Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25839 |
| ensemblid | ENSG00000103051.21 |
| hgncid | 18620 |
| symbol | COG4 |
| name | component of oligomeric golgi complex 4 |
| refseq_nuc | NM_015386.3 |
| refseq_prot | NP_056201.2 |
| ensembl_nuc | ENST00000323786.10 |
| ensembl_prot | ENSP00000315775.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 70480571 |
| end | 70523554 |
| strand | - |
| ver | v1.2 |
| region | chr16:70480571-70523554 |
| region5000 | chr16:70475571-70528554 |
| regionname0 | COG4_chr16_70480571_70523554 |
| regionname5000 | COG4_chr16_70475571_70528554 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 789 | 336 | 74 | 61 | 149 | 14 | 37 | 111 | COG4_chr16_70475571_70528554 | COG4 | MGTKM others(784): Show |
chr16 | 70475571 | 70528554 |
| a0002 | 1/0 | 789 | 13 | 1 | 9 | 0 | 1 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | MGTKM others(784): Show |
chr16 | 70475571 | 70528554 |
| a0003 | 0/0 | 789 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | MGTKM others(784): Show |
chr16 | 70475571 | 70528554 |
| a0004 | 0/0 | 789 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | MGTKM others(784): Show |
chr16 | 70475571 | 70528554 |
| a0005 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | MGTKM others(784): Show |
chr16 | 70475571 | 70528554 |
| a0006 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | MGTKM others(784): Show |
chr16 | 70475571 | 70528554 |
| a0007 | 0/0 | 789 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | MGTKM others(784): Show |
chr16 | 70475571 | 70528554 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2367 | 143 | 15 | 35 | 61 | 9 | 23 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0001c0002 | 0/1 | 2367 | 110 | 30 | 20 | 47 | 3 | 9 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0001c0003 | 0/0 | 2367 | 66 | 27 | 3 | 33 | 0 | 3 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0001c0005 | 0/0 | 2367 | 7 | 0 | 0 | 7 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0001c0006 | 0/0 | 2367 | 2 | 0 | 0 | 0 | 2 | 0 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0001c0007 | 0/0 | 2367 | 2 | 0 | 2 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0001c0008 | 0/0 | 2367 | 2 | 1 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0001c0009 | 0/0 | 2367 | 2 | 0 | 0 | 0 | 0 | 2 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0001c0013 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0001c0014 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0002c0004 | 1/0 | 2367 | 13 | 1 | 9 | 0 | 1 | 1 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0003c0012 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0004c0016 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0005c0010 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0006c0015 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 | ||
| a0007c0011 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | ATGGG others(2362): Show |
chr16 | 70475571 | 70528554 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2820 | 122 | 13 | 31 | 49 | 8 | 21 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0001t0002 | 0/0 | 2820 | 9 | 2 | 4 | 0 | 1 | 2 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0001t0003 | 0/0 | 2820 | 12 | 0 | 0 | 12 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0002t0001 | 0/0 | 2820 | 8 | 5 | 3 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0002t0002 | 0/1 | 2820 | 98 | 21 | 17 | 47 | 3 | 9 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0002t0004 | 0/0 | 2820 | 4 | 4 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0003t0001 | 0/0 | 2820 | 30 | 23 | 2 | 3 | 0 | 2 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0003t0002 | 0/0 | 2820 | 32 | 0 | 1 | 30 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0003t0004 | 0/0 | 2820 | 3 | 3 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0003t0005 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0005t0001 | 0/0 | 2820 | 7 | 0 | 0 | 7 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0006t0002 | 0/0 | 2820 | 2 | 0 | 0 | 0 | 2 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0007t0001 | 0/0 | 2820 | 2 | 0 | 2 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0008t0001 | 0/0 | 2820 | 2 | 1 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0009t0001 | 0/0 | 2820 | 2 | 0 | 0 | 0 | 0 | 2 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0013t0001 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0001c0014t0001 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0002c0004t0001 | 1/0 | 2820 | 13 | 1 | 9 | 0 | 1 | 1 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0003c0012t0001 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0004c0016t0001 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0005c0010t0004 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0006c0015t0001 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| a0007c0011t0001 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | GGAAG others(2815): Show |
chr16 | 70475571 | 70528554 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0321 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0002t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0003t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0005t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0006t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0006t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0007t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0007t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0008t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0008t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0009t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0009t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0013t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0001c0014t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0001 | 1/0 | 4 | 0 | 2 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0002c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0003c0012t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0004c0016t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0005c0010t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0006c0015t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| a0007c0011t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | GBR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00099 | hp2 | a0002 | c0004 | t0001 | g0001 | EUR | GBR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0284 | EUR | FIN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0299 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0274 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0302 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0266 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0314 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0225 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00642 | hp2 | a0002 | c0004 | t0001 | g0238 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0277 | EAS | CHS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0249 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0219 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0271 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0256 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01081 | hp2 | a0002 | c0004 | t0001 | g0001 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0279 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01099 | hp2 | a0002 | c0004 | t0001 | g0235 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01106 | hp1 | a0001 | c0008 | t0001 | g0340 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0337 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0263 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0335 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0336 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0220 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0269 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0234 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0038 | EUR | IBS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0330 | EUR | IBS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0193 | EUR | IBS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01516 | hp2 | a0001 | c0006 | t0002 | g0257 | EUR | IBS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01517 | hp2 | a0001 | c0006 | t0002 | g0215 | EUR | IBS | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0133 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01928 | hp1 | a0002 | c0004 | t0001 | g0241 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01928 | hp2 | a0001 | c0007 | t0001 | g0163 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01934 | hp2 | a0002 | c0004 | t0001 | g0239 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01952 | hp1 | a0001 | c0003 | t0002 | g0035 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01975 | hp2 | a0002 | c0004 | t0001 | g0237 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01993 | hp1 | a0002 | c0004 | t0001 | g0236 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0280 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0275 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0252 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02040 | hp2 | a0001 | c0003 | t0002 | g0300 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0290 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0268 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0083 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02165 | hp1 | a0001 | c0003 | t0002 | g0247 | EAS | CDX | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0135 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02273 | hp2 | a0002 | c0004 | t0001 | g0001 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02300 | hp2 | a0001 | c0007 | t0001 | g0207 | AMR | PEL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0316 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02523 | hp1 | a0001 | c0005 | t0001 | g0170 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0051 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0086 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02683 | hp1 | a0003 | c0012 | t0001 | g0164 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02698 | hp1 | a0004 | c0016 | t0001 | g0343 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0319 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02723 | hp1 | a0001 | c0003 | t0004 | g0134 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0341 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0332 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0244 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0132 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0261 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02895 | hp1 | a0001 | c0008 | t0001 | g0339 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02896 | hp2 | a0001 | c0003 | t0005 | g0125 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0124 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0128 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03098 | hp1 | a0001 | c0013 | t0001 | g0118 | AFR | MSL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | MSL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0123 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0313 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03486 | hp2 | a0001 | c0003 | t0004 | g0342 | AFR | MSL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03491 | hp2 | a0001 | c0003 | t0002 | g0250 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0254 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0136 | AFR | ESN | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0318 | AFR | GWD | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0126 | AFR | MSL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0304 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03669 | hp1 | a0001 | c0009 | t0001 | g0186 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0039 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03704 | hp2 | a0001 | c0009 | t0001 | g0178 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0283 | SAS | PJL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03831 | hp1 | a0002 | c0004 | t0001 | g0222 | SAS | BEB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0288 | SAS | BEB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0293 | EAS | CHB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18612 | hp2 | a0001 | c0005 | t0001 | g0169 | EAS | CHB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | CHB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | YRI | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | YRI | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18942 | hp1 | a0001 | c0005 | t0001 | g0189 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18947 | hp1 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0324 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18951 | hp2 | a0001 | c0005 | t0001 | g0172 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18953 | hp1 | a0001 | c0003 | t0002 | g0265 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0331 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18960 | hp1 | a0001 | c0005 | t0001 | g0322 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0246 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18969 | hp2 | a0001 | c0003 | t0002 | g0272 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0267 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18986 | hp2 | a0001 | c0003 | t0002 | g0223 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18990 | hp1 | a0001 | c0003 | t0002 | g0311 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18997 | hp2 | a0001 | c0005 | t0001 | g0208 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19003 | hp1 | a0001 | c0003 | t0002 | g0309 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19054 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0310 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19062 | hp1 | a0001 | c0003 | t0002 | g0080 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19062 | hp2 | a0001 | c0005 | t0001 | g0173 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19063 | hp1 | a0001 | c0003 | t0002 | g0262 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19066 | hp2 | a0001 | c0003 | t0002 | g0296 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19068 | hp1 | a0006 | c0015 | t0001 | g0327 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19077 | hp2 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19079 | hp1 | a0001 | c0003 | t0002 | g0312 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19084 | hp2 | a0001 | c0014 | t0001 | g0211 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0315 | EAS | JPT | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0303 | AFR | ASW | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ASW | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0037 | EUR | TSI | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20805 | hp2 | a0007 | c0011 | t0001 | g0248 | EUR | TSI | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | GIH | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | GIH | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0285 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0317 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0320 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0258 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0127 | AFR | ACB | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | MSL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0129 | AFR | MSL | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG06807 | hp1 | a0005 | c0010 | t0004 | g0338 | AFR | USA | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | USA | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20300 | hp1 | a0002 | c0004 | t0001 | g0240 | AFR | USA | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | USA | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | LWK | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | LWK | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0321 | REF | REF | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| homoSapiens | grch38p0 | a0002 | c0004 | t0001 | g0001 | REF | REF | COG4_chr16_70475571_70528554 | COG4 | chr16 | 70475571 | 70528554 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:70483921 | G | T | 1 | a0007 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1759C>A | p.Gln587Lys | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/19 | 1770/2820 | 1759/2370 | 587/789 | chr16 | 70483921 | |||
| chr16:70497344 | C | A | 1 | a0006 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1358G>T | p.Ser453Ile | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 11/19 | 1369/2820 | 1358/2370 | 453/789 | chr16 | 70497344 | |||
| chr16:70501019 | C | G | 1 | a0005 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1134G>C | p.Lys378Asn | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/19 | 1145/2820 | 1134/2370 | 378/789 | chr16 | 70501019 | |||
