Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10204 |
| ensemblid | ENSG00000102898.13 |
| hgncid | 13722 |
| symbol | NUTF2 |
| name | nuclear transport factor 2 |
| refseq_nuc | NM_005796.3 |
| refseq_prot | NP_005787.1 |
| ensembl_nuc | ENST00000219169.9 |
| ensembl_prot | ENSP00000219169.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 67846933 |
| end | 67872567 |
| strand | + |
| ver | v1.2 |
| region | chr16:67846933-67872567 |
| region5000 | chr16:67841933-67877567 |
| regionname0 | NUTF2_chr16_67846933_67872567 |
| regionname5000 | NUTF2_chr16_67841933_67877567 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 381 | 246 | 82 | 52 | 72 | 6 | 32 | NUTF2_chr16_67841933_67877567 | NUTF2 | ATGGG others(376): Show |
chr16 | 67841933 | 67877567 | ||
| a0001c0002 | 0/0 | 381 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | ATGGG others(376): Show |
chr16 | 67841933 | 67877567 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2120 | 129 | 21 | 27 | 56 | 3 | 20 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2115): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0002 | 0/0 | 2121 | 56 | 34 | 13 | 4 | 0 | 5 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2116): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0003 | 0/0 | 2119 | 16 | 15 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2114): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0004 | 0/0 | 2120 | 12 | 8 | 3 | 0 | 1 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2115): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0005 | 0/0 | 2119 | 7 | 0 | 3 | 1 | 1 | 2 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2114): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0006 | 0/0 | 2120 | 5 | 0 | 0 | 5 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2115): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0007 | 0/0 | 2122 | 4 | 0 | 3 | 0 | 1 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2117): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0008 | 0/0 | 2119 | 2 | 0 | 0 | 0 | 0 | 2 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2114): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0009 | 0/0 | 2117 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2112): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0010 | 0/0 | 2121 | 2 | 0 | 0 | 2 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2116): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0011 | 0/0 | 2120 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2115): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0012 | 0/0 | 2119 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2114): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0013 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2112): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0014 | 0/0 | 2120 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2115): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0015 | 0/0 | 2120 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2115): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0016 | 0/0 | 2120 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2115): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0017 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2116): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0018 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2116): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0019 | 0/0 | 2121 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2116): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0020 | 0/0 | 2122 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2117): Show |
chr16 | 67841933 | 67877567 |
| a0001c0001t0021 | 0/0 | 2120 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2115): Show |
chr16 | 67841933 | 67877567 |
| a0001c0002t0001 | 0/0 | 2120 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | GCAGA others(2115): Show |
chr16 | 67841933 | 67877567 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0002 | 0/0 | 6 | 1 | 3 | 2 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0006g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0009g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0010g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0011g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0014g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0015g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0016g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0017g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0018g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0019g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0020g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0001t0021g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00438 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | CHS | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0176 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01070 | hp1 | a0001 | c0001 | t0019 | g0030 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0030 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0175 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01496 | hp2 | a0001 | c0001 | t0015 | g0023 | AMR | CLM | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0056 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02056 | hp2 | a0001 | c0001 | t0010 | g0062 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02895 | hp1 | a0001 | c0001 | t0021 | g0164 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0048 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03710 | hp1 | a0001 | c0001 | t0016 | g0063 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | BEB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0086 | SAS | STU | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0071 | SAS | STU | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG04199 | hp2 | a0001 | c0001 | t0020 | g0166 | SAS | STU | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG04204 | hp1 | a0001 | c0001 | t0008 | g0156 | SAS | STU | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | YRI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | YRI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18951 | hp1 | a0001 | c0001 | t0014 | g0019 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18991 | hp1 | a0001 | c0001 | t0017 | g0031 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19009 | hp1 | a0001 | c0001 | t0018 | g0051 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19010 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | LWK | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | LWK | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19055 