Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51617 |
| ensemblid | ENSG00000170091.11 |
| hgncid | 24955 |
| symbol | NSG2 |
| name | neuronal vesicle trafficking associated 2 |
| refseq_nuc | NM_015980.5 |
| refseq_prot | NP_057064.1 |
| ensembl_nuc | ENST00000303177.8 |
| ensembl_prot | ENSP00000307722.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 174045706 |
| end | 174109179 |
| strand | + |
| ver | v1.2 |
| region | chr5:174045706-174109179 |
| region5000 | chr5:174040706-174114179 |
| regionname0 | NSG2_chr5_174045706_174109179 |
| regionname5000 | NSG2_chr5_174040706_174114179 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 513 | 256 | 92 | 55 | 62 | 9 | 36 | NSG2_chr5_174040706_174114179 | NSG2 | ATGGT others(508): Show |
chr5 | 174040706 | 174114179 | ||
| a0001c0002 | 0/0 | 513 | 21 | 0 | 7 | 10 | 1 | 3 | NSG2_chr5_174040706_174114179 | NSG2 | ATGGT others(508): Show |
chr5 | 174040706 | 174114179 | ||
| a0001c0003 | 0/0 | 513 | 16 | 0 | 1 | 14 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | ATGGT others(508): Show |
chr5 | 174040706 | 174114179 | ||
| a0001c0004 | 0/0 | 513 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | ATGGT others(508): Show |
chr5 | 174040706 | 174114179 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2350 | 132 | 26 | 31 | 52 | 4 | 17 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0002 | 0/0 | 2348 | 24 | 10 | 6 | 2 | 2 | 4 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2343): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0003 | 0/0 | 2350 | 39 | 21 | 11 | 0 | 1 | 6 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0004 | 0/0 | 2350 | 24 | 18 | 3 | 1 | 0 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0005 | 0/0 | 2348 | 5 | 5 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2343): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0006 | 0/0 | 2350 | 5 | 2 | 1 | 0 | 0 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0007 | 0/0 | 2350 | 3 | 0 | 1 | 0 | 1 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0008 | 0/0 | 2350 | 3 | 0 | 0 | 0 | 1 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0009 | 0/0 | 2348 | 3 | 2 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2343): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0010 | 0/0 | 2350 | 3 | 0 | 0 | 3 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0011 | 0/0 | 2350 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0012 | 0/0 | 2348 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2343): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0013 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0014 | 0/0 | 2350 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0015 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0016 | 0/0 | 2350 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0017 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0018 | 0/0 | 2350 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0019 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0020 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0021 | 0/0 | 2350 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0022 | 0/0 | 2350 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0023 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0001t0024 | 0/0 | 2350 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0002t0001 | 0/0 | 2350 | 20 | 0 | 7 | 10 | 1 | 2 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0002t0003 | 0/0 | 2350 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| a0001c0003t0002 | 0/0 | 2348 | 16 | 0 | 1 | 14 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2343): Show |
chr5 | 174040706 | 174114179 |
| a0001c0004t0001 | 0/0 | 2350 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | AGAAG others(2345): Show |
chr5 | 174040706 | 174114179 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0008g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0008g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0009g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0009g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0009g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0010g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0010g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0012g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0016g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0017g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0018g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0019g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0020g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0021g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0022g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0023g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0001t0024g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | GBR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0010 | EUR | FIN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0144 | EUR | FIN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0176 | EUR | FIN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00408 | hp2 | a0001 | c0003 | t0002 | g0196 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0203 | EAS | CHS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0268 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0178 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0193 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0225 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0086 | EUR | IBS | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01928 | hp1 | a0001 | c0001 | t0024 | g0245 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0197 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0026 | EAS | CDX | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0270 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0248 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0024 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0029 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0282 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0247 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0228 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02965 | hp1 | a0001 | c0001 | t0015 | g0166 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03098 | hp1 | a0001 | c0001 | t0020 | g0170 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0025 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03492 | hp2 | a0001 | c0001 | t0021 | g0083 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0269 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03579 | hp2 | a0001 | c0001 | t0019 | g0223 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03654 | hp1 | a0001 | c0002 | t0003 | g0235 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0201 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0258 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03927 | hp1 | a0001 | c0001 | t0008 | g0275 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0239 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0251 | SAS | BEB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0173 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0260 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18952 | hp2 | a0001 | c0003 | t0002 | g0199 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18953 | hp1 | a0001 | c0001 | t0012 | g0147 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18953 | hp2 | a0001 | c0001 | t0010 | g0141 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18959 | hp1 | a0001 | c0001 | t0016 | g0067 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18964 | hp1 | a0001 | c0003 | t0002 | g0200 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18964 | hp2 | a0001 | c0001 | t0022 | g0090 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0209 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18999 | hp1 | a0001 | c0003 | t0002 | g0194 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19005 | hp2 | a0001 | c0003 | t0002 | g0202 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0064 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19056 | hp1 | a0001 | c0001 | t0014 | g0213 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0206 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19058 | hp1 | a0001 | c0001 | t0010 | g0130 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19064 | hp2 | a0001 | c0003 | t0002 | g0204 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19070 | hp1 | a0001 | c0003 | t0002 | g0195 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19082 | hp2 | a0001 | c0003 | t0002 | g0009 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19083 | hp1 | a0001 | c0003 | t0002 | g0009 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0121 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | YRI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0233 | EUR | TSI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA20905 | hp1 | a0001 | c0001 | t0018 | g0277 | SAS | GIH | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0010 | SAS | GIH | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | CLM | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | MSL | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | USA | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | USA | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA20300 | hp2 | a0001 | c0001 | t0023 | g0272 | AFR | USA | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | LWK | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0089 | REF | REF | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0149 | REF | REF | NSG2_chr5_174040706_174114179 | NSG2 | chr5 | 174040706 | 174114179 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:174064297 | G | A | 1 | a0001c0002 | 21 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(18): Show |
synonymous_variant | LOW | c.195G>A | p.Pro65Pro | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/5 | 355/2350 | 195/516 | 65/171 | chr5 | 174064297 | |||
| chr5:174107421 | G | A | 1 | a0001c0004 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.432G>A | p.Gln144Gln | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 592/2350 | 432/516 | 144/171 | chr5 | 174107421 | |||
| chr5:174107445 | G | A | 1 | a0001c0003 | 16 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(13): Show |
synonymous_variant | LOW | c.456G>A | p.Pro152Pro | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 616/2350 | 456/516 | 152/171 | chr5 | 174107445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:174045763 | C | G | 1 | a0001c0001t0010 | 3 | NA18953.hp2 NA19058.hp1 NA19086.hp1 |
5_prime_UTR_variant | MODIFIER | c.-103C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/5 | 993 | chr5 | 174045763 | ||||||
| chr5:174045817 | G | T | 6 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0009 others(3): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-49G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/5 | 939 | chr5 | 174045817 | ||||||
| chr5:174045824 | C | G | 1 | a0001c0001t0002 | 1 | HG02559.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/5 | 932 | chr5 | 174045824 | ||||||
| chr5:174107681 | C | T | 1 | a0001c0001t0022 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 176 | chr5 | 174107681 | ||||||
| chr5:174107798 | CTT | C | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(2): Show |
49 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*295_*296delTT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 295 | INFO_REALIGN_3_PRIME | chr5 | 174107798 | |||||
| chr5:174107874 | A | G | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
125 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*369A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 369 | chr5 | 174107874 | ||||||
| chr5:174107932 | C | T | 1 | a0001c0001t0005 | 5 | HG02486.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*427C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 427 | chr5 | 174107932 | ||||||
| chr5:174107933 | G | A | 1 | a0001c0001t0017 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 428 | chr5 | 174107933 | ||||||
| chr5:174108008 | G | A | 1 | a0001c0001t0018 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*503G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 503 | chr5 | 174108008 | ||||||
| chr5:174108041 | G | A | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
121 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*536G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 536 | chr5 | 174108041 | ||||||
| chr5:174108051 | G | C | 1 | a0001c0001t0013 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 546 | chr5 | 174108051 | ||||||
| chr5:174108084 | C | T | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
121 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*579C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 579 | chr5 | 174108084 | ||||||
| chr5:174108129 | C | G | 1 | a0001c0001t0020 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*624C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 624 | chr5 | 174108129 | ||||||
| chr5:174108213 | C | T | 2 | a0001c0001t0005 a0001c0001t0011 |
7 | HG02451.hp2 HG02486.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*708C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 708 | chr5 | 174108213 | ||||||
| chr5:174108311 | C | T | 1 | a0001c0001t0024 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*806C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 806 | chr5 | 174108311 | ||||||
| chr5:174108325 | G | C | 1 | a0001c0001t0014 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 820 | chr5 | 174108325 | ||||||
| chr5:174108434 | T | G | 1 | a0001c0001t0015 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*929T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 929 | chr5 | 174108434 | ||||||
| chr5:174108450 | A | C | 1 | a0001c0001t0016 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*945A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 945 | chr5 | 174108450 | ||||||
| chr5:174108482 | A | G | 1 | a0001c0001t0012 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*977A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 977 | chr5 | 174108482 | ||||||
| chr5:174108717 | G | C | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(13): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1212G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1212 | chr5 | 174108717 | ||||||
| chr5:174108739 | A | G | 1 | a0001c0001t0023 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1234A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1234 | chr5 | 174108739 | ||||||
| chr5:174108815 | A | T | 1 | a0001c0001t0008 | 3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1310A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1310 | chr5 | 174108815 | ||||||
| chr5:174108977 | C | T | 1 | a0001c0001t0019 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1472C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1472 | chr5 | 174108977 | ||||||
| chr5:174109166 | A | G | 1 | a0001c0001t0007 | 3 | HG00323.hp2 HG01258.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1661A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 5/5 | 1661 | chr5 | 174109166 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:174045893 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-23+50C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174045893 | |||||||
| chr5:174046092 | C | CA | 24 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(21): Show |
26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.-23+264dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 174046092 | ||||||
| chr5:174046092 | CA | C | 9 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(6): Show |
11 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23+264delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 174046092 | ||||||
| chr5:174046143 | T | C | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+300T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046143 | |||||||
| chr5:174046155 | A | G | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+312A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046155 | |||||||
| chr5:174046351 | A | G | 71 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0276 others(68): Show |
75 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.-22-383A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046351 | |||||||
| chr5:174046354 | CG | C | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.-22-372delG | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 174046354 | ||||||
| chr5:174046355 | G | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0139 a0001c0001t0002g0022 others(1): Show |
4 | HG01257.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-379G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046355 | |||||||
| chr5:174046359 | G | C | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-22-375G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046359 | |||||||
| chr5:174046376 | C | T | 15 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(12): Show |
15 | HG01099.hp1 HG01109.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-358C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 1/4 | chr5 | 174046376 | |||||||
| chr5:174047099 | G | C | 1 | a0001c0001t0003g0229 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.129+215G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047099 | |||||||
| chr5:174047230 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.129+346G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047230 | |||||||
| chr5:174047436 | T | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0002g0038 |
3 | HG00099.hp2 HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.129+552T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047436 | |||||||
| chr5:174047462 | A | G | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.129+578A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047462 | |||||||
| chr5:174047627 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.129+743G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047627 | |||||||
| chr5:174047728 | G | A | 3 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 |
4 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+844G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047728 | |||||||
| chr5:174047824 | T | C | 6 | a0001c0001t0002g0041 a0001c0001t0004g0040 a0001c0001t0004g0042 others(3): Show |
6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+940T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047824 | |||||||
| chr5:174047884 | T | G | 67 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0276 others(64): Show |
