Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84706 |
| ensemblid | ENSG00000166123.14 |
| hgncid | 18062 |
| symbol | GPT2 |
| name | glutamic--pyruvic transaminase 2 |
| refseq_nuc | NM_133443.4 |
| refseq_prot | NP_597700.1 |
| ensembl_nuc | ENST00000340124.9 |
| ensembl_prot | ENSP00000345282.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 46884362 |
| end | 46931289 |
| strand | + |
| ver | v1.2 |
| region | chr16:46884362-46931289 |
| region5000 | chr16:46879362-46936289 |
| regionname0 | GPT2_chr16_46884362_46931289 |
| regionname5000 | GPT2_chr16_46879362_46936289 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 523 | 190 | 72 | 42 | 36 | 12 | 26 | 24 | GPT2_chr16_46879362_46936289 | GPT2 | MQRAA others(518): Show |
chr16 | 46879362 | 46936289 |
| a0002 | 0/0 | 523 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | MQRAA others(518): Show |
chr16 | 46879362 | 46936289 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1569 | 168 | 59 | 36 | 34 | 12 | 25 | GPT2_chr16_46879362_46936289 | GPT2 | ATGCA others(1564): Show |
chr16 | 46879362 | 46936289 | ||
| a0001c0002 | 0/0 | 1569 | 12 | 11 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | ATGCA others(1564): Show |
chr16 | 46879362 | 46936289 | ||
| a0001c0004 | 0/0 | 1569 | 3 | 0 | 3 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | ATGCA others(1564): Show |
chr16 | 46879362 | 46936289 | ||
| a0001c0005 | 0/0 | 1569 | 3 | 1 | 2 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | ATGCA others(1564): Show |
chr16 | 46879362 | 46936289 | ||
| a0001c0006 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | ATGCA others(1564): Show |
chr16 | 46879362 | 46936289 | ||
| a0001c0007 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | ATGCA others(1564): Show |
chr16 | 46879362 | 46936289 | ||
| a0001c0008 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | ATGCA others(1564): Show |
chr16 | 46879362 | 46936289 | ||
| a0001c0009 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | ATGCA others(1564): Show |
chr16 | 46879362 | 46936289 | ||
| a0002c0003 | 0/0 | 1569 | 4 | 4 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | ATGCA others(1564): Show |
chr16 | 46879362 | 46936289 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3992 | 99 | 47 | 21 | 10 | 9 | 11 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0002 | 0/0 | 3991 | 56 | 9 | 10 | 22 | 3 | 12 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3986): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0003 | 0/0 | 3991 | 2 | 0 | 2 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3986): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0004 | 0/0 | 3992 | 2 | 2 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0005 | 0/0 | 3991 | 2 | 0 | 2 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3986): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0006 | 0/0 | 3991 | 2 | 0 | 0 | 2 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3986): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0007 | 0/0 | 3992 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0008 | 0/0 | 3992 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0009 | 0/0 | 3992 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0012 | 0/1 | 3992 | 1 | 0 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0001t0013 | 0/0 | 3992 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0002t0001 | 0/0 | 3992 | 10 | 9 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0002t0010 | 0/0 | 3992 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0002t0011 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3976): Show |
chr16 | 46879362 | 46936289 |
| a0001c0004t0001 | 0/0 | 3992 | 3 | 0 | 3 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0005t0002 | 0/0 | 3991 | 3 | 1 | 2 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3986): Show |
chr16 | 46879362 | 46936289 |
| a0001c0006t0002 | 0/0 | 3991 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3986): Show |
chr16 | 46879362 | 46936289 |
| a0001c0007t0003 | 0/0 | 3991 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3986): Show |
chr16 | 46879362 | 46936289 |
| a0001c0008t0001 | 0/0 | 3992 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0001c0009t0001 | 0/0 | 3992 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| a0002c0003t0001 | 0/0 | 3992 | 4 | 4 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | GGCGC others(3987): Show |
chr16 | 46879362 | 46936289 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0001 | 0/0 | 10 | 4 | 0 | 3 | 1 | 2 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0012g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0001t0013g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0002t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0004t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0004t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0005t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0005t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0005t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0006t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0007t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0008t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0001c0009t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0002c0003t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0002c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| a0002c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0039 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0137 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0026 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0091 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01496 | hp1 | a0001 | c0005 | t0002 | g0093 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PEL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02148 | hp2 | a0001 | c0005 | t0002 | g0106 | AMR | PEL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02257 | hp1 | a0001 | c0005 | t0002 | g0127 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02257 | hp2 | a0001 | c0002 | t0011 | g0008 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0022 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02622 | hp1 | a0001 | c0009 | t0001 | g0125 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02735 | hp2 | a0001 | c0008 | t0001 | g0066 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0138 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03579 | hp1 | a0001 | c0002 | t0010 | g0021 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03688 | hp1 | a0001 | c0001 | t0013 | g0155 | SAS | STU | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | STU | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | STU | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | STU | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | STU | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0003 | SAS | STU | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | YRI | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA19085 | hp1 | a0001 | c0007 | t0003 | g0115 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA19085 | hp2 | a0001 | c0006 | t0002 | g0001 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ASW | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ASW | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | TSI | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | GIH | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | USA | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | USA | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0012 | g0156 | REF | REF | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0135 | REF | REF | GPT2_chr16_46879362_46936289 | GPT2 | chr16 | 46879362 | 46936289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46928993 | C | T | 1 | a0002 | 4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.1568C>T | p.Ala523Val | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 1696/3992 | 1568/1572 | 523/523 | chr16 | 46928993 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46884721 | G | A | 1 | a0001c0006 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.6G>A | p.Gln2Gln | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/12 | 134/3992 | 6/1572 | 2/523 | chr16 | 46884721 | |||
