Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10693 |
| ensemblid | ENSG00000132141.14 |
| hgncid | 1621 |
| symbol | CCT6B |
| name | chaperonin containing TCP1 subunit 6B |
| refseq_nuc | NM_006584.4 |
| refseq_prot | NP_006575.2 |
| ensembl_nuc | ENST00000314144.10 |
| ensembl_prot | ENSP00000327191.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 34927861 |
| end | 34961460 |
| strand | - |
| ver | v1.2 |
| region | chr17:34927861-34961460 |
| region5000 | chr17:34922861-34966460 |
| regionname0 | CCT6B_chr17_34927861_34961460 |
| regionname5000 | CCT6B_chr17_34922861_34966460 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 530 | 172 | 60 | 38 | 44 | 7 | 21 | 37 | CCT6B_chr17_34922861_34966460 | CCT6B | MAAIK others(525): Show |
chr17 | 34922861 | 34966460 |
| a0002 | 0/0 | 530 | 136 | 15 | 22 | 86 | 4 | 9 | 73 | CCT6B_chr17_34922861_34966460 | CCT6B | MAAIK others(525): Show |
chr17 | 34922861 | 34966460 |
| a0003 | 0/0 | 530 | 81 | 15 | 8 | 43 | 5 | 10 | 35 | CCT6B_chr17_34922861_34966460 | CCT6B | MAAIK others(525): Show |
chr17 | 34922861 | 34966460 |
| a0004 | 0/0 | 530 | 7 | 2 | 0 | 5 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | MAAIK others(525): Show |
chr17 | 34922861 | 34966460 |
| a0005 | 0/0 | 530 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CCT6B_chr17_34922861_34966460 | CCT6B | MAAIK others(525): Show |
chr17 | 34922861 | 34966460 |
| a0006 | 0/0 | 530 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | MAAIK others(525): Show |
chr17 | 34922861 | 34966460 |
| a0007 | 0/0 | 530 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | MAAIK others(525): Show |
chr17 | 34922861 | 34966460 |
| a0008 | 0/0 | 530 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | MAAIK others(525): Show |
chr17 | 34922861 | 34966460 |
| a0009 | 0/0 | 530 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | MAAIK others(525): Show |
chr17 | 34922861 | 34966460 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1590 | 171 | 59 | 38 | 44 | 7 | 21 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0001c0012 | 0/0 | 1590 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0002c0002 | 0/0 | 1590 | 132 | 14 | 21 | 86 | 2 | 9 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0002c0005 | 0/0 | 1590 | 3 | 0 | 1 | 0 | 2 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0002c0007 | 0/0 | 1590 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0003c0003 | 0/0 | 1590 | 81 | 15 | 8 | 43 | 5 | 10 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0004c0004 | 0/0 | 1590 | 7 | 2 | 0 | 5 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0005c0006 | 0/0 | 1590 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0006c0008 | 0/0 | 1590 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0007c0010 | 0/0 | 1590 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0008c0011 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 | ||
| a0009c0009 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | ATGGC others(1585): Show |
chr17 | 34922861 | 34966460 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1847 | 141 | 55 | 37 | 26 | 6 | 15 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0001c0001t0002 | 0/0 | 1847 | 28 | 2 | 1 | 18 | 1 | 6 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0001c0001t0003 | 0/0 | 1847 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | ACATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0001c0001t0004 | 0/0 | 1847 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0001c0012t0001 | 0/0 | 1847 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0002c0002t0001 | 0/0 | 1847 | 132 | 14 | 21 | 86 | 2 | 9 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0002c0005t0001 | 0/0 | 1847 | 3 | 0 | 1 | 0 | 2 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0002c0007t0001 | 0/0 | 1847 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0003c0003t0001 | 0/0 | 1847 | 81 | 15 | 8 | 43 | 5 | 10 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0004c0004t0001 | 0/0 | 1847 | 2 | 2 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0004c0004t0002 | 0/0 | 1847 | 5 | 0 | 0 | 5 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0005c0006t0002 | 0/0 | 1847 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0006c0008t0001 | 0/0 | 1847 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0007c0010t0001 | 0/0 | 1847 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0008c0011t0001 | 0/0 | 1847 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| a0009c0009t0001 | 0/0 | 1847 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | GCATT others(1842): Show |
chr17 | 34922861 | 34966460 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 2 | 8 | 7 | 1 | 4 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 5 | 0 | 2 | 2 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0013 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0006 | 0/0 | 9 | 0 | 0 | 4 | 0 | 5 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0001c0012t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0002 | 0/0 | 21 | 2 | 0 | 19 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0004 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0008 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0009 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0010 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0011 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0005t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0002c0007t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0003 | 0/0 | 17 | 0 | 5 | 11 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0004c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0004c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0004c0004t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0004c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0004c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0004c0004t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0005c0006t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0005c0006t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0006c0008t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0007c0010t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0008c0011t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| a0009c0009t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00099 | hp2 | a0002 | c0005 | t0001 | g0043 | EUR | GBR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00140 | hp1 | a0002 | c0005 | t0001 | g0054 | EUR | GBR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0072 | EUR | GBR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0178 | EUR | FIN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0146 | EUR | FIN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0128 | EUR | FIN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00423 | hp1 | a0004 | c0004 | t0002 | g0124 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0142 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00673 | hp1 | a0004 | c0004 | t0002 | g0037 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | CHS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01069 | hp1 | a0006 | c0008 | t0001 | g0067 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01243 | hp1 | a0002 | c0005 | t0001 | g0043 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01346 | hp2 | a0007 | c0010 | t0001 | g0109 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0138 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0038 | EUR | IBS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0071 | EUR | IBS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0038 | EUR | IBS | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0036 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0136 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0135 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02027 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0039 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0123 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02135 | hp2 | a0004 | c0004 | t0002 | g0125 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CDX | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | CDX | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0129 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02523 | hp2 | a0004 | c0004 | t0002 | g0037 | EAS | KHV | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0099 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0121 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0139 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0117 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0093 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0041 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02818 | hp2 | a0004 | c0004 | t0001 | g0119 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0041 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0118 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02970 | hp1 | a0002 | c0007 | t0001 | g0050 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0148 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0106 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03041 | hp2 | a0001 | c0012 | t0001 | g0223 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0115 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0040 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03195 | hp1 | a0004 | c0004 | t0001 | g0120 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0036 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0122 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03491 | hp2 | a0003 | c0003 | t0001 | g0144 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0149 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0137 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03831 | hp2 | a0003 | c0003 | t0001 | g0133 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03927 | hp1 | a0003 | c0003 | t0001 | g0150 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0110 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | STU | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG04115 | hp2 | a0008 | c0011 | t0001 | g0114 | SAS | STU | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | STU | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG04199 | hp2 | a0009 | c0009 | t0001 | g0101 | SAS | STU | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0131 | SAS | STU | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0092 | SAS | STU | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | YRI | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | YRI | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | CHB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18943 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18944 | hp1 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18945 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18949 | hp1 | a0003 | c0003 | t0001 | g0116 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18962 | hp1 | a0005 | c0006 | t0002 | g0221 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18965 | hp2 | a0003 | c0003 | t0001 | g0112 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18967 | hp2 | a0003 | c0003 | t0001 | g0111 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18970 | hp1 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18978 | hp1 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18985 | hp1 | a0003 | c0003 | t0001 | g0132 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18989 | hp2 | a0005 | c0006 | t0002 | g0163 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18990 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18991 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18993 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19004 | hp1 | a0003 | c0003 | t0001 | g0130 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0040 | AFR | LWK | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | LWK | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0145 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19065 | hp1 | a0004 | c0004 | t0002 | g0126 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19068 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19074 | hp2 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19079 | hp2 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0088 | AFR | YRI | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ASW | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0134 | EUR | TSI | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | USA | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | USA | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | USA | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | USA | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | LWK | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0160 | REF | REF | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0229 | REF | REF | CCT6B_chr17_34922861_34966460 | CCT6B | chr17 | 34922861 | 34966460 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:34932390 | C | A | 1 | a0009 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1324G>T | p.Asp442Tyr | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/14 | 1391/1847 | 1324/1593 | 442/530 | chr17 | 34932390 | |||
| chr17:34932485 | C | T | 1 | a0006 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.1229G>A | p.Gly410Glu | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/14 | 1296/1847 | 1229/1593 | 410/530 | chr17 | 34932485 | |||
| chr17:34942498 | C | T | 1 | a0005 | 2 | NA18962.hp1 NA18989.hp2 |
missense_variant | MODERATE | c.871G>A | p.Val291Ile | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 7/14 | 938/1847 | 871/1593 | 291/530 | chr17 | 34942498 | |||
| chr17:34942629 | C | G | 3 | a0003 a0007 a0008 |
83 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(80): Show |
missense_variant | MODERATE | c.740G>C | p.Gly247Ala | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 7/14 | 807/1847 | 740/1593 | 247/530 | chr17 | 34942629 | |||
| chr17:34958630 | C | T | 1 | a0008 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.266G>A | p.Gly89Glu | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/14 | 333/1847 | 266/1593 | 89/530 | chr17 | 34958630 | |||
| chr17:34959609 | C | T | 1 | a0007 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.179G>A | p.Gly60Asp | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/14 | 246/1847 | 179/1593 | 60/530 | chr17 | 34959609 | |||
| chr17:34959645 | A | G | 3 | a0002 a0006 a0009 |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
missense_variant | MODERATE | c.143T>C | p.Val48Ala | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/14 | 210/1847 | 143/1593 | 48/530 | chr17 | 34959645 | |||
| chr17:34961344 | C | T | 7 | a0002 a0003 a0004 others(4): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
missense_variant | MODERATE | c.50G>A | p.Arg17Gln | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/14 | 117/1847 | 50/1593 | 17/530 | chr17 | 34961344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:34942819 | G | A | 1 | a0001c0012 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.702C>T | p.Asn234Asn | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 6/14 | 769/1847 | 702/1593 | 234/530 | chr17 | 34942819 | |||
| chr17:34959602 | C | T | 1 | a0002c0005 | 3 | HG00099.hp2 HG00140.hp1 HG01243.hp1 |
synonymous_variant | LOW | c.186G>A | p.Val62Val | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/14 | 253/1847 | 186/1593 | 62/530 | chr17 | 34959602 | |||
| chr17:34961289 | C | T | 1 | a0002c0007 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.105G>A | p.Arg35Arg | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/14 | 172/1847 | 105/1593 | 35/530 | chr17 | 34961289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:34927940 | C | T | 3 | a0001c0001t0002 a0004c0004t0002 a0005c0006t0002 |
35 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*108G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 14/14 | 108 | chr17 | 34927940 | ||||||
| chr17:34928006 | C | T | 1 | a0001c0001t0004 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 14/14 | 42 | chr17 | 34928006 | ||||||
| chr17:34961460 | C | T | 1 | a0001c0001t0003 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/14 | 67 | chr17 | 34961460 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:34928224 | T | C | 2 | a0004c0004t0001g0119 a0004c0004t0001g0120 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1524-107A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 13/13 | chr17 | 34928224 | |||||||
| chr17:34928310 | T | C | 1 | a0004c0004t0002g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1524-193A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 13/13 | chr17 | 34928310 | |||||||
| chr17:34928455 | TAG | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0183 |
5 | HG01081.hp2 HG01109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524-340_1524-339d others(4): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 13/13 | chr17 | 34928455 | |||||||
| chr17:34928548 | C | T | 1 | a0008c0011t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1523+414G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 13/13 | chr17 | 34928548 | |||||||
| chr17:34928552 | T | C | 136 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0162 others(133): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1523+410A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 13/13 | chr17 | 34928552 | |||||||
| chr17:34928605 | C | A | 1 | a0002c0002t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1523+357G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 13/13 | chr17 | 34928605 | |||||||
| chr17:34928743 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(189): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1523+219C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 13/13 | chr17 | 34928743 | |||||||
| chr17:34928766 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0182 |
3 | HG02809.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1523+196T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 13/13 | chr17 | 34928766 | |||||||
| chr17:34929491 | C | CT | 18 | a0001c0001t0001g0165 a0001c0001t0001g0225 a0001c0001t0001g0227 others(15): Show |
30 | HG00280.hp1 HG01243.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1451-458dupA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929491 | |||||||
| chr17:34929491 | C | CTT | 5 | a0001c0001t0002g0021 a0001c0001t0002g0166 a0004c0004t0002g0037 others(2): Show |
8 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.1451-459_1451-458d others(4): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929491 | |||||||
| chr17:34929491 | CT | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(52): Show |
