Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22820 |
| ensemblid | ENSG00000181789.14 |
| hgncid | 2236 |
| symbol | COPG1 |
| name | COPI coat complex subunit gamma 1 |
| refseq_nuc | NM_016128.4 |
| refseq_prot | NP_057212.1 |
| ensembl_nuc | ENST00000314797.10 |
| ensembl_prot | ENSP00000325002.6 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 129249606 |
| end | 129277773 |
| strand | + |
| ver | v1.2 |
| region | chr3:129249606-129277773 |
| region5000 | chr3:129244606-129282773 |
| regionname0 | COPG1_chr3_129249606_129277773 |
| regionname5000 | COPG1_chr3_129244606_129282773 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 874 | 307 | 83 | 65 | 112 | 10 | 35 | 76 | COPG1_chr3_129244606_129282773 | COPG1 | MLKKF others(869): Show |
chr3 | 129244606 | 129282773 |
| a0002 | 0/0 | 874 | 14 | 3 | 5 | 1 | 2 | 3 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | MLKKF others(869): Show |
chr3 | 129244606 | 129282773 |
| a0003 | 0/0 | 874 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | MLKKF others(869): Show |
chr3 | 129244606 | 129282773 |
| a0004 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | MLKKF others(869): Show |
chr3 | 129244606 | 129282773 |
| a0005 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | MLKKF others(869): Show |
chr3 | 129244606 | 129282773 |
| a0006 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | MLKKF others(869): Show |
chr3 | 129244606 | 129282773 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2622 | 216 | 31 | 52 | 91 | 10 | 30 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0002 | 0/0 | 2622 | 27 | 6 | 0 | 16 | 0 | 5 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0003 | 0/0 | 2622 | 26 | 25 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0004 | 0/0 | 2622 | 16 | 10 | 6 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0006 | 0/0 | 2622 | 10 | 7 | 3 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0007 | 0/0 | 2622 | 4 | 0 | 0 | 4 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0009 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0010 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0011 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0012 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0013 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0015 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0001c0017 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0002c0005 | 0/0 | 2622 | 14 | 3 | 5 | 1 | 2 | 3 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0003c0008 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0004c0016 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0005c0018 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 | ||
| a0006c0014 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | ATGTT others(2617): Show |
chr3 | 129244606 | 129282773 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3079 | 143 | 18 | 32 | 69 | 6 | 17 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| a0001c0001t0002 | 1/0 | 3078 | 60 | 5 | 20 | 19 | 3 | 12 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0001t0003 | 0/0 | 3077 | 2 | 0 | 0 | 0 | 1 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3072): Show |
chr3 | 129244606 | 129282773 |
| a0001c0001t0004 | 0/0 | 3079 | 8 | 8 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| a0001c0001t0006 | 0/0 | 3078 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0001t0007 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0002t0001 | 0/0 | 3079 | 3 | 1 | 0 | 1 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| a0001c0002t0002 | 0/0 | 3078 | 23 | 4 | 0 | 15 | 0 | 4 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0002t0005 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0003t0001 | 0/0 | 3079 | 3 | 3 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| a0001c0003t0002 | 0/0 | 3078 | 11 | 11 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0003t0003 | 0/0 | 3077 | 12 | 11 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3072): Show |
chr3 | 129244606 | 129282773 |
| a0001c0004t0002 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0004t0003 | 0/0 | 3077 | 15 | 9 | 6 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3072): Show |
chr3 | 129244606 | 129282773 |
| a0001c0006t0002 | 0/0 | 3078 | 10 | 7 | 3 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0007t0002 | 0/0 | 3078 | 4 | 0 | 0 | 4 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0009t0002 | 0/0 | 3078 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0010t0005 | 0/0 | 3078 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0011t0002 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0012t0002 | 0/0 | 3078 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0013t0002 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0001c0015t0001 | 0/0 | 3079 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| a0001c0017t0001 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| a0002c0005t0001 | 0/0 | 3079 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| a0002c0005t0002 | 0/0 | 3078 | 11 | 3 | 2 | 1 | 2 | 3 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0002c0005t0003 | 0/0 | 3077 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3072): Show |
chr3 | 129244606 | 129282773 |
| a0003c0008t0001 | 0/0 | 3079 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| a0004c0016t0002 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3073): Show |
chr3 | 129244606 | 129282773 |
| a0005c0018t0001 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| a0006c0014t0001 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | AGTCG others(3074): Show |
chr3 | 129244606 | 129282773 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 0 | 3 | 13 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0002 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0004 | 0/0 | 10 | 4 | 5 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0006 | 0/0 | 7 | 1 | 4 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0002 | 1/0 | 11 | 1 | 1 | 4 | 1 | 3 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0007 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0005 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0003g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0003g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0004t0003g0003 | 0/0 | 10 | 6 | 4 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0004t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0004t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0004t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0004t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0004t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0006t0002g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0006t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0006t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0006t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0006t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0006t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0007t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0007t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0007t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0007t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0009t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0009t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0010t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0011t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0012t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0013t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0015t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0001c0017t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0002c0005t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0002c0005t0002g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0002c0005t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0002c0005t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0002c0005t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0002c0005t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0002c0005t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0002c0005t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0003c0008t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0003c0008t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0004c0016t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0005c0018t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| a0006c0014t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | FIN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00280 | hp2 | a0002 | c0005 | t0002 | g0045 | EUR | FIN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00408 | hp2 | a0001 | c0017 | t0001 | g0119 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00639 | hp2 | a0001 | c0003 | t0003 | g0031 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00642 | hp2 | a0001 | c0010 | t0005 | g0076 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00735 | hp1 | a0001 | c0004 | t0003 | g0084 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00738 | hp1 | a0001 | c0004 | t0003 | g0003 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01069 | hp1 | a0002 | c0005 | t0002 | g0010 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01071 | hp2 | a0002 | c0005 | t0002 | g0010 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01167 | hp2 | a0001 | c0004 | t0003 | g0003 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01169 | hp1 | a0001 | c0004 | t0003 | g0003 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01175 | hp2 | a0001 | c0004 | t0003 | g0086 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01243 | hp1 | a0001 | c0006 | t0002 | g0012 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01255 | hp2 | a0001 | c0006 | t0002 | g0073 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01261 | hp1 | a0002 | c0005 | t0001 | g0049 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01346 | hp1 | a0001 | c0004 | t0003 | g0003 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01361 | hp2 | a0001 | c0015 | t0001 | g0001 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01496 | hp1 | a0001 | c0012 | t0002 | g0089 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0079 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01884 | hp2 | a0002 | c0005 | t0002 | g0014 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0174 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01934 | hp2 | a0002 | c0005 | t0003 | g0024 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0184 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02055 | hp2 | a0001 | c0006 | t0002 | g0012 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02071 | hp1 | a0004 | c0016 | t0002 | g0023 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CDX | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0075 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02257 | hp2 | a0002 | c0005 | t0002 | g0014 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02258 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02273 | hp1 | a0002 | c0005 | t0003 | g0024 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0055 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0081 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02615 | hp2 | a0001 | c0004 | t0003 | g0003 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0009 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02647 | hp1 | a0001 | c0003 | t0003 | g0009 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02647 | hp2 | a0001 | c0009 | t0002 | g0069 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02698 | hp2 | a0002 | c0005 | t0002 | g0010 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0053 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0082 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02735 | hp2 | a0002 | c0005 | t0002 | g0010 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0064 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02809 | hp2 | a0001 | c0011 | t0002 | g0085 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02818 | hp2 | a0001 | c0004 | t0003 | g0083 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02886 | hp1 | a0001 | c0009 | t0002 | g0070 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02896 | hp1 | a0001 | c0004 | t0003 | g0087 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02896 | hp2 | a0001 | c0006 | t0002 | g0029 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02970 | hp2 | a0003 | c0008 | t0001 | g0134 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02976 | hp2 | a0001 | c0006 | t0002 | g0090 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03098 | hp2 | a0001 | c0003 | t0002 | g0050 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0009 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03139 | hp2 | a0001 | c0004 | t0003 | g0078 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03195 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0030 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03239 | hp1 | a0002 | c0005 | t0002 | g0046 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0031 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03486 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03486 | hp2 | a0001 | c0006 | t0002 | g0029 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03516 | hp1 | a0003 | c0008 | t0001 | g0135 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0052 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0056 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0063 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18522 | hp2 | a0001 | c0006 | t0002 | g0074 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18612 | hp2 | a0002 | c0005 | t0002 | g0047 | EAS | CHB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18747 | hp2 | a0001 | c0007 | t0002 | g0060 | EAS | CHB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18906 | hp1 | a0001 | c0006 | t0002 | g0012 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18906 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18939 | hp1 | a0001 | c0007 | t0002 | g0066 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18954 | hp1 | a0005 | c0018 | t0001 | g0093 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18966 | hp1 | a0001 | c0007 | t0002 | g0028 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18972 | hp2 | a0001 | c0007 | t0002 | g0065 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18973 | hp1 | a0006 | c0014 | t0001 | g0041 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0054 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0061 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20129 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | ASW | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | ASW | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20805 | hp1 | a0002 | c0005 | t0002 | g0048 | EUR | TSI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | GIH | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG01123 | hp2 | a0001 | c0006 | t0002 | g0072 | AMR | CLM | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0025 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02486 | hp1 | a0001 | c0004 | t0003 | g0003 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02486 | hp2 | a0001 | c0006 | t0002 | g0012 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0080 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | MSL | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | USA | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | USA | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20300 | hp1 | a0002 | c0005 | t0002 | g0014 | AFR | USA | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA21309 | hp1 | a0001 | c0013 | t0002 | g0088 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0129 | REF | REF | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | COPG1_chr3_129244606_129282773 | COPG1 | chr3 | 129244606 | 129282773 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129252354 | T | C | 1 | a0003 | 2 | HG02970.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.164T>C | p.Ile55Thr | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 3/24 | 268/3078 | 164/2625 | 55/874 | chr3 | 129252354 | |||
| chr3:129257608 | C | G | 1 | a0002 | 14 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
missense_variant | MODERATE | c.718C>G | p.Leu240Val | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 9/24 | 822/3078 | 718/2625 | 240/874 | chr3 | 129257608 | |||
| chr3:129257791 | T | A | 1 | a0006 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.802T>A | p.Tyr268Asn | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/24 | 906/3078 | 802/2625 | 268/874 | chr3 | 129257791 | |||
| chr3:129271868 | C | T | 1 | a0005 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.1945C>T | p.Arg649Cys | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 19/24 | 2049/3078 | 1945/2625 | 649/874 | chr3 | 129271868 | |||
| chr3:129274944 | C | T | 1 | a0004 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.2363C>T | p.Thr788Met | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 22/24 | 2467/3078 | 2363/2625 | 788/874 | chr3 | 129274944 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129252340 | G | A | 1 | a0001c0010 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.150G>A | p.Lys50Lys | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 3/24 | 254/3078 | 150/2625 | 50/874 | chr3 | 129252340 | |||
| chr3:129252649 | G | A | 1 | a0001c0011 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.198G>A | p.Ala66Ala | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 4/24 | 302/3078 | 198/2625 | 66/874 | chr3 | 129252649 | |||
| chr3:129254716 | C | T | 1 | a0001c0007 | 4 | NA18747.hp2 NA18939.hp1 NA18966.hp1 others(1): Show |
synonymous_variant | LOW | c.372C>T | p.Ala124Ala | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/24 | 476/3078 | 372/2625 | 124/874 | chr3 | 129254716 | |||
| chr3:129257553 | T | C | 11 | a0001c0002 a0001c0003 a0001c0004 others(8): Show |
103 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
synonymous_variant | LOW | c.663T>C | p.His221His | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 9/24 | 767/3078 | 663/2625 | 221/874 | chr3 | 129257553 | |||
| chr3:129257820 | G | A | 2 | a0001c0012 a0001c0013 |
2 | HG01496.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.831G>A | p.Leu277Leu | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/24 | 935/3078 | 831/2625 | 277/874 | chr3 | 129257820 | |||
| chr3:129257850 | G | A | 1 | a0001c0006 | 10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
synonymous_variant | LOW | c.861G>A | p.Pro287Pro | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/24 | 965/3078 | 861/2625 | 287/874 | chr3 | 129257850 | |||
| chr3:129260732 | G | A | 1 | a0001c0015 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.1053G>A | p.Thr351Thr | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/24 | 1157/3078 | 1053/2625 | 351/874 | chr3 | 129260732 | |||
| chr3:129260750 | C | T | 1 | a0001c0013 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1071C>T | p.Ile357Ile | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/24 | 1175/3078 | 1071/2625 | 357/874 | chr3 | 129260750 | |||
| chr3:129265566 | G | A | 2 | a0001c0004 a0001c0011 |
17 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(14): Show |
synonymous_variant | LOW | c.1242G>A | p.Lys414Lys | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/24 | 1346/3078 | 1242/2625 | 414/874 | chr3 | 129265566 | |||
| chr3:129265740 | C | T | 4 | a0001c0002 a0001c0007 a0001c0009 others(1): Show |
34 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(31): Show |
synonymous_variant | LOW | c.1416C>T | p.Tyr472Tyr | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/24 | 1520/3078 | 1416/2625 | 472/874 | chr3 | 129265740 | |||
| chr3:129267976 | C | G | 1 | a0001c0010 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.1584C>G | p.Ala528Ala | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/24 | 1688/3078 | 1584/2625 | 528/874 | chr3 | 129267976 | |||
| chr3:129272366 | C | T | 1 | a0001c0017 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.2109C>T | p.Pro703Pro | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 20/24 | 2213/3078 | 2109/2625 | 703/874 | chr3 | 129272366 | |||
| chr3:129275276 | C | T | 1 | a0001c0009 | 2 | HG02647.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.2478C>T | p.His826His | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/24 | 2582/3078 | 2478/2625 | 826/874 | chr3 | 129275276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129249638 | A | G | 1 | a0001c0001t0006 | 2 | HG02083.hp2 NA18951.hp2 |
5_prime_UTR_variant | MODIFIER | c.-72A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/24 | 72 | chr3 | 129249638 | ||||||
| chr3:129249670 | C | G | 1 | a0001c0001t0007 | 1 | HG02027.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/24 | 40 | chr3 | 129249670 | ||||||
| chr3:129277601 | C | CT | 9 | a0001c0001t0001 a0001c0002t0001 a0001c0003t0001 others(6): Show |
155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*196dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 24/24 | 197 | INFO_REALIGN_3_PRIME | chr3 | 129277601 | |||||
| chr3:129277601 | CT | C | 4 | a0001c0001t0003 a0001c0003t0003 a0001c0004t0003 others(1): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*196delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 24/24 | 196 | INFO_REALIGN_3_PRIME | chr3 | 129277601 | |||||
| chr3:129277620 | T | TA | 1 | a0001c0001t0004 | 8 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*199dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 24/24 | 200 | INFO_REALIGN_3_PRIME | chr3 | 129277620 | |||||
| chr3:129277765 | T | A | 2 | a0001c0002t0005 a0001c0010t0005 |
2 | HG00642.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*341T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 24/24 | 341 | chr3 | 129277765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129249799 | T | C | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.37+53T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249799 | |||||||
