Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56954 |
| ensemblid | ENSG00000114021.12 |
| hgncid | 29878 |
| symbol | NIT2 |
| name | nitrilase family member 2 |
| refseq_nuc | NM_020202.5 |
| refseq_prot | NP_064587.1 |
| ensembl_nuc | ENST00000394140.9 |
| ensembl_prot | ENSP00000377696.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 100334757 |
| end | 100361635 |
| strand | + |
| ver | v1.2 |
| region | chr3:100334757-100361635 |
| region5000 | chr3:100329757-100366635 |
| regionname0 | NIT2_chr3_100334757_100361635 |
| regionname5000 | NIT2_chr3_100329757_100366635 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 276 | 394 | 80 | 72 | 184 | 12 | 46 | 144 | NIT2_chr3_100329757_100366635 | NIT2 | MTSFR others(271): Show |
chr3 | 100329757 | 100366635 |
| a0002 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | MTSFR others(271): Show |
chr3 | 100329757 | 100366635 |
| a0003 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | MTSFR others(271): Show |
chr3 | 100329757 | 100366635 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 828 | 391 | 77 | 72 | 184 | 12 | 46 | NIT2_chr3_100329757_100366635 | NIT2 | ATGAC others(823): Show |
chr3 | 100329757 | 100366635 | ||
| a0001c0002 | 0/0 | 828 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | ATGAC others(823): Show |
chr3 | 100329757 | 100366635 | ||
| a0002c0004 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | ATGAC others(823): Show |
chr3 | 100329757 | 100366635 | ||
| a0003c0003 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | ATGAC others(823): Show |
chr3 | 100329757 | 100366635 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7231 | 91 | 17 | 6 | 65 | 0 | 3 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0002 | 0/0 | 7232 | 63 | 1 | 15 | 32 | 4 | 11 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0003 | 0/0 | 7233 | 59 | 5 | 18 | 19 | 4 | 13 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0004 | 0/0 | 7232 | 37 | 1 | 2 | 32 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0005 | 0/0 | 7232 | 30 | 1 | 15 | 7 | 0 | 7 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0006 | 0/0 | 7232 | 15 | 13 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0007 | 0/0 | 7225 | 5 | 5 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7220): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0008 | 0/0 | 7231 | 5 | 5 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0009 | 0/0 | 7232 | 5 | 0 | 1 | 3 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0010 | 0/0 | 7233 | 4 | 0 | 0 | 4 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0011 | 0/0 | 7232 | 4 | 3 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0012 | 0/0 | 7229 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7224): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0013 | 0/0 | 7232 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0014 | 0/0 | 7232 | 3 | 0 | 2 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0015 | 0/0 | 7231 | 3 | 0 | 3 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0016 | 0/0 | 7231 | 3 | 2 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0017 | 0/0 | 7231 | 3 | 1 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0018 | 0/0 | 7232 | 3 | 0 | 0 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0020 | 0/0 | 7233 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0021 | 0/0 | 7231 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0022 | 0/0 | 7230 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7225): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0023 | 0/0 | 7231 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0024 | 0/0 | 7231 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0025 | 0/0 | 7233 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0026 | 0/0 | 7233 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0027 | 0/0 | 7233 | 2 | 0 | 0 | 1 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0028 | 0/0 | 7232 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0029 | 0/0 | 7232 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0030 | 0/0 | 7209 | 2 | 0 | 0 | 0 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7204): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0032 | 0/0 | 7232 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0033 | 0/0 | 7231 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0034 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0035 | 0/0 | 7225 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7220): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0036 | 0/0 | 7230 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7225): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0037 | 0/0 | 7232 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0038 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0039 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0040 | 0/0 | 7231 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0041 | 0/0 | 7231 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0042 | 0/0 | 7231 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0043 | 0/0 | 7232 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0044 | 0/0 | 7233 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0045 | 0/0 | 7233 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0046 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0047 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0048 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0049 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0050 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0051 | 0/0 | 7232 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0052 | 0/0 | 7231 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7226): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0053 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0054 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0055 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0056 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0057 | 0/0 | 7232 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0058 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0059 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0060 | 0/0 | 7233 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| a0001c0001t0061 | 0/0 | 7234 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | GGTCC others(7229): Show |
chr3 | 100329757 | 100366635 |
| a0001c0002t0019 | 0/0 | 7232 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0001c0002t0031 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0002c0004t0005 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7227): Show |
chr3 | 100329757 | 100366635 |
| a0003c0003t0010 | 0/0 | 7233 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | AGTCC others(7228): Show |
chr3 | 100329757 | 100366635 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 22 | 0 | 0 | 22 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0007 | 0/0 | 11 | 3 | 2 | 6 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0008 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0009 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0001 | 0/0 | 34 | 0 | 4 | 23 | 1 | 6 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0003 | 0/0 | 22 | 0 | 3 | 14 | 2 | 3 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0005 | 0/0 | 18 | 5 | 8 | 0 | 0 | 5 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0004g0002 | 0/0 | 27 | 1 | 2 | 22 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0006 | 0/0 | 12 | 0 | 9 | 0 | 0 | 3 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0006g0002 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0006g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0006g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0007g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0008g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0009g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0009g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0010g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0010g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0011g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0013g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0014g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0015g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0016g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0017g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0018g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0020g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0020g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0021g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0022g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0023g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0024g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0025g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0026g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0027g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0027g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0028g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0029g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0030g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0030g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0032g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0033g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0034g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0035g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0036g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0037g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0038g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0039g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0040g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0041g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0042g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0043g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0044g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0045g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0046g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0047g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0048g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0049g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0050g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0051g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0052g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0053g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0054g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0055g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0056g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0057g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0058g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0059g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0060g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0001t0061g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0002t0019g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0001c0002t0031g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0002c0004t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| a0003c0003t0010g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0061 | EUR | GBR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00280 | hp1 | a0001 | c0001 | t0058 | g0028 | EUR | FIN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00280 | hp2 | a0001 | c0001 | t0059 | g0005 | EUR | FIN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00323 | hp2 | a0001 | c0001 | t0037 | g0006 | EUR | FIN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00544 | hp2 | a0001 | c0001 | t0029 | g0041 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00642 | hp2 | a0001 | c0001 | t0014 | g0015 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00735 | hp2 | a0001 | c0001 | t0016 | g0020 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0107 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0094 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0024 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01346 | hp2 | a0001 | c0001 | t0014 | g0015 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01358 | hp2 | a0001 | c0001 | t0042 | g0026 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01496 | hp1 | a0001 | c0001 | t0015 | g0007 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01516 | hp1 | a0001 | c0001 | t0050 | g0005 | EUR | IBS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0085 | EUR | IBS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0097 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01978 | hp1 | a0001 | c0001 | t0015 | g0007 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01981 | hp2 | a0001 | c0001 | t0032 | g0065 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01993 | hp1 | a0001 | c0001 | t0026 | g0037 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02015 | hp1 | a0001 | c0001 | t0023 | g0009 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02015 | hp2 | a0001 | c0001 | t0021 | g0002 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0024 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02071 | hp2 | a0001 | c0001 | t0023 | g0009 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02074 | hp2 | a0001 | c0001 | t0055 | g0001 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02132 | hp1 | a0001 | c0001 | t0036 | g0013 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02145 | hp2 | a0001 | c0001 | t0045 | g0006 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | CDX | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CDX | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | CDX | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CDX | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02257 | hp1 | a0001 | c0001 | t0025 | g0035 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02280 | hp1 | a0001 | c0001 | t0022 | g0034 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02293 | hp1 | a0001 | c0001 | t0052 | g0003 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02300 | hp2 | a0001 | c0001 | t0015 | g0007 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02572 | hp1 | a0001 | c0001 | t0020 | g0134 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02572 | hp2 | a0001 | c0001 | t0047 | g0106 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02602 | hp2 | a0001 | c0001 | t0043 | g0015 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02615 | hp1 | a0001 | c0001 | t0048 | g0129 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0006 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0020 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02683 | hp2 | a0001 | c0001 | t0030 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02717 | hp2 | a0001 | c0001 | t0013 | g0006 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0024 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0092 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02809 | hp2 | a0001 | c0002 | t0019 | g0023 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0130 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0006 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02970 | hp1 | a0001 | c0001 | t0044 | g0102 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02970 | hp2 | a0001 | c0001 | t0025 | g0035 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03017 | hp1 | a0001 | c0001 | t0054 | g0005 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03041 | hp2 | a0001 | c0002 | t0031 | g0023 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0072 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03098 | hp2 | a0001 | c0001 | t0049 | g0020 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03130 | hp1 | a0001 | c0001 | t0035 | g0068 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0066 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0069 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03209 | hp1 | a0001 | c0001 | t0046 | g0067 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03209 | hp2 | a0001 | c0001 | t0038 | g0070 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03225 | hp1 | a0001 | c0001 | t0022 | g0034 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03486 | hp1 | a0001 | c0001 | t0039 | g0011 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03486 | hp2 | a0001 | c0001 | t0020 | g0073 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03490 | hp1 | a0001 | c0001 | t0051 | g0054 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0133 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03579 | hp1 | a0001 | c0001 | t0061 | g0048 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03669 | hp2 | a0001 | c0001 | t0014 | g0015 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03831 | hp2 | a0001 | c0001 | t0053 | g0003 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0027 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03834 | hp2 | a0001 | c0001 | t0033 | g0125 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04115 | hp2 | a0001 | c0001 | t0009 | g0007 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0093 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0095 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04199 | hp2 | a0001 | c0001 | t0027 | g0010 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04204 | hp2 | a0001 | c0001 | t0030 | g0081 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0020 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18612 | hp2 | a0001 | c0001 | t0024 | g0047 | EAS | CHB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18940 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18940 | hp2 | a0002 | c0004 | t0005 | g0091 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18946 | hp1 | a0001 | c0001 | t0017 | g0080 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18948 | hp2 | a0001 | c0001 | t0040 | g0120 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18956 | hp1 | a0001 | c0001 | t0028 | g0038 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18961 | hp2 | a0001 | c0001 | t0060 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18963 | hp2 | a0001 | c0001 | t0024 | g0047 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18965 | hp1 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18970 | hp2 | a0001 | c0001 | t0041 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18971 | hp1 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18972 | hp1 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18981 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19002 | hp1 | a0001 | c0001 | t0056 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19009 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | LWK | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0063 | AFR | LWK | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | LWK | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19054 | hp1 | a0001 | c0001 | t0021 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19060 | hp2 | a0003 | c0003 | t0010 | g0021 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19064 | hp1 | a0001 | c0001 | t0018 | g0016 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19066 | hp1 | a0001 | c0001 | t0027 | g0087 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19066 | hp2 | a0001 | c0001 | t0029 | g0041 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19067 | hp2 | a0001 | c0001 | t0028 | g0038 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19070 | hp2 | a0001 | c0001 | t0018 | g0016 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19089 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0104 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ASW | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0076 | EUR | TSI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0053 | EUR | TSI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | TSI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | GIH | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01123 | hp1 | a0001 | c0001 | t0057 | g0001 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG01123 | hp2 | a0001 | c0001 | t0026 | g0037 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02559 | hp1 | a0001 | c0001 | t0034 | g0128 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG03471 | hp2 | a0001 | c0002 | t0019 | g0023 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG06807 | hp1 | a0001 | c0001 | t0012 | g0132 | AFR | USA | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | USA | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| NA18955 | hp2 | a0001 | c0001 | t0018 | g0016 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100334767 | GCAGGTGG others(16): Show |