100 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1451-458delA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929491 | |||||||
| chr17:34929491 | CTT | C | 6 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0196 others(3): Show |
6 | HG01099.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1451-459_1451-458d others(4): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929491 | |||||||
| chr17:34929509 | G | T | 9 | a0002c0002t0001g0010 a0002c0002t0001g0083 a0002c0002t0001g0098 others(6): Show |
13 | HG01168.hp2 HG01255.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1451-475C>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929509 | |||||||
| chr17:34929510 | GT | G | 9 | a0002c0002t0001g0010 a0002c0002t0001g0083 a0002c0002t0001g0098 others(6): Show |
13 | HG01168.hp2 HG01255.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1451-477delA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929510 | |||||||
| chr17:34929512 | GTT | G | 120 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0002c0002t0001g0002 others(117): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1451-480_1451-479d others(4): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929512 | |||||||
| chr17:34929514 | T | G | 9 | a0002c0002t0001g0010 a0002c0002t0001g0083 a0002c0002t0001g0098 others(6): Show |
13 | HG01168.hp2 HG01255.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1451-480A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929514 | |||||||
| chr17:34929674 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1451-640G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929674 | |||||||
| chr17:34929898 | A | G | 78 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0002c0002t0001g0002 others(75): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1451-864T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34929898 | |||||||
| chr17:34930009 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1450+940C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34930009 | |||||||
| chr17:34930129 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0155 a0001c0001t0001g0156 |
5 | HG01192.hp1 HG01361.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450+820C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34930129 | |||||||
| chr17:34930177 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0182 |
3 | HG02809.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1450+772G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34930177 | |||||||
| chr17:34930227 | G | A | 2 | a0003c0003t0001g0128 a0003c0003t0001g0136 |
2 | HG00323.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1450+722C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34930227 | |||||||
| chr17:34930501 | C | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0182 |
3 | HG02809.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1450+448G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34930501 | |||||||
| chr17:34930551 | C | T | 1 | a0003c0003t0001g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1450+398G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34930551 | |||||||
| chr17:34930912 | T | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0153 a0001c0001t0001g0155 others(1): Show |
6 | HG01192.hp1 HG01361.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1450+37A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34930912 | |||||||
| chr17:34930925 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1450+24C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 12/13 | chr17 | 34930925 | |||||||
| chr17:34931167 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1348-116A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34931167 | |||||||
| chr17:34931357 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0182 |
3 | HG02809.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1348-306A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34931357 | |||||||
| chr17:34931503 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1348-452T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34931503 | |||||||
| chr17:34931641 | A | C | 1 | a0002c0007t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1348-590T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34931641 | |||||||
| chr17:34931698 | A | T | 1 | a0001c0001t0001g0012 | 4 | HG01884.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1348-647T>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34931698 | |||||||
| chr17:34931704 | C | A | 2 | a0003c0003t0001g0110 a0003c0003t0001g0137 |
2 | HG03669.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1348-653G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34931704 | |||||||
| chr17:34931770 | A | G | 6 | a0002c0002t0001g0004 a0002c0002t0001g0083 a0002c0002t0001g0087 others(3): Show |
15 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1347+597T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34931770 | |||||||
| chr17:34931867 | T | G | 1 | a0001c0001t0001g0012 | 4 | HG01884.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347+500A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34931867 | |||||||
| chr17:34931960 | G | C | 2 | a0003c0003t0001g0110 a0003c0003t0001g0137 |
2 | HG03669.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1347+407C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34931960 | |||||||
| chr17:34932187 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1347+180A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 11/13 | chr17 | 34932187 | |||||||
| chr17:34932927 | G | A | 78 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0002c0002t0001g0002 others(75): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1214-427C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34932927 | |||||||
| chr17:34933070 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1214-570G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34933070 | |||||||
| chr17:34933681 | T | A | 1 | a0004c0004t0002g0126 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1214-1181A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34933681 | |||||||
| chr17:34933701 | T | C | 1 | a0002c0002t0001g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1214-1201A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34933701 | |||||||
| chr17:34933903 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1214-1403A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34933903 | |||||||
| chr17:34933919 | G | A | 129 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0002c0002t0001g0002 others(126): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1214-1419C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34933919 | |||||||
| chr17:34933954 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0232 others(4): Show |
11 | HG00733.hp1 HG01175.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1214-1454G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34933954 | |||||||
| chr17:34933955 | C | T | 19 | a0001c0001t0002g0006 a0001c0001t0002g0020 a0001c0001t0002g0021 others(16): Show |
34 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1214-1455G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34933955 | |||||||
| chr17:34934115 | C | A | 2 | a0004c0004t0001g0119 a0004c0004t0001g0120 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1214-1615G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934115 | |||||||
| chr17:34934116 | G | A | 1 | a0002c0002t0001g0108 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1214-1616C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934116 | |||||||
| chr17:34934134 | GA | G | 7 | a0001c0001t0001g0200 a0002c0002t0001g0064 a0002c0002t0001g0071 others(4): Show |
7 | HG01167.hp1 HG01516.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214-1635delT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934134 | |||||||
| chr17:34934283 | T | C | 7 | a0003c0003t0001g0016 a0003c0003t0001g0036 a0003c0003t0001g0115 others(4): Show |
10 | HG01891.hp2 HG02258.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1214-1783A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934283 | |||||||
| chr17:34934303 | A | G | 1 | a0002c0002t0001g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1214-1803T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934303 | |||||||
| chr17:34934356 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1214-1856A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934356 | |||||||
| chr17:34934379 | T | A | 1 | a0002c0002t0001g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1214-1879A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934379 | |||||||
| chr17:34934469 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0152 others(7): Show |
14 | HG01192.hp1 HG01361.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1214-1969C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934469 | |||||||
| chr17:34934488 | C | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0228 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1214-1988G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934488 | |||||||
| chr17:34934637 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0001g0153 others(3): Show |
8 | HG01192.hp1 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1214-2137C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934637 | |||||||
