||
| chr2:61887253 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127+1128G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887253 | |||||||
| chr2:61887279 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.127+1102G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887279 | |||||||
| chr2:61887284 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.127+1097G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887284 | |||||||
| chr2:61887299 | G | A | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02965.hp2 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+1082C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887299 | |||||||
| chr2:61887322 | T | C | 1 | a0001c0002t0002g0251 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.127+1059A>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887322 | |||||||
| chr2:61887401 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.127+980C>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887401 | |||||||
| chr2:61887501 | ATAC | A | 2 | a0001c0001t0001g0049 a0004c0007t0001g0220 |
3 | HG00423.hp2 NA18994.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.127+877_127+879del others(3): Show |
CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887501 | |||||||
| chr2:61887924 | G | C | 3 | a0001c0002t0002g0252 a0001c0002t0002g0253 a0001c0002t0002g0254 |
3 | HG02055.hp2 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.127+457C>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61887924 | |||||||
| chr2:61888008 | A | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02572.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.127+373T>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61888008 | |||||||
| chr2:61888092 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.127+289G>A | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61888092 | |||||||
| chr2:61888238 | A | C | 1 | a0001c0001t0001g0054 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127+143T>G | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61888238 | |||||||
| chr2:61888345 | C | A | 1 | a0001c0006t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127+36G>T | CCT4 | ENSG00000115484.15 | transcript | ENST00000394440.8 | protein_coding | 1/13 | chr2 | 61888345 |