G | 1 | a0001 | 2 | HG02683.hp2 HG04204.hp2 |
frameshift_variant&start_lost | HIGH | c.-22_1delGGTGGTGCTT others(13): Show |
p.Met1fs | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/10 | 14/7233 | 1/831 | 1/276 | INFO_REALIGN_3_PRIME | chr3 | 100334767 | ||
| chr3:100345601 | T | C | 1 | a0003 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.353T>C | p.Ile118Thr | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/10 | 388/7233 | 353/831 | 118/276 | chr3 | 100345601 | |||
| chr3:100355226 | G | C | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.789G>C | p.Gln263His | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 824/7233 | 789/831 | 263/276 | chr3 | 100355226 | |||
| chr3:100355227 | A | T | 1 | a0002 | 1 | NA18940.hp2 | stop_gained | HIGH | c.790A>T | p.Lys264* | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 825/7233 | 790/831 | 264/276 | chr3 | 100355227 | |||
| chr3:100355229 | G | T | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.792G>T | p.Lys264Asn | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 827/7233 | 792/831 | 264/276 | chr3 | 100355229 | |||
| chr3:100355231 | G | C | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.794G>C | p.Arg265Pro | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 829/7233 | 794/831 | 265/276 | chr3 | 100355231 | |||
| chr3:100355237 | A | T | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.800A>T | p.Asp267Val | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 835/7233 | 800/831 | 267/276 | chr3 | 100355237 | |||
| chr3:100355238 | C | G | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.801C>G | p.Asp267Glu | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 836/7233 | 801/831 | 267/276 | chr3 | 100355238 | |||
| chr3:100355239 | C | A | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.802C>A | p.Leu268Ile | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 837/7233 | 802/831 | 268/276 | chr3 | 100355239 | |||
| chr3:100361634 | A | G | 1 | a0001 | 1 | NA18948.hp2 | splice_region_variant | LOW | c.*6366A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | chr3 | 100361634 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100352488 | C | T | 1 | a0001c0002 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.669C>T | p.Thr223Thr | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/10 | 704/7233 | 669/831 | 223/276 | chr3 | 100352488 | |||
| chr3:100355230 | C | A | 1 | a0002c0004 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.793C>A | p.Arg265Arg | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 828/7233 | 793/831 | 265/276 | chr3 | 100355230 | |||
| chr3:100355241 | C | T | 1 | a0002c0004 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.804C>T | p.Leu268Leu | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 839/7233 | 804/831 | 268/276 | chr3 | 100355241 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100334757 | A | G | 1 | a0001c0001t0061 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/10 | 35 | chr3 | 100334757 | ||||||
| chr3:100355302 | G | A | 2 | a0001c0002t0019 a0001c0002t0031 |
3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*34G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 34 | chr3 | 100355302 | ||||||
| chr3:100355410 | A | G | 1 | a0001c0001t0029 | 2 | HG00544.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*142A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 142 | chr3 | 100355410 | ||||||
| chr3:100355558 | G | A | 1 | a0001c0001t0020 | 2 | HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 290 | chr3 | 100355558 | ||||||
| chr3:100355852 | C | T | 1 | a0001c0002t0031 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*584C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 584 | chr3 | 100355852 | ||||||
| chr3:100355891 | T | C | 1 | a0001c0001t0032 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*623T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 623 | chr3 | 100355891 | ||||||
| chr3:100355915 | G | C | 41 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(38): Show |
243 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*647G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 647 | chr3 | 100355915 | ||||||
| chr3:100355928 | T | C | 1 | a0001c0001t0033 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*660T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 660 | chr3 | 100355928 | ||||||
| chr3:100355940 | G | T | 2 | a0001c0001t0016 a0001c0001t0049 |
4 | HG00735.hp2 HG02622.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*672G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 672 | chr3 | 100355940 | ||||||
| chr3:100356006 | C | T | 1 | a0001c0001t0011 | 4 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*738C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 738 | chr3 | 100356006 | ||||||
| chr3:100356065 | C | T | 2 | a0001c0001t0060 a0001c0002t0031 |
2 | HG03041.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*797C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 797 | chr3 | 100356065 | ||||||
| chr3:100356247 | G | T | 1 | a0001c0001t0015 | 3 | HG01496.hp1 HG01978.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*979G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 979 | chr3 | 100356247 | ||||||
| chr3:100356331 | A | G | 1 | a0001c0001t0025 | 2 | HG02257.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1063A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1063 | chr3 | 100356331 | ||||||
| chr3:100356544 | G | A | 2 | a0001c0001t0012 a0001c0001t0034 |
4 | HG02559.hp1 HG02896.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1276G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1276 | chr3 | 100356544 | ||||||
| chr3:100356675 | A | T | 1 | a0001c0001t0028 | 2 | NA18956.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1407A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1407 | chr3 | 100356675 | ||||||
| chr3:100356811 | A | C | 3 | a0001c0001t0020 a0001c0002t0019 a0001c0002t0031 |
5 | HG02572.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1543A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1543 | chr3 | 100356811 | ||||||
| chr3:100356820 | A | G | 1 | a0001c0001t0059 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1552A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1552 | chr3 | 100356820 | ||||||
| chr3:100356915 | G | T | 2 | a0001c0001t0034 a0001c0001t0048 |
2 | HG02559.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1647G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1647 | chr3 | 100356915 | ||||||
| chr3:100357119 | A | T | 1 | a0001c0001t0058 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1851A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1851 | chr3 | 100357119 | ||||||
| chr3:100357379 | T | A | 1 | a0001c0001t0050 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2111T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2111 | chr3 | 100357379 | ||||||
| chr3:100357637 | C | CT | 12 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0010 others(9): Show |
25 | HG01069.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2391dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2392 | INFO_REALIGN_3_PRIME | chr3 | 100357637 | |||||
| chr3:100357637 | CT | C | 7 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0021 others(4): Show |
12 | HG02015.hp2 HG02132.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2391delT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2391 | INFO_REALIGN_3_PRIME | chr3 | 100357637 | |||||
| chr3:100357637 | CTTTTTTT | C | 2 | a0001c0001t0007 a0001c0001t0035 |
6 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2385_*2391delTTTT others(3): Show |
NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2385 | INFO_REALIGN_3_PRIME | chr3 | 100357637 | |||||
| chr3:100357672 | C | T | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(17): Show |
164 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*2404C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2404 | chr3 | 100357672 | ||||||
| chr3:100357723 | T | G | 1 | a0001c0001t0037 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2455T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2455 | chr3 | 100357723 | ||||||
| chr3:100357726 | A | G | 3 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0046 |
8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2458A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2458 | chr3 | 100357726 | ||||||
| chr3:100357844 | C | G | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(50): Show |
327 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*2576C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2576 | chr3 | 100357844 | ||||||
| chr3:100357979 | T | C | 15 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0012 others(12): Show |
118 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2711T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2711 | chr3 | 100357979 | ||||||
| chr3:100357997 | C | T | 1 | a0001c0001t0042 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2729C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2729 | chr3 | 100357997 | ||||||
| chr3:100357998 | G | A | 1 | a0001c0001t0046 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2730G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2730 | chr3 | 100357998 | ||||||
| chr3:100358019 | C | A | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(5): Show |
64 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2751C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2751 | chr3 | 100358019 | ||||||
| chr3:100358034 | TC | T | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(48): Show |
324 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*2770delC | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2770 | INFO_REALIGN_3_PRIME | chr3 | 100358034 | |||||
| chr3:100358067 | C | T | 1 | a0001c0001t0061 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2799C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2799 | chr3 | 100358067 | ||||||
| chr3:100358136 | A | G | 11 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0017 others(8): Show |
83 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2868A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2868 | chr3 | 100358136 | ||||||