| chr16:46906909 | G | A | 1 | a0001c0004 | 3 | HG00735.hp2 HG01071.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.510G>A | p.Arg170Arg | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/12 | 638/3992 | 510/1572 | 170/523 | chr16 | 46906909 | |||
| chr16:46906927 | G | C | 1 | a0001c0007 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.528G>C | p.Ala176Ala | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/12 | 656/3992 | 528/1572 | 176/523 | chr16 | 46906927 | |||
| chr16:46909833 | G | A | 1 | a0001c0008 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.726G>A | p.Ala242Ala | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/12 | 854/3992 | 726/1572 | 242/523 | chr16 | 46909833 | |||
| chr16:46918695 | C | T | 1 | a0001c0009 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.975C>T | p.Pro325Pro | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/12 | 1103/3992 | 975/1572 | 325/523 | chr16 | 46918695 | |||
| chr16:46922380 | G | C | 1 | a0001c0005 | 3 | HG01496.hp1 HG02148.hp2 HG02257.hp1 |
synonymous_variant | LOW | c.1176G>C | p.Pro392Pro | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 9/12 | 1304/3992 | 1176/1572 | 392/523 | chr16 | 46922380 | |||
| chr16:46924397 | G | A | 1 | a0001c0002 | 12 | HG01106.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
synonymous_variant | LOW | c.1221G>A | p.Glu407Glu | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/12 | 1349/3992 | 1221/1572 | 407/523 | chr16 | 46924397 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46929065 | G | A | 1 | a0001c0001t0007 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 68 | chr16 | 46929065 | ||||||
| chr16:46929096 | A | T | 1 | a0001c0001t0013 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*99A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 99 | chr16 | 46929096 | ||||||
| chr16:46929350 | G | A | 1 | a0001c0001t0008 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 353 | chr16 | 46929350 | ||||||
| chr16:46929496 | C | T | 1 | a0001c0001t0006 | 2 | NA18983.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*499C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 499 | chr16 | 46929496 | ||||||
| chr16:46929518 | G | A | 2 | a0001c0001t0003 a0001c0007t0003 |
3 | HG01258.hp2 HG02004.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*521G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 521 | chr16 | 46929518 | ||||||
| chr16:46929622 | G | A | 1 | a0001c0001t0004 | 2 | HG02717.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*625G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 625 | chr16 | 46929622 | ||||||
| chr16:46929826 | T | A | 2 | a0001c0001t0004 a0001c0001t0009 |
3 | HG02717.hp1 HG02970.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829T>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 829 | chr16 | 46929826 | ||||||
| chr16:46929939 | C | A | 1 | a0001c0001t0006 | 2 | NA18983.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*942C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 942 | chr16 | 46929939 | ||||||
| chr16:46930110 | A | G | 1 | a0001c0001t0005 | 2 | HG01169.hp2 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1113A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 1113 | chr16 | 46930110 | ||||||
| chr16:46930445 | TG | T | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(4): Show |
67 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1449delG | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 1449 | chr16 | 46930445 | ||||||
| chr16:46930511 | CACAGCCC others(4): Show |
C | 1 | a0001c0002t0011 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1515_*1525delACAG others(7): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 1515 | chr16 | 46930511 | ||||||
| chr16:46931215 | C | T | 1 | a0001c0002t0010 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2218C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 12/12 | 2218 | chr16 | 46931215 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46884493 | C | T | 1 | a0001c0001t0002g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-23+26C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 1/11 | chr16 | 46884493 | |||||||
| chr16:46884597 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-22-97C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 1/11 | chr16 | 46884597 | |||||||
| chr16:46884670 | G | C | 1 | a0001c0001t0006g0018 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-22-24G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 1/11 | chr16 | 46884670 | |||||||
| chr16:46884996 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(35): Show |
47 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.243+38T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46884996 | |||||||
| chr16:46885261 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.243+303C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46885261 | |||||||
| chr16:46885399 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.243+441G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46885399 | |||||||
| chr16:46885402 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.243+444G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46885402 | |||||||
| chr16:46885522 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.243+564C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46885522 | |||||||
| chr16:46885535 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.243+577T>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46885535 | |||||||
| chr16:46885547 | C | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG01884.hp1 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+589C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46885547 | |||||||
| chr16:46885964 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.243+1006C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46885964 | |||||||
| chr16:46886267 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.243+1309C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46886267 | |||||||
| chr16:46886333 | A | G | 1 | a0001c0001t0006g0018 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.243+1375A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46886333 | |||||||
| chr16:46886416 | A | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
27 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.243+1458A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46886416 | |||||||
| chr16:46886495 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0054 a0001c0001t0002g0055 others(3): Show |
7 | HG01071.hp1 HG01175.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+1537G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46886495 | |||||||
| chr16:46887011 | A | C | 1 | a0001c0001t0002g0139 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.243+2053A>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46887011 | |||||||
| chr16:46887125 | T | C | 1 | a0001c0001t0002g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.243+2167T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46887125 | |||||||
| chr16:46887341 | G | T | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.243+2383G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46887341 | |||||||
| chr16:46887883 | A | G | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.243+2925A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46887883 | |||||||
| chr16:46887936 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01884.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+2978C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46887936 | |||||||