| chr16:70508436 | C | G | 1 | a0003 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1031G>C | p.Arg344Thr | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/19 | 1042/2820 | 1031/2370 | 344/789 | chr16 | 70508436 | |||
| chr16:70514394 | G | A | 6 | a0001 a0003 a0004 others(3): Show |
340 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(337): Show |
missense_variant | MODERATE | c.485C>T | p.Thr162Ile | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/19 | 496/2820 | 485/2370 | 162/789 | chr16 | 70514394 | |||
| chr16:70523428 | G | C | 1 | a0004 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.116C>G | p.Ser39Cys | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/19 | 127/2820 | 116/2370 | 39/789 | chr16 | 70523428 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:70481070 | G | C | 1 | a0001c0009 | 2 | HG03669.hp1 HG03704.hp2 |
synonymous_variant | LOW | c.2310C>G | p.Arg770Arg | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 19/19 | 2321/2820 | 2310/2370 | 770/789 | chr16 | 70481070 | |||
| chr16:70481133 | G | T | 1 | a0001c0014 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.2247C>A | p.Ile749Ile | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 19/19 | 2258/2820 | 2247/2370 | 749/789 | chr16 | 70481133 | |||
| chr16:70481431 | C | T | 2 | a0001c0008 a0001c0013 |
3 | HG01106.hp1 HG02895.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.2163G>A | p.Thr721Thr | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 18/19 | 2174/2820 | 2163/2370 | 721/789 | chr16 | 70481431 | |||
| chr16:70481452 | C | T | 6 | a0001c0002 a0001c0005 a0001c0006 others(3): Show |
122 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
synonymous_variant | LOW | c.2142G>A | p.Ser714Ser | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 18/19 | 2153/2820 | 2142/2370 | 714/789 | chr16 | 70481452 | |||
| chr16:70483958 | G | C | 1 | a0001c0006 | 2 | HG01516.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.1722C>G | p.Thr574Thr | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/19 | 1733/2820 | 1722/2370 | 574/789 | chr16 | 70483958 | |||
| chr16:70509336 | C | T | 1 | a0001c0007 | 2 | HG01928.hp2 HG02300.hp2 |
synonymous_variant | LOW | c.897G>A | p.Gly299Gly | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 7/19 | 908/2820 | 897/2370 | 299/789 | chr16 | 70509336 | |||
| chr16:70512331 | G | A | 10 | a0001c0001 a0001c0005 a0001c0007 others(7): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
synonymous_variant | LOW | c.646C>T | p.Leu216Leu | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/19 | 657/2820 | 646/2370 | 216/789 | chr16 | 70512331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:70480603 | A | C | 1 | a0001c0001t0003 | 12 | HG02027.hp2 NA18941.hp2 NA18949.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*407T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 19/19 | 407 | chr16 | 70480603 | ||||||
| chr16:70480688 | G | A | 3 | a0001c0002t0004 a0001c0003t0004 a0005c0010t0004 |
8 | HG01891.hp2 HG02723.hp1 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*322C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 19/19 | 322 | chr16 | 70480688 | ||||||
| chr16:70480846 | A | C | 1 | a0001c0003t0005 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*164T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 19/19 | 164 | chr16 | 70480846 | ||||||
| chr16:70480925 | A | C | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(1): Show |
140 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*85T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 19/19 | 85 | chr16 | 70480925 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:70481160 | T | C | 10 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2236-16A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 18/18 | chr16 | 70481160 | |||||||
| chr16:70481691 | T | TG | 6 | a0001c0001t0001g0121 a0001c0002t0002g0084 a0001c0002t0002g0244 others(3): Show |
6 | HG01175.hp2 HG01978.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2106+72dupC | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 17/18 | chr16 | 70481691 | |||||||
| chr16:70481694 | G | C | 3 | a0001c0002t0002g0081 a0001c0002t0002g0286 a0001c0002t0002g0287 |
3 | HG00544.hp2 NA18950.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2106+70C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 17/18 | chr16 | 70481694 | |||||||
| chr16:70481697 | T | G | 205 | a0001c0001t0001g0043 a0001c0001t0001g0057 a0001c0001t0001g0071 others(202): Show |
211 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.2106+67A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 17/18 | chr16 | 70481697 | |||||||
| chr16:70481707 | A | C | 1 | a0001c0002t0001g0328 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2106+57T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 17/18 | chr16 | 70481707 | |||||||
| chr16:70481713 | C | T | 1 | a0001c0002t0001g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2106+51G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 17/18 | chr16 | 70481713 | |||||||
| chr16:70481892 | G | A | 1 | a0001c0002t0002g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2005-27C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 16/18 | chr16 | 70481892 | |||||||
| chr16:70481961 | G | C | 1 | a0001c0002t0002g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2005-96C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 16/18 | chr16 | 70481961 | |||||||
| chr16:70482012 | A | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0203 a0001c0001t0001g0209 |
3 | HG00099.hp1 HG00741.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2004+80T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 16/18 | chr16 | 70482012 | |||||||
| chr16:70482081 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2004+11G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 16/18 | chr16 | 70482081 | |||||||
| chr16:70482206 | G | A | 107 | a0001c0001t0001g0057 a0001c0001t0001g0213 a0001c0002t0001g0335 others(104): Show |
111 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1921-31C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482206 | |||||||
| chr16:70482255 | G | A | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(4): Show |
7 | HG00735.hp2 HG01169.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1921-80C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482255 | |||||||
| chr16:70482325 | C | G | 46 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(43): Show |
48 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.1921-150G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482325 | |||||||
| chr16:70482396 | C | T | 1 | a0001c0002t0002g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1921-221G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482396 | |||||||
| chr16:70482413 | C | T | 5 | a0001c0003t0001g0316 a0001c0003t0001g0317 a0001c0003t0001g0318 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1921-238G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482413 | |||||||
| chr16:70482457 | G | GA | 7 | a0001c0001t0001g0052 a0001c0001t0001g0088 a0001c0001t0001g0326 others(4): Show |
7 | HG02135.hp2 HG02523.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1920+271dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482457 | |||||||
| chr16:70482468 | TTCTAAG | T | 11 | a0001c0002t0001g0130 a0001c0003t0001g0016 a0001c0003t0001g0017 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1920+255_1920+260d others(8): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482468 | |||||||
| chr16:70482487 | G | A | 13 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0131 others(10): Show |
13 | HG01433.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1920+242C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482487 | |||||||
| chr16:70482499 | G | C | 1 | a0002c0004t0001g0235 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1920+230C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482499 | |||||||
| chr16:70482575 | T | C | 12 | a0001c0002t0001g0034 a0001c0002t0001g0130 a0001c0003t0001g0016 others(9): Show |
12 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1920+154A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482575 | |||||||
| chr16:70482619 | G | A | 2 | a0001c0003t0001g0318 a0001c0003t0001g0319 |
2 | HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1920+110C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 15/18 | chr16 | 70482619 | |||||||
| chr16:70482842 | G | C | 1 | a0002c0004t0001g0235 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1828-21C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70482842 | |||||||
| chr16:70482884 | TTCTCCCC others(39): Show |
T | 1 | a0001c0001t0001g0056 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1828-109_1828-64de others(47): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70482884 | |||||||
| chr16:70482923 | T | C | 1 | a0001c0002t0002g0216 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1828-102A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70482923 | |||||||
| chr16:70483095 | T | TACCCATC others(66): Show |
1 | a0001c0003t0002g0309 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1828-275_1828-274i others(75): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483095 | |||||||
| chr16:70483095 | T | TACCCCAC others(63): Show |
1 | a0001c0003t0005g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1828-275_1828-274i others(72): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483095 | |||||||
| chr16:70483095 | T | TACCCCAT others(65): Show |
1 | a0001c0002t0002g0084 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1828-275_1828-274i others(74): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483095 | |||||||
| chr16:70483095 | T | TACCCCAT others(66): Show |
1 | a0001c0003t0002g0080 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1828-275_1828-274i others(75): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483095 | |||||||
| chr16:70483095 | T | TACCCCAT others(65): Show |
117 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0002t0001g0335 others(114): Show |
121 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1828-346_1828-275d others(74): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483095 | |||||||
| chr16:70483095 | T | TACCCCAT others(137): Show |
5 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0039 others(2): Show |
5 | HG01081.hp1 HG01109.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-275_1828-274i others(146): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483095 | |||||||
| chr16:70483095 | T | TACCCCAT others(161): Show |
2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1828-275_1828-274i others(170): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483095 | |||||||
| chr16:70483136 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1828-315C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483136 | |||||||
| chr16:70483173 | T | A | 40 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(37): Show |
42 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1828-352A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483173 | |||||||
| chr16:70483187 | T | TCCCCACC others(66): Show |
1 | a0001c0003t0001g0310 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1828-367_1828-366i others(75): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483187 | |||||||
| chr16:70483195 | C | A | 39 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(36): Show |
41 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.1828-374G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483195 | |||||||
| chr16:70483200 | C | CCT | 39 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(36): Show |
41 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.1828-381_1828-380d others(4): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483200 | |||||||
| chr16:70483206 | A | G | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-385T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483206 | |||||||
| chr16:70483206 | A | GTCTCCCC others(17): Show |
28 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(25): Show |
30 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1828-385delTinsGGA others(22): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483206 | |||||||
| chr16:70483241 | G | C | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-420C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483241 | |||||||
| chr16:70483243 | A | T | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-422T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483243 | |||||||
| chr16:70483248 | C | T | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-427G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483248 | |||||||
| chr16:70483249 | T | C | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-428A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483249 | |||||||
| chr16:70483263 | T | C | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-442A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483263 | |||||||
| chr16:70483267 | T | A | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-446A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483267 | |||||||
| chr16:70483271 | T | C | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-450A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483271 | |||||||
| chr16:70483273 | C | CTCATCTC others(39): Show |
11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-453_1828-452i others(48): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483273 | |||||||
| chr16:70483280 | C | T | 1 | a0001c0002t0002g0288 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1828-459G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483280 | |||||||
| chr16:70483287 | C | T | 40 | a0001c0001t0001g0147 a0001c0002t0001g0034 a0001c0002t0001g0072 others(37): Show |
42 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1828-466G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483287 | |||||||
| chr16:70483291 | A | T | 40 | a0001c0001t0001g0147 a0001c0002t0001g0034 a0001c0002t0001g0072 others(37): Show |
42 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1828-470T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483291 | |||||||
| chr16:70483295 | T | C | 29 | a0001c0001t0001g0147 a0001c0002t0002g0002 a0001c0002t0002g0008 others(26): Show |
31 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1828-474A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483295 | |||||||
| chr16:70483296 | C | T | 40 | a0001c0001t0001g0147 a0001c0002t0001g0034 a0001c0002t0001g0072 others(37): Show |
42 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1828-475G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483296 | |||||||
| chr16:70483302 | C | T | 1 | a0001c0003t0002g0309 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1828-481G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483302 | |||||||
| chr16:70483303 | T | C | 1 | a0001c0003t0002g0309 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1828-482A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483303 | |||||||
| chr16:70483311 | T | C | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-490A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483311 | |||||||
| chr16:70483311 | TCCCTTCC others(18): Show |
T | 1 | a0001c0003t0005g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1828-515_1828-491d others(27): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483311 | |||||||
| chr16:70483315 | T | A | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-494A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483315 | |||||||
| chr16:70483319 | C | T | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-498G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483319 | |||||||
| chr16:70483320 | T | C | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1828-499A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483320 | |||||||
| chr16:70483349 | G | A | 1 | a0001c0002t0002g0243 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1827+504C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483349 | |||||||
| chr16:70483422 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1827+431C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483422 | |||||||
| chr16:70483738 | G | A | 31 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(28): Show |
31 | HG00323.hp2 HG00544.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1827+115C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483738 | |||||||
| chr16:70483826 | C | T | 1 | a0001c0003t0001g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1827+27G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 14/18 | chr16 | 70483826 | |||||||
| chr16:70484109 | C | G | 4 | a0001c0002t0004g0124 a0001c0002t0004g0132 a0001c0002t0004g0133 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1711-140G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70484109 | |||||||