| chr3:100358377 | C | T | 1 | a0001c0001t0057 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3109C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3109 | chr3 | 100358377 | ||||||
| chr3:100358633 | A | G | 1 | a0001c0001t0024 | 2 | NA18612.hp2 NA18963.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3365A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3365 | chr3 | 100358633 | ||||||
| chr3:100358795 | C | T | 1 | a0001c0001t0041 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3527C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3527 | chr3 | 100358795 | ||||||
| chr3:100358800 | G | A | 1 | a0001c0001t0025 | 2 | HG02257.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3532G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3532 | chr3 | 100358800 | ||||||
| chr3:100358894 | C | T | 1 | a0001c0001t0054 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3626C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3626 | chr3 | 100358894 | ||||||
| chr3:100359217 | T | G | 1 | a0001c0001t0011 | 4 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3949T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3949 | chr3 | 100359217 | ||||||
| chr3:100359239 | C | T | 1 | a0001c0001t0047 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3971C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3971 | chr3 | 100359239 | ||||||
| chr3:100359541 | C | A | 1 | a0001c0001t0026 | 2 | HG01123.hp2 HG01993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4273C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4273 | chr3 | 100359541 | ||||||
| chr3:100359542 | C | T | 1 | a0001c0001t0023 | 2 | HG02015.hp1 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4274C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4274 | chr3 | 100359542 | ||||||
| chr3:100359566 | CCT | C | 5 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0022 others(2): Show |
12 | HG02109.hp2 HG02280.hp1 HG02293.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4304_*4305delTC | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4304 | INFO_REALIGN_3_PRIME | chr3 | 100359566 | |||||
| chr3:100359777 | C | T | 1 | a0001c0001t0013 | 3 | HG02615.hp2 HG02717.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4509C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4509 | chr3 | 100359777 | ||||||
| chr3:100359850 | G | C | 3 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0046 |
8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4582G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4582 | chr3 | 100359850 | ||||||
| chr3:100360460 | C | T | 1 | a0001c0001t0053 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5192C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5192 | chr3 | 100360460 | ||||||
| chr3:100360544 | T | C | 1 | a0001c0001t0018 | 3 | NA18955.hp2 NA19064.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5276T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5276 | chr3 | 100360544 | ||||||
| chr3:100360575 | C | A | 3 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0046 |
8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5307C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5307 | chr3 | 100360575 | ||||||
| chr3:100360603 | G | T | 14 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0015 others(11): Show |
114 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*5335G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5335 | chr3 | 100360603 | ||||||
| chr3:100360638 | C | T | 1 | a0001c0001t0056 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5370C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5370 | chr3 | 100360638 | ||||||
| chr3:100360795 | C | T | 3 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0046 |
8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5527C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5527 | chr3 | 100360795 | ||||||
| chr3:100360892 | G | A | 1 | a0001c0001t0013 | 3 | HG02615.hp2 HG02717.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5624G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5624 | chr3 | 100360892 | ||||||
| chr3:100361289 | T | A | 1 | a0001c0001t0043 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6021T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6021 | chr3 | 100361289 | ||||||
| chr3:100361302 | AT | A | 14 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0015 others(11): Show |
114 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*6035delT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6035 | chr3 | 100361302 | ||||||
| chr3:100361354 | T | G | 7 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0029 others(4): Show |
39 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*6086T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6086 | chr3 | 100361354 | ||||||
| chr3:100361495 | G | A | 1 | a0001c0001t0055 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6227G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6227 | chr3 | 100361495 | ||||||
| chr3:100361602 | T | C | 2 | a0001c0001t0014 a0001c0001t0043 |
4 | HG00642.hp2 HG01346.hp2 HG02602.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6334T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6334 | chr3 | 100361602 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100334807 | C | T | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7+9C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100334807 | |||||||
| chr3:100334808 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0061g0048 |
2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.7+10G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100334808 | |||||||
| chr3:100334840 | C | CG | 138 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
320 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(317): Show |
intron_variant | MODIFIER | c.7+47dupG | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100334840 | ||||||
| chr3:100334892 | C | A | 1 | a0001c0001t0001g0062 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.7+94C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100334892 | |||||||
| chr3:100334960 | C | G | 1 | a0001c0001t0008g0133 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7+162C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100334960 | |||||||
| chr3:100335044 | C | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0132 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+246C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335044 | |||||||
| chr3:100335157 | T | A | 1 | a0001c0001t0017g0063 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7+359T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335157 | |||||||
| chr3:100335276 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7+478A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335276 | |||||||
| chr3:100335316 | A | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.7+518A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335316 | |||||||
| chr3:100335342 | G | A | 1 | a0001c0001t0009g0107 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.7+544G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335342 | |||||||
| chr3:100335408 | A | C | 1 | a0001c0001t0047g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7+610A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335408 | |||||||
| chr3:100335472 | T | C | 1 | a0001c0001t0005g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7+674T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335472 | |||||||
| chr3:100335646 | G | T | 34 | a0001c0001t0001g0040 a0001c0001t0004g0002 a0001c0001t0004g0042 others(31): Show |
94 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.7+848G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335646 | |||||||
| chr3:100335779 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0032g0065 |
5 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+981G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335779 | |||||||
| chr3:100335784 | G | T | 2 | a0001c0001t0001g0126 a0001c0001t0033g0125 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.7+986G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335784 | |||||||
| chr3:100335802 | A | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(42): Show |
110 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.7+1004A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335802 | |||||||
| chr3:100335890 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7+1092A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335890 | |||||||
| chr3:100336004 | G | T | 1 | a0001c0001t0002g0039 | 2 | HG01258.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.7+1206G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336004 | |||||||
| chr3:100336007 | C | A | 2 | a0001c0001t0034g0128 a0001c0001t0048g0129 |
2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.7+1209C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336007 | |||||||
| chr3:100336169 | C | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02155.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.7+1371C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336169 | |||||||
| chr3:100336197 | C | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0132 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+1399C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336197 | |||||||
| chr3:100336281 | C | T | 33 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0016 others(30): Show |
78 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.7+1483C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336281 | |||||||
| chr3:100336302 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(42): Show |
110 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.7+1504A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336302 | |||||||
| chr3:100336429 | G | A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(126): Show |
307 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(304): Show |
intron_variant | MODIFIER | c.7+1631G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336429 | |||||||
| chr3:100336471 | T | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(42): Show |
110 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.7+1673T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336471 | |||||||
| chr3:100336493 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.7+1695A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336493 | |||||||