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19091 | hp2 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | YRI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0085 | AFR | YRI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ASW | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0177 | EUR | TSI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0006 | EUR | TSI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0168 | EUR | TSI | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | GIH | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0167 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ACB | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | MSL | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | USA | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | USA | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0136 | REF | REF | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0106 | REF | REF | NUTF2_chr16_67841933_67877567 | NUTF2 | chr16 | 67841933 | 67877567 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67870839 | C | T | 1 | a0001c0002 | 2 | HG02451.hp1 HG02615.hp1 |
synonymous_variant | LOW | c.310C>T | p.Leu104Leu | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 392/2120 | 310/384 | 104/127 | chr16 | 67870839 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67871019 | G | C | 1 | a0001c0001t0011 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*106G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 106 | chr16 | 67871019 | ||||||
| chr16:67871033 | C | T | 1 | a0001c0001t0021 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 120 | chr16 | 67871033 | ||||||
| chr16:67871162 | C | CT | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(2): Show |
61 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*271dupT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 272 | INFO_REALIGN_3_PRIME | chr16 | 67871162 | |||||
| chr16:67871162 | C | CTT | 2 | a0001c0001t0007 a0001c0001t0020 |
5 | HG00741.hp2 HG01071.hp1 HG01346.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*270_*271dupTT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 272 | INFO_REALIGN_3_PRIME | chr16 | 67871162 | |||||
| chr16:67871162 | CT | C | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(3): Show |
29 | HG01109.hp1 HG01168.hp1 HG01168.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*271delT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 271 | INFO_REALIGN_3_PRIME | chr16 | 67871162 | |||||
| chr16:67871311 | T | A | 2 | a0001c0001t0006 a0001c0001t0017 |
6 | HG00438.hp1 NA18940.hp1 NA18991.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*398T>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 398 | chr16 | 67871311 | ||||||
| chr16:67871504 | A | G | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(9): Show |
102 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*591A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 591 | chr16 | 67871504 | ||||||
| chr16:67871615 | G | A | 1 | a0001c0001t0018 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*702G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 702 | chr16 | 67871615 | ||||||
| chr16:67871743 | G | T | 1 | a0001c0001t0009 | 2 | HG03041.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*830G>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 830 | chr16 | 67871743 | ||||||
| chr16:67871745 | C | T | 1 | a0001c0001t0016 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 832 | chr16 | 67871745 | ||||||
| chr16:67872009 | CCT | C | 2 | a0001c0001t0009 a0001c0001t0013 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1102_*1103delTC | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 1102 | INFO_REALIGN_3_PRIME | chr16 | 67872009 | |||||
| chr16:67872049 | A | G | 1 | a0001c0001t0012 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1136A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 1136 | chr16 | 67872049 | ||||||
| chr16:67872055 | C | T | 1 | a0001c0001t0015 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1142C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 1142 | chr16 | 67872055 | ||||||
| chr16:67872091 | G | A | 2 | a0001c0001t0007 a0001c0001t0019 |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1178G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 1178 | chr16 | 67872091 | ||||||
| chr16:67872293 | C | G | 1 | a0001c0001t0008 | 2 | HG04115.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1380C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 1380 | chr16 | 67872293 | ||||||
| chr16:67872307 | G | T | 1 | a0001c0001t0014 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1394G>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 5/5 | 1394 | chr16 | 67872307 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67847088 | T | TC | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(49): Show |
62 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-30+114dupC | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67847088 | ||||||
| chr16:67847088 | TC | T | 36 | a0001c0001t0001g0183 a0001c0001t0002g0002 a0001c0001t0002g0011 others(33): Show |
46 | HG00438.hp1 HG00639.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.-30+114delC | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67847088 | ||||||
| chr16:67847143 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-30+158G>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67847143 | |||||||
| chr16:67847176 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30+191G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67847176 | |||||||
| chr16:67847403 | A | G | 1 | a0001c0001t0020g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-30+418A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67847403 | |||||||
| chr16:67847527 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-30+542G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67847527 | |||||||
| chr16:67847757 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-30+772A>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67847757 | |||||||
| chr16:67847807 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-30+822A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67847807 | |||||||
| chr16:67847954 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-30+969C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67847954 | |||||||
| chr16:67847977 | G | A | 1 | a0001c0001t0004g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-30+992G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67847977 | |||||||
| chr16:67848082 | C | A | 1 | a0001c0001t0004g0168 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-30+1097C>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848082 | |||||||