| chr16:70484298 | G | C | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(3): Show |
6 | HG00735.hp2 HG01169.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1711-329C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70484298 | |||||||
| chr16:70484505 | T | C | 1 | a0007c0011t0001g0248 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1711-536A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70484505 | |||||||
| chr16:70484554 | T | C | 9 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1711-585A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70484554 | |||||||
| chr16:70484679 | C | T | 1 | a0001c0005t0001g0170 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1711-710G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70484679 | |||||||
| chr16:70484770 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1711-801C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70484770 | |||||||
| chr16:70484804 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1711-835G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70484804 | |||||||
| chr16:70485031 | A | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(213): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1711-1062T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485031 | |||||||
| chr16:70485134 | C | G | 1 | a0001c0003t0002g0250 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1711-1165G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485134 | |||||||
| chr16:70485205 | C | CT | 48 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0062 others(45): Show |
50 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1711-1237dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485205 | |||||||
| chr16:70485205 | C | CTT | 6 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(3): Show |
6 | HG01243.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1711-1238_1711-123 others(6): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485205 | |||||||
| chr16:70485205 | CT | C | 7 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0001c0001t0002g0111 others(4): Show |
7 | HG01884.hp2 HG01975.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1711-1237delA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485205 | |||||||
| chr16:70485207 | T | C | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG01099.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1711-1238A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485207 | |||||||
| chr16:70485281 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1711-1312C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485281 | |||||||
| chr16:70485348 | C | T | 1 | a0001c0009t0001g0178 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1711-1379G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485348 | |||||||
| chr16:70485376 | C | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1711-1407G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485376 | |||||||
| chr16:70485486 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1711-1517C>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485486 | |||||||
| chr16:70485536 | G | A | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1711-1567C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485536 | |||||||
| chr16:70485587 | G | GT | 51 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0061 others(48): Show |
51 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1711-1619dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485587 | |||||||
| chr16:70485587 | G | T | 2 | a0001c0001t0001g0046 a0001c0002t0002g0224 |
2 | HG02300.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1711-1618C>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485587 | |||||||
| chr16:70485587 | GT | G | 24 | a0001c0001t0002g0111 a0001c0002t0002g0002 a0001c0002t0002g0008 others(21): Show |
26 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1711-1619delA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485587 | |||||||
| chr16:70485644 | G | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1711-1675C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485644 | |||||||
| chr16:70485691 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1711-1722G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485691 | |||||||
| chr16:70485735 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1711-1766T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485735 | |||||||
| chr16:70485826 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1711-1857G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485826 | |||||||
| chr16:70485868 | A | T | 1 | a0001c0003t0002g0080 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1711-1899T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485868 | |||||||
| chr16:70485880 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1711-1911G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485880 | |||||||
| chr16:70485897 | C | CT | 216 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(213): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1711-1929dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70485897 | |||||||
| chr16:70486068 | T | A | 1 | a0001c0003t0002g0080 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1711-2099A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486068 | |||||||
| chr16:70486099 | G | T | 10 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1711-2130C>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486099 | |||||||
| chr16:70486117 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1711-2148C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486117 | |||||||
| chr16:70486125 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(146): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1711-2156C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486125 | |||||||
| chr16:70486130 | T | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0183 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1711-2161A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486130 | |||||||
| chr16:70486163 | A | G | 3 | a0001c0002t0002g0012 a0001c0002t0002g0013 a0001c0002t0002g0015 |
3 | HG02486.hp2 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1711-2194T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486163 | |||||||
| chr16:70486296 | A | G | 1 | a0001c0002t0002g0278 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1711-2327T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486296 | |||||||
| chr16:70486376 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1711-2407G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486376 | |||||||
| chr16:70486462 | C | T | 1 | a0001c0002t0002g0305 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1711-2493G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486462 | |||||||
| chr16:70486576 | A | C | 211 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(208): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1711-2607T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486576 | |||||||
| chr16:70486617 | A | T | 19 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(16): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1711-2648T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486617 | |||||||
| chr16:70486619 | T | C | 13 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(10): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1711-2650A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486619 | |||||||
| chr16:70486714 | C | T | 1 | a0001c0002t0002g0291 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1711-2745G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486714 | |||||||
| chr16:70486763 | G | A | 6 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1711-2794C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486763 | |||||||
| chr16:70486793 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1711-2824T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486793 | |||||||
| chr16:70486802 | C | T | 2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1711-2833G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486802 | |||||||
| chr16:70486897 | A | G | 19 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(16): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1711-2928T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486897 | |||||||
| chr16:70486935 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0095 |
2 | NA18949.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1711-2966G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486935 | |||||||
| chr16:70486943 | C | T | 2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1711-2974G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486943 | |||||||
| chr16:70486951 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1711-2982G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486951 | |||||||
| chr16:70486995 | C | CA | 6 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0001g0209 others(3): Show |
6 | HG00099.hp1 HG01175.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1711-3027dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70486995 | |||||||
| chr16:70487163 | T | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1710+3167A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487163 | |||||||
| chr16:70487288 | A | T | 2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1710+3042T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487288 | |||||||
| chr16:70487289 | A | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1710+3041T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487289 | |||||||
| chr16:70487290 | T | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(206): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1710+3040A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487290 | |||||||
| chr16:70487291 | A | T | 7 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0001g0089 others(4): Show |
7 | HG00597.hp1 HG01346.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1710+3039T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487291 | |||||||
| chr16:70487292 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1710+3038T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487292 | |||||||
| chr16:70487296 | T | A | 5 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0232 others(2): Show |
5 | HG02523.hp1 NA18957.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1710+3034A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487296 | |||||||
| chr16:70487296 | T | TA | 6 | a0001c0002t0002g0081 a0001c0002t0002g0082 a0001c0002t0002g0291 others(3): Show |
6 | HG02015.hp1 NA18949.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.1710+3033dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487296 | |||||||
| chr16:70487297 | A | T | 2 | a0001c0002t0002g0270 a0001c0005t0001g0170 |
2 | HG02523.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1710+3033T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487297 | |||||||
| chr16:70487302 | A | T | 2 | a0001c0002t0002g0078 a0001c0002t0002g0256 |
2 | HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1710+3028T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487302 | |||||||
| chr16:70487388 | G | A | 1 | a0001c0003t0004g0341 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1710+2942C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487388 | |||||||
| chr16:70487403 | C | G | 1 | a0005c0010t0004g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1710+2927G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487403 | |||||||
| chr16:70487532 | A | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1710+2798T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487532 | |||||||
| chr16:70487536 | C | G | 1 | a0001c0005t0001g0322 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1710+2794G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487536 | |||||||
| chr16:70487561 | G | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1710+2769C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487561 | |||||||
| chr16:70487734 | C | T | 2 | a0001c0002t0002g0253 a0001c0002t0002g0260 |
2 | NA18952.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1710+2596G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487734 | |||||||
| chr16:70487848 | G | A | 39 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(36): Show |
39 | HG00597.hp1 HG00733.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1710+2482C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487848 | |||||||
| chr16:70487927 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1710+2403G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70487927 | |||||||
| chr16:70488071 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0049 |
2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1710+2259G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70488071 | |||||||
| chr16:70488115 | A | T | 2 | a0001c0001t0002g0111 a0001c0001t0002g0112 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1710+2215T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70488115 | |||||||
| chr16:70488194 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1710+2136G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70488194 | |||||||
| chr16:70488881 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1710+1449T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70488881 | |||||||
| chr16:70489057 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1710+1273T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489057 | |||||||
| chr16:70489107 | T | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1710+1223A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489107 | |||||||
| chr16:70489220 | A | AT | 13 | a0001c0001t0001g0075 a0001c0001t0001g0151 a0001c0001t0001g0206 others(10): Show |
13 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1710+1109dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489220 | |||||||
| chr16:70489220 | AT | A | 11 | a0001c0001t0001g0054 a0001c0001t0003g0074 a0001c0002t0002g0230 others(8): Show |
11 | HG01993.hp2 HG03471.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.1710+1109delA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489220 | |||||||
| chr16:70489362 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1710+968G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489362 | |||||||
| chr16:70489418 | C | T | 2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1710+912G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489418 | |||||||
| chr16:70489501 | G | A | 1 | a0001c0013t0001g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1710+829C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489501 | |||||||
| chr16:70489529 | T | TA | 7 | a0001c0001t0001g0167 a0001c0002t0002g0244 a0001c0003t0001g0316 others(4): Show |
7 | HG01071.hp1 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1710+800dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489529 | |||||||
| chr16:70489529 | TA | T | 34 | a0001c0001t0001g0052 a0001c0001t0001g0145 a0001c0001t0001g0171 others(31): Show |
36 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1710+800delT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489529 | |||||||
| chr16:70489543 | G | GT | 13 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0069 others(10): Show |
13 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.1710+786dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489543 | |||||||
| chr16:70489645 | A | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(208): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1710+685T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489645 | |||||||
| chr16:70489731 | T | C | 16 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(13): Show |
18 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1710+599A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489731 | |||||||
| chr16:70489761 | G | GA | 157 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1710+568_1710+569i others(3): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489761 | |||||||
| chr16:70489804 | A | G | 2 | a0001c0003t0001g0318 a0001c0003t0001g0319 |
2 | HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1710+526T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70489804 | |||||||
| chr16:70490313 | G | C | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0137 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1710+17C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 13/18 | chr16 | 70490313 | |||||||
| chr16:70490518 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1648-126G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70490518 | |||||||
| chr16:70490817 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1648-425C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70490817 | |||||||
| chr16:70490957 | C | T | 1 | a0001c0002t0002g0037 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1648-565G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70490957 | |||||||