| chr3:100336497 | A | AT | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0132 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+1700dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100336497 | ||||||
| chr3:100336506 | C | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0132 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+1708C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336506 | |||||||
| chr3:100336520 | G | A | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0132 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+1722G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336520 | |||||||
| chr3:100336610 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | NA18975.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.7+1812G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336610 | |||||||
| chr3:100336760 | C | T | 6 | a0001c0001t0011g0024 a0001c0001t0011g0072 a0001c0001t0017g0063 others(3): Show |
9 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+1962C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336760 | |||||||
| chr3:100336770 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0061g0048 |
2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.7+1972C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336770 | |||||||
| chr3:100336833 | G | A | 1 | a0001c0001t0011g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7+2035G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336833 | |||||||
| chr3:100336835 | T | G | 1 | a0001c0001t0011g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7+2037T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336835 | |||||||
| chr3:100336876 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.7+2078C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336876 | |||||||
| chr3:100337030 | T | G | 1 | a0001c0001t0002g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.8-2057T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337030 | |||||||
| chr3:100337160 | A | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1927A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337160 | |||||||
| chr3:100337162 | T | G | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.8-1925T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337162 | |||||||
| chr3:100337173 | T | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1914T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337173 | |||||||
| chr3:100337234 | G | A | 1 | a0001c0001t0001g0019 | 4 | HG02109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1853G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337234 | |||||||
| chr3:100337334 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.8-1753G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337334 | |||||||
| chr3:100337482 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1605C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337482 | |||||||
| chr3:100337510 | G | T | 2 | a0001c0001t0017g0063 a0001c0001t0020g0073 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8-1577G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337510 | |||||||
| chr3:100337541 | A | T | 1 | a0001c0001t0027g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.8-1546A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337541 | |||||||
| chr3:100337655 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1432C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337655 | |||||||
| chr3:100337656 | G | A | 1 | a0001c0001t0034g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.8-1431G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337656 | |||||||
| chr3:100337748 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0024g0047 |
4 | NA18612.hp2 NA18963.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1339C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337748 | |||||||
| chr3:100337765 | T | C | 2 | a0001c0002t0019g0023 a0001c0002t0031g0023 |
3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.8-1322T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337765 | |||||||
| chr3:100337771 | A | T | 1 | a0001c0001t0002g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.8-1316A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337771 | |||||||
| chr3:100337772 | T | G | 3 | a0001c0001t0002g0010 a0001c0001t0002g0076 a0001c0001t0027g0010 |
7 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1315T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337772 | |||||||
| chr3:100337943 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.8-1144T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337943 | |||||||
| chr3:100338001 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.8-1086G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338001 | |||||||
| chr3:100338049 | C | T | 5 | a0001c0001t0007g0011 a0001c0001t0007g0069 a0001c0001t0035g0068 others(2): Show |
8 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-1038C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338049 | |||||||
| chr3:100338050 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1037G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338050 | |||||||
| chr3:100338163 | T | C | 1 | a0001c0001t0012g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.8-924T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338163 | |||||||
| chr3:100338265 | A | G | 21 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0031 others(18): Show |
64 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.8-822A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338265 | |||||||
| chr3:100338359 | A | G | 141 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(138): Show |
324 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(321): Show |
intron_variant | MODIFIER | c.8-728A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338359 | |||||||
| chr3:100338425 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-662C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338425 | |||||||
| chr3:100338573 | T | G | 52 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.8-514T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338573 | |||||||
| chr3:100338826 | C | T | 1 | a0001c0001t0002g0033 | 2 | HG00741.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.8-261C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338826 | |||||||
| chr3:100338859 | G | A | 1 | a0001c0001t0061g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.8-228G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338859 | |||||||
| chr3:100338940 | C | G | 1 | a0001c0001t0034g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.8-147C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338940 | |||||||
| chr3:100338991 | CG | C | 3 | a0001c0001t0001g0040 a0001c0001t0020g0134 a0001c0001t0047g0106 |
4 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-92delG | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100338991 | ||||||
| chr3:100338999 | TAA | T | 3 | a0001c0001t0001g0040 a0001c0001t0020g0134 a0001c0001t0047g0106 |
4 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-87_8-86delAA | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338999 | |||||||
| chr3:100339002 | C | A | 2 | a0001c0001t0004g0021 a0003c0003t0010g0021 |
3 | NA18988.hp2 NA19060.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.8-85C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100339002 | |||||||
| chr3:100339002 | C | T | 52 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.8-85C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100339002 | |||||||
| chr3:100339048 | G | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | NA18950.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.8-39G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100339048 | |||||||
| chr3:100339258 | G | A | 52 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.126+53G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339258 | |||||||
| chr3:100339294 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.126+89G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339294 | |||||||
| chr3:100339361 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(24): Show |
54 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.126+156G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339361 | |||||||
| chr3:100339456 | T | C | 24 | a0001c0001t0001g0040 a0001c0001t0005g0006 a0001c0001t0005g0012 others(21): Show |
48 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.126+251T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339456 | |||||||
| chr3:100339472 | A | C | 1 | a0001c0001t0029g0041 | 2 | HG00544.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.126+267A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339472 | |||||||
| chr3:100339566 | A | AT | 6 | a0001c0001t0011g0024 a0001c0001t0011g0072 a0001c0001t0017g0063 others(3): Show |
9 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-239dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100339566 | ||||||
| chr3:100339577 | A | T | 3 | a0001c0001t0001g0040 a0001c0001t0020g0134 a0001c0001t0047g0106 |
4 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-238A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339577 | |||||||
| chr3:100339622 | C | G | 45 | a0001c0001t0001g0040 a0001c0001t0004g0002 a0001c0001t0004g0021 others(42): Show |
112 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.127-193C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339622 | |||||||
| chr3:100339698 | T | A | 1 | a0001c0001t0004g0042 | 2 | NA18956.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.127-117T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339698 | |||||||
| chr3:100339772 | T | A | 1 | a0001c0001t0002g0036 | 2 | HG01099.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.127-43T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339772 | |||||||
| chr3:100340272 | C | G | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.247+337C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340272 | |||||||
| chr3:100340324 | C | G | 21 | a0001c0001t0005g0006 a0001c0001t0005g0012 a0001c0001t0005g0025 others(18): Show |
44 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.247+389C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340324 | |||||||
| chr3:100340391 | T | C | 10 | a0001c0001t0008g0022 a0001c0001t0008g0066 a0001c0001t0008g0133 others(7): Show |