| chr16:67848086 | T | G | 9 | a0001c0001t0002g0029 a0001c0001t0002g0079 a0001c0001t0002g0169 others(6): Show |
10 | HG01175.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+1101T>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848086 | |||||||
| chr16:67848314 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-30+1329G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848314 | |||||||
| chr16:67848340 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-30+1355T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848340 | |||||||
| chr16:67848444 | G | A | 1 | a0001c0001t0005g0082 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-30+1459G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848444 | |||||||
| chr16:67848510 | G | C | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-30+1525G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848510 | |||||||
| chr16:67848611 | G | A | 3 | a0001c0001t0009g0017 a0001c0001t0013g0085 a0001c0001t0021g0164 |
4 | HG02895.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+1626G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848611 | |||||||
| chr16:67848666 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-30+1681C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848666 | |||||||
| chr16:67848671 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-30+1686G>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848671 | |||||||
| chr16:67848757 | G | GA | 6 | a0001c0001t0007g0030 a0001c0001t0007g0175 a0001c0001t0007g0176 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+1785dupA | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67848757 | ||||||
| chr16:67848972 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-30+1987C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67848972 | |||||||
| chr16:67849029 | A | G | 14 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0073 others(11): Show |
16 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+2044A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67849029 | |||||||
| chr16:67849291 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0004g0178 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-30+2306G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67849291 | |||||||
| chr16:67849303 | G | C | 1 | a0001c0001t0002g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-30+2318G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67849303 | |||||||
| chr16:67849359 | C | A | 5 | a0001c0001t0007g0030 a0001c0001t0007g0175 a0001c0001t0007g0176 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+2374C>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67849359 | |||||||
| chr16:67849594 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+2609C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67849594 | |||||||
| chr16:67849653 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30+2668T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67849653 | |||||||
| chr16:67849703 | G | C | 1 | a0001c0001t0002g0087 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-30+2718G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67849703 | |||||||
| chr16:67849860 | G | A | 2 | a0001c0001t0002g0088 a0001c0001t0004g0033 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-30+2875G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67849860 | |||||||
| chr16:67849880 | G | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0160 others(4): Show |
9 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30+2895G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67849880 | |||||||
| chr16:67850079 | A | C | 1 | a0001c0001t0002g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-30+3094A>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850079 | |||||||
| chr16:67850112 | A | T | 16 | a0001c0001t0002g0075 a0001c0001t0003g0027 a0001c0001t0003g0028 others(13): Show |
19 | HG01109.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-30+3127A>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850112 | |||||||
| chr16:67850137 | A | T | 1 | a0001c0001t0021g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-30+3152A>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850137 | |||||||
| chr16:67850138 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0162 |
2 | HG01433.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-30+3153C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850138 | |||||||
| chr16:67850205 | C | CT | 7 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0073 others(4): Show |
9 | HG01433.hp2 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30+3222dupT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67850205 | ||||||
| chr16:67850205 | C | CTT | 5 | a0001c0001t0007g0030 a0001c0001t0007g0175 a0001c0001t0007g0176 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+3221_-30+3222d others(4): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67850205 | ||||||
| chr16:67850208 | C | T | 36 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0073 others(33): Show |
42 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-30+3223C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850208 | |||||||
| chr16:67850265 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-30+3280C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850265 | |||||||
| chr16:67850365 | C | T | 2 | a0001c0001t0002g0179 a0001c0001t0004g0178 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-30+3380C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850365 | |||||||
| chr16:67850370 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-30+3385A>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850370 | |||||||
| chr16:67850427 | C | G | 5 | a0001c0001t0002g0151 a0001c0001t0002g0158 a0001c0001t0003g0026 others(2): Show |
6 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+3442C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850427 | |||||||
| chr16:67850465 | C | A | 5 | a0001c0001t0002g0151 a0001c0001t0002g0158 a0001c0001t0003g0026 others(2): Show |
6 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+3480C>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850465 | |||||||
| chr16:67850508 | T | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-30+3523T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850508 | |||||||
| chr16:67850655 | C | G | 1 | a0001c0001t0021g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-30+3670C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850655 | |||||||
| chr16:67850716 | C | T | 79 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0010 others(76): Show |
98 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.-30+3731C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850716 | |||||||