| chr16:70491089 | A | T | 17 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(14): Show |
19 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1648-697T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491089 | |||||||
| chr16:70491174 | C | T | 6 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1648-782G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491174 | |||||||
| chr16:70491212 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1648-820G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491212 | |||||||
| chr16:70491275 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1648-883T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491275 | |||||||
| chr16:70491343 | T | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1648-951A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491343 | |||||||
| chr16:70491390 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1648-998C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491390 | |||||||
| chr16:70491454 | G | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1648-1062C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491454 | |||||||
| chr16:70491520 | C | CA | 234 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0042 others(231): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1648-1129dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491520 | |||||||
| chr16:70491520 | C | CAA | 61 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0054 others(58): Show |
61 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1648-1130_1648-112 others(6): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491520 | |||||||
| chr16:70491520 | C | CAAA | 20 | a0001c0001t0002g0191 a0001c0001t0002g0193 a0001c0001t0002g0194 others(17): Show |
22 | HG00639.hp1 HG01243.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1648-1131_1648-112 others(7): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491520 | |||||||
| chr16:70491520 | C | CAAAA | 13 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0002t0002g0012 others(10): Show |
13 | HG01123.hp2 HG01934.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1648-1132_1648-112 others(8): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491520 | |||||||
| chr16:70491556 | A | G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(205): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1648-1164T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491556 | |||||||
| chr16:70491591 | G | A | 1 | a0001c0002t0002g0298 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1648-1199C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491591 | |||||||
| chr16:70491657 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1648-1265A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491657 | |||||||
| chr16:70491717 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1648-1325C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491717 | |||||||
| chr16:70491824 | C | CA | 24 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0069 others(21): Show |
24 | HG00438.hp1 HG00597.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1648-1433dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491824 | |||||||
| chr16:70491824 | CA | C | 40 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0065 others(37): Show |
40 | HG00558.hp1 HG01109.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.1648-1433delT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491824 | |||||||
| chr16:70491824 | CAAAA | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1648-1436_1648-143 others(8): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70491824 | |||||||
| chr16:70492208 | T | C | 2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1648-1816A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492208 | |||||||
| chr16:70492333 | T | C | 17 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(14): Show |
19 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1648-1941A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492333 | |||||||
| chr16:70492369 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1648-1977T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492369 | |||||||
| chr16:70492384 | C | T | 1 | a0005c0010t0004g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1648-1992G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492384 | |||||||
| chr16:70492424 | C | T | 4 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0183 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648-2032G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492424 | |||||||
| chr16:70492430 | G | A | 4 | a0001c0002t0004g0124 a0001c0002t0004g0132 a0001c0002t0004g0133 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648-2038C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492430 | |||||||
| chr16:70492507 | C | T | 5 | a0001c0001t0001g0138 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1648-2115G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492507 | |||||||
| chr16:70492517 | C | T | 1 | a0001c0008t0001g0340 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1648-2125G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492517 | |||||||
| chr16:70492588 | C | A | 1 | a0001c0003t0001g0271 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1648-2196G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492588 | |||||||
| chr16:70492593 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1648-2201T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492593 | |||||||
| chr16:70492622 | T | C | 5 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648-2230A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492622 | |||||||
| chr16:70492781 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1648-2389C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492781 | |||||||
| chr16:70492894 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1648-2502G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492894 | |||||||
| chr16:70492950 | C | T | 3 | a0001c0005t0001g0169 a0001c0005t0001g0172 a0001c0005t0001g0173 |
3 | NA18612.hp2 NA18951.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1648-2558G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492950 | |||||||
| chr16:70492986 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1648-2594G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70492986 | |||||||
| chr16:70493042 | C | T | 193 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(190): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1648-2650G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493042 | |||||||
| chr16:70493121 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1648-2729G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493121 | |||||||
| chr16:70493122 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1648-2730T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493122 | |||||||
| chr16:70493154 | C | T | 6 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1648-2762G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493154 | |||||||
| chr16:70493351 | T | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1647+2915A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493351 | |||||||
| chr16:70493402 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0168 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1647+2864T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493402 | |||||||
| chr16:70493551 | A | G | 1 | a0001c0014t0001g0211 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1647+2715T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493551 | |||||||
| chr16:70493813 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1647+2453A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493813 | |||||||
| chr16:70493887 | T | C | 1 | a0001c0001t0003g0094 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1647+2379A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493887 | |||||||
| chr16:70493926 | G | A | 1 | a0001c0002t0002g0294 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1647+2340C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70493926 | |||||||
| chr16:70494146 | C | G | 1 | a0001c0002t0001g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1647+2120G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494146 | |||||||
| chr16:70494318 | A | G | 1 | a0001c0002t0001g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1647+1948T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494318 | |||||||
| chr16:70494321 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1647+1945G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494321 | |||||||
| chr16:70494351 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1647+1915G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494351 | |||||||
| chr16:70494461 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1647+1805C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494461 | |||||||
| chr16:70494537 | C | A | 1 | a0001c0001t0001g0088 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1647+1729G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494537 | |||||||
| chr16:70494588 | G | A | 1 | a0001c0003t0001g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1647+1678C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494588 | |||||||
| chr16:70494614 | T | C | 1 | a0001c0002t0002g0308 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1647+1652A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494614 | |||||||
| chr16:70494702 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1647+1564G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494702 | |||||||
| chr16:70494743 | T | TA | 6 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647+1522dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494743 | |||||||
| chr16:70494842 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1647+1424G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494842 | |||||||
| chr16:70494971 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0198 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1647+1295T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70494971 | |||||||
| chr16:70495088 | A | G | 3 | a0001c0005t0001g0169 a0001c0005t0001g0172 a0001c0005t0001g0173 |
3 | NA18612.hp2 NA18951.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1647+1178T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495088 | |||||||
| chr16:70495228 | T | TA | 6 | a0001c0001t0001g0069 a0001c0002t0002g0038 a0001c0002t0002g0295 others(3): Show |
6 | HG00597.hp1 HG01515.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647+1037dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495228 | |||||||
| chr16:70495228 | TA | T | 9 | a0001c0001t0001g0180 a0001c0001t0001g0333 a0001c0001t0002g0111 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1647+1037delT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495228 | |||||||
| chr16:70495228 | TAAA | T | 10 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1647+1035_1647+103 others(7): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495228 | |||||||
| chr16:70495321 | T | C | 1 | a0001c0002t0002g0220 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1647+945A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495321 | |||||||
| chr16:70495390 | T | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1647+876A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495390 | |||||||
| chr16:70495397 | C | CA | 149 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(146): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1647+868dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495397 | |||||||
| chr16:70495397 | C | CAAAAAAA others(12): Show |
7 | a0001c0003t0001g0016 a0001c0003t0001g0018 a0001c0003t0001g0019 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1647+868_1647+869i others(21): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495397 | |||||||
| chr16:70495397 | C | CAAAAAAA others(13): Show |
3 | a0001c0003t0001g0017 a0001c0003t0001g0024 a0001c0003t0001g0025 |
3 | HG02886.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1647+868_1647+869i others(22): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495397 | |||||||
| chr16:70495606 | G | A | 1 | a0001c0002t0001g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1647+660C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495606 | |||||||
| chr16:70495607 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1647+659G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495607 | |||||||
| chr16:70495871 | C | T | 6 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647+395G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70495871 | |||||||
| chr16:70496189 | A | G | 1 | a0001c0003t0002g0309 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1647+77T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70496189 | |||||||
| chr16:70496217 | T | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0183 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647+49A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 12/18 | chr16 | 70496217 | |||||||
| chr16:70496456 | A | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(188): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1482-25T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 11/18 | chr16 | 70496456 | |||||||
| chr16:70496481 | C | T | 16 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(13): Show |
18 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1482-50G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 11/18 | chr16 | 70496481 | |||||||
| chr16:70496532 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1482-101G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 11/18 | chr16 | 70496532 | |||||||
| chr16:70496644 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1482-213C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 11/18 | chr16 | 70496644 | |||||||
| chr16:70496751 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1482-320C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 11/18 | chr16 | 70496751 | |||||||
| chr16:70496799 | G | A | 1 | a0001c0002t0002g0253 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1482-368C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 11/18 | chr16 | 70496799 | |||||||
| chr16:70496869 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1481+352A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 11/18 | chr16 | 70496869 | |||||||
| chr16:70497463 | C | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(152): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1315-76G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 10/18 | chr16 | 70497463 | |||||||
| chr16:70497471 | C | G | 1 | a0001c0002t0002g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1315-84G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 10/18 | chr16 | 70497471 | |||||||
| chr16:70497573 | AATATTTC others(17): Show |
A | 1 | a0001c0002t0002g0217 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1315-210_1315-187d others(26): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 10/18 | chr16 | 70497573 | |||||||
| chr16:70497614 | G | A | 3 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0006c0015t0001g0327 |
3 | HG02129.hp1 HG02135.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1315-227C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 10/18 | chr16 | 70497614 | |||||||
| chr16:70497683 | G | C | 1 | a0001c0003t0001g0129 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1314+254C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 10/18 | chr16 | 70497683 | |||||||
| chr16:70497740 | G | A | 2 | a0001c0001t0002g0111 a0001c0001t0002g0112 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1314+197C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 10/18 | chr16 | 70497740 | |||||||
| chr16:70497851 | T | G | 250 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(247): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1314+86A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 10/18 | chr16 | 70497851 | |||||||
| chr16:70497883 | C | T | 1 | a0001c0003t0005g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1314+54G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 10/18 | chr16 | 70497883 | |||||||
| chr16:70498270 | CTA | C | 10 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1196-217_1196-216d others(4): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498270 | |||||||
| chr16:70498351 | G | C | 1 | a0001c0013t0001g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1196-296C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498351 | |||||||
| chr16:70498406 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1196-351C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498406 | |||||||
| chr16:70498485 | C | T | 10 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1196-430G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498485 | |||||||
| chr16:70498550 | C | T | 19 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(16): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1196-495G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498550 | |||||||