71 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.129+1000T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047884 | |||||||
| chr5:174047890 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.129+1006C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174047890 | |||||||
| chr5:174048003 | A | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.129+1119A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048003 | |||||||
| chr5:174048073 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.129+1189G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048073 | |||||||
| chr5:174048083 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0219 others(1): Show |
4 | HG01891.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+1199G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048083 | |||||||
| chr5:174048147 | A | G | 6 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0215 others(3): Show |
6 | HG02083.hp1 NA18979.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+1263A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048147 | |||||||
| chr5:174048375 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.129+1491G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048375 | |||||||
| chr5:174048613 | A | G | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+1729A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048613 | |||||||
| chr5:174048698 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.129+1814C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048698 | |||||||
| chr5:174048805 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.129+1921C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048805 | |||||||
| chr5:174048922 | C | T | 49 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(46): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.129+2038C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048922 | |||||||
| chr5:174048939 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.129+2055G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174048939 | |||||||
| chr5:174049078 | G | C | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.129+2194G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049078 | |||||||
| chr5:174049114 | C | T | 3 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0017g0029 |
3 | HG02572.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.129+2230C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049114 | |||||||
| chr5:174049135 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.129+2251C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049135 | |||||||
| chr5:174049136 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.129+2252G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049136 | |||||||
| chr5:174049155 | C | G | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+2271C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049155 | |||||||
| chr5:174049165 | G | C | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.129+2281G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049165 | |||||||
| chr5:174049204 | G | A | 1 | a0001c0001t0004g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.129+2320G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049204 | |||||||
| chr5:174049211 | G | C | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.129+2327G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049211 | |||||||
| chr5:174049264 | T | C | 7 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0005g0033 others(4): Show |
9 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+2380T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049264 | |||||||
| chr5:174049340 | AAAACAAA others(1): Show |
A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(13): Show |
17 | HG00099.hp2 HG00621.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.129+2476_129+2483d others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174049340 | ||||||
| chr5:174049432 | TGCACGC | T | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.129+2554_129+2559d others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174049432 | ||||||
| chr5:174049437 | G | A | 2 | a0001c0002t0001g0180 a0001c0002t0001g0187 |
2 | HG02523.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.129+2553G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049437 | |||||||
| chr5:174049443 | G | A | 6 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0232 others(3): Show |
6 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+2559G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049443 | |||||||
| chr5:174049449 | A | G | 1 | a0001c0003t0002g0209 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.129+2565A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049449 | |||||||
| chr5:174049647 | C | G | 1 | a0001c0001t0001g0208 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.129+2763C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049647 | |||||||
| chr5:174049736 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.129+2852G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049736 | |||||||
| chr5:174049936 | C | G | 6 | a0001c0001t0002g0041 a0001c0001t0004g0040 a0001c0001t0004g0042 others(3): Show |
6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+3052C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174049936 | |||||||
| chr5:174050032 | T | C | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.129+3148T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050032 | |||||||
| chr5:174050070 | C | T | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129+3186C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050070 | |||||||
| chr5:174050155 | T | C | 3 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0062 |
3 | HG02257.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.129+3271T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050155 | |||||||
| chr5:174050366 | C | T | 20 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0004g0013 others(17): Show |
21 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.129+3482C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050366 | |||||||
| chr5:174050400 | G | T | 10 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(7): Show |
10 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+3516G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050400 | |||||||
| chr5:174050554 | C | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.129+3670C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050554 | |||||||
| chr5:174050566 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.129+3682C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050566 | |||||||
| chr5:174050718 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0046 |
3 | HG00099.hp2 HG01099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.129+3834G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050718 | |||||||
| chr5:174050871 | G | A | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+3987G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050871 | |||||||
| chr5:174050964 | C | T | 11 | a0001c0002t0001g0008 a0001c0002t0001g0179 a0001c0002t0001g0180 others(8): Show |
12 | HG01934.hp1 HG01981.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.129+4080C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174050964 | |||||||
| chr5:174051022 | C | T | 2 | a0001c0001t0011g0024 a0001c0001t0011g0025 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.129+4138C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051022 | |||||||
| chr5:174051048 | G | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.129+4164G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051048 | |||||||
| chr5:174051168 | A | T | 1 | a0001c0001t0003g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.129+4284A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051168 | |||||||
| chr5:174051241 | G | T | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+4357G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051241 | |||||||
| chr5:174051255 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0007g0176 a0001c0001t0007g0178 |
3 | HG00323.hp2 HG01258.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.129+4371C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051255 | |||||||
| chr5:174051259 | T | C | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+4375T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051259 | |||||||
| chr5:174051575 | T | TCATC | 21 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0004g0013 others(18): Show |
22 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.129+4710_129+4713d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174051575 | ||||||
| chr5:174051595 | C | T | 2 | a0001c0002t0001g0174 a0001c0002t0001g0175 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.129+4711C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051595 | |||||||
| chr5:174051656 | G | A | 1 | a0001c0002t0001g0179 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.129+4772G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051656 | |||||||
| chr5:174051786 | G | T | 1 | a0001c0001t0007g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.129+4902G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051786 | |||||||
| chr5:174051935 | G | T | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
53 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.129+5051G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051935 | |||||||
| chr5:174051979 | A | T | 71 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0276 others(68): Show |
75 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.129+5095A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174051979 | |||||||
| chr5:174052075 | G | T | 4 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0279 others(1): Show |
4 | HG01928.hp2 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+5191G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052075 | |||||||
| chr5:174052087 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0013g0064 |
3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.129+5203G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052087 | |||||||
| chr5:174052088 | G | A | 1 | a0001c0001t0004g0011 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.129+5204G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052088 | |||||||
| chr5:174052123 | C | T | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
5 | HG02622.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+5239C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052123 | |||||||
| chr5:174052379 | C | T | 1 | a0001c0003t0002g0206 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.129+5495C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052379 | |||||||
| chr5:174052477 | C | T | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+5593C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052477 | |||||||
| chr5:174052564 | A | C | 1 | a0001c0001t0007g0178 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.129+5680A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052564 | |||||||
| chr5:174052672 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.129+5788C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052672 | |||||||
| chr5:174052806 | G | A | 1 | a0001c0001t0004g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.129+5922G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052806 | |||||||
| chr5:174052829 | G | C | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.129+5945G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052829 | |||||||
| chr5:174052893 | G | A | 1 | a0001c0001t0016g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.129+6009G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174052893 | |||||||
| chr5:174053225 | G | C | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.129+6341G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053225 | |||||||
| chr5:174053444 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.129+6560A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053444 | |||||||
| chr5:174053503 | C | T | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.129+6619C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053503 | |||||||
| chr5:174053822 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.129+6938C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053822 | |||||||
| chr5:174053904 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.129+7020A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174053904 | |||||||
| chr5:174054066 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02683.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.129+7182C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054066 | |||||||
| chr5:174054145 | C | T | 2 | a0001c0001t0003g0273 a0001c0001t0023g0272 |
2 | HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.129+7261C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054145 | |||||||
| chr5:174054339 | T | C | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.129+7455T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054339 | |||||||
| chr5:174054530 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.129+7646A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054530 | |||||||
| chr5:174054535 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.129+7651A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054535 | |||||||
| chr5:174054539 | C | T | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.129+7655C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054539 | |||||||
| chr5:174054710 | A | G | 77 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0041 others(74): Show |
81 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.129+7826A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054710 | |||||||
| chr5:174054936 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.129+8052T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054936 | |||||||
| chr5:174054978 | A | G | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+8094A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174054978 | |||||||
| chr5:174055057 | C | G | 17 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0003t0002g0009 others(14): Show |
18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.129+8173C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055057 | |||||||
| chr5:174055081 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.129+8197G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055081 | |||||||
| chr5:174055132 | T | C | 71 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0276 others(68): Show |
75 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.129+8248T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055132 | |||||||
| chr5:174055265 | C | T | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129+8381C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055265 | |||||||
| chr5:174055310 | T | G | 1 | a0001c0002t0001g0180 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.129+8426T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055310 | |||||||
| chr5:174055369 | G | A | 4 | a0001c0001t0003g0229 a0001c0001t0003g0236 a0001c0001t0003g0237 others(1): Show |
4 | HG01884.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+8485G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055369 | |||||||
| chr5:174055409 | C | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.129+8525C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055409 | |||||||
| chr5:174055411 | G | C | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129+8527G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055411 | |||||||
| chr5:174055429 | TA | T | 77 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0041 others(74): Show |
81 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.129+8555delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174055429 | ||||||
| chr5:174055467 | A | G | 46 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(43): Show |
46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.129+8583A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055467 | |||||||
| chr5:174055490 | C | T | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.129+8606C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055490 | |||||||
| chr5:174055578 | C | T | 49 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(46): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-8654C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055578 | |||||||
| chr5:174055651 | G | A | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130-8581G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055651 | |||||||
| chr5:174055925 | C | G | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-8307C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174055925 | |||||||
| chr5:174056117 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | NA18952.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.130-8115C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056117 | |||||||
| chr5:174056140 | A | G | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-8092A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056140 | |||||||
| chr5:174056171 | A | T | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130-8061A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056171 | |||||||
| chr5:174056256 | CCTT | C | 49 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(46): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-7975_130-7973d others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056256 | |||||||
| chr5:174056299 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.130-7933G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056299 | |||||||
| chr5:174056450 | A | G | 1 | a0001c0001t0002g0007 | 2 | HG01069.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.130-7782A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056450 | |||||||
| chr5:174056468 | G | A | 1 | a0001c0001t0004g0226 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.130-7764G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056468 | |||||||
| chr5:174056608 | T | C | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-7624T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056608 | |||||||
| chr5:174056615 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.130-7617G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056615 | |||||||
| chr5:174056678 | T | C | 3 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0062 |
3 | HG02257.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.130-7554T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056678 | |||||||