| chr17:34934669 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1214-2169C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934669 | |||||||
| chr17:34934737 | A | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0228 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1214-2237T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34934737 | |||||||
| chr17:34935134 | A | G | 1 | a0002c0002t0001g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1214-2634T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935134 | |||||||
| chr17:34935312 | T | C | 1 | a0002c0007t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1214-2812A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935312 | |||||||
| chr17:34935404 | T | G | 58 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0232 others(55): Show |
96 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1214-2904A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935404 | |||||||
| chr17:34935405 | T | C | 1 | a0002c0002t0001g0033 | 2 | NA18955.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1214-2905A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935405 | |||||||
| chr17:34935571 | G | A | 1 | a0003c0003t0001g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1214-3071C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935571 | |||||||
| chr17:34935581 | T | G | 10 | a0003c0003t0001g0005 a0003c0003t0001g0112 a0003c0003t0001g0113 others(7): Show |
18 | NA18945.hp2 NA18946.hp1 NA18949.hp1 others(15): Show |
intron_variant | MODIFIER | c.1214-3081A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935581 | |||||||
| chr17:34935813 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1214-3313G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935813 | |||||||
| chr17:34935838 | C | T | 48 | a0003c0003t0001g0003 a0003c0003t0001g0005 a0003c0003t0001g0016 others(45): Show |
82 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1214-3338G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935838 | |||||||
| chr17:34935861 | G | GA | 77 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0002c0002t0001g0002 others(74): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1213+3321dupT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935861 | |||||||
| chr17:34935924 | C | CGT | 25 | a0001c0001t0001g0212 a0001c0001t0002g0006 a0001c0001t0002g0021 others(22): Show |
41 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1213+3257_1213+325 others(6): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935924 | |||||||
| chr17:34935924 | C | CGTGT | 7 | a0001c0001t0001g0192 a0001c0001t0002g0020 a0001c0001t0002g0167 others(4): Show |
9 | HG02155.hp1 NA18946.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.1213+3255_1213+325 others(8): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935924 | |||||||
| chr17:34935924 | CGT | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0193 |
3 | NA18960.hp1 NA18995.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1213+3257_1213+325 others(6): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935924 | |||||||
| chr17:34935958 | AAAC | A | 21 | a0001c0001t0001g0192 a0001c0001t0002g0006 a0001c0001t0002g0020 others(18): Show |
36 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.1213+3222_1213+322 others(7): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935958 | |||||||
| chr17:34935973 | G | C | 1 | a0002c0002t0001g0069 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1213+3210C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34935973 | |||||||
| chr17:34936038 | C | A | 1 | a0002c0002t0001g0069 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1213+3145G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34936038 | |||||||
| chr17:34936060 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1213+3123G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34936060 | |||||||
| chr17:34936202 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1213+2981C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34936202 | |||||||
| chr17:34936302 | C | T | 2 | a0002c0002t0001g0066 a0002c0002t0001g0080 |
2 | NA18959.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1213+2881G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34936302 | |||||||
| chr17:34936360 | T | C | 1 | a0002c0002t0001g0034 | 2 | NA19058.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1213+2823A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34936360 | |||||||
| chr17:34936457 | A | G | 1 | a0003c0003t0001g0133 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1213+2726T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34936457 | |||||||
| chr17:34936499 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1213+2684C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34936499 | |||||||
| chr17:34937229 | C | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0232 others(4): Show |
11 | HG00733.hp1 HG01175.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1213+1954G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34937229 | |||||||
| chr17:34937279 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0183 a0001c0001t0001g0184 |
6 | HG01081.hp2 HG01109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1213+1904A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34937279 | |||||||
| chr17:34937292 | G | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0185 |
5 | HG00733.hp2 HG01109.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213+1891C>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34937292 | |||||||
| chr17:34937704 | T | C | 79 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0001c0001t0001g0201 others(76): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1213+1479A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34937704 | |||||||
| chr17:34937735 | T | C | 1 | a0003c0003t0001g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1213+1448A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34937735 | |||||||
| chr17:34937768 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1213+1415G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34937768 | |||||||
| chr17:34937827 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1213+1356A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34937827 | |||||||
| chr17:34937871 | TTTTTC | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0232 others(5): Show |
12 | HG00621.hp2 HG00733.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1213+1307_1213+131 others(9): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34937871 | |||||||
| chr17:34937946 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1213+1237A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34937946 | |||||||
| chr17:34938053 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1213+1130G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938053 | |||||||
| chr17:34938283 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1213+900C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938283 | |||||||
| chr17:34938321 | C | T | 51 | a0003c0003t0001g0003 a0003c0003t0001g0005 a0003c0003t0001g0016 others(48): Show |
85 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1213+862G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938321 | |||||||
| chr17:34938487 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0182 |
3 | HG02809.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1213+696A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938487 | |||||||
| chr17:34938509 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1213+674A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938509 | |||||||
| chr17:34938592 | G | A | 3 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0064 |
3 | NA18977.hp2 NA18986.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1213+591C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938592 | |||||||
| chr17:34938703 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1213+480G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938703 | |||||||
| chr17:34938972 | T | A | 1 | a0003c0003t0001g0040 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1213+211A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938972 | |||||||
| chr17:34938978 | G | C | 1 | a0003c0003t0001g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1213+205C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938978 | |||||||
| chr17:34938983 | C | A | 1 | a0002c0002t0001g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1213+200G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34938983 | |||||||
| chr17:34939061 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1213+122C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34939061 | |||||||
| chr17:34939062 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1213+121G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34939062 | |||||||
| chr17:34939086 | AATATACA others(31): Show |
A | 1 | a0001c0001t0002g0022 | 3 | HG01243.hp2 HG02280.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1213+59_1213+96del others(38): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34939086 | |||||||
| chr17:34939096 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1213+87A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34939096 | |||||||
| chr17:34939119 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1213+64T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34939119 | |||||||