| chr16:46888135 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.243+3177G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46888135 | |||||||
| chr16:46888766 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0163 |
2 | NA18984.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.243+3808C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46888766 | |||||||
| chr16:46889135 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.243+4177T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46889135 | |||||||
| chr16:46889246 | A | AT | 30 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0048 others(27): Show |
31 | HG00735.hp1 HG01074.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.243+4314dupT | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 46889246 | ||||||
| chr16:46889246 | A | ATT | 79 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(76): Show |
92 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.243+4313_243+4314d others(4): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 46889246 | ||||||
| chr16:46889246 | A | ATTT | 8 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
10 | HG01261.hp2 HG01433.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+4312_243+4314d others(5): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 46889246 | ||||||
| chr16:46889246 | AT | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0044 others(2): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+4314delT | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 46889246 | ||||||
| chr16:46889594 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
6 | HG00280.hp1 HG01516.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+4636G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46889594 | |||||||
| chr16:46889607 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.243+4649G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46889607 | |||||||
| chr16:46889692 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.243+4734C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46889692 | |||||||
| chr16:46889743 | G | A | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.243+4785G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46889743 | |||||||
| chr16:46889853 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0040 others(2): Show |
7 | HG02895.hp2 HG02897.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.243+4895C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46889853 | |||||||
| chr16:46890057 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(35): Show |
47 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.243+5099C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46890057 | |||||||
| chr16:46890140 | T | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(118): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.243+5182T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46890140 | |||||||
| chr16:46890222 | C | A | 2 | a0001c0001t0001g0080 a0001c0001t0002g0079 |
2 | NA18939.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.243+5264C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46890222 | |||||||
| chr16:46890745 | A | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(35): Show |
47 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.243+5787A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46890745 | |||||||
| chr16:46890948 | A | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01884.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+5990A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46890948 | |||||||
| chr16:46891000 | C | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.243+6042C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46891000 | |||||||
| chr16:46891076 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.243+6118T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46891076 | |||||||
| chr16:46891213 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.243+6255A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46891213 | |||||||
| chr16:46891528 | C | T | 2 | a0001c0001t0002g0058 a0001c0001t0008g0137 |
2 | HG01109.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.244-6120C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46891528 | |||||||
| chr16:46891531 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.244-6117G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46891531 | |||||||
| chr16:46891644 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.244-6004C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46891644 | |||||||
| chr16:46891749 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.244-5899T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46891749 | |||||||
| chr16:46892168 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0123 others(6): Show |
9 | HG01261.hp2 HG01433.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-5480A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46892168 | |||||||
| chr16:46892176 | C | T | 2 | a0001c0001t0003g0121 a0001c0001t0003g0122 |
2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.244-5472C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46892176 | |||||||
| chr16:46892342 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244-5306A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46892342 | |||||||
| chr16:46892507 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0076 |
3 | HG02818.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.244-5141A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46892507 | |||||||
| chr16:46892897 | G | A | 1 | a0001c0002t0010g0021 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244-4751G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46892897 | |||||||
| chr16:46893122 | TG | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.244-4525delG | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46893122 | |||||||
| chr16:46893200 | G | C | 5 | a0001c0001t0001g0082 a0001c0001t0002g0012 a0001c0001t0002g0063 others(2): Show |
6 | HG02735.hp1 HG03654.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-4448G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46893200 | |||||||
| chr16:46893612 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.244-4036G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46893612 | |||||||
| chr16:46893642 | A | G | 1 | a0001c0004t0001g0039 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.244-4006A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46893642 | |||||||
| chr16:46893671 | G | C | 1 | a0001c0001t0002g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.244-3977G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46893671 | |||||||
| chr16:46893995 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.244-3653G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46893995 | |||||||
| chr16:46894223 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.244-3425A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46894223 | |||||||
| chr16:46894342 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-3306A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46894342 | |||||||
| chr16:46894447 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.244-3201C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46894447 | |||||||
| chr16:46894728 | A | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.244-2920A>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46894728 | |||||||
| chr16:46894814 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.244-2834C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46894814 | |||||||
| chr16:46895083 | T | A | 1 | a0001c0001t0001g0016 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.244-2565T>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46895083 | |||||||
| chr16:46895497 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.244-2151T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46895497 | |||||||