| chr3:129249812 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.37+66C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249812 | |||||||
| chr3:129249911 | C | T | 17 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(14): Show |
32 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.37+165C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249911 | |||||||
| chr3:129249964 | G | A | 8 | a0002c0005t0001g0049 a0002c0005t0002g0010 a0002c0005t0002g0014 others(5): Show |
14 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.37+218G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249964 | |||||||
| chr3:129249972 | C | T | 1 | a0001c0002t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.37+226C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249972 | |||||||
| chr3:129249973 | A | AC | 17 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0177 others(14): Show |
23 | HG00323.hp2 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+238dupC | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr3 | 129249973 | ||||||
| chr3:129249973 | ACC | A | 43 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(40): Show |
72 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.37+237_37+238delCC | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr3 | 129249973 | ||||||
| chr3:129249973 | ACCC | A | 17 | a0001c0003t0001g0025 a0001c0003t0002g0011 a0001c0003t0002g0025 others(14): Show |
26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.37+236_37+238delCC others(1): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr3 | 129249973 | ||||||
| chr3:129249982 | C | A | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.37+236C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249982 | |||||||
| chr3:129249987 | G | A | 2 | a0001c0002t0005g0075 a0001c0010t0005g0076 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.37+241G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129249987 | |||||||
| chr3:129250069 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.37+323G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250069 | |||||||
| chr3:129250304 | G | C | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.38-378G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250304 | |||||||
| chr3:129250315 | G | C | 2 | a0001c0003t0002g0050 a0001c0003t0002g0051 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.38-367G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250315 | |||||||
| chr3:129250438 | T | C | 1 | a0001c0002t0002g0056 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.38-244T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250438 | |||||||
| chr3:129250668 | G | T | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.38-14G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 1/23 | chr3 | 129250668 | |||||||
| chr3:129250810 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.90+76A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250810 | |||||||
| chr3:129250863 | T | C | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.90+129T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250863 | |||||||
| chr3:129250896 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.90+162T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250896 | |||||||
| chr3:129250912 | CT | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(69): Show |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.90+205delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129250912 | ||||||
| chr3:129250912 | CTT | C | 9 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0006t0002g0012 others(6): Show |
13 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.90+204_90+205delTT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129250912 | ||||||
| chr3:129250912 | CTTT | C | 10 | a0001c0002t0002g0071 a0001c0003t0003g0030 a0001c0003t0003g0031 others(7): Show |
21 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.90+203_90+205delTT others(1): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129250912 | ||||||
| chr3:129250912 | CTTTT | C | 45 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(42): Show |
68 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.90+202_90+205delTT others(2): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129250912 | ||||||
| chr3:129250947 | A | G | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.90+213A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250947 | |||||||
| chr3:129250952 | C | A | 1 | a0001c0002t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.90+218C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250952 | |||||||
| chr3:129250969 | G | T | 3 | a0001c0001t0001g0137 a0001c0012t0002g0089 a0001c0013t0002g0088 |
3 | HG01433.hp1 HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.90+235G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250969 | |||||||
| chr3:129250992 | C | T | 2 | a0001c0003t0001g0136 a0001c0003t0001g0174 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.90+258C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250992 | |||||||
| chr3:129250993 | G | A | 1 | a0002c0005t0002g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.90+259G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129250993 | |||||||
| chr3:129251016 | C | G | 2 | a0001c0012t0002g0089 a0001c0013t0002g0088 |
2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.90+282C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251016 | |||||||
| chr3:129251054 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0138 |
4 | NA18941.hp1 NA18970.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+320G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251054 | |||||||
| chr3:129251178 | C | T | 2 | a0001c0009t0002g0069 a0001c0009t0002g0070 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.90+444C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251178 | |||||||
| chr3:129251212 | C | T | 17 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(14): Show |
26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.90+478C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251212 | |||||||
| chr3:129251269 | A | G | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.90+535A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251269 | |||||||
| chr3:129251326 | G | A | 4 | a0001c0002t0005g0075 a0001c0009t0002g0069 a0001c0009t0002g0070 others(1): Show |
4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+592G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251326 | |||||||
| chr3:129251327 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0091 |
4 | HG00609.hp2 NA18944.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+593G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251327 | |||||||
| chr3:129251368 | T | A | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.90+634T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251368 | |||||||
| chr3:129251371 | T | A | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0139 others(3): Show |
6 | NA18955.hp1 NA18959.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+637T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251371 | |||||||
| chr3:129251371 | TTA | T | 23 | a0001c0003t0001g0025 a0001c0003t0002g0011 a0001c0003t0002g0025 others(20): Show |
36 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.90+653_90+654delAT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129251371 | ||||||
| chr3:129251371 | TTATA | T | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.90+651_90+654delAT others(2): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr3 | 129251371 | ||||||
| chr3:129251508 | A | G | 57 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(54): Show |
91 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.91-773A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251508 | |||||||
| chr3:129251582 | G | C | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.91-699G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251582 | |||||||
| chr3:129251607 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.91-674G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251607 | |||||||
| chr3:129251675 | C | T | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.91-606C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251675 | |||||||
| chr3:129251805 | G | A | 2 | a0001c0003t0003g0030 a0001c0003t0003g0082 |
3 | HG02145.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.91-476G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251805 | |||||||
| chr3:129251812 | C | G | 2 | a0003c0008t0001g0134 a0003c0008t0001g0135 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.91-469C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251812 | |||||||
| chr3:129251877 | G | A | 1 | a0001c0006t0002g0090 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.91-404G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251877 | |||||||
| chr3:129251985 | G | A | 4 | a0001c0002t0005g0075 a0001c0009t0002g0069 a0001c0009t0002g0070 others(1): Show |
4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-296G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129251985 | |||||||
| chr3:129252059 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.91-222A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129252059 | |||||||
| chr3:129252150 | A | G | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.91-131A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129252150 | |||||||
| chr3:129252270 | T | C | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.91-11T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 2/23 | chr3 | 129252270 | |||||||
| chr3:129252403 | G | T | 2 | a0001c0001t0001g0036 a0001c0001t0002g0036 |
2 | NA18952.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.171+42G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 3/23 | chr3 | 129252403 | |||||||
| chr3:129252416 | G | C | 2 | a0001c0002t0005g0075 a0001c0010t0005g0076 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.171+55G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 3/23 | chr3 | 129252416 | |||||||
| chr3:129253315 | A | G | 65 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(62): Show |
103 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.323+360A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129253315 | |||||||
| chr3:129253750 | A | G | 2 | a0001c0003t0001g0136 a0001c0003t0001g0174 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.323+795A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129253750 | |||||||
| chr3:129253807 | C | G | 1 | a0001c0001t0002g0132 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.323+852C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129253807 | |||||||
| chr3:129253994 | G | C | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.324-674G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129253994 | |||||||
| chr3:129254000 | C | CA | 13 | a0001c0001t0001g0094 a0001c0001t0001g0143 a0001c0001t0001g0144 others(10): Show |