| chr5:174056824 | G | C | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-7408G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056824 | |||||||
| chr5:174056879 | T | C | 1 | a0001c0001t0011g0024 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.130-7353T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056879 | |||||||
| chr5:174056886 | T | C | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-7346T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174056886 | |||||||
| chr5:174057027 | C | T | 2 | a0001c0001t0011g0024 a0001c0001t0011g0025 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130-7205C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057027 | |||||||
| chr5:174057163 | G | C | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-7069G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057163 | |||||||
| chr5:174057417 | A | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0020g0170 |
3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130-6815A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057417 | |||||||
| chr5:174057490 | CTA | C | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-6741_130-6740d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057490 | |||||||
| chr5:174057491 | T | C | 2 | a0001c0001t0011g0024 a0001c0001t0011g0025 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130-6741T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057491 | |||||||
| chr5:174057534 | T | C | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-6698T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057534 | |||||||
| chr5:174057575 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.130-6657A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057575 | |||||||
| chr5:174057695 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.130-6537C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057695 | |||||||
| chr5:174057722 | T | C | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.130-6510T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057722 | |||||||
| chr5:174057808 | A | G | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130-6424A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057808 | |||||||
| chr5:174057823 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.130-6409G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057823 | |||||||
| chr5:174057857 | C | T | 6 | a0001c0001t0002g0041 a0001c0001t0004g0040 a0001c0001t0004g0042 others(3): Show |
6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-6375C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057857 | |||||||
| chr5:174057858 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.130-6374C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174057858 | |||||||
| chr5:174058086 | A | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130-6146A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058086 | |||||||
| chr5:174058405 | T | G | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-5827T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058405 | |||||||
| chr5:174058412 | A | C | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-5820A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058412 | |||||||
| chr5:174058586 | G | A | 1 | a0001c0001t0004g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.130-5646G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058586 | |||||||
| chr5:174058646 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.130-5586G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058646 | |||||||
| chr5:174058809 | C | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-5423C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174058809 | |||||||
| chr5:174059116 | C | T | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-5116C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059116 | |||||||
| chr5:174059280 | A | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.130-4952A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059280 | |||||||
| chr5:174059466 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.130-4766G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059466 | |||||||
| chr5:174059486 | G | A | 6 | a0001c0001t0002g0041 a0001c0001t0004g0040 a0001c0001t0004g0042 others(3): Show |
6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-4746G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059486 | |||||||
| chr5:174059562 | G | C | 2 | a0001c0001t0005g0016 a0001c0001t0005g0017 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.130-4670G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059562 | |||||||
| chr5:174059636 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0013g0064 |
3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.130-4596C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059636 | |||||||
| chr5:174059695 | A | G | 2 | a0001c0001t0005g0016 a0001c0001t0005g0017 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.130-4537A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059695 | |||||||
| chr5:174059697 | G | C | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-4535G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059697 | |||||||
| chr5:174059896 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.130-4336C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174059896 | |||||||
| chr5:174060065 | G | A | 3 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 |
4 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-4167G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060065 | |||||||
| chr5:174060109 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
16 | HG00099.hp2 HG00621.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.130-4123G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060109 | |||||||
| chr5:174060266 | G | A | 2 | a0001c0001t0017g0029 a0001c0001t0019g0223 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.130-3966G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060266 | |||||||
| chr5:174060341 | C | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-3891C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060341 | |||||||
| chr5:174060373 | AT | A | 9 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0004g0225 others(6): Show |
11 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-3847delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174060373 | ||||||
| chr5:174060526 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.130-3706G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060526 | |||||||
| chr5:174060536 | G | T | 17 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0003t0002g0009 others(14): Show |
18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.130-3696G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060536 | |||||||
| chr5:174060643 | AC | A | 111 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0198 others(108): Show |
117 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.130-3587delC | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174060643 | ||||||
| chr5:174060685 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.130-3547G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060685 | |||||||
| chr5:174060768 | G | C | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-3464G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060768 | |||||||
| chr5:174060779 | T | A | 7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-3453T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060779 | |||||||
| chr5:174060891 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130-3341C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174060891 | |||||||
| chr5:174061116 | T | C | 1 | a0001c0001t0013g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130-3116T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061116 | |||||||
| chr5:174061134 | T | TAC | 49 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(46): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-3084_130-3083d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174061134 | ||||||
| chr5:174061244 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.130-2988G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061244 | |||||||
| chr5:174061458 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.130-2774G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061458 | |||||||
| chr5:174061628 | A | G | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-2604A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061628 | |||||||
| chr5:174061672 | T | G | 4 | a0001c0001t0001g0012 a0001c0001t0002g0007 a0001c0001t0002g0015 others(1): Show |
5 | HG00099.hp1 HG01069.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-2560T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061672 | |||||||
| chr5:174061717 | C | T | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.130-2515C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061717 | |||||||
| chr5:174061816 | G | T | 1 | a0001c0001t0003g0271 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.130-2416G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061816 | |||||||
| chr5:174061883 | G | A | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-2349G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061883 | |||||||
| chr5:174061897 | C | T | 1 | a0001c0001t0003g0238 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.130-2335C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174061897 | |||||||
| chr5:174061909 | C | CT | 60 | a0001c0001t0001g0039 a0001c0001t0001g0150 a0001c0001t0001g0151 others(57): Show |
62 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.130-2301dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174061909 | ||||||
| chr5:174061909 | C | CTT | 11 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0003g0257 others(8): Show |
11 | HG01891.hp1 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-2302_130-2301d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174061909 | ||||||
| chr5:174061909 | CT | C | 48 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0001c0001t0001g0063 others(45): Show |
50 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.130-2301delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174061909 | ||||||
| chr5:174062456 | T | G | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-1776T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062456 | |||||||
| chr5:174062548 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0018 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.130-1684G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062548 | |||||||
| chr5:174062669 | G | A | 2 | a0001c0001t0002g0276 a0001c0001t0018g0277 |
2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.130-1563G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062669 | |||||||
| chr5:174062673 | T | TGG | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-1556_130-1555d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174062673 | ||||||
| chr5:174062762 | C | T | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-1470C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062762 | |||||||
| chr5:174062766 | G | A | 49 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(46): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-1466G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062766 | |||||||
| chr5:174062779 | C | G | 1 | a0001c0002t0001g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.130-1453C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062779 | |||||||
| chr5:174062898 | C | T | 1 | a0001c0001t0003g0256 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.130-1334C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062898 | |||||||
| chr5:174062917 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.130-1315G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062917 | |||||||
| chr5:174062923 | T | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-1309T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062923 | |||||||
| chr5:174062946 | G | A | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-1286G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062946 | |||||||
| chr5:174062963 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.130-1269A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062963 | |||||||
| chr5:174062990 | G | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-1242G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174062990 | |||||||
| chr5:174063107 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.130-1125T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063107 | |||||||
| chr5:174063257 | C | G | 1 | a0001c0001t0004g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.130-975C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063257 | |||||||
| chr5:174063446 | C | T | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-786C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063446 | |||||||
| chr5:174063517 | C | T | 11 | a0001c0001t0001g0012 a0001c0001t0002g0005 a0001c0001t0002g0006 others(8): Show |
14 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.130-715C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063517 | |||||||
| chr5:174063521 | C | CTATTT | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0139 others(7): Show |
10 | HG00621.hp2 HG01255.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.130-665_130-661dup others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | ||||||
| chr5:174063521 | C | CTATTTTA others(3): Show |
1 | a0001c0001t0004g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.130-670_130-661dup others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | ||||||
| chr5:174063521 | CTATTT | C | 115 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(112): Show |
116 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.130-665_130-661del others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | ||||||
| chr5:174063521 | CTATTTTA others(3): Show |
C | 24 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(21): Show |
26 | HG00408.hp2 HG01358.hp1 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.130-670_130-661del others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | ||||||
| chr5:174063521 | CTATTTTA others(8): Show |
C | 6 | a0001c0001t0001g0079 a0001c0001t0001g0278 a0001c0001t0002g0071 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-675_130-661del others(15): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | ||||||
| chr5:174063521 | CTATTTTA others(13): Show |
C | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0013g0064 |
3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.130-680_130-661del others(20): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063521 | ||||||
| chr5:174063543 | ATTTTATT others(14): Show |
A | 49 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(46): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.130-685_130-665del others(21): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063543 | ||||||
| chr5:174063548 | ATTTTATT others(9): Show |
A | 7 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0005g0033 others(4): Show |
9 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.130-680_130-665del others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 174063548 | ||||||
| chr5:174063573 | T | C | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-659T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063573 | |||||||
| chr5:174063574 | T | A | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-658T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063574 | |||||||
| chr5:174063577 | C | T | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-655C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063577 | |||||||
| chr5:174063578 | A | T | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.130-654A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063578 | |||||||
| chr5:174063610 | G | C | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.130-622G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063610 | |||||||
| chr5:174063612 | A | G | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-620A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063612 | |||||||
| chr5:174063614 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.130-618A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 2/4 | chr5 | 174063614 | |||||||
| chr5:174064450 | G | A | 1 | a0001c0001t0004g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.213+135G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064450 | |||||||
| chr5:174064843 | G | T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+528G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064843 | |||||||
| chr5:174064927 | A | G | 1 | a0001c0001t0006g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.213+612A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064927 | |||||||
| chr5:174064935 | T | G | 54 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(51): Show |
57 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.213+620T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064935 | |||||||
| chr5:174064989 | G | T | 1 | a0001c0001t0020g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.213+674G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174064989 | |||||||
| chr5:174065124 | C | T | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+809C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065124 | |||||||
| chr5:174065282 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.213+967C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065282 | |||||||
| chr5:174065308 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.213+993A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065308 | |||||||
| chr5:174065353 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.213+1038G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065353 | |||||||
| chr5:174065382 | A | C | 1 | a0001c0002t0001g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.213+1067A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065382 | |||||||
| chr5:174065555 | A | G | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.213+1240A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065555 | |||||||
| chr5:174065822 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0046 others(1): Show |
4 | HG00099.hp2 HG01099.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+1507C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065822 | |||||||
| chr5:174065920 | C | T | 17 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0003t0002g0009 others(14): Show |
18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+1605C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174065920 | |||||||