| chr16:46895538 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.244-2110C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46895538 | |||||||
| chr16:46895578 | A | G | 1 | a0001c0001t0001g0014 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.244-2070A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46895578 | |||||||
| chr16:46896349 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.244-1299C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46896349 | |||||||
| chr16:46896452 | CT | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0002c0003t0001g0005 others(2): Show |
6 | HG01496.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-1184delT | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 46896452 | ||||||
| chr16:46896492 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244-1156T>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46896492 | |||||||
| chr16:46896583 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.244-1065C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46896583 | |||||||
| chr16:46896688 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01884.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-960C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46896688 | |||||||
| chr16:46896754 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(35): Show |
47 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.244-894G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46896754 | |||||||
| chr16:46896865 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244-783C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46896865 | |||||||
| chr16:46897280 | C | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0118 others(2): Show |
5 | HG00438.hp2 HG02129.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-368C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46897280 | |||||||
| chr16:46897297 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG00735.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.244-351C>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46897297 | |||||||
| chr16:46897364 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.244-284C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 2/11 | chr16 | 46897364 | |||||||
| chr16:46897773 | C | T | 5 | a0001c0001t0002g0114 a0001c0001t0002g0116 a0001c0001t0003g0121 others(2): Show |
5 | HG01258.hp2 HG02004.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+36C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46897773 | |||||||
| chr16:46898196 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.333+459C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898196 | |||||||
| chr16:46898215 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.333+478C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898215 | |||||||
| chr16:46898357 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.333+620G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898357 | |||||||
| chr16:46898871 | C | CAT | 5 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0111 others(2): Show |
5 | HG02055.hp2 HG02129.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+1150_333+1151d others(4): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898871 | ||||||
| chr16:46898877 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.333+1142_333+1165d others(26): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898877 | ||||||
| chr16:46898887 | T | C | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.333+1150T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898887 | |||||||
| chr16:46898932 | A | G | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.333+1195A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898932 | |||||||
| chr16:46898947 | C | CAT | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.333+1215_333+1216d others(4): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898947 | ||||||
| chr16:46898947 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.333+1210C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898947 | |||||||
| chr16:46898954 | G | A | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.333+1217G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898954 | |||||||
| chr16:46898958 | A | G | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.333+1221A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898958 | |||||||
| chr16:46898965 | T | TAC | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01884.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+1238_333+1239d others(4): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898965 | ||||||
| chr16:46898967 | C | T | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.333+1230C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898967 | |||||||
| chr16:46898975 | C | CAT | 32 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(29): Show |
41 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.333+1254_333+1255d others(4): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898975 | ||||||
| chr16:46898975 | C | CATAT | 2 | a0001c0002t0001g0035 a0001c0002t0001g0036 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.333+1252_333+1255d others(6): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898975 | ||||||
| chr16:46898975 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
5 | HG00642.hp2 HG00735.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+1238C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898975 | |||||||
| chr16:46898975 | CATAT | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(115): Show |
134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.333+1252_333+1255d others(6): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898975 | ||||||
| chr16:46898979 | T | TATGTGTA others(17): Show |
4 | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG00642.hp2 HG00735.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+1244_333+1245i others(26): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898979 | ||||||
| chr16:46898979 | T | TATGTGTA others(73): Show |
1 | a0001c0001t0002g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.333+1244_333+1245i others(82): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898979 | ||||||
| chr16:46898998 | C | CATAT | 1 | a0001c0001t0001g0014 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.333+1296_333+1299d others(6): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898998 | ||||||
| chr16:46898998 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0009g0138 |
2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.333+1261C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46898998 | |||||||
| chr16:46898998 | CATATATA others(11): Show |
C | 1 | a0001c0001t0002g0087 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.333+1282_333+1299d others(20): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898998 | ||||||
| chr16:46898998 | CATATATA others(13): Show |
C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(104): Show |
122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.333+1280_333+1299d others(22): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898998 | ||||||
| chr16:46898998 | CATATATA others(15): Show |
C | 1 | a0001c0001t0001g0080 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.333+1278_333+1299d others(24): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46898998 | ||||||
| chr16:46899000 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.333+1263T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899000 | |||||||
| chr16:46899002 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.333+1265T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899002 | |||||||
| chr16:46899016 | TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.333+1280_333+1298d others(21): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899016 | |||||||
| chr16:46899017 | ATATATAT others(12): Show |