13 | HG01891.hp2 HG02572.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.324-651dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr3 | 129254000 | ||||||
| chr3:129254000 | CA | C | 16 | a0001c0003t0001g0025 a0001c0003t0002g0011 a0001c0003t0002g0025 others(13): Show |
25 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.324-651delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr3 | 129254000 | ||||||
| chr3:129254000 | CAA | C | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-652_324-651del others(2): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr3 | 129254000 | ||||||
| chr3:129254032 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.324-636C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254032 | |||||||
| chr3:129254087 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.324-581G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254087 | |||||||
| chr3:129254104 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.324-564C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254104 | |||||||
| chr3:129254154 | G | A | 1 | a0001c0013t0002g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.324-514G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254154 | |||||||
| chr3:129254217 | T | C | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.324-451T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254217 | |||||||
| chr3:129254248 | C | T | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-420C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254248 | |||||||
| chr3:129254295 | C | CA | 41 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(38): Show |
66 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.324-362dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr3 | 129254295 | ||||||
| chr3:129254609 | T | A | 1 | a0001c0004t0003g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.324-59T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 5/23 | chr3 | 129254609 | |||||||
| chr3:129254750 | C | T | 1 | a0001c0002t0001g0077 | 1 | HG03471.hp2 | splice_region_variant&intron_variant | LOW | c.399+7C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254750 | |||||||
| chr3:129254755 | C | G | 20 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(17): Show |
30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.399+12C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254755 | |||||||
| chr3:129254783 | A | C | 2 | a0001c0002t0005g0075 a0001c0010t0005g0076 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.399+40A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254783 | |||||||
| chr3:129254820 | T | C | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.399+77T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254820 | |||||||
| chr3:129254838 | C | T | 8 | a0001c0001t0004g0018 a0001c0001t0004g0098 a0001c0001t0004g0125 others(5): Show |
10 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.399+95C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254838 | |||||||
| chr3:129254904 | A | C | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.400-81A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 6/23 | chr3 | 129254904 | |||||||
| chr3:129255135 | A | C | 65 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(62): Show |
103 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.492+58A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255135 | |||||||
| chr3:129255135 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.492+58A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255135 | |||||||
| chr3:129255141 | C | T | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.492+64C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255141 | |||||||
| chr3:129255179 | C | CT | 45 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(42): Show |
74 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.492+115dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr3 | 129255179 | ||||||
| chr3:129255201 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.492+124C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255201 | |||||||
| chr3:129255297 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.492+220G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255297 | |||||||
| chr3:129255321 | G | T | 1 | a0001c0001t0002g0132 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.492+244G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255321 | |||||||
| chr3:129255346 | T | C | 1 | a0001c0002t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.492+269T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255346 | |||||||
| chr3:129255350 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.492+273T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255350 | |||||||
| chr3:129255478 | C | T | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.492+401C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255478 | |||||||
| chr3:129255487 | C | CT | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(37): Show |
68 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.492+423dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr3 | 129255487 | ||||||
| chr3:129255773 | C | T | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.493-295C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255773 | |||||||
| chr3:129255968 | C | T | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.493-100C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 7/23 | chr3 | 129255968 | |||||||
| chr3:129256169 | A | G | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.579+15A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256169 | |||||||
| chr3:129256201 | G | C | 1 | a0001c0002t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.579+47G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256201 | |||||||
| chr3:129256202 | T | G | 19 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(16): Show |
29 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.579+48T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256202 | |||||||
| chr3:129256237 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.579+83C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256237 | |||||||
| chr3:129256275 | C | A | 20 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(17): Show |
30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.579+121C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256275 | |||||||
| chr3:129256491 | C | T | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.579+337C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256491 | |||||||
| chr3:129256657 | C | G | 1 | a0001c0001t0001g0173 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.579+503C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256657 | |||||||
| chr3:129256702 | C | T | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.579+548C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256702 | |||||||
| chr3:129256714 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.579+560G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256714 | |||||||
| chr3:129256814 | A | G | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-656A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129256814 | |||||||
| chr3:129257028 | C | T | 2 | a0001c0002t0005g0075 a0001c0010t0005g0076 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.580-442C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 8/23 | chr3 | 129257028 | |||||||
| chr3:129257702 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG03654.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.738-25C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 9/23 | chr3 | 129257702 | |||||||
| chr3:129257886 | C | G | 4 | a0002c0005t0002g0010 a0002c0005t0002g0046 a0002c0005t0002g0047 others(1): Show |
8 | HG01069.hp1 HG01071.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.871+26C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129257886 | |||||||
| chr3:129257897 | A | G | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.871+37A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129257897 | |||||||
| chr3:129258315 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.871+455G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129258315 | |||||||
| chr3:129258448 | C | T | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.871+588C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129258448 | |||||||
| chr3:129258800 | G | C | 1 | a0001c0007t0002g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.871+940G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129258800 | |||||||
| chr3:129259439 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02602.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.872-894C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259439 | |||||||
| chr3:129259460 | C | CA | 7 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0001g0139 others(4): Show |
8 | HG01081.hp2 HG02145.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.872-853dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr3 | 129259460 | ||||||
| chr3:129259460 | CA | C | 5 | a0001c0001t0001g0034 a0001c0001t0001g0121 a0001c0001t0001g0177 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.872-853delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr3 | 129259460 | ||||||
| chr3:129259477 | AAAAG | A | 9 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(6): Show |
15 | HG00639.hp2 HG01175.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.872-852_872-849del others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr3 | 129259477 | ||||||
| chr3:129259478 | AAAG | A | 27 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(24): Show |
46 | HG00408.hp1 HG00544.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.872-852_872-850del others(3): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr3 | 129259478 | ||||||
| chr3:129259487 | G | A | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.872-846G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259487 | |||||||
| chr3:129259612 | T | A | 19 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(16): Show |
29 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.872-721T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259612 | |||||||
| chr3:129259763 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.872-570G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259763 | |||||||
| chr3:129259845 | A | C | 1 | a0001c0002t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.872-488A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259845 | |||||||
| chr3:129259958 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.872-375C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129259958 | |||||||
| chr3:129260153 | A | G | 1 | a0001c0002t0002g0068 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.872-180A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260153 | |||||||
| chr3:129260165 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(50): Show |
86 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.872-168C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260165 | |||||||