| chr16:67850785 | A | G | 5 | a0001c0001t0007g0030 a0001c0001t0007g0175 a0001c0001t0007g0176 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+3800A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850785 | |||||||
| chr16:67850838 | T | C | 16 | a0001c0001t0002g0075 a0001c0001t0003g0027 a0001c0001t0003g0028 others(13): Show |
19 | HG01109.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-30+3853T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67850838 | |||||||
| chr16:67850981 | AGTAGAGA others(4): Show |
A | 1 | a0001c0001t0002g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-30+3999_-30+4009d others(13): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67850981 | ||||||
| chr16:67851047 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-30+4062C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67851047 | |||||||
| chr16:67851207 | GTGCGGTG others(5): Show |
G | 2 | a0001c0001t0007g0175 a0001c0001t0007g0176 |
2 | HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-30+4226_-30+4237d others(14): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67851207 | ||||||
| chr16:67851413 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-30+4428G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67851413 | |||||||
| chr16:67851505 | G | GT | 5 | a0001c0001t0007g0030 a0001c0001t0007g0175 a0001c0001t0007g0176 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+4528dupT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67851505 | ||||||
| chr16:67851554 | C | T | 16 | a0001c0001t0002g0075 a0001c0001t0003g0027 a0001c0001t0003g0028 others(13): Show |
19 | HG01109.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-30+4569C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67851554 | |||||||
| chr16:67851624 | A | G | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG01175.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-30+4639A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67851624 | |||||||
| chr16:67851659 | A | AC | 5 | a0001c0001t0001g0035 a0001c0001t0001g0089 a0001c0001t0003g0149 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+4679dupC | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67851659 | ||||||
| chr16:67851681 | C | T | 1 | a0001c0001t0021g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-30+4696C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67851681 | |||||||
| chr16:67851689 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-30+4704G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67851689 | |||||||
| chr16:67851877 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0018 others(18): Show |
25 | HG00673.hp1 HG00673.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-30+4892G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67851877 | |||||||
| chr16:67851907 | T | C | 14 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0073 others(11): Show |
16 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+4922T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67851907 | |||||||
| chr16:67851948 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | NA18946.hp1 NA18968.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-30+4963G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67851948 | |||||||
| chr16:67852233 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-30+5248T>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67852233 | |||||||
| chr16:67852354 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-30+5369T>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67852354 | |||||||
| chr16:67852449 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-30+5464C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67852449 | |||||||
| chr16:67852748 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-30+5763C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67852748 | |||||||
| chr16:67853591 | T | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0029 others(28): Show |
39 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-30+6606T>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67853591 | |||||||
| chr16:67853629 | C | A | 36 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0073 others(33): Show |
42 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-30+6644C>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67853629 | |||||||
| chr16:67853692 | G | A | 1 | a0001c0001t0004g0168 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-30+6707G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67853692 | |||||||
| chr16:67854043 | C | T | 1 | a0001c0001t0002g0007 | 3 | HG02622.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-30+7058C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854043 | |||||||
| chr16:67854196 | G | A | 5 | a0001c0001t0007g0030 a0001c0001t0007g0175 a0001c0001t0007g0176 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+7211G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854196 | |||||||
| chr16:67854426 | G | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-30+7441G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854426 | |||||||
| chr16:67854610 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-30+7625G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854610 | |||||||
| chr16:67854764 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-30+7779T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854764 | |||||||
| chr16:67854896 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-30+7911C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854896 | |||||||
| chr16:67854921 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01070.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-30+7936G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854921 | |||||||
| chr16:67854923 | C | T | 1 | a0001c0001t0021g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-30+7938C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854923 | |||||||
| chr16:67854925 | A | G | 1 | a0001c0001t0002g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-30+7940A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854925 | |||||||
| chr16:67854928 | G | C | 1 | a0001c0001t0002g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-30+7943G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854928 | |||||||
| chr16:67854937 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-30+7952T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854937 | |||||||
| chr16:67854941 | T | TCAAAAAA others(15): Show |
1 | a0001c0001t0002g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-30+7956_-30+7957i others(24): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854941 | |||||||