A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0157 a0001c0001t0002g0120 |
3 | HG00558.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.333+1282_333+1300d others(21): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46899017 | ||||||
| chr16:46899017 | ATATATAT others(13): Show |
A | 5 | a0001c0001t0001g0075 a0001c0001t0001g0118 a0001c0001t0002g0064 others(2): Show |
5 | HG00438.hp2 HG01993.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+1282_333+1301d others(22): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46899017 | ||||||
| chr16:46899017 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0076 |
3 | HG02818.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.333+1282_333+1302d others(23): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46899017 | ||||||
| chr16:46899019 | ATATATAT others(10): Show |
A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(24): Show |
29 | HG01106.hp1 HG01496.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.333+1284_333+1300d others(19): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46899019 | ||||||
| chr16:46899019 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0074 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.333+1284_333+1301d others(20): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46899019 | ||||||
| chr16:46899021 | ATATATAT others(8): Show |
A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(7): Show |
17 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+1286_333+1300d others(17): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46899021 | ||||||
| chr16:46899021 | ATATATAT others(9): Show |
A | 1 | a0001c0002t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.333+1286_333+1301d others(18): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46899021 | ||||||
| chr16:46899035 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.333+1299_333+1300i others(31): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 46899035 | ||||||
| chr16:46899035 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.333+1298A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899035 | |||||||
| chr16:46899037 | T | A | 1 | a0001c0001t0001g0014 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.333+1300T>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899037 | |||||||
| chr16:46899087 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0002g0063 |
2 | HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.333+1350G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899087 | |||||||
| chr16:46899253 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.334-1429C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899253 | |||||||
| chr16:46899355 | G | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.334-1327G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899355 | |||||||
| chr16:46899386 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0118 |
2 | HG00438.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.334-1296G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899386 | |||||||
| chr16:46899505 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(10): Show |
21 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.334-1177G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899505 | |||||||
| chr16:46899806 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.334-876C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899806 | |||||||
| chr16:46899833 | G | A | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.334-849G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899833 | |||||||
| chr16:46899950 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.334-732G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899950 | |||||||
| chr16:46899997 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.334-685T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46899997 | |||||||
| chr16:46900012 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-670G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46900012 | |||||||
| chr16:46900085 | A | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(36): Show |
48 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.334-597A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46900085 | |||||||
| chr16:46900253 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.334-429G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46900253 | |||||||
| chr16:46900370 | G | C | 1 | a0001c0001t0002g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.334-312G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46900370 | |||||||
| chr16:46900495 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.334-187C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 3/11 | chr16 | 46900495 | |||||||
| chr16:46900893 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442+103C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46900893 | |||||||
| chr16:46901082 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.442+292C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46901082 | |||||||
| chr16:46901125 | C | T | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.442+335C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46901125 | |||||||
| chr16:46901904 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.442+1114G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46901904 | |||||||
| chr16:46901935 | G | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(19): Show |
25 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.442+1145G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46901935 | |||||||
| chr16:46902069 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442+1279T>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902069 | |||||||
| chr16:46902106 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.442+1316C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902106 | |||||||
| chr16:46902115 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.442+1325G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902115 | |||||||
| chr16:46902248 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.442+1458T>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902248 | |||||||
| chr16:46902361 | C | G | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.442+1571C>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902361 | |||||||
| chr16:46902589 | T | C | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.442+1799T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902589 | |||||||
| chr16:46902601 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.442+1811A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902601 | |||||||
| chr16:46902729 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442+1939G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902729 | |||||||
| chr16:46902784 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.442+1994C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902784 | |||||||
| chr16:46902970 | C | T | 9 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0001g0070 others(6): Show |
9 | HG00438.hp2 HG00738.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.442+2180C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46902970 | |||||||
| chr16:46903212 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.442+2422G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46903212 | |||||||
| chr16:46903266 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442+2476T>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46903266 | |||||||
| chr16:46903384 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.442+2594C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46903384 | |||||||
| chr16:46903388 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442+2598A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46903388 | |||||||
| chr16:46903518 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.442+2728G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46903518 | |||||||