13 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.247+456T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340391 | |||||||
| chr3:100340590 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.248-483G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340590 | |||||||
| chr3:100340623 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.248-450C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340623 | |||||||
| chr3:100340644 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.248-429T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340644 | |||||||
| chr3:100340674 | GAATTC | G | 33 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0016 others(30): Show |
78 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.248-396_248-392del others(5): Show |
NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 100340674 | ||||||
| chr3:100340694 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.248-379G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340694 | |||||||
| chr3:100340714 | A | G | 2 | a0001c0001t0011g0024 a0001c0001t0011g0072 |
4 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-359A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340714 | |||||||
| chr3:100340822 | T | C | 32 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0016 others(29): Show |
76 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.248-251T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340822 | |||||||
| chr3:100340849 | T | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0050 |
5 | HG01358.hp1 HG01943.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-224T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340849 | |||||||
| chr3:100341250 | C | T | 1 | a0001c0001t0001g0044 | 2 | NA18970.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.336+89C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341250 | |||||||
| chr3:100341291 | G | A | 52 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.336+130G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341291 | |||||||
| chr3:100341448 | T | A | 52 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.336+287T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341448 | |||||||
| chr3:100341637 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.336+476G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341637 | |||||||
| chr3:100341717 | G | C | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+556G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341717 | |||||||
| chr3:100341724 | G | T | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+563G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341724 | |||||||
| chr3:100341726 | G | T | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+565G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341726 | |||||||
| chr3:100341727 | T | A | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+566T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341727 | |||||||
| chr3:100341729 | G | T | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+568G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341729 | |||||||
| chr3:100341731 | C | A | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+570C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341731 | |||||||
| chr3:100341734 | C | G | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+573C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341734 | |||||||
| chr3:100341735 | T | A | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+574T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341735 | |||||||
| chr3:100341736 | T | A | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+575T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341736 | |||||||
| chr3:100341737 | T | A | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+576T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341737 | |||||||
| chr3:100341741 | G | C | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+580G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341741 | |||||||
| chr3:100341744 | T | A | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+583T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341744 | |||||||
| chr3:100341750 | G | A | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+589G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341750 | |||||||
| chr3:100341752 | G | A | 1 | a0002c0004t0005g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+591G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341752 | |||||||
| chr3:100341935 | C | T | 62 | a0001c0001t0001g0040 a0001c0001t0002g0001 a0001c0001t0002g0010 others(59): Show |
131 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.336+774C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341935 | |||||||
| chr3:100341978 | C | T | 2 | a0001c0001t0003g0030 a0001c0001t0003g0058 |
3 | HG02155.hp1 NA18977.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.336+817C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341978 | |||||||
| chr3:100342027 | A | G | 1 | a0001c0001t0028g0038 | 2 | NA18956.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.336+866A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342027 | |||||||
| chr3:100342177 | A | G | 1 | a0001c0001t0003g0057 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.336+1016A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342177 | |||||||
| chr3:100342200 | C | G | 1 | a0001c0001t0003g0029 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.336+1039C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342200 | |||||||
| chr3:100342407 | A | G | 28 | a0001c0001t0001g0040 a0001c0001t0005g0006 a0001c0001t0005g0012 others(25): Show |
52 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.336+1246A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342407 | |||||||
| chr3:100342519 | CT | C | 7 | a0001c0001t0003g0030 a0001c0001t0003g0058 a0001c0001t0008g0022 others(4): Show |
11 | HG02109.hp2 HG02155.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.336+1371delT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 100342519 | ||||||
| chr3:100342897 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.336+1736A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342897 | |||||||
| chr3:100342946 | A | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0045 others(14): Show |
53 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.336+1785A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342946 | |||||||
| chr3:100343001 | A | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0043 others(10): Show |
22 | HG00423.hp1 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.336+1840A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343001 | |||||||
| chr3:100343062 | T | C | 1 | a0001c0001t0005g0025 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.336+1901T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343062 | |||||||
| chr3:100343084 | A | G | 1 | a0001c0001t0032g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.336+1923A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343084 | |||||||
| chr3:100343096 | T | G | 5 | a0001c0001t0007g0011 a0001c0001t0007g0069 a0001c0001t0035g0068 others(2): Show |
8 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.336+1935T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343096 | |||||||
| chr3:100343105 | G | A | 5 | a0001c0001t0008g0022 a0001c0001t0008g0066 a0001c0001t0008g0133 others(2): Show |
8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.336+1944G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343105 | |||||||
| chr3:100343253 | C | G | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.336+2092C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343253 | |||||||
| chr3:100343363 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.336+2202C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343363 | |||||||
| chr3:100343407 | T | A | 22 | a0001c0001t0002g0071 a0001c0001t0004g0002 a0001c0001t0004g0021 others(19): Show |
65 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.337-2178T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343407 | |||||||
| chr3:100343482 | C | T | 1 | a0001c0001t0026g0037 | 2 | HG01123.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.337-2103C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343482 | |||||||
| chr3:100343483 | G | A | 1 | a0001c0001t0005g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.337-2102G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343483 | |||||||
| chr3:100343606 | C | T | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.337-1979C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343606 | |||||||
| chr3:100343785 | G | A | 2 | a0001c0002t0019g0023 a0001c0002t0031g0023 |
3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.337-1800G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343785 | |||||||
| chr3:100343934 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.337-1651G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343934 | |||||||
| chr3:100344008 | T | A | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.337-1577T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344008 | |||||||
| chr3:100344267 | G | A | 1 | a0001c0001t0047g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.337-1318G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344267 | |||||||
| chr3:100344285 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.337-1300A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344285 | |||||||
| chr3:100344296 | C | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0116 a0001c0001t0009g0013 others(1): Show |
6 | HG00423.hp1 HG02027.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-1289C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344296 | |||||||
| chr3:100344327 | G | T | 1 | a0001c0001t0003g0123 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.337-1258G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344327 | |||||||
| chr3:100344533 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.337-1052C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344533 | |||||||
| chr3:100344557 | T | A | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.337-1028T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344557 | |||||||
| chr3:100344642 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.337-943C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344642 | |||||||