| chr16:67854942 | T | A | 1 | a0001c0001t0002g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-30+7957T>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854942 | |||||||
| chr16:67854943 | T | A | 1 | a0001c0001t0002g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-30+7958T>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854943 | |||||||
| chr16:67854990 | A | T | 1 | a0001c0001t0002g0087 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-30+8005A>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67854990 | |||||||
| chr16:67855174 | GCCAGCAG others(11): Show |
G | 3 | a0001c0001t0002g0151 a0001c0001t0003g0026 a0001c0001t0003g0149 |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+8190_-30+8207d others(20): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67855174 | |||||||
| chr16:67855218 | A | G | 1 | a0001c0001t0004g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-30+8233A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67855218 | |||||||
| chr16:67855244 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-30+8259C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67855244 | |||||||
| chr16:67855887 | C | CG | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(47): Show |
59 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-30+8913dupG | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67855887 | ||||||
| chr16:67855890 | G | C | 44 | a0001c0001t0001g0103 a0001c0001t0002g0002 a0001c0001t0002g0007 others(41): Show |
57 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.-30+8905G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67855890 | |||||||
| chr16:67855891 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-30+8906G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67855891 | |||||||
| chr16:67855892 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-30+8907G>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67855892 | |||||||
| chr16:67856003 | G | A | 4 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(1): Show |
4 | HG02559.hp2 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+9018G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67856003 | |||||||
| chr16:67856156 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-29-8946C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67856156 | |||||||
| chr16:67856469 | C | T | 6 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0160 others(3): Show |
8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-8633C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67856469 | |||||||
| chr16:67856483 | C | A | 1 | a0001c0001t0002g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-29-8619C>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67856483 | |||||||
| chr16:67856485 | T | C | 36 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0073 others(33): Show |
42 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-29-8617T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67856485 | |||||||
| chr16:67856492 | G | GT | 49 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(46): Show |
62 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.-29-8595dupT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67856492 | ||||||
| chr16:67857010 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-29-8092C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67857010 | |||||||
| chr16:67857065 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-29-8037G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67857065 | |||||||
| chr16:67857171 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-29-7931A>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67857171 | |||||||
| chr16:67857403 | C | G | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-29-7699C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67857403 | |||||||
| chr16:67857666 | A | G | 4 | a0001c0001t0001g0089 a0001c0001t0001g0126 a0001c0001t0001g0134 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-7436A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67857666 | |||||||
| chr16:67857755 | C | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(28): Show |
37 | HG00140.hp1 HG00673.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.-29-7347C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67857755 | |||||||
| chr16:67857829 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-29-7273G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67857829 | |||||||
| chr16:67857878 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-29-7224G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67857878 | |||||||
| chr16:67857931 | C | T | 2 | a0001c0001t0007g0030 a0001c0001t0019g0030 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-29-7171C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67857931 | |||||||
| chr16:67858074 | G | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0078 |
2 | HG02129.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-29-7028G>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67858074 | |||||||
| chr16:67858217 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-29-6885G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67858217 | |||||||
| chr16:67858237 | G | A | 5 | a0001c0001t0007g0030 a0001c0001t0007g0175 a0001c0001t0007g0176 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-6865G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67858237 | |||||||
| chr16:67858459 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-29-6643A>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67858459 | |||||||
| chr16:67858803 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-29-6299G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67858803 | |||||||
| chr16:67859000 | CT | C | 43 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0010 others(40): Show |
56 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.-29-6090delT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67859000 | ||||||
| chr16:67859103 | C | T | 1 | a0001c0001t0005g0048 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-29-5999C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859103 | |||||||
| chr16:67859153 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0052 |
2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-29-5949G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859153 | |||||||
| chr16:67859349 | A | AT | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
199 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.-29-5736dupT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67859349 | ||||||
| chr16:67859349 | A | ATT | 6 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0132 others(3): Show |
7 | HG00558.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-5737_-29-5736d others(4): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67859349 | ||||||