| chr3:129260221 | G | A | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.872-112G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260221 | |||||||
| chr3:129260265 | T | C | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.872-68T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260265 | |||||||
| chr3:129260272 | C | T | 1 | a0001c0003t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.872-61C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260272 | |||||||
| chr3:129260319 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.872-14C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 10/23 | chr3 | 129260319 | |||||||
| chr3:129260413 | C | G | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.939+13C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 11/23 | chr3 | 129260413 | |||||||
| chr3:129260954 | G | C | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1128+147G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129260954 | |||||||
| chr3:129261189 | G | A | 8 | a0002c0005t0001g0049 a0002c0005t0002g0010 a0002c0005t0002g0014 others(5): Show |
14 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1128+382G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261189 | |||||||
| chr3:129261268 | A | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0164 |
5 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+461A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261268 | |||||||
| chr3:129261397 | G | T | 2 | a0001c0002t0005g0075 a0001c0010t0005g0076 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1128+590G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261397 | |||||||
| chr3:129261449 | T | C | 17 | a0001c0003t0001g0025 a0001c0003t0002g0011 a0001c0003t0002g0025 others(14): Show |
26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1128+642T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261449 | |||||||
| chr3:129261620 | A | G | 20 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(17): Show |
30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.1128+813A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261620 | |||||||
| chr3:129261625 | C | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0150 a0001c0001t0001g0152 others(1): Show |
5 | HG03490.hp1 HG03492.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+818C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261625 | |||||||
| chr3:129261628 | CT | C | 17 | a0001c0003t0001g0025 a0001c0003t0002g0011 a0001c0003t0002g0025 others(14): Show |
26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1128+822delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261628 | |||||||
| chr3:129261658 | G | T | 17 | a0001c0003t0001g0025 a0001c0003t0002g0011 a0001c0003t0002g0025 others(14): Show |
26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1128+851G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261658 | |||||||
| chr3:129261681 | C | T | 1 | a0001c0017t0001g0119 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1128+874C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261681 | |||||||
| chr3:129261836 | T | C | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1128+1029T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261836 | |||||||
| chr3:129261855 | G | C | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1128+1048G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261855 | |||||||
| chr3:129261983 | A | G | 2 | a0001c0012t0002g0089 a0001c0013t0002g0088 |
2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1128+1176A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129261983 | |||||||
| chr3:129262013 | T | C | 4 | a0001c0002t0005g0075 a0001c0009t0002g0069 a0001c0009t0002g0070 others(1): Show |
4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+1206T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262013 | |||||||
| chr3:129262065 | T | C | 1 | a0001c0002t0002g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1128+1258T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262065 | |||||||
| chr3:129262074 | C | T | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1128+1267C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262074 | |||||||
| chr3:129262133 | T | G | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1128+1326T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262133 | |||||||
| chr3:129262250 | CA | C | 16 | a0001c0003t0001g0025 a0001c0003t0002g0011 a0001c0003t0002g0025 others(13): Show |
25 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1128+1446delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262250 | ||||||
| chr3:129262253 | A | T | 1 | a0001c0003t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1128+1446A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262253 | |||||||
| chr3:129262253 | AT | A | 50 | a0001c0001t0001g0095 a0001c0001t0001g0103 a0001c0001t0001g0113 others(47): Show |
79 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1128+1463delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262253 | ||||||
| chr3:129262256 | T | A | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1128+1449T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262256 | |||||||
| chr3:129262256 | T | G | 1 | a0001c0001t0002g0141 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1128+1449T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262256 | |||||||
| chr3:129262401 | C | T | 5 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(2): Show |
9 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1129-1503C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262401 | |||||||
| chr3:129262472 | C | G | 1 | a0001c0001t0002g0163 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1129-1432C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262472 | |||||||
| chr3:129262542 | C | T | 2 | a0001c0012t0002g0089 a0001c0013t0002g0088 |
2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1129-1362C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262542 | |||||||
| chr3:129262575 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1129-1329T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262575 | |||||||
| chr3:129262665 | G | C | 1 | a0001c0001t0002g0104 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1129-1239G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262665 | |||||||
| chr3:129262722 | G | GAA | 34 | a0001c0002t0001g0063 a0001c0002t0001g0077 a0001c0002t0002g0005 others(31): Show |
57 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1129-1170_1129-116 others(6): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262722 | ||||||
| chr3:129262722 | G | GAAA | 5 | a0001c0002t0002g0027 a0001c0002t0002g0058 a0001c0002t0002g0062 others(2): Show |
7 | HG00408.hp1 HG02080.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-1171_1129-116 others(7): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262722 | ||||||
| chr3:129262722 | GA | G | 10 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0039 others(7): Show |
18 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1129-1169delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129262722 | ||||||
| chr3:129262736 | T | C | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1129-1168T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262736 | |||||||
| chr3:129262788 | G | T | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1129-1116G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262788 | |||||||
| chr3:129262977 | C | A | 1 | a0001c0002t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1129-927C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129262977 | |||||||
| chr3:129263014 | C | CA | 25 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0099 others(22): Show |
39 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1129-869dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263014 | ||||||
| chr3:129263033 | AAAGAGTC others(6): Show |
A | 1 | a0001c0007t0002g0066 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1129-870_1129-858d others(15): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263033 | |||||||
| chr3:129263034 | AAGAGTCC others(5): Show |
A | 12 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(9): Show |
20 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1129-869_1129-858d others(14): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263034 | |||||||
| chr3:129263034 | AAGAGTCC others(6): Show |
A | 1 | a0001c0007t0002g0065 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1129-867_1129-855d others(15): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263034 | ||||||
| chr3:129263035 | AGAGTCCT others(3): Show |
A | 5 | a0001c0002t0001g0077 a0001c0002t0002g0026 a0001c0002t0002g0057 others(2): Show |
6 | HG00642.hp2 HG02257.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-867_1129-858d others(12): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263035 | ||||||
| chr3:129263035 | AGAGTCCT others(4): Show |
A | 6 | a0001c0002t0002g0005 a0001c0002t0002g0056 a0001c0002t0002g0064 others(3): Show |
6 | HG02647.hp2 HG02738.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-865_1129-855d others(13): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263035 | ||||||
| chr3:129263036 | G | A | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1129-868G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263036 | |||||||
| chr3:129263037 | A | T | 17 | a0001c0003t0001g0025 a0001c0003t0002g0011 a0001c0003t0002g0025 others(14): Show |
26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1129-867A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263037 | |||||||
| chr3:129263037 | AGTCCTTC others(1): Show |
A | 12 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(9): Show |
27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1129-865_1129-858d others(10): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263037 | ||||||
| chr3:129263037 | AGTCCTTC others(2): Show |
A | 3 | a0001c0004t0002g0081 a0001c0012t0002g0089 a0001c0013t0002g0088 |
3 | HG01496.hp1 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1129-865_1129-857d others(11): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263037 | ||||||
| chr3:129263045 | T | A | 1 | a0001c0004t0003g0086 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1129-859T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263045 | |||||||
| chr3:129263046 | G | A | 18 | a0001c0002t0001g0077 a0001c0002t0002g0026 a0001c0002t0002g0057 others(15): Show |
34 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1129-858G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263046 | |||||||
| chr3:129263099 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1129-805G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263099 | |||||||
| chr3:129263105 | A | T | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1129-799A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263105 | |||||||
| chr3:129263121 | C | G | 1 | a0001c0007t0002g0065 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1129-783C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263121 | |||||||