| chr3:100344667 | A | G | 1 | a0001c0001t0004g0105 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.337-918A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344667 | |||||||
| chr3:100344685 | G | A | 21 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0031 others(18): Show |
64 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.337-900G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344685 | |||||||
| chr3:100344851 | G | C | 1 | a0001c0001t0006g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.337-734G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344851 | |||||||
| chr3:100344901 | C | T | 1 | a0001c0001t0010g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.337-684C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344901 | |||||||
| chr3:100344911 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.337-674C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344911 | |||||||
| chr3:100344959 | C | T | 2 | a0001c0001t0006g0017 a0001c0001t0006g0099 |
5 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-626C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344959 | |||||||
| chr3:100344959 | CT | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
317 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(314): Show |
intron_variant | MODIFIER | c.337-615delT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 100344959 | ||||||
| chr3:100344960 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0006g0017 a0001c0001t0006g0099 |
6 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-625T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344960 | |||||||
| chr3:100345050 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.337-535G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345050 | |||||||
| chr3:100345101 | C | T | 1 | a0001c0001t0048g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337-484C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345101 | |||||||
| chr3:100345161 | T | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
193 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.337-424T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345161 | |||||||
| chr3:100345210 | C | T | 4 | a0001c0001t0011g0024 a0001c0001t0011g0072 a0001c0001t0017g0063 others(1): Show |
6 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-375C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345210 | |||||||
| chr3:100345254 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.337-331C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345254 | |||||||
| chr3:100345383 | A | G | 5 | a0001c0001t0007g0011 a0001c0001t0007g0069 a0001c0001t0035g0068 others(2): Show |
8 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-202A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345383 | |||||||
| chr3:100345439 | G | T | 1 | a0001c0001t0051g0054 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.337-146G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345439 | |||||||
| chr3:100345758 | G | A | 5 | a0001c0001t0002g0036 a0001c0001t0011g0024 a0001c0001t0011g0072 others(2): Show |
8 | HG01099.hp1 HG01243.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+80G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/9 | chr3 | 100345758 | |||||||
| chr3:100345897 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
192 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.430+219C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/9 | chr3 | 100345897 | |||||||
| chr3:100345985 | C | G | 32 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0016 others(29): Show |
76 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.431-196C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/9 | chr3 | 100345985 | |||||||
| chr3:100346058 | C | T | 31 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0016 others(28): Show |
75 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.431-123C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/9 | chr3 | 100346058 | |||||||
| chr3:100346401 | G | A | 2 | a0001c0001t0020g0073 a0001c0001t0020g0134 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.505+146G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346401 | |||||||
| chr3:100346454 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0042g0026 |
3 | HG01346.hp1 HG01358.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.505+199T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346454 | |||||||
| chr3:100346698 | T | G | 1 | a0001c0001t0001g0045 | 2 | NA18978.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.505+443T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346698 | |||||||
| chr3:100346733 | C | G | 22 | a0001c0001t0002g0071 a0001c0001t0004g0002 a0001c0001t0004g0021 others(19): Show |
65 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.505+478C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346733 | |||||||
| chr3:100346788 | G | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
195 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.505+533G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346788 | |||||||
| chr3:100346936 | TG | T | 1 | a0001c0001t0006g0017 | 4 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+684delG | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 100346936 | ||||||
| chr3:100346982 | C | G | 141 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(138): Show |
324 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(321): Show |
intron_variant | MODIFIER | c.505+727C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346982 | |||||||
| chr3:100346995 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.505+740C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346995 | |||||||
| chr3:100347039 | T | C | 3 | a0001c0001t0008g0022 a0001c0001t0008g0066 a0001c0001t0008g0133 |
5 | HG02109.hp2 HG02630.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.505+784T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347039 | |||||||
| chr3:100347061 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.505+806T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347061 | |||||||
| chr3:100347089 | G | T | 1 | a0001c0001t0001g0009 | 2 | HG02083.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.505+834G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347089 | |||||||
| chr3:100347109 | T | G | 1 | a0001c0001t0035g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.505+854T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347109 | |||||||
| chr3:100347385 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.505+1130C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347385 | |||||||
| chr3:100347647 | C | T | 3 | a0001c0001t0003g0028 a0001c0001t0003g0053 a0001c0001t0058g0028 |
3 | HG00280.hp1 HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.506-1156C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347647 | |||||||
| chr3:100347731 | A | T | 1 | a0001c0001t0002g0036 | 2 | HG01099.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.506-1072A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347731 | |||||||
| chr3:100347784 | G | T | 17 | a0001c0001t0003g0003 a0001c0001t0003g0014 a0001c0001t0003g0028 others(14): Show |
42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.506-1019G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347784 | |||||||
| chr3:100347860 | C | T | 1 | a0001c0001t0061g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.506-943C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347860 | |||||||
| chr3:100347897 | C | CT | 5 | a0001c0001t0002g0083 a0001c0001t0011g0024 a0001c0001t0011g0072 others(2): Show |
7 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-895dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 100347897 | ||||||
| chr3:100347937 | C | G | 1 | a0001c0001t0008g0066 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.506-866C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347937 | |||||||
| chr3:100347953 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0018g0016 |
4 | NA18955.hp2 NA18962.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-850C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347953 | |||||||
| chr3:100347954 | G | A | 2 | a0001c0001t0034g0128 a0001c0001t0048g0129 |
2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.506-849G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347954 | |||||||
| chr3:100348013 | C | T | 2 | a0001c0002t0019g0023 a0001c0002t0031g0023 |
3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.506-790C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348013 | |||||||
| chr3:100348036 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.506-767G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348036 | |||||||
| chr3:100348089 | A | C | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.506-714A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348089 | |||||||
| chr3:100348125 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.506-678C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348125 | |||||||
| chr3:100348143 | C | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0132 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.506-660C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348143 | |||||||
| chr3:100348312 | A | C | 1 | a0001c0001t0006g0018 | 4 | HG01106.hp1 HG02257.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-491A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348312 | |||||||
| chr3:100348533 | G | A | 1 | a0001c0001t0010g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.506-270G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348533 | |||||||
| chr3:100348624 | C | T | 142 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
325 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.506-179C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348624 | |||||||
| chr3:100348927 | G | A | 2 | a0001c0001t0011g0024 a0001c0001t0011g0072 |
4 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.584+46G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100348927 | |||||||
| chr3:100348957 | C | T | 2 | a0001c0001t0034g0128 a0001c0001t0048g0129 |
2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.584+76C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100348957 | |||||||