| chr16:67859418 | C | T | 6 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0160 others(3): Show |
8 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-5684C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859418 | |||||||
| chr16:67859509 | A | G | 5 | a0001c0001t0002g0151 a0001c0001t0002g0158 a0001c0001t0003g0026 others(2): Show |
6 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-5593A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859509 | |||||||
| chr16:67859529 | T | G | 1 | a0001c0001t0002g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-29-5573T>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859529 | |||||||
| chr16:67859602 | C | T | 1 | a0001c0001t0021g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-29-5500C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859602 | |||||||
| chr16:67859685 | G | A | 2 | a0001c0001t0009g0017 a0001c0001t0013g0085 |
3 | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-29-5417G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859685 | |||||||
| chr16:67859795 | C | CT | 6 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0059 others(3): Show |
6 | HG01106.hp1 HG01169.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-5280dupT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67859795 | ||||||
| chr16:67859795 | CT | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(47): Show |
57 | HG00438.hp1 HG00738.hp2 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.-29-5280delT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67859795 | ||||||
| chr16:67859795 | CTT | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
89 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-29-5281_-29-5280d others(4): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67859795 | ||||||
| chr16:67859795 | CTTT | C | 37 | a0001c0001t0001g0089 a0001c0001t0001g0107 a0001c0001t0001g0126 others(34): Show |
47 | HG00639.hp2 HG00738.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.-29-5282_-29-5280d others(5): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67859795 | ||||||
| chr16:67859795 | CTTTT | C | 30 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0073 others(27): Show |
35 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-29-5283_-29-5280d others(6): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67859795 | ||||||
| chr16:67859795 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-29-5289_-29-5280d others(12): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67859795 | ||||||
| chr16:67859821 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0035 |
3 | HG03704.hp2 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-29-5281T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859821 | |||||||
| chr16:67859868 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-29-5234C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859868 | |||||||
| chr16:67859869 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(7): Show |
13 | HG02040.hp1 HG02135.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.-29-5233G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859869 | |||||||
| chr16:67859936 | G | A | 36 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0073 others(33): Show |
42 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-29-5166G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859936 | |||||||
| chr16:67859975 | T | TG | 3 | a0001c0001t0002g0073 a0001c0001t0002g0162 a0001c0001t0004g0150 |
3 | HG01433.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-29-5127_-29-5126i others(3): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859975 | |||||||
| chr16:67859976 | A | G | 79 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0010 others(76): Show |
98 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.-29-5126A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859976 | |||||||
| chr16:67859976 | A | T | 3 | a0001c0001t0002g0073 a0001c0001t0002g0162 a0001c0001t0004g0150 |
3 | HG01433.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-29-5126A>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859976 | |||||||
| chr16:67859977 | T | G | 1 | a0001c0001t0004g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-5125T>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859977 | |||||||
| chr16:67859978 | T | G | 16 | a0001c0001t0002g0075 a0001c0001t0003g0027 a0001c0001t0003g0028 others(13): Show |
19 | HG01109.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-5124T>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859978 | |||||||
| chr16:67859979 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-29-5123T>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67859979 | |||||||
| chr16:67860718 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-29-4384C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67860718 | |||||||
| chr16:67860723 | G | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0112 |
2 | HG01496.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-29-4379G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67860723 | |||||||
| chr16:67860779 | T | C | 15 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0068 others(12): Show |
18 | HG01109.hp1 HG02451.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29-4323T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67860779 | |||||||
| chr16:67861058 | C | G | 1 | a0001c0001t0004g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-29-4044C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67861058 | |||||||
| chr16:67861063 | T | C | 18 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0068 others(15): Show |
21 | HG00438.hp1 HG01109.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-29-4039T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67861063 | |||||||
| chr16:67861158 | A | G | 1 | a0001c0001t0003g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-29-3944A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67861158 | |||||||
| chr16:67861273 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-29-3829C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67861273 | |||||||
| chr16:67861526 | G | C | 1 | a0001c0001t0003g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-29-3576G>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67861526 | |||||||
| chr16:67861862 | C | CCCT | 5 | a0001c0001t0001g0015 a0001c0001t0001g0101 a0001c0001t0001g0119 others(2): Show |
6 | HG01175.hp1 HG03490.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-3237_-29-3235d others(5): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67861862 | ||||||
| chr16:67862300 | C | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0123 |