| chr3:129263122 | G | C | 1 | a0001c0007t0002g0065 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1129-782G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263122 | |||||||
| chr3:129263244 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0120 a0001c0001t0002g0036 others(1): Show |
4 | HG02040.hp1 NA18952.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-660C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263244 | |||||||
| chr3:129263262 | G | A | 3 | a0001c0001t0004g0018 a0001c0001t0004g0098 a0001c0001t0004g0125 |
5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129-642G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263262 | |||||||
| chr3:129263378 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1129-526G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263378 | |||||||
| chr3:129263394 | A | T | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1129-510A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263394 | |||||||
| chr3:129263395 | G | A | 3 | a0001c0003t0003g0009 a0001c0003t0003g0079 a0001c0003t0003g0080 |
7 | HG01884.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-509G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263395 | |||||||
| chr3:129263459 | A | C | 1 | a0001c0002t0005g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1129-445A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263459 | |||||||
| chr3:129263507 | G | A | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1129-397G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263507 | |||||||
| chr3:129263725 | G | T | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1129-179G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263725 | |||||||
| chr3:129263740 | CCTTCAAG | C | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1129-155_1129-149d others(9): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr3 | 129263740 | ||||||
| chr3:129263898 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02523.hp2 | splice_region_variant&intron_variant | LOW | c.1129-6A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 12/23 | chr3 | 129263898 | |||||||
| chr3:129264008 | CA | C | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1224+10delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264008 | |||||||
| chr3:129264018 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG00323.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1224+19C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264018 | |||||||
| chr3:129264067 | C | T | 1 | a0001c0001t0002g0043 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1224+68C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264067 | |||||||
| chr3:129264135 | C | T | 2 | a0001c0012t0002g0089 a0001c0013t0002g0088 |
2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1224+136C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264135 | |||||||
| chr3:129264357 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1224+358C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264357 | |||||||
| chr3:129264381 | C | T | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1224+382C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264381 | |||||||
| chr3:129264421 | C | T | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1224+422C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264421 | |||||||
| chr3:129264453 | A | C | 1 | a0002c0005t0002g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1224+454A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264453 | |||||||
| chr3:129264467 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1224+468A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264467 | |||||||
| chr3:129264616 | T | C | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1224+617T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264616 | |||||||
| chr3:129264640 | T | C | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224+641T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264640 | |||||||
| chr3:129264676 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1224+677G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264676 | |||||||
| chr3:129264775 | G | C | 1 | a0001c0007t0002g0065 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1225-774G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264775 | |||||||
| chr3:129264776 | C | G | 1 | a0001c0007t0002g0065 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1225-773C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264776 | |||||||
| chr3:129264821 | G | GT | 7 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0101 others(4): Show |
7 | HG02145.hp2 HG02738.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225-715dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr3 | 129264821 | ||||||
| chr3:129264837 | G | T | 57 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(54): Show |
91 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1225-712G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264837 | |||||||
| chr3:129264850 | C | T | 16 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(13): Show |
31 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1225-699C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264850 | |||||||
| chr3:129264852 | C | T | 2 | a0001c0003t0001g0136 a0001c0003t0001g0174 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1225-697C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129264852 | |||||||
| chr3:129265010 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1225-539A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265010 | |||||||
| chr3:129265100 | C | T | 1 | a0001c0002t0002g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1225-449C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265100 | |||||||
| chr3:129265117 | G | A | 17 | a0001c0003t0001g0025 a0001c0003t0002g0011 a0001c0003t0002g0025 others(14): Show |
26 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1225-432G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265117 | |||||||
| chr3:129265315 | T | C | 63 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(60): Show |
101 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1225-234T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265315 | |||||||
| chr3:129265335 | A | G | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1225-214A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265335 | |||||||
| chr3:129265497 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1225-52A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 13/23 | chr3 | 129265497 | |||||||
| chr3:129265891 | G | A | 2 | a0001c0012t0002g0089 a0001c0013t0002g0088 |
2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1468+99G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129265891 | |||||||
| chr3:129265974 | GT | G | 8 | a0002c0005t0001g0049 a0002c0005t0002g0010 a0002c0005t0002g0014 others(5): Show |
14 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1468+186delT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr3 | 129265974 | ||||||
| chr3:129266221 | C | T | 20 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(17): Show |
30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.1468+429C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266221 | |||||||
| chr3:129266222 | G | A | 1 | a0001c0013t0002g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1468+430G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266222 | |||||||
| chr3:129266237 | C | T | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1468+445C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266237 | |||||||
| chr3:129266315 | G | A | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1468+523G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266315 | |||||||
| chr3:129266320 | G | T | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1468+528G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266320 | |||||||
| chr3:129266490 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1469-534G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266490 | |||||||
| chr3:129266536 | T | G | 1 | a0001c0003t0003g0030 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1469-488T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266536 | |||||||
| chr3:129266659 | T | A | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1469-365T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266659 | |||||||
| chr3:129266719 | T | G | 2 | a0001c0012t0002g0089 a0001c0013t0002g0088 |
2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1469-305T>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266719 | |||||||
| chr3:129266738 | C | T | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1469-286C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266738 | |||||||
| chr3:129266804 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1469-220C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266804 | |||||||
| chr3:129266806 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1469-218C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266806 | |||||||
| chr3:129266838 | G | A | 2 | a0001c0002t0005g0075 a0001c0010t0005g0076 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1469-186G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266838 | |||||||
| chr3:129266849 | T | C | 40 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(37): Show |
65 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1469-175T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266849 | |||||||
| chr3:129266875 | C | T | 10 | a0001c0002t0001g0063 a0001c0002t0002g0027 a0001c0002t0002g0028 others(7): Show |
11 | HG00408.hp1 HG02056.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1469-149C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266875 | |||||||
| chr3:129266932 | T | A | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1469-92T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266932 | |||||||
| chr3:129266965 | G | A | 2 | a0001c0002t0005g0075 a0001c0010t0005g0076 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1469-59G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 14/23 | chr3 | 129266965 | |||||||
| chr3:129267169 | TA | T | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1544+71delA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267169 | |||||||
| chr3:129267236 | G | A | 1 | a0001c0003t0003g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1544+137G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267236 | |||||||
| chr3:129267317 | T | A | 1 | a0001c0001t0002g0142 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1544+218T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267317 | |||||||
| chr3:129267388 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1544+289A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267388 | |||||||
| chr3:129267423 | C | T | 1 | a0001c0010t0005g0076 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1544+324C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267423 | |||||||
| chr3:129267424 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1544+325G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267424 | |||||||