| chr16:70498553 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1196-498C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498553 | |||||||
| chr16:70498577 | A | G | 10 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1196-522T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498577 | |||||||
| chr16:70498606 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1196-551A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498606 | |||||||
| chr16:70498731 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1196-676T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498731 | |||||||
| chr16:70498775 | A | G | 2 | a0001c0009t0001g0178 a0001c0009t0001g0186 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1196-720T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498775 | |||||||
| chr16:70498983 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1196-928C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498983 | |||||||
| chr16:70498985 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(245): Show |
252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1196-930G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498985 | |||||||
| chr16:70498987 | C | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1196-932G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70498987 | |||||||
| chr16:70499131 | G | A | 1 | a0001c0003t0002g0035 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1196-1076C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70499131 | |||||||
| chr16:70499667 | T | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0117 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1195+1291A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70499667 | |||||||
| chr16:70499809 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0202 |
2 | HG01496.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1195+1149C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70499809 | |||||||
| chr16:70499859 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1195+1099T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70499859 | |||||||
| chr16:70499903 | G | A | 1 | a0001c0002t0002g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1195+1055C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70499903 | |||||||
| chr16:70499926 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1195+1032G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70499926 | |||||||
| chr16:70499965 | A | T | 1 | a0001c0008t0001g0340 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1195+993T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70499965 | |||||||
| chr16:70499966 | T | A | 1 | a0001c0002t0002g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1195+992A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70499966 | |||||||
| chr16:70500265 | C | G | 1 | a0001c0003t0001g0109 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1195+693G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500265 | |||||||
| chr16:70500365 | C | CT | 20 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0137 others(17): Show |
20 | HG01175.hp2 HG01361.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1195+592dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500365 | |||||||
| chr16:70500365 | C | CTTTTTTT others(1): Show |
22 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(19): Show |
24 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1195+585_1195+592d others(10): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500365 | |||||||
| chr16:70500365 | CT | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(153): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1195+592delA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500365 | |||||||
| chr16:70500365 | CTT | C | 7 | a0001c0001t0001g0054 a0001c0001t0001g0097 a0001c0001t0001g0104 others(4): Show |
7 | HG00733.hp2 HG01257.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195+591_1195+592d others(4): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500365 | |||||||
| chr16:70500365 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0107 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1195+580_1195+592d others(15): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500365 | |||||||
| chr16:70500385 | T | C | 2 | a0001c0001t0001g0174 a0003c0012t0001g0164 |
2 | HG01192.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1195+573A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500385 | |||||||
| chr16:70500560 | C | T | 2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1195+398G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500560 | |||||||
| chr16:70500928 | C | T | 1 | a0001c0002t0001g0328 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1195+30G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500928 | |||||||
| chr16:70500950 | G | A | 10 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1195+8C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 9/18 | chr16 | 70500950 | |||||||
| chr16:70501136 | T | C | 1 | a0001c0005t0001g0189 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1062-45A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501136 | |||||||
| chr16:70501216 | G | A | 1 | a0001c0002t0002g0039 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1062-125C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501216 | |||||||
| chr16:70501378 | G | C | 1 | a0001c0002t0002g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1062-287C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501378 | |||||||
| chr16:70501417 | G | A | 1 | a0001c0002t0002g0084 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1062-326C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501417 | |||||||
| chr16:70501454 | C | T | 11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0137 others(8): Show |
11 | HG01433.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1062-363G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501454 | |||||||
| chr16:70501515 | C | T | 1 | a0001c0001t0003g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1062-424G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501515 | |||||||
| chr16:70501590 | G | A | 1 | a0001c0002t0002g0313 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1062-499C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501590 | |||||||
| chr16:70501636 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1062-545C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501636 | |||||||
| chr16:70501818 | A | AT | 22 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0071 others(19): Show |
22 | HG00544.hp2 HG00642.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1062-728dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501818 | |||||||
| chr16:70501818 | AT | A | 28 | a0001c0001t0001g0061 a0001c0002t0002g0002 a0001c0002t0002g0008 others(25): Show |
30 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1062-728delA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501818 | |||||||
| chr16:70501915 | T | C | 1 | a0001c0003t0001g0051 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1062-824A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70501915 | |||||||
| chr16:70502054 | C | T | 1 | a0001c0002t0002g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1062-963G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502054 | |||||||
| chr16:70502059 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1062-968C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502059 | |||||||
| chr16:70502236 | C | T | 1 | a0001c0002t0002g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1062-1145G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502236 | |||||||
| chr16:70502280 | C | CA | 111 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0049 others(108): Show |
114 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1062-1190dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502280 | |||||||
| chr16:70502280 | C | CAA | 74 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-1191_1062-119 others(6): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502280 | |||||||
| chr16:70502280 | C | CAAA | 15 | a0001c0001t0001g0101 a0001c0001t0001g0138 a0001c0001t0001g0148 others(12): Show |
15 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1062-1192_1062-119 others(7): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502280 | |||||||
| chr16:70502280 | CA | C | 12 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(9): Show |
12 | HG00639.hp1 HG01257.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1062-1190delT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502280 | |||||||
| chr16:70502280 | CAAAAAAA others(1): Show |
C | 25 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(22): Show |
27 | HG01891.hp1 HG02280.hp1 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.1062-1197_1062-119 others(12): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502280 | |||||||
| chr16:70502316 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0171 |
2 | NA18942.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1062-1225G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502316 | |||||||
| chr16:70502445 | T | C | 1 | a0001c0003t0002g0277 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1062-1354A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502445 | |||||||
| chr16:70502525 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1062-1434G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502525 | |||||||
| chr16:70502526 | G | GA | 155 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(152): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1062-1436dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502526 | |||||||
| chr16:70502596 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1062-1505G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502596 | |||||||
| chr16:70502601 | T | TAAA | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1062-1513_1062-151 others(7): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502601 | |||||||
| chr16:70502857 | G | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0055 |
2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1062-1766C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502857 | |||||||
| chr16:70502933 | T | G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(205): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1062-1842A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70502933 | |||||||
| chr16:70503240 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1062-2149G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503240 | |||||||
| chr16:70503337 | C | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0144 a0001c0001t0001g0209 |
3 | HG00099.hp1 HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1062-2246G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503337 | |||||||
| chr16:70503426 | T | G | 210 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(207): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1062-2335A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503426 | |||||||
| chr16:70503438 | T | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1062-2347A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503438 | |||||||
| chr16:70503498 | C | T | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG00639.hp1 HG01123.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1062-2407G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503498 | |||||||
| chr16:70503537 | T | G | 9 | a0001c0002t0002g0082 a0001c0002t0002g0289 a0001c0002t0002g0291 others(6): Show |
9 | HG00544.hp1 HG02015.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1062-2446A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503537 | |||||||
| chr16:70503580 | TAACTCCT others(306): Show |
T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1062-2802_1062-249 others(4): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503580 | |||||||
| chr16:70503595 | C | CTTTTTTT others(1): Show |
15 | a0001c0002t0001g0072 a0001c0002t0001g0130 a0001c0002t0001g0131 others(12): Show |
15 | HG01891.hp2 HG02258.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062-2512_1062-250 others(12): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503595 | |||||||
| chr16:70503595 | CT | C | 7 | a0001c0003t0001g0316 a0001c0003t0001g0317 a0001c0003t0001g0318 others(4): Show |
7 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1062-2505delA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503595 | |||||||
| chr16:70503595 | CTTTTT | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(156): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1062-2509_1062-250 others(9): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503595 | |||||||
| chr16:70503784 | C | T | 1 | a0001c0002t0002g0229 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1062-2693G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503784 | |||||||
| chr16:70503841 | G | A | 1 | a0001c0003t0001g0129 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1062-2750C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503841 | |||||||
| chr16:70503889 | C | T | 13 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(10): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1062-2798G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70503889 | |||||||
| chr16:70504095 | C | T | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1062-3004G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504095 | |||||||
| chr16:70504119 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0190 |
2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1062-3028G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504119 | |||||||
| chr16:70504295 | T | A | 2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1062-3204A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504295 | |||||||
| chr16:70504515 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1062-3424C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504515 | |||||||
| chr16:70504578 | G | C | 1 | a0001c0003t0002g0312 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1062-3487C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504578 | |||||||
| chr16:70504609 | T | TA | 7 | a0001c0002t0002g0217 a0001c0003t0001g0316 a0001c0003t0001g0317 others(4): Show |
7 | HG02027.hp1 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1062-3519dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504609 | |||||||
| chr16:70504609 | T | TAAAAAAA others(3): Show |
11 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(8): Show |
11 | HG01433.hp2 HG01891.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1062-3528_1062-351 others(14): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504609 | |||||||
| chr16:70504609 | T | TAAAAAAA others(4): Show |
14 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1062-3529_1062-351 others(15): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504609 | |||||||
| chr16:70504609 | T | TAAAAAAA others(5): Show |
3 | a0001c0001t0002g0191 a0001c0002t0001g0131 a0001c0002t0001g0328 |
3 | HG01257.hp2 HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1062-3530_1062-351 others(16): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504609 | |||||||
| chr16:70504609 | T | TAAAAAAA others(6): Show |
4 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(1): Show |
4 | HG01516.hp1 HG01934.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062-3531_1062-351 others(17): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504609 | |||||||
| chr16:70504609 | T | TAAAAAAA others(7): Show |
2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG00639.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1062-3532_1062-351 others(18): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504609 | |||||||
| chr16:70504609 | T | TAAAAAAA others(10): Show |
2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1062-3535_1062-351 others(21): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504609 | |||||||
| chr16:70504609 | TAAAAAA | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1062-3524_1062-351 others(10): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504609 | |||||||
| chr16:70504678 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1062-3587T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504678 | |||||||
| chr16:70504682 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1062-3591G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504682 | |||||||
| chr16:70504797 | G | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(24): Show |
29 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.1061+3609C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504797 | |||||||
| chr16:70504908 | C | CA | 22 | a0001c0001t0002g0197 a0001c0002t0001g0328 a0001c0002t0002g0084 others(19): Show |
22 | HG00423.hp1 HG00558.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1061+3497dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504908 | |||||||