| chr17:34939158 | A | C | 1 | a0002c0002t0001g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1213+25T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 10/13 | chr17 | 34939158 | |||||||
| chr17:34939412 | A | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0232 others(4): Show |
11 | HG00733.hp1 HG01175.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1066-82T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 9/13 | chr17 | 34939412 | |||||||
| chr17:34939514 | G | C | 2 | a0004c0004t0001g0119 a0004c0004t0001g0120 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1065+103C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 9/13 | chr17 | 34939514 | |||||||
| chr17:34939553 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1065+64A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 9/13 | chr17 | 34939553 | |||||||
| chr17:34939569 | A | G | 1 | a0002c0002t0001g0105 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1065+48T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 9/13 | chr17 | 34939569 | |||||||
| chr17:34939577 | T | C | 1 | a0002c0005t0001g0054 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1065+40A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 9/13 | chr17 | 34939577 | |||||||
| chr17:34940026 | G | A | 2 | a0002c0002t0001g0086 a0002c0002t0001g0095 |
2 | HG00609.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.969-313C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 8/13 | chr17 | 34940026 | |||||||
| chr17:34940170 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.968+369C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 8/13 | chr17 | 34940170 | |||||||
| chr17:34940305 | A | C | 1 | a0003c0003t0001g0132 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.968+234T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 8/13 | chr17 | 34940305 | |||||||
| chr17:34940345 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.968+194T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 8/13 | chr17 | 34940345 | |||||||
| chr17:34940891 | A | C | 1 | a0002c0007t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.886-270T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 7/13 | chr17 | 34940891 | |||||||
| chr17:34941121 | A | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0194 others(6): Show |
12 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.886-500T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 7/13 | chr17 | 34941121 | |||||||
| chr17:34941495 | G | A | 15 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0031 others(12): Show |
28 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.886-874C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 7/13 | chr17 | 34941495 | |||||||
| chr17:34941653 | T | A | 1 | a0001c0001t0003g0218 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.885+831A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 7/13 | chr17 | 34941653 | |||||||
| chr17:34941858 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.885+626T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 7/13 | chr17 | 34941858 | |||||||
| chr17:34941862 | C | T | 1 | a0003c0003t0001g0040 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.885+622G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 7/13 | chr17 | 34941862 | |||||||
| chr17:34942286 | C | T | 1 | a0003c0003t0001g0041 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.885+198G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 7/13 | chr17 | 34942286 | |||||||
| chr17:34942729 | A | G | 1 | a0002c0002t0001g0070 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.725+67T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 6/13 | chr17 | 34942729 | |||||||
| chr17:34942908 | T | C | 1 | a0002c0002t0001g0096 | 1 | NA19066.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.615-2A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34942908 | |||||||
| chr17:34942941 | T | A | 1 | a0002c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.615-35A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34942941 | |||||||
| chr17:34943171 | C | T | 1 | a0002c0002t0001g0053 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.615-265G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34943171 | |||||||
| chr17:34943359 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.615-453A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34943359 | |||||||
| chr17:34943475 | A | G | 51 | a0003c0003t0001g0003 a0003c0003t0001g0005 a0003c0003t0001g0016 others(48): Show |
85 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.615-569T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34943475 | |||||||
| chr17:34943680 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0186 |
4 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.615-774C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34943680 | |||||||
| chr17:34943791 | TA | T | 7 | a0001c0001t0002g0164 a0001c0001t0002g0178 a0001c0001t0002g0180 others(4): Show |
8 | HG00280.hp1 HG02071.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.615-886delT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34943791 | |||||||
| chr17:34943792 | A | T | 1 | a0001c0001t0002g0006 | 3 | NA18968.hp2 NA18984.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.615-886T>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34943792 | |||||||
| chr17:34943832 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.615-926C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34943832 | |||||||
| chr17:34943933 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.615-1027A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34943933 | |||||||
| chr17:34944110 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.615-1204A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944110 | |||||||
| chr17:34944416 | C | A | 1 | a0002c0002t0001g0078 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.615-1510G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944416 | |||||||
| chr17:34944426 | A | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0001g0153 others(3): Show |
8 | HG01192.hp1 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.615-1520T>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944426 | |||||||
| chr17:34944586 | T | C | 1 | a0001c0001t0003g0218 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.615-1680A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944586 | |||||||
| chr17:34944653 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.615-1747C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944653 | |||||||
| chr17:34944761 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.615-1855G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944761 | |||||||
| chr17:34944781 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(229): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.615-1875A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944781 | |||||||
| chr17:34944842 | C | T | 2 | a0003c0003t0001g0131 a0008c0011t0001g0114 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.615-1936G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944842 | |||||||
| chr17:34944913 | G | A | 1 | a0003c0003t0001g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.615-2007C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944913 | |||||||
| chr17:34944970 | C | T | 2 | a0002c0005t0001g0043 a0002c0005t0001g0054 |
3 | HG00099.hp2 HG00140.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.615-2064G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34944970 | |||||||
| chr17:34945148 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.615-2242G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34945148 | |||||||
| chr17:34945166 | A | C | 7 | a0003c0003t0001g0016 a0003c0003t0001g0036 a0003c0003t0001g0115 others(4): Show |
10 | HG01891.hp2 HG02258.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.615-2260T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34945166 | |||||||
| chr17:34945488 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
92 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.615-2582G>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34945488 | |||||||
| chr17:34945525 | C | T | 1 | a0002c0002t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.615-2619G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34945525 | |||||||
| chr17:34945537 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.615-2631G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34945537 | |||||||
| chr17:34945716 | C | T | 1 | a0007c0010t0001g0109 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.615-2810G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34945716 | |||||||
| chr17:34946144 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0183 a0001c0001t0001g0184 |
6 | HG01081.hp2 HG01109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.615-3238A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34946144 | |||||||
| chr17:34946189 | C | T | 1 | a0001c0001t0004g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.615-3283G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34946189 | |||||||
| chr17:34946445 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.615-3539G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34946445 | |||||||
| chr17:34946474 | T | C | 15 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0031 others(12): Show |