| chr3:129267438 | G | A | 1 | a0001c0003t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1544+339G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267438 | |||||||
| chr3:129267439 | C | G | 1 | a0001c0003t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1544+340C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267439 | |||||||
| chr3:129267830 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1545-107T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267830 | |||||||
| chr3:129267872 | A | C | 66 | a0001c0001t0002g0038 a0001c0001t0002g0118 a0001c0001t0002g0146 others(63): Show |
105 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1545-65A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 15/23 | chr3 | 129267872 | |||||||
| chr3:129268183 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1648+143G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | chr3 | 129268183 | |||||||
| chr3:129268231 | T | TGAATTGA others(3): Show |
1 | a0001c0006t0002g0073 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1648+193_1648+202d others(12): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr3 | 129268231 | ||||||
| chr3:129268241 | C | T | 1 | a0001c0004t0003g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1648+201C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | chr3 | 129268241 | |||||||
| chr3:129268260 | CTT | C | 3 | a0001c0003t0001g0025 a0001c0003t0002g0025 a0001c0003t0002g0053 |
3 | HG02109.hp2 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1648+222_1648+223d others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr3 | 129268260 | ||||||
| chr3:129268316 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0137 a0001c0001t0002g0008 |
7 | HG00609.hp1 HG01081.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1649-179C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | chr3 | 129268316 | |||||||
| chr3:129268347 | G | A | 24 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(21): Show |
34 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1649-148G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 16/23 | chr3 | 129268347 | |||||||
| chr3:129268826 | C | T | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1775-106C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 17/23 | chr3 | 129268826 | |||||||
| chr3:129268887 | G | A | 65 | a0001c0001t0002g0038 a0001c0001t0002g0146 a0001c0001t0002g0158 others(62): Show |
104 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1775-45G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 17/23 | chr3 | 129268887 | |||||||
| chr3:129269056 | T | A | 59 | a0001c0001t0002g0038 a0001c0001t0002g0146 a0001c0001t0002g0158 others(56): Show |
94 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1843+56T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269056 | |||||||
| chr3:129269202 | A | G | 59 | a0001c0001t0002g0038 a0001c0001t0002g0146 a0001c0001t0002g0158 others(56): Show |
94 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1843+202A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269202 | |||||||
| chr3:129269209 | G | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0130 a0001c0001t0001g0161 |
3 | HG03654.hp1 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1843+209G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269209 | |||||||
| chr3:129269287 | G | C | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1843+287G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269287 | |||||||
| chr3:129269332 | A | G | 4 | a0002c0005t0002g0010 a0002c0005t0002g0046 a0002c0005t0002g0047 others(1): Show |
8 | HG01069.hp1 HG01071.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1843+332A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269332 | |||||||
| chr3:129269382 | C | T | 21 | a0001c0001t0002g0038 a0001c0001t0002g0146 a0001c0001t0002g0158 others(18): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1843+382C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269382 | |||||||
| chr3:129269449 | G | A | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1843+449G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269449 | |||||||
| chr3:129269606 | C | T | 2 | a0001c0002t0005g0075 a0001c0010t0005g0076 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1843+606C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269606 | |||||||
| chr3:129269660 | T | C | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1843+660T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269660 | |||||||
| chr3:129269699 | C | T | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1843+699C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269699 | |||||||
| chr3:129269708 | A | G | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1843+708A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269708 | |||||||
| chr3:129269797 | T | C | 17 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(14): Show |
26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.1843+797T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269797 | |||||||
| chr3:129269853 | C | T | 1 | a0001c0003t0002g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1843+853C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269853 | |||||||
| chr3:129269968 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG00438.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1843+968C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269968 | |||||||
| chr3:129269969 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1843+969G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269969 | |||||||
| chr3:129269983 | C | T | 1 | a0001c0002t0002g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1843+983C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129269983 | |||||||
| chr3:129270060 | C | G | 1 | a0001c0009t0002g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1843+1060C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270060 | |||||||
| chr3:129270110 | C | A | 1 | a0001c0006t0002g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1843+1110C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270110 | |||||||
| chr3:129270116 | T | C | 1 | a0003c0008t0001g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1843+1116T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270116 | |||||||
| chr3:129270122 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1843+1122A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270122 | |||||||
| chr3:129270134 | C | A | 1 | a0001c0001t0007g0184 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1843+1134C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270134 | |||||||
| chr3:129270194 | A | G | 2 | a0001c0009t0002g0069 a0001c0009t0002g0070 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1843+1194A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270194 | |||||||
| chr3:129270278 | G | T | 17 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(14): Show |
26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.1843+1278G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270278 | |||||||
| chr3:129270388 | C | T | 2 | a0001c0009t0002g0069 a0001c0009t0002g0070 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1844-1379C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270388 | |||||||
| chr3:129270428 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1844-1339T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270428 | |||||||
| chr3:129270474 | C | A | 4 | a0001c0001t0004g0018 a0001c0001t0004g0098 a0001c0001t0004g0125 others(1): Show |
6 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1844-1293C>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270474 | |||||||
| chr3:129270618 | A | G | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1844-1149A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270618 | |||||||
| chr3:129270911 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1844-856A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129270911 | |||||||
| chr3:129270943 | TGTA | T | 17 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(14): Show |
26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.1844-819_1844-817d others(5): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr3 | 129270943 | ||||||
| chr3:129271239 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1844-528C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271239 | |||||||
| chr3:129271426 | C | T | 1 | a0001c0002t0002g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1844-341C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271426 | |||||||
| chr3:129271574 | A | G | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1844-193A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271574 | |||||||
| chr3:129271578 | G | A | 2 | a0001c0012t0002g0089 a0001c0013t0002g0088 |
2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1844-189G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271578 | |||||||
| chr3:129271629 | T | C | 1 | a0001c0003t0002g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1844-138T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 18/23 | chr3 | 129271629 | |||||||
| chr3:129272155 | T | C | 65 | a0001c0001t0002g0038 a0001c0001t0002g0146 a0001c0001t0002g0158 others(62): Show |
104 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1987-89T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 19/23 | chr3 | 129272155 | |||||||
| chr3:129272163 | A | C | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1987-81A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 19/23 | chr3 | 129272163 | |||||||
| chr3:129272193 | C | T | 2 | a0001c0009t0002g0069 a0001c0009t0002g0070 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1987-51C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 19/23 | chr3 | 129272193 | |||||||
| chr3:129272565 | CTCT | C | 4 | a0001c0002t0005g0075 a0001c0009t0002g0069 a0001c0009t0002g0070 others(1): Show |
4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158+155_2158+157d others(5): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr3 | 129272565 | ||||||
| chr3:129272577 | A | T | 1 | a0001c0002t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2158+162A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 20/23 | chr3 | 129272577 | |||||||
| chr3:129272578 | A | T | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2158+163A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 20/23 | chr3 | 129272578 | |||||||
| chr3:129273085 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2256+181C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273085 | |||||||
| chr3:129273104 | C | T | 17 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(14): Show |
26 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.2256+200C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273104 | |||||||
| chr3:129273163 | C | T | 2 | a0001c0001t0001g0120 a0005c0018t0001g0093 |
2 | HG02040.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2256+259C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273163 | |||||||