| chr16:70504908 | CA | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(162): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1061+3497delT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504908 | |||||||
| chr16:70504941 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1061+3465G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70504941 | |||||||
| chr16:70505197 | C | CT | 38 | a0001c0001t0001g0062 a0001c0001t0001g0116 a0001c0001t0001g0185 others(35): Show |
40 | HG00438.hp2 HG01243.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.1061+3208dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505197 | |||||||
| chr16:70505197 | CT | C | 7 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0199 others(4): Show |
7 | HG00673.hp2 HG01517.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1061+3208delA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505197 | |||||||
| chr16:70505228 | C | T | 28 | a0001c0001t0001g0176 a0001c0002t0002g0002 a0001c0002t0002g0008 others(25): Show |
30 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1061+3178G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505228 | |||||||
| chr16:70505290 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1061+3116G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505290 | |||||||
| chr16:70505299 | G | A | 2 | a0001c0002t0002g0303 a0001c0002t0002g0313 |
2 | HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1061+3107C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505299 | |||||||
| chr16:70505427 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1061+2979A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505427 | |||||||
| chr16:70505481 | C | T | 1 | a0003c0012t0001g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1061+2925G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505481 | |||||||
| chr16:70505482 | G | A | 19 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(16): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1061+2924C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505482 | |||||||
| chr16:70505553 | G | A | 1 | a0001c0005t0001g0322 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1061+2853C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505553 | |||||||
| chr16:70505778 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0190 |
2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1061+2628C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505778 | |||||||
| chr16:70505846 | G | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(212): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1061+2560C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505846 | |||||||
| chr16:70505922 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1061+2484T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505922 | |||||||
| chr16:70505923 | A | G | 1 | a0001c0003t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1061+2483T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70505923 | |||||||
| chr16:70506262 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1061+2144C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506262 | |||||||
| chr16:70506275 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1061+2131G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506275 | |||||||
| chr16:70506320 | G | A | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1061+2086C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506320 | |||||||
| chr16:70506357 | C | A | 1 | a0001c0013t0001g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1061+2049G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506357 | |||||||
| chr16:70506398 | G | A | 1 | a0001c0003t0001g0271 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1061+2008C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506398 | |||||||
| chr16:70506507 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1061+1899C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506507 | |||||||
| chr16:70506593 | C | CA | 57 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0092 others(54): Show |
58 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1061+1812dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAA | 55 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0076 others(52): Show |
55 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1061+1811_1061+181 others(6): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAAA | 59 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0043 others(56): Show |
62 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1061+1810_1061+181 others(7): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAAAA | 43 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0045 others(40): Show |
44 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1061+1809_1061+181 others(8): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAAAAA | 12 | a0001c0001t0001g0047 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
12 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1061+1808_1061+181 others(9): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAAAAAA | 7 | a0001c0002t0001g0072 a0001c0002t0002g0278 a0001c0003t0001g0067 others(4): Show |
7 | HG00544.hp1 HG01928.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1061+1807_1061+181 others(10): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAAAAAAA | 7 | a0001c0001t0001g0161 a0001c0003t0001g0126 a0001c0003t0001g0127 others(4): Show |
7 | HG00642.hp1 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1061+1806_1061+181 others(11): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0001g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1061+1803_1061+181 others(14): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1061+1802_1061+181 others(15): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAAAAAAA others(9): Show |
2 | a0001c0002t0004g0124 a0001c0002t0004g0132 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1061+1797_1061+181 others(20): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506593 | C | CAAAAAAA others(10): Show |
1 | a0001c0003t0004g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1061+1796_1061+181 others(21): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506593 | |||||||
| chr16:70506595 | AAAAAAAA others(16): Show |
A | 7 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(4): Show |
7 | HG00639.hp1 HG01123.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1061+1788_1061+181 others(27): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506595 | |||||||
| chr16:70506598 | AAAAAAAA others(13): Show |
A | 2 | a0001c0003t0002g0079 a0001c0003t0002g0247 |
2 | HG02165.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1061+1788_1061+180 others(24): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506598 | |||||||
| chr16:70506599 | AAAAAAAA others(12): Show |
A | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1061+1788_1061+180 others(23): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506599 | |||||||
| chr16:70506600 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0206 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1061+1788_1061+180 others(22): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506600 | |||||||
| chr16:70506603 | AAAAAAAA others(8): Show |
A | 3 | a0001c0001t0001g0113 a0001c0002t0002g0289 a0001c0005t0001g0170 |
3 | HG02523.hp1 HG02717.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1061+1788_1061+180 others(19): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506603 | |||||||
| chr16:70506606 | AAAAAAAA others(5): Show |
A | 3 | a0001c0002t0002g0244 a0001c0002t0002g0337 a0001c0003t0002g0250 |
3 | HG01169.hp2 HG02738.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1061+1788_1061+179 others(16): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506606 | |||||||
| chr16:70506607 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0002g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1061+1788_1061+179 others(15): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506607 | |||||||
| chr16:70506608 | AAAAAAAA others(3): Show |
A | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0003t0001g0016 others(5): Show |
8 | HG00735.hp2 HG01169.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+1788_1061+179 others(14): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506608 | |||||||
| chr16:70506609 | AAAAAAAA others(2): Show |
A | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0002g0002 others(5): Show |
8 | HG01358.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1061+1788_1061+179 others(13): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506609 | |||||||
| chr16:70506610 | AAAAAAAA others(1): Show |
A | 15 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(12): Show |
16 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1061+1788_1061+179 others(12): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506610 | |||||||
| chr16:70506618 | C | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(270): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1061+1788G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506618 | |||||||
| chr16:70506680 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1061+1726C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506680 | |||||||
| chr16:70506701 | G | A | 1 | a0002c0004t0001g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1061+1705C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506701 | |||||||
| chr16:70506702 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1061+1704G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506702 | |||||||
| chr16:70506795 | TA | T | 29 | a0001c0001t0001g0092 a0001c0001t0001g0106 a0001c0002t0002g0002 others(26): Show |
31 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1061+1610delT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506795 | |||||||
| chr16:70506796 | A | T | 1 | a0003c0012t0001g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1061+1610T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70506796 | |||||||
| chr16:70507025 | T | C | 1 | a0001c0002t0002g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1061+1381A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507025 | |||||||
| chr16:70507046 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1061+1360C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507046 | |||||||
| chr16:70507114 | A | G | 6 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1061+1292T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507114 | |||||||
| chr16:70507130 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1061+1276G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507130 | |||||||
| chr16:70507151 | T | C | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1061+1255A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507151 | |||||||
| chr16:70507192 | C | A | 1 | a0001c0002t0002g0301 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1061+1214G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507192 | |||||||
| chr16:70507208 | A | G | 1 | a0001c0002t0002g0313 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1061+1198T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507208 | |||||||
| chr16:70507272 | C | CA | 14 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(11): Show |
14 | HG01433.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1061+1133dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507272 | |||||||
| chr16:70507275 | A | C | 33 | a0001c0001t0001g0052 a0001c0001t0001g0090 a0001c0001t0001g0091 others(30): Show |
35 | HG01243.hp2 HG01358.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.1061+1131T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507275 | |||||||
| chr16:70507321 | C | A | 1 | a0001c0003t0002g0302 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1061+1085G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507321 | |||||||
| chr16:70507405 | C | T | 6 | a0001c0001t0001g0138 a0001c0001t0001g0165 a0001c0001t0001g0166 others(3): Show |
6 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+1001G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507405 | |||||||
| chr16:70507636 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(24): Show |
29 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.1061+770C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507636 | |||||||
| chr16:70507678 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1061+728A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507678 | |||||||
| chr16:70507951 | C | T | 17 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(14): Show |
19 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1061+455G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507951 | |||||||
| chr16:70507971 | A | T | 1 | a0001c0002t0001g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1061+435T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70507971 | |||||||
| chr16:70508006 | C | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(158): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1061+400G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70508006 | |||||||
| chr16:70508065 | C | T | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1061+341G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70508065 | |||||||
| chr16:70508118 | A | G | 6 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1061+288T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70508118 | |||||||
| chr16:70508173 | T | G | 3 | a0001c0002t0002g0231 a0001c0002t0002g0232 a0001c0002t0002g0233 |
3 | NA18957.hp1 NA18960.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1061+233A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70508173 | |||||||
| chr16:70508201 | G | A | 1 | a0002c0004t0001g0241 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1061+205C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70508201 | |||||||
| chr16:70508224 | T | G | 1 | a0001c0013t0001g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1061+182A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70508224 | |||||||
| chr16:70508257 | T | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1061+149A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 8/18 | chr16 | 70508257 | |||||||
| chr16:70508494 | C | G | 10 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1003-30G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 7/18 | chr16 | 70508494 | |||||||
| chr16:70508675 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0330 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1003-211A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 7/18 | chr16 | 70508675 | |||||||
| chr16:70508818 | C | T | 31 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(28): Show |
31 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1003-354G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 7/18 | chr16 | 70508818 | |||||||
| chr16:70508851 | A | G | 2 | a0001c0002t0002g0081 a0001c0002t0002g0286 |
2 | NA18950.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1002+380T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 7/18 | chr16 | 70508851 | |||||||
| chr16:70508913 | T | C | 19 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(16): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1002+318A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 7/18 | chr16 | 70508913 | |||||||
| chr16:70508961 | A | G | 1 | a0001c0001t0003g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1002+270T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 7/18 | chr16 | 70508961 | |||||||
| chr16:70509180 | G | A | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG01099.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1002+51C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 7/18 | chr16 | 70509180 | |||||||
| chr16:70509208 | T | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1002+23A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 7/18 | chr16 | 70509208 | |||||||
| chr16:70509406 | A | G | 11 | a0001c0002t0001g0072 a0001c0002t0001g0137 a0001c0002t0002g0245 others(8): Show |
11 | HG02258.hp1 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.845-18T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 6/18 | chr16 | 70509406 | |||||||
| chr16:70509422 | A | C | 1 | a0001c0002t0004g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.845-34T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 6/18 | chr16 | 70509422 | |||||||
| chr16:70509476 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.845-88C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 6/18 | chr16 | 70509476 | |||||||
| chr16:70509742 | A | C | 1 | a0001c0002t0001g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.844+174T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 6/18 | chr16 | 70509742 | |||||||
| chr16:70510030 | G | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.739-9C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70510030 | |||||||
| chr16:70510597 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.739-576A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70510597 | |||||||