28 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.615-3568A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34946474 | |||||||
| chr17:34946482 | T | A | 6 | a0003c0003t0001g0017 a0003c0003t0001g0052 a0003c0003t0001g0123 others(3): Show |
8 | HG00621.hp1 HG02074.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.615-3576A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34946482 | |||||||
| chr17:34946634 | G | A | 78 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0002c0002t0001g0002 others(75): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.615-3728C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34946634 | |||||||
| chr17:34946933 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.615-4027G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34946933 | |||||||
| chr17:34947058 | G | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0177 |
2 | HG02155.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.615-4152C>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34947058 | |||||||
| chr17:34947238 | G | T | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0008 others(73): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.615-4332C>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34947238 | |||||||
| chr17:34947750 | G | A | 1 | a0002c0002t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.614+4200C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34947750 | |||||||
| chr17:34947880 | G | C | 1 | a0001c0001t0002g0167 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.614+4070C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34947880 | |||||||
| chr17:34947906 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.614+4044T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34947906 | |||||||
| chr17:34947975 | C | CA | 7 | a0001c0001t0001g0192 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
8 | HG03041.hp1 HG04199.hp2 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.614+3974dupT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34947975 | |||||||
| chr17:34947975 | CA | C | 6 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0215 others(3): Show |
6 | HG01070.hp1 HG06807.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.614+3974delT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34947975 | |||||||
| chr17:34947986 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0182 |
3 | HG02809.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.614+3964T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34947986 | |||||||
| chr17:34948093 | G | C | 1 | a0003c0003t0001g0140 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.614+3857C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948093 | |||||||
| chr17:34948115 | T | G | 1 | a0001c0001t0001g0206 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.614+3835A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948115 | |||||||
| chr17:34948481 | G | A | 1 | a0002c0002t0001g0086 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.614+3469C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948481 | |||||||
| chr17:34948662 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0224 a0001c0012t0001g0223 |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.614+3288G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948662 | |||||||
| chr17:34948713 | T | TC | 11 | a0001c0001t0001g0183 a0002c0002t0001g0035 a0002c0002t0001g0063 others(8): Show |
12 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.614+3236_614+3237i others(3): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948713 | |||||||
| chr17:34948714 | A | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(217): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.614+3236T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948714 | |||||||
| chr17:34948715 | A | C | 1 | a0005c0006t0002g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.614+3235T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948715 | |||||||
| chr17:34948726 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.614+3224T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948726 | |||||||
| chr17:34948731 | C | A | 77 | a0001c0001t0001g0225 a0002c0002t0001g0002 a0002c0002t0001g0004 others(74): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.614+3219G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948731 | |||||||
| chr17:34948798 | C | A | 1 | a0001c0001t0002g0180 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.614+3152G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948798 | |||||||
| chr17:34948904 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0004g0171 |
2 | HG01192.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.614+3046C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34948904 | |||||||
| chr17:34949087 | G | T | 2 | a0003c0003t0001g0150 a0003c0003t0001g0151 |
2 | HG03927.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.614+2863C>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949087 | |||||||
| chr17:34949095 | G | GGAAAAGA others(3): Show |
173 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0019 others(170): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.614+2845_614+2854d others(12): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949095 | |||||||
| chr17:34949095 | G | GGGAGGGA others(8): Show |
56 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(53): Show |
100 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.614+2854_614+2855i others(17): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949095 | |||||||
| chr17:34949098 | A | AAAGAAAA others(3): Show |
1 | a0002c0002t0001g0071 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.614+2851_614+2852i others(12): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949098 | |||||||
| chr17:34949108 | G | A | 1 | a0005c0006t0002g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.614+2842C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949108 | |||||||
| chr17:34949109 | A | AAGAAAAG others(4): Show |
1 | a0005c0006t0002g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.614+2840_614+2841i others(13): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949109 | |||||||
| chr17:34949131 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.614+2819C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949131 | |||||||
| chr17:34949322 | C | T | 1 | a0003c0003t0001g0130 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.614+2628G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949322 | |||||||
| chr17:34949389 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.614+2561C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949389 | |||||||
| chr17:34949460 | CA | C | 6 | a0001c0001t0001g0189 a0001c0001t0001g0215 a0001c0001t0002g0176 others(3): Show |
6 | HG03239.hp2 HG03491.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.614+2489delT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949460 | |||||||
| chr17:34949509 | G | GAGGA | 82 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0001c0001t0001g0225 others(79): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.614+2440_614+2441i others(6): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949509 | |||||||
| chr17:34949513 | G | A | 49 | a0003c0003t0001g0003 a0003c0003t0001g0005 a0003c0003t0001g0016 others(46): Show |
83 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.614+2437C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949513 | |||||||
| chr17:34949894 | G | T | 22 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0001c0001t0002g0006 others(19): Show |
37 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.614+2056C>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34949894 | |||||||
| chr17:34950213 | T | C | 1 | a0002c0002t0001g0105 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.614+1737A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34950213 | |||||||
| chr17:34950378 | A | G | 1 | a0003c0003t0001g0039 | 2 | HG02056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.614+1572T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34950378 | |||||||
| chr17:34950625 | C | G | 1 | a0001c0001t0001g0222 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.614+1325G>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34950625 | |||||||
| chr17:34950656 | C | T | 2 | a0004c0004t0001g0119 a0004c0004t0001g0120 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.614+1294G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34950656 | |||||||
| chr17:34951310 | CA | C | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0008 others(73): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.614+639delT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34951310 | |||||||
| chr17:34951629 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.614+321G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34951629 | |||||||
| chr17:34951632 | T | G | 37 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0015 others(34): Show |
56 | HG00140.hp2 HG00639.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.614+318A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34951632 | |||||||
| chr17:34951695 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.614+255C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 5/13 | chr17 | 34951695 | |||||||
| chr17:34952106 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0232 others(4): Show |