| chr5:174066011 | G | A | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+1696G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066011 | |||||||
| chr5:174066334 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.213+2019C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066334 | |||||||
| chr5:174066487 | A | G | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+2172A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066487 | |||||||
| chr5:174066497 | A | G | 2 | a0001c0001t0005g0016 a0001c0001t0005g0017 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.213+2182A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066497 | |||||||
| chr5:174066694 | T | TA | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
6 | HG00280.hp1 HG02071.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+2388dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066694 | ||||||
| chr5:174066695 | A | T | 7 | a0001c0001t0001g0172 a0001c0001t0002g0022 a0001c0001t0002g0023 others(4): Show |
8 | HG01257.hp2 HG02055.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+2380A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066695 | |||||||
| chr5:174066924 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.213+2609A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066924 | |||||||
| chr5:174066938 | C | T | 1 | a0001c0001t0009g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.213+2623C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066938 | |||||||
| chr5:174066949 | C | T | 46 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(43): Show |
46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+2634C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066949 | |||||||
| chr5:174066984 | T | C | 112 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0198 others(109): Show |
118 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.213+2669T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174066984 | |||||||
| chr5:174066989 | C | CA | 97 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0039 others(94): Show |
102 | HG00408.hp2 HG00642.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.213+2701dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | ||||||
| chr5:174066989 | C | CAA | 19 | a0001c0001t0001g0221 a0001c0001t0003g0031 a0001c0001t0003g0230 others(16): Show |
19 | HG01109.hp2 HG01243.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.213+2700_213+2701d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | ||||||
| chr5:174066989 | CA | C | 8 | a0001c0001t0001g0087 a0001c0001t0001g0094 a0001c0001t0001g0124 others(5): Show |
8 | HG01123.hp2 HG02735.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.213+2701delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | ||||||
| chr5:174066989 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0278 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.213+2692_213+2701d others(12): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | ||||||
| chr5:174066989 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.213+2691_213+2701d others(13): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | ||||||
| chr5:174066989 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.213+2690_213+2701d others(14): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174066989 | ||||||
| chr5:174067035 | T | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.213+2720T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067035 | |||||||
| chr5:174067057 | TAAAG | T | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+2744_213+2747d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174067057 | ||||||
| chr5:174067182 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.213+2867G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067182 | |||||||
| chr5:174067342 | CCT | C | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.213+3032_213+3033d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174067342 | ||||||
| chr5:174067461 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0219 others(1): Show |
4 | HG01891.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+3146G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067461 | |||||||
| chr5:174067463 | G | A | 1 | a0001c0001t0011g0024 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.213+3148G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067463 | |||||||
| chr5:174067549 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.213+3234G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067549 | |||||||
| chr5:174067810 | G | A | 17 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0003t0002g0009 others(14): Show |
18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+3495G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067810 | |||||||
| chr5:174067845 | G | T | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213+3530G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067845 | |||||||
| chr5:174067913 | A | T | 2 | a0001c0001t0005g0016 a0001c0001t0005g0017 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.213+3598A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067913 | |||||||
| chr5:174067983 | G | A | 1 | a0001c0001t0007g0176 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.213+3668G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174067983 | |||||||
| chr5:174068132 | A | C | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+3817A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068132 | |||||||
| chr5:174068242 | A | G | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+3927A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068242 | |||||||
| chr5:174068541 | G | GATGTGGA others(13): Show |
56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+4230_213+4231i others(22): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174068541 | ||||||
| chr5:174068600 | T | C | 46 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(43): Show |
46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+4285T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068600 | |||||||
| chr5:174068676 | TCTGGTGC others(46): Show |
T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0018 others(253): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.213+4512_213+4564d others(55): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174068676 | ||||||
| chr5:174068708 | AGGTGCTG others(52): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.213+4398_213+4456d others(61): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174068708 | ||||||
| chr5:174068771 | G | A | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+4456G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068771 | |||||||
| chr5:174068778 | G | A | 4 | a0001c0003t0002g0009 a0001c0003t0002g0194 a0001c0003t0002g0199 others(1): Show |
5 | HG03704.hp1 NA18952.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+4463G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068778 | |||||||
| chr5:174068827 | ATGGGAAT others(46): Show |
A | 1 | a0001c0001t0013g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.213+4565_213+4617d others(55): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174068827 | ||||||
| chr5:174068886 | A | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+4571A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174068886 | |||||||
| chr5:174069114 | G | A | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.213+4799G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069114 | |||||||
| chr5:174069401 | G | A | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.213+5086G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069401 | |||||||
| chr5:174069472 | C | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+5157C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069472 | |||||||
| chr5:174069498 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213+5183C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069498 | |||||||
| chr5:174069507 | A | G | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+5192A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069507 | |||||||
| chr5:174069564 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.213+5249A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069564 | |||||||
| chr5:174069755 | G | C | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+5440G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069755 | |||||||
| chr5:174069836 | C | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+5521C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069836 | |||||||
| chr5:174069843 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0013g0064 |
3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.213+5528G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069843 | |||||||
| chr5:174069874 | A | AT | 60 | a0001c0001t0001g0021 a0001c0001t0001g0120 a0001c0001t0001g0132 others(57): Show |
62 | HG01099.hp1 HG01109.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.213+5580dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174069874 | ||||||
| chr5:174069874 | A | ATT | 8 | a0001c0001t0002g0276 a0001c0001t0003g0273 a0001c0001t0004g0011 others(5): Show |
9 | HG01167.hp2 HG01169.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.213+5579_213+5580d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174069874 | ||||||
| chr5:174069874 | A | T | 1 | a0001c0001t0004g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.213+5559A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069874 | |||||||
| chr5:174069874 | AT | A | 31 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0126 others(28): Show |
32 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.213+5580delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174069874 | ||||||
| chr5:174069897 | A | C | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+5582A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069897 | |||||||
| chr5:174069996 | G | A | 5 | a0001c0001t0001g0205 a0001c0003t0002g0009 a0001c0003t0002g0194 others(2): Show |
6 | HG03704.hp1 NA18952.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+5681G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174069996 | |||||||
| chr5:174070003 | A | G | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+5688A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070003 | |||||||
| chr5:174070039 | G | A | 6 | a0001c0001t0002g0041 a0001c0001t0004g0040 a0001c0001t0004g0042 others(3): Show |
6 | HG02559.hp2 HG03130.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+5724G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070039 | |||||||
| chr5:174070054 | G | A | 2 | a0001c0001t0011g0024 a0001c0001t0011g0025 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.213+5739G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070054 | |||||||
| chr5:174070140 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213+5825G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070140 | |||||||
| chr5:174070162 | C | CA | 6 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0256 others(3): Show |
6 | HG01261.hp1 HG01928.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+5848dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174070162 | ||||||
| chr5:174070184 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0219 others(1): Show |
4 | HG01891.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+5869G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070184 | |||||||
| chr5:174070189 | G | C | 49 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(46): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.213+5874G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070189 | |||||||
| chr5:174070389 | T | C | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.213+6074T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070389 | |||||||
| chr5:174070391 | T | A | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+6076T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070391 | |||||||
| chr5:174070570 | T | C | 1 | a0001c0002t0001g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.213+6255T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070570 | |||||||
| chr5:174070653 | A | G | 2 | a0001c0001t0004g0002 a0001c0001t0004g0030 |
3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.213+6338A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070653 | |||||||
| chr5:174070793 | C | T | 11 | a0001c0001t0001g0012 a0001c0001t0002g0005 a0001c0001t0002g0006 others(8): Show |
14 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.213+6478C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070793 | |||||||
| chr5:174070800 | C | T | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+6485C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070800 | |||||||
| chr5:174070889 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.213+6574G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070889 | |||||||
| chr5:174070908 | G | A | 5 | a0001c0001t0002g0041 a0001c0001t0004g0042 a0001c0001t0004g0043 others(2): Show |
5 | HG02559.hp2 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+6593G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174070908 | |||||||
| chr5:174071003 | G | A | 49 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(46): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.213+6688G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071003 | |||||||
| chr5:174071092 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.213+6777C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071092 | |||||||
| chr5:174071119 | A | C | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0008g0010 others(2): Show |
7 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+6804A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071119 | |||||||
| chr5:174071283 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00408.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.213+6968C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071283 | |||||||
| chr5:174071442 | G | A | 1 | a0001c0001t0003g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.213+7127G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071442 | |||||||
| chr5:174071619 | G | A | 1 | a0001c0001t0006g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.213+7304G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071619 | |||||||
| chr5:174071625 | C | T | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+7310C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071625 | |||||||
| chr5:174071683 | G | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0279 others(1): Show |
4 | HG01928.hp2 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+7368G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071683 | |||||||
| chr5:174071683 | G | C | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.213+7368G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071683 | |||||||
| chr5:174071691 | G | T | 1 | a0001c0001t0002g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.213+7376G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071691 | |||||||
| chr5:174071944 | G | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0046 others(3): Show |
6 | HG00099.hp2 HG01099.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+7629G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071944 | |||||||
| chr5:174071996 | G | A | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+7681G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174071996 | |||||||
| chr5:174072022 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.213+7707A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072022 | |||||||
| chr5:174072358 | G | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+8043G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072358 | |||||||
| chr5:174072431 | A | G | 6 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0256 others(3): Show |
6 | HG01261.hp1 HG01928.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+8116A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072431 | |||||||
| chr5:174072570 | G | A | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+8255G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072570 | |||||||
| chr5:174072795 | G | A | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.213+8480G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072795 | |||||||
| chr5:174072882 | G | C | 4 | a0001c0001t0004g0002 a0001c0001t0004g0027 a0001c0001t0004g0028 others(1): Show |
5 | HG02630.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+8567G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072882 | |||||||
| chr5:174072933 | C | T | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+8618C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072933 | |||||||
| chr5:174072983 | CAAAT | C | 3 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 |
3 | HG01433.hp1 HG03041.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.213+8669_213+8672d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072983 | |||||||
| chr5:174072984 | A | AAATGAAT others(1): Show |
2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+8686_213+8693d others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174072984 | ||||||
| chr5:174072987 | T | G | 6 | a0001c0002t0001g0008 a0001c0002t0001g0181 a0001c0002t0001g0182 others(3): Show |
7 | HG01934.hp1 HG01981.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+8672T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174072987 | |||||||
| chr5:174073043 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.213+8728G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073043 | |||||||
| chr5:174073488 | G | C | 1 | a0001c0001t0002g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.213+9173G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073488 | |||||||
| chr5:174073515 | G | T | 46 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(43): Show |
46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+9200G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073515 | |||||||
| chr5:174073528 | T | C | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+9213T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073528 | |||||||
| chr5:174073703 | T | C | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+9388T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073703 | |||||||
| chr5:174073886 | G | A | 1 | a0001c0001t0006g0247 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.213+9571G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174073886 | |||||||
| chr5:174074046 | C | T | 2 | a0001c0001t0004g0002 a0001c0001t0004g0030 |
3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.213+9731C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074046 | |||||||
| chr5:174074124 | C | T | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+9809C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074124 | |||||||