| chr16:46903938 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.443-2904T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46903938 | |||||||
| chr16:46903949 | G | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0076 |
3 | HG02818.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.443-2893G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46903949 | |||||||
| chr16:46904000 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.443-2842G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46904000 | |||||||
| chr16:46904019 | G | A | 1 | a0001c0001t0005g0091 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.443-2823G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46904019 | |||||||
| chr16:46904049 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.443-2793G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46904049 | |||||||
| chr16:46904179 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.443-2663G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46904179 | |||||||
| chr16:46904224 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0007g0003 |
3 | HG03492.hp1 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.443-2618G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46904224 | |||||||
| chr16:46905059 | CT | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0080 others(6): Show |
10 | HG00099.hp1 HG01099.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.443-1767delT | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 46905059 | ||||||
| chr16:46905203 | C | A | 3 | a0001c0001t0004g0053 a0001c0001t0004g0113 a0001c0001t0009g0138 |
3 | HG02717.hp1 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.443-1639C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46905203 | |||||||
| chr16:46905220 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(26): Show |
37 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.443-1622C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46905220 | |||||||
| chr16:46905314 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.443-1528G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46905314 | |||||||
| chr16:46905492 | C | G | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.443-1350C>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46905492 | |||||||
| chr16:46905535 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443-1307G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46905535 | |||||||
| chr16:46905688 | C | A | 7 | a0001c0002t0001g0008 a0001c0002t0001g0028 a0001c0002t0001g0030 others(4): Show |
7 | HG01106.hp1 HG02257.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-1154C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46905688 | |||||||
| chr16:46906081 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.443-761A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46906081 | |||||||
| chr16:46906178 | A | G | 1 | a0001c0005t0002g0106 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.443-664A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46906178 | |||||||
| chr16:46906225 | A | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0105 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.443-617A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46906225 | |||||||
| chr16:46906232 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0070 |
2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.443-610C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46906232 | |||||||
| chr16:46906369 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.443-473A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46906369 | |||||||
| chr16:46906564 | C | T | 1 | a0001c0002t0010g0021 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.443-278C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 4/11 | chr16 | 46906564 | |||||||
| chr16:46907171 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.576+196G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46907171 | |||||||
| chr16:46907220 | G | C | 2 | a0001c0001t0006g0018 a0001c0001t0006g0065 |
2 | NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.576+245G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46907220 | |||||||
| chr16:46907410 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.576+435G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46907410 | |||||||
| chr16:46907494 | T | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0117 a0001c0008t0001g0066 |
3 | HG02735.hp2 HG03704.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.576+519T>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46907494 | |||||||
| chr16:46907655 | G | A | 2 | a0001c0002t0001g0028 a0001c0002t0001g0031 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.576+680G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46907655 | |||||||
| chr16:46907700 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(120): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.576+725A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46907700 | |||||||
| chr16:46907933 | TC | T | 3 | a0001c0001t0004g0053 a0001c0001t0004g0113 a0001c0001t0009g0138 |
3 | HG02717.hp1 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.576+959delC | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46907933 | |||||||
| chr16:46907968 | G | A | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0118 others(2): Show |
5 | HG00438.hp2 HG02129.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+993G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46907968 | |||||||
| chr16:46908232 | C | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(5): Show |
14 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.576+1257C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46908232 | |||||||
| chr16:46908235 | G | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(120): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.576+1260G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46908235 | |||||||
| chr16:46908341 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.577-1343C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46908341 | |||||||
| chr16:46908383 | TG | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(31): Show |
43 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.577-1297delG | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 46908383 | ||||||
| chr16:46908394 | G | A | 1 | a0001c0004t0001g0026 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.577-1290G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46908394 | |||||||
| chr16:46908709 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.577-975A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46908709 | |||||||
| chr16:46908895 | G | A | 1 | a0001c0001t0008g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.577-789G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46908895 | |||||||
| chr16:46909177 | G | C | 1 | a0001c0001t0002g0096 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.577-507G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46909177 | |||||||
| chr16:46909524 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.577-160C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46909524 | |||||||
| chr16:46909525 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.577-159G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 5/11 | chr16 | 46909525 | |||||||
| chr16:46910380 | C | CA | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.820+481dupA | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 46910380 | ||||||
| chr16:46910380 | C | CAA | 38 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0045 others(35): Show |
40 | HG00673.hp1 HG00673.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.820+480_820+481dup others(2): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 46910380 | ||||||
| chr16:46911016 | G | A | 2 | a0001c0001t0005g0091 a0001c0001t0005g0103 |