| chr3:129273204 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.2256+300G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273204 | |||||||
| chr3:129273284 | A | G | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2256+380A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273284 | |||||||
| chr3:129273315 | C | T | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2256+411C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273315 | |||||||
| chr3:129273316 | G | A | 3 | a0002c0005t0001g0049 a0002c0005t0002g0045 a0002c0005t0002g0048 |
3 | HG00280.hp2 HG01261.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2256+412G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273316 | |||||||
| chr3:129273357 | T | C | 20 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(17): Show |
30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.2256+453T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273357 | |||||||
| chr3:129273505 | T | C | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2256+601T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273505 | |||||||
| chr3:129273532 | A | G | 65 | a0001c0001t0002g0038 a0001c0001t0002g0146 a0001c0001t0002g0158 others(62): Show |
104 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.2256+628A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273532 | |||||||
| chr3:129273655 | A | C | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2256+751A>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273655 | |||||||
| chr3:129273881 | T | C | 4 | a0001c0002t0005g0075 a0001c0009t0002g0069 a0001c0009t0002g0070 others(1): Show |
4 | HG00642.hp2 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257-957T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273881 | |||||||
| chr3:129273980 | T | C | 24 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(21): Show |
34 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.2257-858T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129273980 | |||||||
| chr3:129274020 | G | A | 1 | a0001c0001t0002g0038 | 2 | HG01358.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2257-818G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274020 | |||||||
| chr3:129274104 | A | ATGACCCC others(214): Show |
1 | a0001c0001t0002g0112 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2257-731_2257-511d others(223): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr3 | 129274104 | ||||||
| chr3:129274161 | C | G | 1 | a0001c0011t0002g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2257-677C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274161 | |||||||
| chr3:129274186 | G | GA | 8 | a0001c0001t0002g0007 a0001c0001t0002g0043 a0001c0001t0002g0104 others(5): Show |
16 | HG00639.hp2 HG01123.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.2257-640dupA | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr3 | 129274186 | ||||||
| chr3:129274199 | G | A | 37 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0002g0005 others(34): Show |
62 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2257-639G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274199 | |||||||
| chr3:129274628 | C | T | 20 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(17): Show |
30 | HG00408.hp1 HG00544.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.2257-210C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274628 | |||||||
| chr3:129274803 | A | G | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2257-35A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274803 | |||||||
| chr3:129274816 | A | T | 1 | a0001c0006t0002g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2257-22A>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 21/23 | chr3 | 129274816 | |||||||
| chr3:129275035 | T | C | 1 | a0001c0002t0005g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2395+59T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 22/23 | chr3 | 129275035 | |||||||
| chr3:129275040 | G | A | 2 | a0001c0009t0002g0069 a0001c0009t0002g0070 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2395+64G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 22/23 | chr3 | 129275040 | |||||||
| chr3:129275359 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2494+67C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275359 | |||||||
| chr3:129275532 | G | A | 14 | a0001c0003t0003g0009 a0001c0003t0003g0030 a0001c0003t0003g0031 others(11): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2494+240G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275532 | |||||||
| chr3:129275564 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2494+272C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275564 | |||||||
| chr3:129275667 | A | G | 2 | a0001c0009t0002g0069 a0001c0009t0002g0070 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2494+375A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275667 | |||||||
| chr3:129275790 | C | G | 1 | a0001c0001t0002g0112 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2494+498C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275790 | |||||||
| chr3:129275862 | T | C | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2494+570T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275862 | |||||||
| chr3:129275967 | C | T | 2 | a0001c0002t0005g0075 a0001c0010t0005g0076 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2494+675C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275967 | |||||||
| chr3:129275968 | G | A | 1 | a0001c0002t0002g0064 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2494+676G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129275968 | |||||||
| chr3:129275971 | T | TAC | 7 | a0001c0001t0001g0032 a0001c0001t0001g0100 a0001c0001t0001g0101 others(4): Show |
7 | HG01934.hp1 HG02145.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.2494+705_2494+706d others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | ||||||
| chr3:129275971 | TAC | T | 9 | a0001c0001t0001g0091 a0001c0001t0001g0182 a0001c0001t0002g0158 others(6): Show |
9 | HG01891.hp2 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2494+705_2494+706d others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | ||||||
| chr3:129275971 | TACAC | T | 27 | a0001c0001t0001g0178 a0001c0001t0002g0038 a0001c0001t0002g0146 others(24): Show |
41 | HG00280.hp2 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+703_2494+706d others(6): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | ||||||
| chr3:129275971 | TACACAC | T | 32 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(29): Show |
56 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2494+701_2494+706d others(8): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | ||||||
| chr3:129275971 | TACACACA others(1): Show |
T | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2494+699_2494+706d others(10): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129275971 | ||||||
| chr3:129276099 | C | T | 21 | a0001c0001t0002g0038 a0001c0001t0002g0146 a0001c0001t0002g0158 others(18): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2494+807C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276099 | |||||||
| chr3:129276234 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2494+942T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276234 | |||||||
| chr3:129276505 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2495-789T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276505 | |||||||
| chr3:129276530 | T | A | 1 | a0002c0005t0002g0010 | 4 | HG01069.hp1 HG01071.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-764T>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276530 | |||||||
| chr3:129276542 | C | T | 1 | a0001c0002t0002g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2495-752C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276542 | |||||||
| chr3:129276687 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2495-607A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276687 | |||||||
| chr3:129276698 | G | C | 6 | a0001c0006t0002g0012 a0001c0006t0002g0029 a0001c0006t0002g0072 others(3): Show |
10 | HG01123.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2495-596G>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276698 | |||||||
| chr3:129276760 | T | C | 2 | a0001c0012t0002g0089 a0001c0013t0002g0088 |
2 | HG01496.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2495-534T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276760 | |||||||
| chr3:129276779 | A | G | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2495-515A>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276779 | |||||||
| chr3:129276793 | G | A | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2495-501G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276793 | |||||||
| chr3:129276823 | C | CT | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
120 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2495-453dupT | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129276823 | ||||||
| chr3:129276823 | C | CTT | 21 | a0001c0001t0002g0158 a0001c0001t0002g0186 a0001c0002t0001g0063 others(18): Show |
30 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.2495-454_2495-453d others(4): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129276823 | ||||||
| chr3:129276823 | C | CTTTT | 12 | a0001c0002t0001g0077 a0001c0003t0003g0009 a0001c0003t0003g0030 others(9): Show |
27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2495-456_2495-453d others(6): Show |
COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr3 | 129276823 | ||||||
| chr3:129276846 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2495-448C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276846 | |||||||
| chr3:129276940 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2495-354C>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276940 | |||||||
| chr3:129276955 | C | G | 21 | a0001c0001t0002g0038 a0001c0001t0002g0146 a0001c0001t0002g0158 others(18): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2495-339C>G | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276955 | |||||||
| chr3:129276970 | T | C | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2495-324T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129276970 | |||||||
| chr3:129277039 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2495-255G>T | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129277039 | |||||||
| chr3:129277064 | T | C | 38 | a0001c0002t0001g0063 a0001c0002t0001g0067 a0001c0002t0001g0077 others(35): Show |
63 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2495-230T>C | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129277064 | |||||||
| chr3:129277185 | G | A | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
3 | HG02922.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2495-109G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129277185 | |||||||
| chr3:129277262 | G | A | 1 | a0001c0002t0005g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2495-32G>A | COPG1 | ENSG00000181789.14 | transcript | ENST00000314797.10 | protein_coding | 23/23 | chr3 | 129277262 |