| chr5:174074309 | G | A | 7 | a0001c0001t0001g0056 a0001c0001t0002g0041 a0001c0001t0004g0040 others(4): Show |
7 | HG01496.hp1 HG02559.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+9994G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074309 | |||||||
| chr5:174074375 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.213+10060A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074375 | |||||||
| chr5:174074538 | A | T | 1 | a0001c0001t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.213+10223A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074538 | |||||||
| chr5:174074587 | A | C | 1 | a0001c0001t0001g0039 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.213+10272A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074587 | |||||||
| chr5:174074640 | G | A | 4 | a0001c0001t0004g0002 a0001c0001t0004g0027 a0001c0001t0004g0028 others(1): Show |
5 | HG02630.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+10325G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074640 | |||||||
| chr5:174074750 | A | G | 17 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0003t0002g0009 others(14): Show |
18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+10435A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074750 | |||||||
| chr5:174074863 | G | T | 2 | a0001c0001t0011g0024 a0001c0001t0011g0025 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.213+10548G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174074863 | |||||||
| chr5:174075281 | C | G | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+10966C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075281 | |||||||
| chr5:174075288 | G | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+10973G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075288 | |||||||
| chr5:174075307 | C | G | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+10992C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075307 | |||||||
| chr5:174075428 | C | T | 1 | a0001c0001t0013g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.213+11113C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075428 | |||||||
| chr5:174075441 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.213+11126T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075441 | |||||||
| chr5:174075488 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0139 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.213+11173G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075488 | |||||||
| chr5:174075508 | G | A | 49 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(46): Show |
50 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.213+11193G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075508 | |||||||
| chr5:174075646 | C | T | 1 | a0001c0002t0001g0184 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.213+11331C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075646 | |||||||
| chr5:174075749 | T | C | 2 | a0001c0001t0003g0003 a0001c0001t0003g0032 |
3 | HG02145.hp2 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.213+11434T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174075749 | |||||||
| chr5:174076085 | T | G | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+11770T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076085 | |||||||
| chr5:174076153 | C | T | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+11838C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076153 | |||||||
| chr5:174076233 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.213+11918C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076233 | |||||||
| chr5:174076285 | A | G | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+11970A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076285 | |||||||
| chr5:174076314 | AG | A | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+12001delG | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174076314 | ||||||
| chr5:174076336 | AAAG | A | 51 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.213+12022_213+1202 others(7): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076336 | |||||||
| chr5:174076447 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.213+12132G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076447 | |||||||
| chr5:174076735 | G | C | 1 | a0001c0001t0002g0023 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.213+12420G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076735 | |||||||
| chr5:174076915 | C | A | 1 | a0001c0003t0002g0206 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.213+12600C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076915 | |||||||
| chr5:174076932 | G | A | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.213+12617G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076932 | |||||||
| chr5:174076950 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.213+12635C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076950 | |||||||
| chr5:174076995 | T | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG02015.hp2 NA18951.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+12680T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174076995 | |||||||
| chr5:174077014 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.213+12699A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077014 | |||||||
| chr5:174077125 | C | T | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+12810C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077125 | |||||||
| chr5:174077519 | C | T | 230 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(227): Show |
237 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.213+13204C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077519 | |||||||
| chr5:174077713 | T | C | 46 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(43): Show |
46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+13398T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077713 | |||||||
| chr5:174077747 | G | GT | 3 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0062 |
3 | HG02257.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.213+13437dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174077747 | ||||||
| chr5:174077906 | T | C | 56 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.213+13591T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174077906 | |||||||
| chr5:174078093 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.213+13778C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078093 | |||||||
| chr5:174078247 | G | A | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+13932G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078247 | |||||||
| chr5:174078276 | CCA | C | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+13978_213+1397 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174078276 | ||||||
| chr5:174078289 | C | T | 1 | a0001c0003t0002g0209 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.213+13974C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078289 | |||||||
| chr5:174078453 | G | A | 43 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(40): Show |
43 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.213+14138G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078453 | |||||||
| chr5:174078964 | C | T | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+14649C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174078964 | |||||||
| chr5:174079019 | A | G | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+14704A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079019 | |||||||
| chr5:174079029 | C | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0013g0064 |
3 | HG02809.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.213+14714C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079029 | |||||||
| chr5:174079029 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.213+14714C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079029 | |||||||
| chr5:174079107 | C | G | 2 | a0001c0003t0002g0009 a0001c0003t0002g0194 |
3 | NA18999.hp1 NA19082.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.213+14792C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079107 | |||||||
| chr5:174079132 | C | T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+14817C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079132 | |||||||
| chr5:174079247 | T | TTC | 47 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(44): Show |
48 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.213+14948_213+1494 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174079247 | ||||||
| chr5:174079247 | TTCTC | T | 16 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0003t0002g0009 others(13): Show |
17 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.213+14946_213+1494 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174079247 | ||||||
| chr5:174079257 | C | G | 9 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(6): Show |
11 | HG00280.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+14942C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079257 | |||||||
| chr5:174079263 | C | CT | 12 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(9): Show |
15 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.213+14961dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174079263 | ||||||
| chr5:174079263 | C | CTT | 11 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.213+14960_213+1496 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174079263 | ||||||
| chr5:174079269 | T | A | 2 | a0001c0001t0001g0066 a0001c0001t0013g0064 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.213+14954T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079269 | |||||||
| chr5:174079331 | C | G | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.213+15016C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079331 | |||||||
| chr5:174079360 | C | T | 17 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0003t0002g0009 others(14): Show |
18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+15045C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079360 | |||||||
| chr5:174079547 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.213+15232T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079547 | |||||||
| chr5:174079607 | G | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+15292G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079607 | |||||||
| chr5:174079658 | A | C | 7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+15343A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079658 | |||||||
| chr5:174079769 | G | A | 48 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(45): Show |
49 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.213+15454G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079769 | |||||||
| chr5:174079849 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.213+15534G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079849 | |||||||
| chr5:174079857 | T | C | 48 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(45): Show |
49 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.213+15542T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174079857 | |||||||
| chr5:174080047 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.213+15732T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080047 | |||||||
| chr5:174080077 | A | G | 9 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(6): Show |
11 | HG00280.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+15762A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080077 | |||||||
| chr5:174080214 | A | G | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+15899A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080214 | |||||||
| chr5:174080258 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.213+15943C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080258 | |||||||
| chr5:174080449 | G | C | 1 | a0001c0002t0001g0186 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.213+16134G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080449 | |||||||
| chr5:174080467 | T | TTTTCTTT others(9): Show |
29 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0221 others(26): Show |
30 | HG01167.hp1 HG01257.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.213+16197_213+1621 others(20): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080467 | ||||||
| chr5:174080467 | T | TTTTCTTT others(25): Show |
1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+16181_213+1621 others(36): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080467 | ||||||
| chr5:174080501 | TTCTTTCT others(5): Show |
T | 2 | a0001c0001t0001g0215 a0001c0001t0004g0011 |
3 | HG01167.hp2 HG01169.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.213+16197_213+1620 others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080501 | ||||||
| chr5:174080511 | CCCTCTTT others(7): Show |
C | 1 | a0001c0001t0001g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.213+16197_213+1621 others(18): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080511 | |||||||
| chr5:174080513 | CTCTT | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
15 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.213+16210_213+1621 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080513 | ||||||
| chr5:174080517 | T | TTCTTTCT others(5): Show |
17 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0003t0002g0009 others(14): Show |
18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+16212_213+1621 others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080517 | ||||||
| chr5:174080521 | T | C | 2 | a0001c0001t0002g0276 a0001c0001t0018g0277 |
2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.213+16206T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080521 | |||||||
| chr5:174080525 | T | C | 3 | a0001c0001t0001g0215 a0001c0001t0002g0276 a0001c0001t0018g0277 |
3 | HG02083.hp1 HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.213+16210T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080525 | |||||||
| chr5:174080525 | T | TTC | 45 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0068 others(42): Show |
46 | HG00323.hp2 HG00621.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+16234_213+1623 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080525 | T | TTCCCTCT others(11): Show |
7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+16212_213+1621 others(22): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080525 | T | TTCTTTCT others(31): Show |
2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+16213_213+1621 others(42): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080525 | T | TTCTTTCT others(29): Show |
1 | a0001c0001t0003g0234 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.213+16213_213+1621 others(40): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080525 | T | TTCTTTCT others(23): Show |
5 | a0001c0001t0003g0229 a0001c0001t0003g0236 a0001c0001t0003g0237 others(2): Show |
5 | HG01884.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+16213_213+1621 others(34): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080525 | T | TTCTTTCT others(27): Show |
25 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0232 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.213+16213_213+1621 others(38): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080525 | T | TTCTTTCT others(29): Show |
1 | a0001c0001t0003g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.213+16213_213+1621 others(40): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080525 | T | TTCTTTCT others(31): Show |
8 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0252 others(5): Show |
8 | HG01261.hp1 HG01928.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+16213_213+1621 others(42): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080525 | T | TTCTTTCT others(33): Show |
3 | a0001c0001t0003g0242 a0001c0001t0003g0251 a0001c0001t0006g0247 |
3 | HG02683.hp2 HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.213+16213_213+1621 others(44): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080525 | TTCTC | T | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0070 others(10): Show |
13 | HG00280.hp2 HG00408.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.213+16232_213+1623 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080525 | ||||||
| chr5:174080527 | C | CTT | 3 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 |
4 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+16213_213+1621 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080527 | ||||||
| chr5:174080529 | C | T | 28 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0001g0221 others(25): Show |
30 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.213+16214C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080529 | |||||||
| chr5:174080551 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0004g0011 |
3 | HG01167.hp2 HG01169.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.213+16236T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080551 | |||||||
| chr5:174080554 | T | TCTCTCTC others(18): Show |
2 | a0001c0001t0003g0003 a0001c0001t0003g0032 |
3 | HG02145.hp2 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.213+16239_213+1624 others(29): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080554 | |||||||
| chr5:174080554 | T | TCTCTCTC others(20): Show |
1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.213+16239_213+1624 others(31): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080554 | |||||||
| chr5:174080556 | T | C | 4 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(1): Show |
6 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+16241T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080556 | |||||||
| chr5:174080567 | CTTTCTTT others(3): Show |
C | 2 | a0001c0001t0002g0276 a0001c0001t0018g0277 |
2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.213+16255_213+1626 others(14): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174080567 | ||||||
| chr5:174080674 | G | T | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.213+16359G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080674 | |||||||
| chr5:174080766 | T | C | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+16451T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080766 | |||||||
| chr5:174080805 | C | T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+16490C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080805 | |||||||
| chr5:174080809 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213+16494C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080809 | |||||||
| chr5:174080917 | A | T | 5 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0009g0268 others(2): Show |