2 | HG01169.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.820+1089G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46911016 | |||||||
| chr16:46911415 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.820+1488C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46911415 | |||||||
| chr16:46911512 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.820+1585A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46911512 | |||||||
| chr16:46911522 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.820+1595A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46911522 | |||||||
| chr16:46911873 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.820+1946A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46911873 | |||||||
| chr16:46912334 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.820+2407C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46912334 | |||||||
| chr16:46912406 | C | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(22): Show |
34 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.820+2479C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46912406 | |||||||
| chr16:46912769 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG03098.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.820+2842G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46912769 | |||||||
| chr16:46912976 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.820+3049G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46912976 | |||||||
| chr16:46913005 | C | T | 1 | a0001c0001t0002g0012 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.820+3078C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46913005 | |||||||
| chr16:46913140 | T | G | 3 | a0001c0001t0004g0053 a0001c0001t0004g0113 a0001c0001t0009g0138 |
3 | HG02717.hp1 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.820+3213T>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46913140 | |||||||
| chr16:46913374 | A | C | 4 | a0001c0001t0001g0099 a0001c0001t0002g0090 a0001c0001t0002g0100 others(1): Show |
4 | HG03490.hp2 HG03654.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-3254A>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46913374 | |||||||
| chr16:46913403 | G | T | 1 | a0001c0002t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.821-3225G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46913403 | |||||||
| chr16:46913463 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.821-3165T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46913463 | |||||||
| chr16:46913849 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.821-2779G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46913849 | |||||||
| chr16:46914164 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.821-2464C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46914164 | |||||||
| chr16:46914184 | T | C | 5 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-2444T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46914184 | |||||||
| chr16:46914586 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.821-2042G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46914586 | |||||||
| chr16:46914601 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(22): Show |
34 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.821-2027G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46914601 | |||||||
| chr16:46914812 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.821-1816C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46914812 | |||||||
| chr16:46914952 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.821-1676C>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46914952 | |||||||
| chr16:46915270 | CACACACA others(8): Show |
C | 1 | a0001c0002t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.821-1343_821-1329d others(17): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 46915270 | ||||||
| chr16:46915293 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.821-1335C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46915293 | |||||||
| chr16:46915361 | CAT | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(120): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.821-1266_821-1265d others(4): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46915361 | |||||||
| chr16:46915370 | G | GCA | 2 | a0001c0002t0001g0035 a0001c0002t0001g0036 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.821-1246_821-1245d others(4): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 46915370 | ||||||
| chr16:46915380 | ACAC | A | 56 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0099 others(53): Show |
68 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.821-1241_821-1239d others(5): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 46915380 | ||||||
| chr16:46915429 | C | G | 1 | a0001c0005t0002g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.821-1199C>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46915429 | |||||||
| chr16:46915449 | GACAC | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0107 |
2 | NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.821-1172_821-1169d others(6): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 46915449 | ||||||
| chr16:46915568 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG00735.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.821-1060C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46915568 | |||||||
| chr16:46915705 | TACAC | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0070 |
2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.821-916_821-913del others(4): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 46915705 | ||||||
| chr16:46916003 | CCACCACA others(13): Show |
C | 1 | a0001c0001t0009g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.821-611_821-592del others(20): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 46916003 | ||||||
| chr16:46916038 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.821-590A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46916038 | |||||||
| chr16:46916121 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.821-507C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46916121 | |||||||
| chr16:46916270 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0150 |
3 | HG01109.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.821-358C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 6/11 | chr16 | 46916270 | |||||||
| chr16:46916713 | A | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0126 |
2 | HG02615.hp1 NA19043.hp2 |
splice_region_variant&intron_variant | LOW | c.900+6A>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 7/11 | chr16 | 46916713 | |||||||
| chr16:46917139 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.900+432A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 7/11 | chr16 | 46917139 | |||||||
| chr16:46917745 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.901-876C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 7/11 | chr16 | 46917745 | |||||||
| chr16:46917841 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.901-780T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 7/11 | chr16 | 46917841 | |||||||
| chr16:46918119 | T | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(111): Show |
129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.901-502T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 7/11 | chr16 | 46918119 | |||||||
| chr16:46918406 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.901-215C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 7/11 | chr16 | 46918406 | |||||||
| chr16:46919249 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0152 others(1): Show |
4 | HG01123.hp2 HG02683.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037+492C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46919249 | |||||||
| chr16:46919513 | C | A | 1 | a0001c0001t0002g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1037+756C>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46919513 | |||||||