11 | HG00733.hp1 HG01175.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-53G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34952106 | |||||||
| chr17:34952198 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.511-145A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34952198 | |||||||
| chr17:34952317 | C | T | 1 | a0002c0002t0001g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.511-264G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34952317 | |||||||
| chr17:34952630 | C | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(214): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.511-577G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34952630 | |||||||
| chr17:34952694 | C | T | 1 | a0003c0003t0001g0127 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.511-641G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34952694 | |||||||
| chr17:34952817 | C | T | 1 | a0002c0002t0001g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.511-764G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34952817 | |||||||
| chr17:34952825 | G | A | 1 | a0003c0003t0001g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.511-772C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34952825 | |||||||
| chr17:34953043 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.511-990C>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953043 | |||||||
| chr17:34953055 | C | T | 1 | a0003c0003t0001g0039 | 2 | HG02056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.511-1002G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953055 | |||||||
| chr17:34953318 | A | AATATAT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0161 others(4): Show |
17 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+1102_510+1107d others(8): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953318 | |||||||
| chr17:34953318 | A | AATATATA others(3): Show |
3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0219 |
3 | HG01175.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.510+1098_510+1107d others(12): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953318 | |||||||
| chr17:34953334 | TA | T | 5 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0064 others(2): Show |
5 | HG03017.hp1 NA18977.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+1091delT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953334 | |||||||
| chr17:34953336 | TA | T | 61 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0008 others(58): Show |
119 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.510+1089delT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953336 | |||||||
| chr17:34953337 | A | T | 9 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0002c0002t0001g0031 others(6): Show |
11 | HG03017.hp1 HG03041.hp1 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+1089T>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953337 | |||||||
| chr17:34953338 | TA | T | 6 | a0002c0002t0001g0015 a0002c0002t0001g0028 a0002c0002t0001g0051 others(3): Show |
9 | NA18951.hp2 NA18963.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+1087delT | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953338 | |||||||
| chr17:34953339 | A | T | 89 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0049 others(86): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.510+1087T>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953339 | |||||||
| chr17:34953341 | A | T | 180 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(177): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.510+1085T>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953341 | |||||||
| chr17:34953343 | T | A | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG02970.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+1083A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953343 | |||||||
| chr17:34953359 | T | A | 1 | a0001c0001t0004g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510+1067A>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953359 | |||||||
| chr17:34953363 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.510+1063G>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953363 | |||||||
| chr17:34953419 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0186 |
4 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1007G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953419 | |||||||
| chr17:34953645 | C | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0073 |
3 | HG01070.hp2 HG01071.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.510+781G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953645 | |||||||
| chr17:34953649 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510+777G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953649 | |||||||
| chr17:34953695 | T | G | 1 | a0002c0005t0001g0054 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.510+731A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953695 | |||||||
| chr17:34953855 | G | A | 1 | a0003c0003t0001g0041 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.510+571C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953855 | |||||||
| chr17:34953885 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0232 a0001c0001t0001g0236 |
4 | HG01175.hp1 HG01258.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+541G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953885 | |||||||
| chr17:34953920 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0183 |
5 | HG01081.hp2 HG01109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+506G>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34953920 | |||||||
| chr17:34954040 | A | G | 1 | a0003c0003t0001g0038 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510+386T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34954040 | |||||||
| chr17:34954118 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.510+308T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34954118 | |||||||
| chr17:34954210 | G | A | 1 | a0001c0001t0004g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510+216C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34954210 | |||||||
| chr17:34954323 | G | A | 22 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0001t0002g0006 others(19): Show |
37 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.510+103C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 4/13 | chr17 | 34954323 | |||||||
| chr17:34954697 | A | G | 18 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0002c0002t0001g0009 others(15): Show |
26 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.337-98T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34954697 | |||||||
| chr17:34954704 | C | T | 2 | a0002c0002t0001g0061 a0002c0002t0001g0064 |
2 | NA18977.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.337-105G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34954704 | |||||||
| chr17:34954908 | A | G | 1 | a0002c0002t0001g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.337-309T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34954908 | |||||||
| chr17:34955000 | G | A | 2 | a0003c0003t0001g0144 a0003c0003t0001g0149 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.337-401C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34955000 | |||||||
| chr17:34955160 | A | G | 22 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0001c0001t0002g0006 others(19): Show |
37 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.337-561T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34955160 | |||||||
| chr17:34955499 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0182 |
3 | HG02809.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.337-900G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34955499 | |||||||
| chr17:34955900 | C | T | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0008 others(73): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.337-1301G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34955900 | |||||||
| chr17:34955962 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.337-1363A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34955962 | |||||||
| chr17:34956090 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.337-1491G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34956090 | |||||||
| chr17:34956165 | T | G | 1 | a0001c0001t0001g0214 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.337-1566A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34956165 | |||||||
| chr17:34956635 | T | C | 22 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0001c0001t0002g0006 others(19): Show |
37 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.336+1925A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34956635 | |||||||
| chr17:34956661 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(47): Show |
91 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.336+1899A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34956661 | |||||||
| chr17:34956816 | C | A | 2 | a0002c0002t0001g0015 a0002c0002t0001g0079 |
4 | NA18963.hp1 NA18965.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.336+1744G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34956816 | |||||||
| chr17:34956932 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.336+1628G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34956932 | |||||||
| chr17:34956973 | AT | A | 24 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0001g0173 others(21): Show |