| chr16:70510610 | C | A | 2 | a0001c0002t0002g0244 a0001c0002t0002g0337 |
2 | HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.739-589G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70510610 | |||||||
| chr16:70510655 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.739-634C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70510655 | |||||||
| chr16:70510704 | A | C | 1 | a0001c0002t0002g0244 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.739-683T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70510704 | |||||||
| chr16:70510767 | C | CT | 45 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(42): Show |
45 | HG00597.hp1 HG00733.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.739-747dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70510767 | |||||||
| chr16:70510840 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.739-819A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70510840 | |||||||
| chr16:70510866 | C | A | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.739-845G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70510866 | |||||||
| chr16:70511009 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.739-988G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511009 | |||||||
| chr16:70511019 | C | G | 16 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(13): Show |
18 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.739-998G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511019 | |||||||
| chr16:70511054 | C | T | 1 | a0001c0002t0002g0284 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.739-1033G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511054 | |||||||
| chr16:70511108 | C | T | 1 | a0001c0002t0002g0243 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.739-1087G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511108 | |||||||
| chr16:70511114 | A | C | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.739-1093T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511114 | |||||||
| chr16:70511305 | C | CCT | 208 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(205): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.738+933_738+934ins others(2): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511305 | |||||||
| chr16:70511371 | A | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.738+868T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511371 | |||||||
| chr16:70511549 | T | TA | 15 | a0001c0001t0001g0116 a0001c0002t0001g0034 a0001c0002t0001g0072 others(12): Show |
15 | HG01433.hp2 HG02258.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.738+689dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511549 | |||||||
| chr16:70511550 | A | T | 1 | a0001c0002t0002g0026 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.738+689T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511550 | |||||||
| chr16:70511626 | T | C | 17 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(14): Show |
19 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.738+613A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511626 | |||||||
| chr16:70511659 | G | A | 5 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.738+580C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511659 | |||||||
| chr16:70511708 | G | T | 1 | a0001c0002t0002g0217 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.738+531C>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511708 | |||||||
| chr16:70511776 | T | C | 11 | a0001c0002t0002g0026 a0001c0003t0001g0016 a0001c0003t0001g0017 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.738+463A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511776 | |||||||
| chr16:70511789 | G | A | 1 | a0001c0002t0002g0331 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.738+450C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70511789 | |||||||
| chr16:70512030 | T | TA | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.738+208_738+209ins others(1): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 5/18 | chr16 | 70512030 | |||||||
| chr16:70512473 | G | C | 1 | a0001c0005t0001g0322 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.545-41C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70512473 | |||||||
| chr16:70512493 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.545-61G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70512493 | |||||||
| chr16:70512638 | T | C | 1 | a0002c0004t0001g0222 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.545-206A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70512638 | |||||||
| chr16:70512762 | A | G | 48 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(45): Show |
50 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.545-330T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70512762 | |||||||
| chr16:70512847 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.545-415T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70512847 | |||||||
| chr16:70512855 | G | A | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.545-423C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70512855 | |||||||
| chr16:70513090 | A | G | 5 | a0001c0002t0002g0284 a0001c0002t0002g0285 a0001c0002t0002g0303 others(2): Show |
5 | HG00323.hp2 HG01123.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.545-658T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513090 | |||||||
| chr16:70513174 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.545-742C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513174 | |||||||
| chr16:70513264 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.545-832T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513264 | |||||||
| chr16:70513331 | A | T | 19 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(16): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.545-899T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513331 | |||||||
| chr16:70513434 | G | A | 1 | a0001c0002t0002g0303 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.544+901C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513434 | |||||||
| chr16:70513507 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.544+828G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513507 | |||||||
| chr16:70513511 | C | T | 48 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(45): Show |
50 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.544+824G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513511 | |||||||
| chr16:70513614 | G | A | 1 | a0001c0002t0002g0282 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.544+721C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513614 | |||||||
| chr16:70513816 | C | A | 1 | a0006c0015t0001g0327 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.544+519G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513816 | |||||||
| chr16:70513837 | C | A | 44 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(41): Show |
44 | HG00597.hp1 HG00733.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.544+498G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513837 | |||||||
| chr16:70513934 | G | A | 1 | a0005c0010t0004g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.544+401C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513934 | |||||||
| chr16:70513978 | C | G | 1 | a0001c0002t0002g0242 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.544+357G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70513978 | |||||||
| chr16:70514057 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.544+278T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70514057 | |||||||
| chr16:70514202 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.544+133C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70514202 | |||||||
| chr16:70514295 | A | G | 7 | a0001c0003t0001g0067 a0001c0003t0001g0126 a0001c0003t0001g0127 others(4): Show |
7 | HG02258.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544+40T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70514295 | |||||||
| chr16:70514316 | A | T | 17 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(14): Show |
17 | HG00642.hp1 HG00735.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.544+19T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 4/18 | chr16 | 70514316 | |||||||
| chr16:70514632 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.370-123G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70514632 | |||||||
| chr16:70514658 | T | C | 1 | a0001c0002t0002g0283 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.370-149A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70514658 | |||||||
| chr16:70514684 | A | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(213): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.370-175T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70514684 | |||||||
| chr16:70514914 | A | G | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.370-405T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70514914 | |||||||
| chr16:70514968 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.370-459G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70514968 | |||||||
| chr16:70514998 | G | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.370-489C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70514998 | |||||||
| chr16:70515012 | C | CT | 20 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(17): Show |
20 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.370-504dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515012 | |||||||
| chr16:70515012 | C | CTTT | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.370-506_370-504dup others(3): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515012 | |||||||
| chr16:70515027 | T | C | 1 | a0001c0003t0001g0109 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.370-518A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515027 | |||||||
| chr16:70515087 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.370-578G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515087 | |||||||
| chr16:70515274 | G | A | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.370-765C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515274 | |||||||
| chr16:70515293 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.370-784T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515293 | |||||||
| chr16:70515444 | C | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.370-935G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515444 | |||||||
| chr16:70515553 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.370-1044C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515553 | |||||||
| chr16:70515557 | G | A | 33 | a0001c0002t0002g0036 a0001c0002t0002g0044 a0001c0002t0002g0081 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.370-1048C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515557 | |||||||
| chr16:70515684 | A | AAATC | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.370-1179_370-1176d others(6): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515684 | |||||||
| chr16:70515704 | C | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0002t0002g0304 |
3 | HG00438.hp2 HG02015.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.370-1195G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515704 | |||||||
| chr16:70515708 | A | C | 30 | a0001c0001t0001g0050 a0001c0001t0001g0117 a0001c0001t0001g0140 others(27): Show |
32 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.370-1199T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515708 | |||||||
| chr16:70515712 | A | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.370-1203T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515712 | |||||||
| chr16:70515723 | GCTTGCTT others(3): Show |
G | 6 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0107 others(3): Show |
6 | HG00597.hp1 NA18954.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-1224_370-1215d others(12): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515723 | |||||||
| chr16:70515876 | A | G | 39 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(36): Show |
39 | HG00597.hp1 HG00733.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.370-1367T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70515876 | |||||||
| chr16:70516047 | C | T | 19 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(16): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.370-1538G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516047 | |||||||
| chr16:70516055 | T | C | 48 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(45): Show |
50 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.370-1546A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516055 | |||||||
| chr16:70516210 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.369+1416A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516210 | |||||||
| chr16:70516301 | A | ATT | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.369+1323_369+1324d others(4): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516301 | |||||||
| chr16:70516319 | G | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.369+1307C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516319 | |||||||
| chr16:70516406 | C | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.369+1220G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516406 | |||||||
| chr16:70516531 | T | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.369+1095A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516531 | |||||||
| chr16:70516542 | C | T | 29 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(26): Show |
31 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.369+1084G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516542 | |||||||
| chr16:70516546 | T | C | 1 | a0001c0002t0002g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.369+1080A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516546 | |||||||
| chr16:70516688 | T | C | 1 | a0001c0002t0002g0305 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.369+938A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516688 | |||||||
| chr16:70516727 | C | CT | 6 | a0001c0002t0001g0328 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG02647.hp2 HG02818.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+898dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516727 | |||||||
| chr16:70516776 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.369+850T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516776 | |||||||
| chr16:70516811 | T | A | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.369+815A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516811 | |||||||
| chr16:70516857 | G | C | 1 | a0001c0002t0001g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.369+769C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516857 | |||||||
| chr16:70516908 | T | G | 6 | a0001c0002t0004g0123 a0001c0002t0004g0124 a0001c0002t0004g0132 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+718A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70516908 | |||||||
| chr16:70517018 | G | A | 211 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(208): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.369+608C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517018 | |||||||
| chr16:70517052 | C | T | 1 | a0001c0002t0002g0229 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.369+574G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517052 | |||||||
| chr16:70517063 | T | A | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.369+563A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517063 | |||||||
| chr16:70517087 | T | C | 48 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(45): Show |
50 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.369+539A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517087 | |||||||
| chr16:70517190 | C | T | 1 | a0001c0002t0002g0004 | 2 | HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.369+436G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517190 | |||||||
| chr16:70517296 | C | T | 2 | a0001c0001t0001g0089 a0001c0002t0004g0132 |
2 | HG02809.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.369+330G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517296 | |||||||
| chr16:70517310 | C | T | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.369+316G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517310 | |||||||
| chr16:70517381 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.369+245T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517381 | |||||||
| chr16:70517413 | C | A | 13 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(10): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.369+213G>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517413 | |||||||
| chr16:70517444 | T | A | 13 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(10): Show |
13 | HG01433.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.369+182A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517444 | |||||||