| chr16:46919597 | G | A | 3 | a0002c0003t0001g0005 a0002c0003t0001g0022 a0002c0003t0001g0025 |
4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037+840G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46919597 | |||||||
| chr16:46919625 | G | C | 1 | a0001c0001t0001g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1037+868G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46919625 | |||||||
| chr16:46919631 | T | C | 5 | a0001c0001t0001g0052 a0001c0001t0004g0053 a0001c0001t0004g0113 others(2): Show |
5 | HG02717.hp1 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037+874T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46919631 | |||||||
| chr16:46919928 | C | T | 4 | a0001c0001t0002g0068 a0001c0001t0002g0098 a0001c0001t0002g0114 others(1): Show |
4 | HG00673.hp2 NA18955.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037+1171C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46919928 | |||||||
| chr16:46920383 | C | G | 1 | a0001c0001t0002g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1037+1626C>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46920383 | |||||||
| chr16:46920436 | G | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1037+1679G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46920436 | |||||||
| chr16:46920478 | G | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0067 others(6): Show |
10 | HG00280.hp1 HG00642.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037+1721G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46920478 | |||||||
| chr16:46921229 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1038-1013C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46921229 | |||||||
| chr16:46921271 | T | G | 1 | a0001c0001t0002g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1038-971T>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46921271 | |||||||
| chr16:46921336 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1038-906G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46921336 | |||||||
| chr16:46921401 | G | T | 1 | a0001c0001t0002g0087 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1038-841G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46921401 | |||||||
| chr16:46921562 | T | C | 1 | a0001c0007t0003g0115 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1038-680T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46921562 | |||||||
| chr16:46921741 | G | T | 1 | a0001c0001t0002g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1038-501G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46921741 | |||||||
| chr16:46921885 | G | A | 2 | a0001c0001t0004g0053 a0001c0001t0004g0113 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1038-357G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 8/11 | chr16 | 46921885 | |||||||
| chr16:46922603 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1212+187A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 9/11 | chr16 | 46922603 | |||||||
| chr16:46922725 | A | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0105 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1212+309A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 9/11 | chr16 | 46922725 | |||||||
| chr16:46922781 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1212+365G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 9/11 | chr16 | 46922781 | |||||||
| chr16:46923390 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1212+974G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 9/11 | chr16 | 46923390 | |||||||
| chr16:46923789 | G | C | 3 | a0002c0003t0001g0005 a0002c0003t0001g0022 a0002c0003t0001g0025 |
4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1213-600G>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 9/11 | chr16 | 46923789 | |||||||
| chr16:46924567 | GCT | G | 2 | a0001c0001t0002g0100 a0001c0001t0002g0102 |
2 | HG03490.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1368+30_1368+31del others(2): Show |
GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 46924567 | ||||||
| chr16:46924831 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1368+287G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46924831 | |||||||
| chr16:46924833 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1368+289G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46924833 | |||||||
| chr16:46924952 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0124 others(5): Show |
8 | HG01261.hp2 HG01433.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368+408G>A | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46924952 | |||||||
| chr16:46925038 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1368+494C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46925038 | |||||||
| chr16:46925079 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1368+535T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46925079 | |||||||
| chr16:46925109 | A | T | 1 | a0001c0002t0001g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1368+565A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46925109 | |||||||
| chr16:46925212 | G | GT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(32): Show |
44 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.1368+675dupT | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 46925212 | ||||||
| chr16:46925613 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1368+1069T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46925613 | |||||||
| chr16:46925834 | A | T | 3 | a0001c0001t0004g0053 a0001c0001t0004g0113 a0001c0001t0009g0138 |
3 | HG02717.hp1 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1369-1091A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46925834 | |||||||
| chr16:46925974 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1369-951A>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46925974 | |||||||
| chr16:46926130 | CA | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1369-774delA | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 46926130 | ||||||
| chr16:46926468 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0076 |
3 | HG02818.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1369-457C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46926468 | |||||||
| chr16:46926763 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1369-162C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 10/11 | chr16 | 46926763 | |||||||
| chr16:46927285 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1481+248C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 11/11 | chr16 | 46927285 | |||||||
| chr16:46927335 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1481+298T>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 11/11 | chr16 | 46927335 | |||||||
| chr16:46927619 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(34): Show |
46 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.1481+582A>G | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 11/11 | chr16 | 46927619 | |||||||
| chr16:46927751 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1481+714C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 11/11 | chr16 | 46927751 | |||||||
| chr16:46927857 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1481+820G>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 11/11 | chr16 | 46927857 | |||||||
| chr16:46928203 | C | T | 1 | a0001c0008t0001g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1482-704C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 11/11 | chr16 | 46928203 | |||||||
| chr16:46928310 | A | C | 1 | a0001c0001t0001g0015 | 2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1482-597A>C | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 11/11 | chr16 | 46928310 | |||||||
| chr16:46928708 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1482-199C>T | GPT2 | ENSG00000166123.14 | transcript | ENST00000340124.9 | protein_coding | 11/11 | chr16 | 46928708 |