39 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.336+1586delA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34956973 | |||||||
| chr17:34957143 | A | AT | 12 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0153 others(9): Show |
16 | HG01192.hp1 HG01361.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.336+1416dupA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34957143 | |||||||
| chr17:34957143 | AT | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(103): Show |
188 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.336+1416delA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34957143 | |||||||
| chr17:34957143 | ATT | A | 76 | a0001c0001t0004g0171 a0002c0002t0001g0002 a0002c0002t0001g0004 others(73): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.336+1415_336+1416d others(4): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34957143 | |||||||
| chr17:34957301 | C | T | 1 | a0003c0003t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.336+1259G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34957301 | |||||||
| chr17:34957407 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.336+1153C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34957407 | |||||||
| chr17:34957588 | G | C | 1 | a0003c0003t0001g0041 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.336+972C>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34957588 | |||||||
| chr17:34957834 | T | C | 1 | a0003c0003t0001g0146 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.336+726A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34957834 | |||||||
| chr17:34957839 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.336+721C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34957839 | |||||||
| chr17:34957883 | T | C | 2 | a0004c0004t0001g0119 a0004c0004t0001g0120 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.336+677A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34957883 | |||||||
| chr17:34958002 | T | C | 2 | a0003c0003t0001g0042 a0003c0003t0001g0147 |
3 | NA18942.hp2 NA18944.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.336+558A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34958002 | |||||||
| chr17:34958095 | C | G | 1 | a0001c0001t0001g0012 | 4 | HG01884.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.336+465G>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34958095 | |||||||
| chr17:34958200 | C | T | 1 | a0001c0001t0004g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.336+360G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34958200 | |||||||
| chr17:34958393 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(214): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.336+167T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34958393 | |||||||
| chr17:34958408 | C | A | 1 | a0002c0002t0001g0108 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.336+152G>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34958408 | |||||||
| chr17:34958422 | C | T | 2 | a0004c0004t0001g0119 a0004c0004t0001g0120 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.336+138G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 3/13 | chr17 | 34958422 | |||||||
| chr17:34958714 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | NA18939.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.202-20C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34958714 | |||||||
| chr17:34958885 | C | T | 3 | a0003c0003t0001g0036 a0003c0003t0001g0117 a0003c0003t0001g0118 |
4 | HG01891.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-191G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34958885 | |||||||
| chr17:34958977 | A | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0232 others(4): Show |
11 | HG00733.hp1 HG01175.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-283T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34958977 | |||||||
| chr17:34959009 | A | G | 1 | a0002c0002t0001g0031 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.202-315T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959009 | |||||||
| chr17:34959042 | A | G | 1 | a0002c0002t0001g0031 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.202-348T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959042 | |||||||
| chr17:34959123 | C | CT | 184 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(181): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.202-430dupA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959123 | |||||||
| chr17:34959123 | C | CTT | 28 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0161 others(25): Show |
34 | HG00609.hp1 HG00621.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.202-431_202-430dup others(2): Show |
CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959123 | |||||||
| chr17:34959123 | C | T | 1 | a0002c0002t0001g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.202-429G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959123 | |||||||
| chr17:34959269 | G | A | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0008 others(73): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.201+318C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959269 | |||||||
| chr17:34959291 | A | AT | 19 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0232 others(16): Show |
19 | HG01169.hp2 HG01346.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.201+295dupA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959291 | |||||||
| chr17:34959291 | AT | A | 12 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0001g0153 others(9): Show |
14 | HG01192.hp1 HG01361.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.201+295delA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959291 | |||||||
| chr17:34959304 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.201+283A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959304 | |||||||
| chr17:34959340 | A | C | 1 | a0001c0001t0001g0018 | 3 | HG02145.hp2 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.201+247T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959340 | |||||||
| chr17:34959379 | C | T | 36 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0015 others(33): Show |
55 | HG00140.hp2 HG00639.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.201+208G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959379 | |||||||
| chr17:34959546 | A | G | 1 | a0002c0007t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.201+41T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 2/13 | chr17 | 34959546 | |||||||
| chr17:34959989 | T | G | 1 | a0002c0007t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-339A>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34959989 | |||||||
| chr17:34960043 | C | T | 1 | a0002c0002t0001g0053 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.138-393G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34960043 | |||||||
| chr17:34960049 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.138-399T>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34960049 | |||||||
| chr17:34960081 | A | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(214): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.138-431T>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34960081 | |||||||
| chr17:34960528 | T | C | 2 | a0003c0003t0001g0150 a0003c0003t0001g0151 |
2 | HG03927.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.137+729A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34960528 | |||||||
| chr17:34960632 | A | G | 131 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0008 others(128): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.137+625T>C | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34960632 | |||||||
| chr17:34960663 | T | C | 1 | a0002c0005t0001g0043 | 2 | HG00099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.137+594A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34960663 | |||||||
| chr17:34960681 | T | C | 1 | a0002c0002t0001g0044 | 2 | NA18971.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.137+576A>G | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34960681 | |||||||
| chr17:34960843 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.137+414T>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34960843 | |||||||
| chr17:34961084 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0232 others(4): Show |
11 | HG00733.hp1 HG01175.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+173C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34961084 | |||||||
| chr17:34961143 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.137+114C>T | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34961143 | |||||||
| chr17:34961182 | G | T | 1 | a0003c0003t0001g0052 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.137+75C>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34961182 | |||||||
| chr17:34961184 | C | T | 1 | a0002c0002t0001g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.137+73G>A | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34961184 | |||||||
| chr17:34961250 | GTC | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0152 others(5): Show |
12 | HG01192.hp1 HG01361.hp1 HG02055.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.137+5_137+6delGA | CCT6B | ENSG00000132141.14 | transcript | ENST00000314144.10 | protein_coding | 1/13 | chr17 | 34961250 |