| chr16:70517566 | T | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.369+60A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517566 | |||||||
| chr16:70517587 | C | CA | 173 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(170): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.369+38dupT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517587 | |||||||
| chr16:70517587 | C | CAA | 40 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0064 others(37): Show |
40 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.369+37_369+38dupTT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517587 | |||||||
| chr16:70517587 | CA | C | 13 | a0001c0002t0001g0328 a0001c0002t0002g0216 a0001c0002t0002g0224 others(10): Show |
13 | HG00639.hp2 HG01517.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.369+38delT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517587 | |||||||
| chr16:70517587 | CAAAAAAA others(4): Show |
C | 1 | a0005c0010t0004g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.369+28_369+38delTT others(9): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517587 | |||||||
| chr16:70517611 | A | T | 1 | a0001c0002t0002g0221 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.369+15T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 3/18 | chr16 | 70517611 | |||||||
| chr16:70517768 | A | G | 1 | a0001c0001t0003g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.255-28T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70517768 | |||||||
| chr16:70517802 | T | C | 1 | a0001c0002t0002g0313 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.255-62A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70517802 | |||||||
| chr16:70517893 | C | T | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.255-153G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70517893 | |||||||
| chr16:70517937 | C | CT | 29 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(26): Show |
31 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.255-198dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70517937 | |||||||
| chr16:70517969 | T | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.255-229A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70517969 | |||||||
| chr16:70517971 | G | A | 1 | a0004c0016t0001g0343 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.255-231C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70517971 | |||||||
| chr16:70518064 | G | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.255-324C>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518064 | |||||||
| chr16:70518132 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.255-392G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518132 | |||||||
| chr16:70518163 | C | T | 2 | a0001c0002t0002g0219 a0001c0002t0002g0220 |
2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.255-423G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518163 | |||||||
| chr16:70518629 | T | C | 19 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(16): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.255-889A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518629 | |||||||
| chr16:70518695 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.254+954G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518695 | |||||||
| chr16:70518775 | G | C | 1 | a0005c0010t0004g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.254+874C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518775 | |||||||
| chr16:70518902 | G | A | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.254+747C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518902 | |||||||
| chr16:70518907 | G | C | 2 | a0001c0003t0002g0314 a0001c0003t0002g0315 |
2 | HG00597.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.254+742C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518907 | |||||||
| chr16:70518926 | G | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.254+723C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518926 | |||||||
| chr16:70518960 | A | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.254+689T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518960 | |||||||
| chr16:70518977 | CA | C | 42 | a0001c0001t0001g0049 a0001c0001t0001g0073 a0001c0001t0001g0087 others(39): Show |
44 | HG00621.hp2 HG01243.hp2 HG01515.hp2 others(41): Show |
intron_variant | MODIFIER | c.254+671delT | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70518977 | |||||||
| chr16:70519014 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.254+635C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70519014 | |||||||
| chr16:70519033 | T | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.254+616A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70519033 | |||||||
| chr16:70519106 | TAGGATTT others(313): Show |
T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(208): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.254+223_254+542del | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70519106 | |||||||
| chr16:70519120 | C | CTTTTTTT others(3): Show |
5 | a0001c0003t0001g0316 a0001c0003t0001g0317 a0001c0003t0001g0318 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.254+519_254+528dup others(10): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70519120 | |||||||
| chr16:70519187 | C | T | 3 | a0001c0002t0002g0244 a0001c0002t0002g0337 a0001c0003t0002g0250 |
3 | HG01169.hp2 HG02738.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.254+462G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70519187 | |||||||
| chr16:70519202 | T | C | 5 | a0001c0003t0001g0316 a0001c0003t0001g0317 a0001c0003t0001g0318 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.254+447A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70519202 | |||||||
| chr16:70519319 | G | T | 1 | a0001c0003t0002g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.254+330C>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70519319 | |||||||
| chr16:70519422 | C | T | 1 | a0001c0002t0002g0289 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.254+227G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70519422 | |||||||
| chr16:70519479 | G | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(213): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.254+170C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 2/18 | chr16 | 70519479 | |||||||
| chr16:70519999 | G | A | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.172-268C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70519999 | |||||||
| chr16:70520164 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01256.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.172-433C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520164 | |||||||
| chr16:70520198 | G | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(158): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.172-467C>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520198 | |||||||
| chr16:70520205 | G | A | 1 | a0001c0003t0001g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.172-474C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520205 | |||||||
| chr16:70520219 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.172-488T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520219 | |||||||
| chr16:70520374 | T | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG00642.hp1 HG01346.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-643A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520374 | |||||||
| chr16:70520374 | T | TG | 76 | a0001c0001t0001g0043 a0001c0001t0001g0088 a0001c0001t0001g0139 others(73): Show |
78 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.172-644dupC | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520374 | |||||||
| chr16:70520374 | T | TGG | 69 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0063 others(66): Show |
69 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.172-645_172-644dup others(2): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520374 | |||||||
| chr16:70520374 | T | TGGG | 73 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0052 others(70): Show |
75 | HG00323.hp1 HG00438.hp2 HG01106.hp1 others(72): Show |
intron_variant | MODIFIER | c.172-646_172-644dup others(3): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520374 | |||||||
| chr16:70520374 | T | TGGGG | 27 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0042 others(24): Show |
27 | HG01358.hp1 HG01496.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.172-647_172-644dup others(4): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520374 | |||||||
| chr16:70520377 | G | C | 6 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-646C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520377 | |||||||
| chr16:70520378 | G | C | 8 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0022 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-647C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520378 | |||||||
| chr16:70520379 | G | C | 13 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0011 others(10): Show |
15 | HG02280.hp1 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-648C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520379 | |||||||
| chr16:70520501 | G | A | 1 | a0001c0002t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.172-770C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520501 | |||||||
| chr16:70520513 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.172-782A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520513 | |||||||
| chr16:70520596 | C | T | 2 | a0001c0003t0001g0016 a0001c0003t0001g0017 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.172-865G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520596 | |||||||
| chr16:70520613 | CAA | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.172-884_172-883del others(2): Show |
COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520613 | |||||||
| chr16:70520638 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.172-907T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520638 | |||||||
| chr16:70520707 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.172-976C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520707 | |||||||
| chr16:70520877 | T | C | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.172-1146A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70520877 | |||||||
| chr16:70521022 | T | C | 5 | a0001c0001t0001g0071 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG00733.hp2 HG01106.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1291A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521022 | |||||||
| chr16:70521090 | G | T | 7 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(4): Show |
7 | HG01243.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-1359C>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521090 | |||||||
| chr16:70521101 | T | A | 1 | a0001c0005t0001g0322 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.172-1370A>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521101 | |||||||
| chr16:70521357 | A | G | 19 | a0001c0002t0001g0034 a0001c0002t0001g0072 a0001c0002t0001g0130 others(16): Show |
19 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.172-1626T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521357 | |||||||
| chr16:70521363 | G | C | 1 | a0001c0003t0002g0085 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.172-1632C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521363 | |||||||
| chr16:70521416 | T | G | 1 | a0001c0001t0001g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.172-1685A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521416 | |||||||
| chr16:70521424 | G | A | 1 | a0001c0003t0002g0324 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.172-1693C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521424 | |||||||
| chr16:70521455 | C | T | 44 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(41): Show |
44 | HG00597.hp1 HG00733.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.172-1724G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521455 | |||||||
| chr16:70521468 | C | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.172-1737G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521468 | |||||||
| chr16:70521507 | A | C | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.172-1776T>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521507 | |||||||
| chr16:70521614 | G | A | 3 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0006c0015t0001g0327 |
3 | HG02129.hp1 HG02135.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.171+1759C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521614 | |||||||
| chr16:70521659 | G | A | 1 | a0001c0003t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.171+1714C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521659 | |||||||
| chr16:70521671 | G | C | 2 | a0001c0002t0001g0328 a0001c0003t0001g0086 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.171+1702C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521671 | |||||||
| chr16:70521699 | A | AT | 22 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(19): Show |
22 | HG00597.hp1 HG00621.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.171+1673dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521699 | |||||||
| chr16:70521699 | A | T | 1 | a0001c0003t0001g0067 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.171+1674T>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521699 | |||||||
| chr16:70521699 | AT | A | 33 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0329 others(30): Show |
35 | HG01243.hp2 HG01256.hp2 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.171+1673delA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521699 | |||||||
| chr16:70521743 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(25): Show |
30 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.171+1630G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521743 | |||||||
| chr16:70521959 | C | T | 1 | a0001c0002t0002g0044 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.171+1414G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521959 | |||||||
| chr16:70521999 | C | CT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
8 | HG00323.hp1 HG00741.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.171+1373dupA | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70521999 | |||||||
| chr16:70522011 | T | G | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.171+1362A>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70522011 | |||||||
| chr16:70522155 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.171+1218T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70522155 | |||||||
| chr16:70522446 | G | A | 2 | a0001c0002t0001g0335 a0001c0002t0001g0336 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.171+927C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70522446 | |||||||
| chr16:70522567 | C | T | 3 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG01515.hp1 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.171+806G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70522567 | |||||||
| chr16:70522636 | C | T | 1 | a0001c0002t0002g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.171+737G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70522636 | |||||||
| chr16:70522639 | G | A | 1 | a0001c0002t0002g0337 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.171+734C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70522639 | |||||||
| chr16:70522823 | G | C | 1 | a0005c0010t0004g0338 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.171+550C>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70522823 | |||||||
| chr16:70522841 | G | A | 2 | a0001c0008t0001g0339 a0001c0008t0001g0340 |
2 | HG01106.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.171+532C>T | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70522841 | |||||||
| chr16:70522913 | C | T | 1 | a0001c0002t0002g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.171+460G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70522913 | |||||||
| chr16:70523076 | C | T | 1 | a0001c0003t0002g0035 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.171+297G>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70523076 | |||||||
| chr16:70523115 | T | C | 2 | a0001c0003t0004g0341 a0001c0003t0004g0342 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.171+258A>G | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70523115 | |||||||
| chr16:70523212 | G | T | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.171+161C>A | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70523212 | |||||||
| chr16:70523310 | C | G | 1 | a0001c0002t0001g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.171+63G>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70523310 | |||||||
| chr16:70523355 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): Show |
29 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.171+18T>C | COG4 | ENSG00000103051.21 | transcript | ENST00000323786.10 | protein_coding | 1/18 | chr16 | 70523355 |