5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+16602A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174080917 | |||||||
| chr5:174081388 | A | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+17073A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081388 | |||||||
| chr5:174081494 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.213+17179C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081494 | |||||||
| chr5:174081523 | G | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+17208G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081523 | |||||||
| chr5:174081637 | G | A | 53 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(50): Show |
56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.213+17322G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081637 | |||||||
| chr5:174081641 | A | AT | 7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+17333dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174081641 | ||||||
| chr5:174081648 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.213+17333T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081648 | |||||||
| chr5:174081677 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.213+17362T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081677 | |||||||
| chr5:174081882 | C | T | 3 | a0001c0001t0003g0241 a0001c0001t0006g0255 a0001c0001t0017g0029 |
3 | HG01243.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.213+17567C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081882 | |||||||
| chr5:174081887 | C | CA | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
8 | HG00099.hp2 HG01099.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.213+17593dupA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174081887 | ||||||
| chr5:174081887 | CA | C | 65 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0117 others(62): Show |
69 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.213+17593delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174081887 | ||||||
| chr5:174081887 | CAA | C | 45 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0229 others(42): Show |
46 | HG00642.hp1 HG01071.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+17592_213+1759 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174081887 | ||||||
| chr5:174081907 | A | G | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+17592A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174081907 | |||||||
| chr5:174082099 | C | G | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+17784C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082099 | |||||||
| chr5:174082365 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.213+18050A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082365 | |||||||
| chr5:174082539 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0097 others(1): Show |
4 | HG01192.hp2 HG01243.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+18224G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082539 | |||||||
| chr5:174082565 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.213+18250G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082565 | |||||||
| chr5:174082585 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.213+18270C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082585 | |||||||
| chr5:174082874 | C | T | 2 | a0001c0001t0004g0002 a0001c0001t0004g0030 |
3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.213+18559C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082874 | |||||||
| chr5:174082918 | C | T | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+18603C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082918 | |||||||
| chr5:174082928 | G | A | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+18613G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082928 | |||||||
| chr5:174082936 | C | A | 55 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(52): Show |
58 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.213+18621C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174082936 | |||||||
| chr5:174083018 | A | G | 2 | a0001c0001t0004g0002 a0001c0001t0004g0030 |
3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.213+18703A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083018 | |||||||
| chr5:174083231 | C | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.213+18916C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083231 | |||||||
| chr5:174083266 | A | G | 111 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0198 others(108): Show |
117 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.213+18951A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083266 | |||||||
| chr5:174083542 | A | G | 53 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(50): Show |
56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.213+19227A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083542 | |||||||
| chr5:174083774 | T | C | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+19459T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083774 | |||||||
| chr5:174083807 | G | A | 6 | a0001c0001t0001g0205 a0001c0001t0022g0090 a0001c0003t0002g0009 others(3): Show |
7 | HG03704.hp1 NA18952.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+19492G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083807 | |||||||
| chr5:174083832 | G | C | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+19517G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083832 | |||||||
| chr5:174083834 | C | T | 4 | a0001c0001t0002g0023 a0001c0001t0009g0268 a0001c0001t0009g0269 others(1): Show |
4 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+19519C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083834 | |||||||
| chr5:174083954 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.213+19639G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083954 | |||||||
| chr5:174083963 | G | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+19648G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174083963 | |||||||
| chr5:174084000 | A | C | 1 | a0001c0001t0003g0254 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.213+19685A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084000 | |||||||
| chr5:174084009 | G | A | 17 | a0001c0002t0001g0008 a0001c0002t0001g0060 a0001c0002t0001g0061 others(14): Show |
18 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.213+19694G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084009 | |||||||
| chr5:174084093 | A | C | 53 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(50): Show |
56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.213+19778A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084093 | |||||||
| chr5:174084454 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG02015.hp2 NA18951.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-19774G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084454 | |||||||
| chr5:174084518 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.214-19710G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084518 | |||||||
| chr5:174084736 | G | C | 10 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(7): Show |
11 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-19492G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084736 | |||||||
| chr5:174084742 | G | A | 1 | a0001c0001t0003g0261 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.214-19486G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084742 | |||||||
| chr5:174084816 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.214-19412A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174084816 | |||||||
| chr5:174085021 | G | C | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.214-19207G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085021 | |||||||
| chr5:174085313 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.214-18915G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085313 | |||||||
| chr5:174085388 | C | G | 46 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(43): Show |
47 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.214-18840C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085388 | |||||||
| chr5:174085431 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
16 | HG00099.hp2 HG00621.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.214-18797C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085431 | |||||||
| chr5:174085432 | A | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0216 a0001c0001t0010g0141 |
3 | NA18953.hp2 NA19058.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.214-18796A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085432 | |||||||
| chr5:174085728 | C | T | 8 | a0001c0001t0002g0041 a0001c0001t0004g0040 a0001c0001t0004g0042 others(5): Show |
8 | HG02451.hp2 HG02559.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.214-18500C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085728 | |||||||
| chr5:174085915 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.214-18313T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174085915 | |||||||
| chr5:174086068 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.214-18160G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086068 | |||||||
| chr5:174086078 | C | T | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214-18150C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086078 | |||||||
| chr5:174086157 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.214-18071A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086157 | |||||||
| chr5:174086186 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.214-18042A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086186 | |||||||
| chr5:174086235 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.214-17993C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086235 | |||||||
| chr5:174086393 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.214-17835T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086393 | |||||||
| chr5:174086514 | G | A | 5 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0009g0268 others(2): Show |
5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-17714G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086514 | |||||||
| chr5:174086528 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.214-17700A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086528 | |||||||
| chr5:174086718 | C | T | 11 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-17510C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174086718 | |||||||
| chr5:174087000 | C | T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-17228C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087000 | |||||||
| chr5:174087070 | T | C | 11 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-17158T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087070 | |||||||
| chr5:174087237 | G | T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-16991G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087237 | |||||||
| chr5:174087518 | G | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0157 a0001c0001t0001g0217 |
3 | NA18966.hp2 NA19060.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.214-16710G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087518 | |||||||
| chr5:174087704 | C | A | 7 | a0001c0001t0002g0004 a0001c0001t0002g0071 a0001c0001t0002g0072 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-16524C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087704 | |||||||
| chr5:174087787 | CA | C | 9 | a0001c0001t0001g0105 a0001c0001t0001g0123 a0001c0001t0002g0276 others(6): Show |
10 | HG01167.hp2 HG01169.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-16427delA | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174087787 | ||||||
| chr5:174087856 | A | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.214-16372A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087856 | |||||||
| chr5:174087889 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.214-16339G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087889 | |||||||
| chr5:174087890 | G | A | 2 | a0001c0003t0002g0203 a0001c0003t0002g0206 |
2 | HG00673.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.214-16338G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174087890 | |||||||
| chr5:174088309 | C | T | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0005g0033 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-15919C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088309 | |||||||
| chr5:174088319 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.214-15909G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088319 | |||||||
| chr5:174088346 | C | T | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0005g0033 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-15882C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088346 | |||||||
| chr5:174088372 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.214-15856G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088372 | |||||||
| chr5:174088541 | G | A | 1 | a0001c0001t0011g0024 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.214-15687G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088541 | |||||||
| chr5:174088737 | G | A | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-15491G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088737 | |||||||
| chr5:174088765 | G | A | 53 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(50): Show |
56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.214-15463G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088765 | |||||||
| chr5:174088957 | A | C | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214-15271A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174088957 | |||||||
| chr5:174089178 | G | A | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-15050G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089178 | |||||||
| chr5:174089179 | C | T | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0002 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-15049C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089179 | |||||||
| chr5:174089235 | C | T | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.214-14993C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089235 | |||||||
| chr5:174089314 | C | T | 10 | a0001c0001t0001g0132 a0001c0001t0001g0154 a0001c0001t0001g0189 others(7): Show |
10 | HG00673.hp1 HG02071.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-14914C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089314 | |||||||
| chr5:174089367 | G | A | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-14861G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089367 | |||||||
| chr5:174089517 | G | A | 1 | a0001c0001t0004g0011 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.214-14711G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089517 | |||||||
| chr5:174089517 | G | T | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-14711G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089517 | |||||||
| chr5:174089567 | T | C | 53 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0031 others(50): Show |
56 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.214-14661T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089567 | |||||||
| chr5:174089681 | A | G | 46 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(43): Show |
47 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.214-14547A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089681 | |||||||
| chr5:174089731 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.214-14497C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089731 | |||||||
| chr5:174089776 | G | A | 5 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0009g0268 others(2): Show |
5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-14452G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089776 | |||||||
| chr5:174089776 | G | C | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-14452G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089776 | |||||||
| chr5:174089786 | T | C | 17 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0003t0002g0009 others(14): Show |
18 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.214-14442T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089786 | |||||||
| chr5:174089798 | T | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0259 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.214-14430T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089798 | |||||||
| chr5:174089811 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.214-14417G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089811 | |||||||
| chr5:174089872 | C | T | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-14356C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174089872 | |||||||
| chr5:174090032 | G | A | 5 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0005g0033 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-14196G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090032 | |||||||
| chr5:174090112 | C | T | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.214-14116C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090112 | |||||||
| chr5:174090263 | C | T | 3 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0003g0267 |
3 | HG01891.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.214-13965C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090263 | |||||||
| chr5:174090322 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0278 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.214-13906C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090322 | |||||||
| chr5:174090341 | T | C | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-13887T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090341 | |||||||
| chr5:174090353 | G | A | 1 | a0001c0001t0015g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.214-13875G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090353 | |||||||
| chr5:174090620 | G | A | 4 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0062 others(1): Show |
4 | HG02257.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-13608G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090620 | |||||||
| chr5:174090740 | C | T | 45 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(42): Show |
47 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.214-13488C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090740 | |||||||
| chr5:174090801 | A | G | 39 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0066 others(36): Show |
43 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.214-13427A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090801 | |||||||