| chr3:100349053 | C | T | 1 | a0001c0001t0046g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.584+172C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100349053 | |||||||
| chr3:100349108 | C | CT | 9 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0004g0059 others(6): Show |
12 | HG02027.hp1 HG02135.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.584+245dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 100349108 | ||||||
| chr3:100349192 | C | T | 1 | a0001c0001t0005g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.584+311C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100349192 | |||||||
| chr3:100349954 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.584+1073A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100349954 | |||||||
| chr3:100349962 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.584+1081A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100349962 | |||||||
| chr3:100350414 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.584+1533G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350414 | |||||||
| chr3:100350593 | T | C | 1 | a0001c0001t0004g0100 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.584+1712T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350593 | |||||||
| chr3:100350596 | G | A | 2 | a0001c0002t0019g0023 a0001c0002t0031g0023 |
3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.584+1715G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350596 | |||||||
| chr3:100350784 | C | T | 1 | a0001c0001t0012g0132 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.585-1620C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350784 | |||||||
| chr3:100350848 | T | C | 144 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(141): Show |
328 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(325): Show |
intron_variant | MODIFIER | c.585-1556T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350848 | |||||||
| chr3:100350855 | C | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(46): Show |
115 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.585-1549C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350855 | |||||||
| chr3:100350900 | C | T | 5 | a0001c0001t0008g0022 a0001c0001t0008g0066 a0001c0001t0008g0133 others(2): Show |
8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.585-1504C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350900 | |||||||
| chr3:100350918 | C | T | 2 | a0001c0002t0019g0023 a0001c0002t0031g0023 |
3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.585-1486C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350918 | |||||||
| chr3:100350934 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG00597.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.585-1470C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350934 | |||||||
| chr3:100350939 | G | A | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.585-1465G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350939 | |||||||
| chr3:100351174 | C | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0132 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.585-1230C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351174 | |||||||
| chr3:100351200 | A | G | 3 | a0001c0001t0005g0012 a0001c0001t0005g0096 a0002c0004t0005g0091 |
7 | NA18940.hp2 NA18953.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.585-1204A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351200 | |||||||
| chr3:100351220 | C | A | 1 | a0001c0001t0004g0101 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.585-1184C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351220 | |||||||
| chr3:100351418 | A | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0043 others(12): Show |
25 | HG00423.hp1 HG00642.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.585-986A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351418 | |||||||
| chr3:100351452 | G | A | 1 | a0001c0001t0044g0102 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.585-952G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351452 | |||||||
| chr3:100351620 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.585-784A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351620 | |||||||
| chr3:100351846 | C | T | 1 | a0001c0001t0003g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.585-558C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351846 | |||||||
| chr3:100351847 | G | A | 21 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0031 others(18): Show |
64 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.585-557G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351847 | |||||||
| chr3:100351884 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.585-520T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351884 | |||||||
| chr3:100351901 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(46): Show |
115 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.585-503C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351901 | |||||||
| chr3:100351911 | A | C | 1 | a0001c0001t0030g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.585-493A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351911 | |||||||
| chr3:100351912 | G | T | 1 | a0001c0001t0001g0114 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.585-492G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351912 | |||||||
| chr3:100352022 | G | C | 105 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
241 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.585-382G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100352022 | |||||||
| chr3:100352226 | G | C | 33 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0016 others(30): Show |
77 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.585-178G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100352226 | |||||||
| chr3:100352310 | T | C | 1 | a0001c0001t0005g0093 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.585-94T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100352310 | |||||||
| chr3:100352372 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
18 | HG00544.hp1 HG00558.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.585-32C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100352372 | |||||||
| chr3:100352938 | A | G | 1 | a0001c0001t0020g0073 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.683+436A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100352938 | |||||||
| chr3:100353191 | G | A | 2 | a0001c0002t0019g0023 a0001c0002t0031g0023 |
3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.683+689G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353191 | |||||||
| chr3:100353392 | C | T | 2 | a0001c0001t0005g0093 a0001c0001t0005g0095 |
2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.683+890C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353392 | |||||||
| chr3:100353488 | G | A | 51 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0031 others(48): Show |
120 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.683+986G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353488 | |||||||
| chr3:100353601 | T | G | 2 | a0001c0002t0019g0023 a0001c0002t0031g0023 |
3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.683+1099T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353601 | |||||||
| chr3:100353765 | AGTTTC | A | 5 | a0001c0001t0008g0022 a0001c0001t0008g0066 a0001c0001t0008g0133 others(2): Show |
8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.684-1006_684-1002d others(7): Show |
NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353765 | |||||||
| chr3:100353777 | C | CT | 139 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
319 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.684-981dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 100353777 | ||||||
| chr3:100354051 | C | T | 1 | a0001c0001t0061g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.684-721C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354051 | |||||||
| chr3:100354197 | C | T | 1 | a0001c0001t0020g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.684-575C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354197 | |||||||
| chr3:100354418 | T | C | 1 | a0001c0001t0005g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.684-354T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354418 | |||||||
| chr3:100354489 | C | T | 17 | a0001c0001t0005g0006 a0001c0001t0005g0012 a0001c0001t0005g0025 others(14): Show |
38 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.684-283C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354489 | |||||||
| chr3:100354633 | C | T | 1 | a0001c0001t0038g0070 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.684-139C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354633 | |||||||
| chr3:100354737 | G | A | 4 | a0001c0001t0020g0073 a0001c0001t0020g0134 a0001c0002t0019g0023 others(1): Show |
5 | HG02572.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.684-35G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354737 | |||||||
| chr3:100354880 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.739+53G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100354880 | |||||||
| chr3:100354881 | C | G | 22 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0031 others(19): Show |
65 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.739+54C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100354881 | |||||||
| chr3:100354939 | C | T | 1 | a0001c0001t0003g0052 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.739+112C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100354939 | |||||||
| chr3:100354982 | T | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
325 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.739+155T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100354982 | |||||||
| chr3:100355048 | A | G | 1 | a0001c0001t0005g0096 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.740-129A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100355048 | |||||||
| chr3:100355062 | TA | T | 22 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0031 others(19): Show |
65 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.740-114delA | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100355062 | |||||||
| chr3:100355097 | T | C | 1 | a0001c0001t0002g0089 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.740-80T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100355097 |