| chr5:174090890 | G | A | 1 | a0001c0001t0015g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.214-13338G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090890 | |||||||
| chr5:174090920 | G | A | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.214-13308G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090920 | |||||||
| chr5:174090983 | C | T | 1 | a0001c0001t0004g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214-13245C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174090983 | |||||||
| chr5:174091039 | C | CT | 81 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(78): Show |
82 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.214-13169dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091039 | ||||||
| chr5:174091039 | CT | C | 53 | a0001c0001t0001g0012 a0001c0001t0001g0128 a0001c0001t0001g0139 others(50): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.214-13169delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091039 | ||||||
| chr5:174091088 | T | G | 1 | a0001c0001t0016g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.214-13140T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091088 | |||||||
| chr5:174091100 | A | C | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-13128A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091100 | |||||||
| chr5:174091220 | A | C | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-13008A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091220 | |||||||
| chr5:174091236 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.214-12992G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091236 | |||||||
| chr5:174091311 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG00099.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.214-12917A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091311 | |||||||
| chr5:174091483 | C | T | 1 | a0001c0003t0002g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.214-12745C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091483 | |||||||
| chr5:174091595 | G | A | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-12633G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091595 | |||||||
| chr5:174091615 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0218 |
2 | HG01168.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.214-12613A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091615 | |||||||
| chr5:174091644 | G | GGT | 21 | a0001c0001t0001g0070 a0001c0001t0001g0125 a0001c0001t0001g0126 others(18): Show |
22 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.214-12543_214-1254 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | ||||||
| chr5:174091644 | G | GGTGT | 4 | a0001c0001t0001g0085 a0001c0001t0001g0108 a0001c0001t0001g0167 others(1): Show |
4 | HG01074.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-12545_214-1254 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | ||||||
| chr5:174091644 | GGT | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0034 others(124): Show |
133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.214-12543_214-1254 others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | ||||||
| chr5:174091644 | GGTGT | G | 75 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(72): Show |
76 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.214-12545_214-1254 others(8): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | ||||||
| chr5:174091644 | GGTGTGT | G | 7 | a0001c0001t0001g0165 a0001c0001t0002g0276 a0001c0001t0004g0011 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-12547_214-1254 others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | ||||||
| chr5:174091644 | GGTGTGTG others(5): Show |
G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0216 a0001c0001t0010g0141 |
3 | NA18953.hp2 NA19058.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.214-12553_214-1254 others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | ||||||
| chr5:174091644 | GGTGTGTG others(13): Show |
G | 1 | a0001c0002t0001g0174 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.214-12561_214-1254 others(24): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174091644 | ||||||
| chr5:174091819 | T | C | 1 | a0001c0001t0016g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.214-12409T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091819 | |||||||
| chr5:174091957 | A | C | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-12271A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174091957 | |||||||
| chr5:174092059 | C | A | 3 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 |
4 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-12169C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092059 | |||||||
| chr5:174092386 | C | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02040.hp2 NA18955.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-11842C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092386 | |||||||
| chr5:174092691 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.214-11537A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092691 | |||||||
| chr5:174092719 | C | T | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-11509C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092719 | |||||||
| chr5:174092748 | T | C | 5 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0009g0268 others(2): Show |
5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-11480T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092748 | |||||||
| chr5:174092921 | G | C | 5 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0085 others(2): Show |
5 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-11307G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174092921 | |||||||
| chr5:174093034 | C | G | 3 | a0001c0001t0005g0033 a0001c0001t0005g0207 a0001c0001t0005g0259 |
3 | HG02886.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214-11194C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093034 | |||||||
| chr5:174093041 | G | A | 1 | a0001c0001t0004g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.214-11187G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093041 | |||||||
| chr5:174093185 | A | G | 45 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(42): Show |
47 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.214-11043A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093185 | |||||||
| chr5:174093214 | C | T | 1 | a0001c0001t0004g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.214-11014C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093214 | |||||||
| chr5:174093226 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.214-11002G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093226 | |||||||
| chr5:174093251 | A | T | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-10977A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093251 | |||||||
| chr5:174093348 | C | T | 4 | a0001c0001t0004g0042 a0001c0001t0004g0043 a0001c0001t0004g0044 others(1): Show |
4 | HG03471.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-10880C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093348 | |||||||
| chr5:174093363 | A | G | 1 | a0001c0003t0002g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.214-10865A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093363 | |||||||
| chr5:174093392 | C | T | 3 | a0001c0001t0005g0033 a0001c0001t0005g0207 a0001c0001t0005g0259 |
3 | HG02886.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214-10836C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093392 | |||||||
| chr5:174093542 | A | T | 2 | a0001c0002t0001g0182 a0001c0002t0001g0184 |
2 | NA18943.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.214-10686A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093542 | |||||||
| chr5:174093824 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.214-10404G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093824 | |||||||
| chr5:174093826 | A | T | 4 | a0001c0001t0004g0002 a0001c0001t0004g0027 a0001c0001t0004g0028 others(1): Show |
5 | HG02630.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-10402A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174093826 | |||||||
| chr5:174094815 | C | T | 1 | a0001c0001t0004g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.214-9413C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174094815 | |||||||
| chr5:174095009 | A | G | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-9219A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095009 | |||||||
| chr5:174095054 | C | T | 9 | a0001c0001t0004g0002 a0001c0001t0004g0027 a0001c0001t0004g0028 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-9174C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095054 | |||||||
| chr5:174095055 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.214-9173A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095055 | |||||||
| chr5:174095093 | C | T | 1 | a0001c0001t0017g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.214-9135C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095093 | |||||||
| chr5:174095095 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214-9133A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095095 | |||||||
| chr5:174095150 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.214-9078G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095150 | |||||||
| chr5:174095229 | G | A | 1 | a0001c0001t0022g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.214-8999G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095229 | |||||||
| chr5:174095484 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.214-8744C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095484 | |||||||
| chr5:174095485 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0046 |
2 | HG01099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.214-8743G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095485 | |||||||
| chr5:174095530 | T | C | 7 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-8698T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095530 | |||||||
| chr5:174095600 | A | G | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-8628A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095600 | |||||||
| chr5:174095754 | C | T | 4 | a0001c0001t0004g0042 a0001c0001t0004g0043 a0001c0001t0004g0044 others(1): Show |
4 | HG03471.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-8474C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174095754 | |||||||
| chr5:174096061 | T | G | 1 | a0001c0003t0002g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.214-8167T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096061 | |||||||
| chr5:174096064 | T | C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG00280.hp2 HG01255.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-8164T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096064 | |||||||
| chr5:174096238 | A | C | 2 | a0001c0001t0011g0024 a0001c0001t0011g0025 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.214-7990A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096238 | |||||||
| chr5:174096286 | C | T | 2 | a0001c0001t0005g0016 a0001c0001t0005g0017 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.214-7942C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096286 | |||||||
| chr5:174096444 | A | C | 1 | a0001c0001t0005g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214-7784A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096444 | |||||||
| chr5:174096537 | G | A | 49 | a0001c0001t0001g0012 a0001c0001t0002g0004 a0001c0001t0002g0005 others(46): Show |
54 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.214-7691G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096537 | |||||||
| chr5:174096806 | G | A | 10 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(7): Show |
10 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-7422G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174096806 | |||||||
| chr5:174097033 | A | G | 1 | a0001c0001t0004g0011 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.214-7195A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097033 | |||||||
| chr5:174097089 | T | C | 45 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(42): Show |
46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.214-7139T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097089 | |||||||
| chr5:174097159 | C | A | 1 | a0001c0001t0003g0032 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214-7069C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097159 | |||||||
| chr5:174097162 | G | T | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214-7066G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097162 | |||||||
| chr5:174097266 | A | G | 121 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0221 others(118): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.214-6962A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097266 | |||||||
| chr5:174097314 | G | A | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-6914G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097314 | |||||||
| chr5:174097404 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.214-6824C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097404 | |||||||
| chr5:174097413 | G | A | 2 | a0001c0001t0005g0016 a0001c0001t0005g0017 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.214-6815G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097413 | |||||||
| chr5:174097453 | G | A | 26 | a0001c0001t0001g0012 a0001c0001t0002g0005 a0001c0001t0002g0006 others(23): Show |
30 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.214-6775G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097453 | |||||||
| chr5:174097463 | G | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG01891.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-6765G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097463 | |||||||
| chr5:174097508 | T | C | 1 | a0001c0001t0004g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.214-6720T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097508 | |||||||
| chr5:174097537 | A | G | 47 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(44): Show |
49 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.214-6691A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097537 | |||||||
| chr5:174097557 | CTG | C | 12 | a0001c0001t0001g0012 a0001c0001t0002g0005 a0001c0001t0002g0006 others(9): Show |
15 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.214-6663_214-6662d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097557 | ||||||
| chr5:174097581 | CTG | C | 50 | a0001c0001t0001g0012 a0001c0001t0002g0004 a0001c0001t0002g0005 others(47): Show |
55 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.214-6637_214-6636d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097581 | ||||||
| chr5:174097631 | CTG | C | 5 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0033 others(2): Show |
5 | HG02486.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-6587_214-6586d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097631 | ||||||
| chr5:174097643 | TTC | T | 11 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(8): Show |
11 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.214-6578_214-6577d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097643 | ||||||
| chr5:174097679 | CTCTG | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0002g0276 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-6543_214-6540d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097679 | ||||||
| chr5:174097807 | G | A | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-6421G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097807 | |||||||
| chr5:174097833 | T | G | 45 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(42): Show |
46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.214-6395T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097833 | |||||||
| chr5:174097843 | C | G | 5 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0033 others(2): Show |
5 | HG02486.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-6385C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097843 | |||||||
| chr5:174097843 | CTG | C | 5 | a0001c0001t0001g0217 a0001c0001t0004g0040 a0001c0001t0008g0010 others(2): Show |
6 | HG00280.hp1 HG03130.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-6365_214-6364d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174097843 | ||||||
| chr5:174097947 | A | G | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214-6281A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174097947 | |||||||
| chr5:174098018 | G | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214-6210G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098018 | |||||||
| chr5:174098042 | G | A | 1 | a0001c0001t0003g0243 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-6186G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098042 | |||||||
| chr5:174098069 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214-6159A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098069 | |||||||
| chr5:174098071 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.214-6157C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098071 | |||||||
| chr5:174098208 | C | T | 11 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.214-6020C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098208 | |||||||
| chr5:174098214 | C | G | 7 | a0001c0003t0002g0026 a0001c0003t0002g0200 a0001c0003t0002g0202 others(4): Show |
7 | HG00673.hp2 HG02155.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-6014C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098214 | |||||||
| chr5:174098438 | T | TCTC | 121 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0221 others(118): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.214-5787_214-5785d others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174098438 | ||||||
| chr5:174098688 | ACT | A | 15 | a0001c0003t0002g0009 a0001c0003t0002g0026 a0001c0003t0002g0193 others(12): Show |
16 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.214-5534_214-5533d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174098688 | ||||||
| chr5:174098728 | C | G | 49 | a0001c0001t0001g0012 a0001c0001t0002g0004 a0001c0001t0002g0005 others(46): Show |
54 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.214-5500C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098728 | |||||||
| chr5:174098732 | G | A | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-5496G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098732 | |||||||
| chr5:174098833 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0005g0033 others(2): Show |
5 | HG02886.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-5395G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098833 | |||||||
| chr5:174098869 | G | T | 121 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0221 others(118): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.214-5359G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098869 | |||||||
| chr5:174098887 | C | T | 1 | a0001c0001t0022g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.214-5341C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098887 | |||||||
| chr5:174098925 | G | A | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-5303G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174098925 | |||||||
| chr5:174099233 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.214-4995C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099233 | |||||||
| chr5:174099241 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.214-4987C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099241 | |||||||
| chr5:174099242 | G | A | 3 | a0001c0001t0002g0276 a0001c0001t0004g0011 a0001c0001t0018g0277 |
4 | HG01167.hp2 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-4986G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099242 | |||||||
| chr5:174099482 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.214-4746T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099482 | |||||||
| chr5:174099615 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214-4613C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099615 | |||||||
| chr5:174099711 | T | A | 120 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(117): Show |
129 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.214-4517T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099711 | |||||||
| chr5:174099776 | A | T | 8 | a0001c0001t0003g0229 a0001c0001t0003g0236 a0001c0001t0003g0237 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-4452A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099776 | |||||||
| chr5:174099798 | C | A | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01433.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-4430C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174099798 | |||||||
| chr5:174100017 | T | C | 48 | a0001c0001t0002g0041 a0001c0001t0003g0003 a0001c0001t0003g0031 others(45): Show |
49 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.214-4211T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100017 | |||||||
| chr5:174100126 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0136 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.214-4102T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100126 | |||||||
| chr5:174100442 | G | A | 5 | a0001c0001t0002g0023 a0001c0001t0002g0041 a0001c0001t0009g0268 others(2): Show |
5 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-3786G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100442 | |||||||
| chr5:174100679 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.214-3549C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100679 | |||||||
| chr5:174100685 | T | C | 1 | a0001c0001t0004g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214-3543T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100685 | |||||||
| chr5:174100802 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.214-3426G>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100802 | |||||||
| chr5:174100843 | T | C | 120 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(117): Show |
129 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.214-3385T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174100843 | |||||||
| chr5:174101073 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.214-3155G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101073 | |||||||
| chr5:174101111 | C | T | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-3117C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101111 | |||||||
| chr5:174101247 | G | T | 56 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(53): Show |
58 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.214-2981G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101247 | |||||||
| chr5:174101351 | C | T | 4 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0062 others(1): Show |
4 | HG02257.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-2877C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101351 | |||||||
| chr5:174101784 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.214-2444T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101784 | |||||||
| chr5:174101966 | C | A | 1 | a0001c0001t0011g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.214-2262C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174101966 | |||||||
| chr5:174102204 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.214-2024C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102204 | |||||||
| chr5:174102276 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.214-1952A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102276 | |||||||
| chr5:174102461 | T | G | 48 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(45): Show |
53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.214-1767T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102461 | |||||||
| chr5:174102509 | C | T | 1 | a0001c0001t0021g0083 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.214-1719C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102509 | |||||||
| chr5:174102590 | TAACC | T | 42 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(39): Show |
42 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.214-1635_214-1632d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102590 | ||||||
| chr5:174102625 | GC | G | 4 | a0001c0001t0001g0070 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG00280.hp2 HG01255.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-1598delC | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102625 | ||||||
| chr5:174102632 | CT | C | 118 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(115): Show |
126 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.214-1593delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102632 | ||||||
| chr5:174102730 | C | A | 7 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0043 others(4): Show |
7 | HG02451.hp2 HG03130.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-1498C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102730 | |||||||
| chr5:174102749 | GTTTT | G | 87 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(84): Show |
94 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.214-1474_214-1471d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102749 | ||||||
| chr5:174102750 | TTTTTTTT others(1): Show |
T | 8 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(5): Show |
8 | HG01891.hp1 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-1474_214-1467d others(10): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102750 | ||||||
| chr5:174102750 | TTTTTTTT others(5): Show |
T | 2 | a0001c0001t0003g0031 a0001c0003t0002g0202 |
2 | HG02055.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.214-1474_214-1463d others(14): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102750 | ||||||
| chr5:174102750 | TTTTTTTT others(9): Show |
T | 2 | a0001c0001t0005g0016 a0001c0001t0005g0017 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.214-1474_214-1459d others(18): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102750 | ||||||
| chr5:174102754 | T | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0080 a0001c0001t0001g0092 others(20): Show |
24 | HG00408.hp2 HG01167.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.214-1474T>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102754 | |||||||
| chr5:174102754 | T | TTTTA | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0039 others(11): Show |
14 | HG00408.hp1 HG00639.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.214-1433_214-1430d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102754 | ||||||
| chr5:174102754 | TTTTA | T | 9 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0101 others(6): Show |
10 | HG00280.hp1 HG00323.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-1433_214-1430d others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102754 | ||||||
| chr5:174102754 | TTTTATTT others(5): Show |
T | 1 | a0001c0001t0001g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.214-1441_214-1430d others(14): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102754 | ||||||
| chr5:174102941 | C | CTT | 16 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(13): Show |
18 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.214-1269_214-1268d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102941 | ||||||
| chr5:174102941 | C | CTTT | 51 | a0001c0001t0002g0276 a0001c0001t0003g0031 a0001c0001t0003g0229 others(48): Show |
52 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.214-1270_214-1268d others(5): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102941 | ||||||
| chr5:174102941 | CT | C | 26 | a0001c0001t0001g0047 a0001c0001t0001g0101 a0001c0001t0001g0191 others(23): Show |
27 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.214-1268delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102941 | ||||||
| chr5:174102941 | CTT | C | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(37): Show |
45 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.214-1269_214-1268d others(4): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 174102941 | ||||||
| chr5:174102992 | T | C | 1 | a0001c0001t0013g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.214-1236T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174102992 | |||||||
| chr5:174103009 | G | A | 9 | a0001c0001t0001g0096 a0001c0001t0001g0100 a0001c0001t0001g0102 others(6): Show |
9 | HG00639.hp2 HG00642.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.214-1219G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103009 | |||||||
| chr5:174103130 | G | A | 4 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0062 others(1): Show |
4 | HG02257.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-1098G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103130 | |||||||
| chr5:174103136 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0205 |
2 | NA18998.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.214-1092T>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103136 | |||||||
| chr5:174103410 | G | A | 67 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0034 others(64): Show |
67 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.214-818G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103410 | |||||||
| chr5:174103439 | A | C | 3 | a0001c0001t0005g0033 a0001c0001t0005g0207 a0001c0001t0005g0259 |
3 | HG02886.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214-789A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103439 | |||||||
| chr5:174103439 | A | G | 109 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(106): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.214-789A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103439 | |||||||
| chr5:174103465 | A | T | 7 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0043 others(4): Show |
7 | HG02451.hp2 HG03130.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-763A>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103465 | |||||||
| chr5:174103823 | G | T | 1 | a0001c0001t0016g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.214-405G>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103823 | |||||||
| chr5:174103905 | C | T | 2 | a0001c0002t0001g0174 a0001c0002t0001g0175 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.214-323C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174103905 | |||||||
| chr5:174104007 | C | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
8 | HG00621.hp2 HG01099.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.214-221C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174104007 | |||||||
| chr5:174104050 | G | A | 45 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(42): Show |
46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.214-178G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174104050 | |||||||
| chr5:174104078 | A | G | 15 | a0001c0003t0002g0009 a0001c0003t0002g0026 a0001c0003t0002g0193 others(12): Show |
16 | HG00408.hp2 HG00673.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.214-150A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174104078 | |||||||
| chr5:174104120 | C | T | 2 | a0001c0001t0004g0002 a0001c0001t0004g0030 |
3 | HG02630.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.214-108C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 3/4 | chr5 | 174104120 | |||||||
| chr5:174104538 | A | G | 1 | a0001c0001t0003g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.324+200A>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104538 | |||||||
| chr5:174104579 | G | A | 44 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(41): Show |
45 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.324+241G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104579 | |||||||
| chr5:174104657 | G | A | 63 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(60): Show |
65 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.324+319G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104657 | |||||||
| chr5:174104748 | G | A | 1 | a0001c0003t0002g0202 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.324+410G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104748 | |||||||
| chr5:174104766 | C | G | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.324+428C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104766 | |||||||
| chr5:174104777 | C | A | 12 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(9): Show |
15 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.324+439C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104777 | |||||||
| chr5:174104808 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.324+470G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104808 | |||||||
| chr5:174104913 | C | G | 1 | a0001c0003t0002g0203 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.324+575C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174104913 | |||||||
| chr5:174105027 | A | ATACTAT | 119 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(116): Show |
128 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.324+691_324+692ins others(6): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174105027 | ||||||
| chr5:174105110 | G | A | 41 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 others(38): Show |
41 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.324+772G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105110 | |||||||
| chr5:174105277 | A | C | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.324+939A>C | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105277 | |||||||
| chr5:174105556 | C | T | 6 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0041 others(3): Show |
6 | HG01167.hp1 HG01257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+1218C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105556 | |||||||
| chr5:174105718 | T | G | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.324+1380T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105718 | |||||||
| chr5:174105788 | T | G | 3 | a0001c0001t0001g0065 a0001c0001t0008g0010 a0001c0001t0008g0275 |
4 | HG00280.hp1 HG02809.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+1450T>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105788 | |||||||
| chr5:174105894 | C | T | 31 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(28): Show |
35 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-1420C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174105894 | |||||||
| chr5:174106034 | C | T | 3 | a0001c0001t0004g0002 a0001c0001t0004g0030 a0001c0001t0004g0073 |
4 | HG02630.hp1 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-1280C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106034 | |||||||
| chr5:174106283 | C | A | 119 | a0001c0001t0001g0065 a0001c0001t0001g0221 a0001c0001t0001g0222 others(116): Show |
128 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.325-1031C>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106283 | |||||||
| chr5:174106551 | C | T | 7 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0043 others(4): Show |
7 | HG02451.hp2 HG03130.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-763C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106551 | |||||||
| chr5:174106583 | C | CT | 59 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0020 others(56): Show |
60 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.325-702dupT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174106583 | ||||||
| chr5:174106583 | CT | C | 32 | a0001c0001t0001g0140 a0001c0001t0003g0003 a0001c0001t0003g0031 others(29): Show |
33 | HG00642.hp1 HG01071.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.325-702delT | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174106583 | ||||||
| chr5:174106583 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.325-713_325-702del others(12): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174106583 | ||||||
| chr5:174106583 | CTTTTTTT others(9): Show |
C | 48 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(45): Show |
53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.325-717_325-702del others(16): Show |
NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 174106583 | ||||||
| chr5:174106639 | C | T | 2 | a0001c0001t0008g0010 a0001c0001t0008g0275 |
3 | HG00280.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.325-675C>T | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106639 | |||||||
| chr5:174106882 | C | G | 45 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 others(42): Show |
46 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.325-432C>G | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174106882 | |||||||
| chr5:174107023 | G | A | 111 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(108): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.325-291G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174107023 | |||||||
| chr5:174107220 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.325-94G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174107220 | |||||||
| chr5:174107280 | G | A | 10 | a0001c0001t0001g0095 a0001c0001t0001g0129 a0001c0001t0001g0157 others(7): Show |
10 | HG02683.hp1 HG03654.hp2 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.325-34G>A | NSG2 | ENSG00000170091.11 | transcript | ENST00000303177.8 | protein_coding | 4/4 | chr5 | 174107280 |