2 | HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-29-2802C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67862300 | |||||||
| chr16:67862520 | G | T | 1 | a0001c0001t0021g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-29-2582G>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67862520 | |||||||
| chr16:67862522 | C | A | 1 | a0001c0001t0021g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-29-2580C>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67862522 | |||||||
| chr16:67862814 | G | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0118 a0001c0001t0001g0128 |
3 | NA18943.hp2 NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-29-2288G>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67862814 | |||||||
| chr16:67863311 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-29-1791A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67863311 | |||||||
| chr16:67863583 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-29-1519C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67863583 | |||||||
| chr16:67863584 | C | T | 43 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0010 others(40): Show |
56 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.-29-1518C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67863584 | |||||||
| chr16:67863729 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-29-1373A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67863729 | |||||||
| chr16:67863858 | A | G | 1 | a0001c0001t0004g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-29-1244A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67863858 | |||||||
| chr16:67864128 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0123 |
2 | HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-29-974C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67864128 | |||||||
| chr16:67864449 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-29-653C>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67864449 | |||||||
| chr16:67864509 | C | CA | 22 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0060 others(19): Show |
24 | HG00741.hp2 HG01099.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.-29-569dupA | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67864509 | ||||||
| chr16:67864509 | CA | C | 5 | a0001c0001t0001g0097 a0001c0001t0001g0117 a0001c0001t0001g0120 others(2): Show |
5 | HG01256.hp2 HG02735.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-569delA | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67864509 | ||||||
| chr16:67864509 | CAAAAAAA | C | 16 | a0001c0001t0002g0075 a0001c0001t0003g0027 a0001c0001t0003g0028 others(13): Show |
19 | HG01109.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-575_-29-569del others(7): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 67864509 | ||||||
| chr16:67864589 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0004g0178 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-29-513G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67864589 | |||||||
| chr16:67864593 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-29-509C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67864593 | |||||||
| chr16:67864894 | G | A | 21 | a0001c0001t0002g0012 a0001c0001t0002g0072 a0001c0001t0002g0073 others(18): Show |
24 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-29-208G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 1/4 | chr16 | 67864894 | |||||||
| chr16:67865503 | T | C | 3 | a0001c0001t0004g0054 a0001c0001t0004g0083 a0001c0001t0004g0084 |
3 | HG01884.hp1 HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.99+274T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67865503 | |||||||
| chr16:67865616 | T | G | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.99+387T>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67865616 | |||||||
| chr16:67865635 | T | A | 3 | a0001c0001t0001g0102 a0001c0002t0001g0036 a0001c0002t0001g0127 |
3 | HG02451.hp1 HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.99+406T>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67865635 | |||||||
| chr16:67865719 | C | CT | 8 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0060 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+508dupT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 67865719 | ||||||
| chr16:67865719 | CT | C | 16 | a0001c0001t0001g0114 a0001c0001t0003g0027 a0001c0001t0003g0028 others(13): Show |
19 | HG01109.hp1 HG02451.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+508delT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 67865719 | ||||||
| chr16:67866240 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99+1011T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67866240 | |||||||
| chr16:67866306 | G | GT | 10 | a0001c0001t0001g0104 a0001c0001t0001g0110 a0001c0001t0002g0145 others(7): Show |
10 | HG00741.hp2 HG02257.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+1095dupT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 67866306 | ||||||
| chr16:67866306 | GT | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0115 a0001c0001t0001g0165 others(2): Show |
5 | HG03491.hp1 NA18747.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+1095delT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 67866306 | ||||||
| chr16:67866654 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+1425A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67866654 | |||||||
| chr16:67866774 | A | G | 4 | a0001c0001t0004g0054 a0001c0001t0004g0083 a0001c0001t0004g0084 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1545A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67866774 | |||||||
| chr16:67866947 | C | T | 5 | a0001c0001t0007g0030 a0001c0001t0007g0175 a0001c0001t0007g0176 others(2): Show |
5 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-1393C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67866947 | |||||||
| chr16:67866976 | C | CT | 7 | a0001c0001t0002g0186 a0001c0001t0004g0168 a0001c0001t0007g0030 others(4): Show |
7 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-1351dupT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 67866976 | ||||||
| chr16:67866977 | T | C | 3 | a0001c0001t0002g0151 a0001c0001t0003g0026 a0001c0001t0003g0149 |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-1363T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67866977 | |||||||
| chr16:67867229 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.100-1111C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67867229 | |||||||
| chr16:67867260 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.100-1080C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67867260 | |||||||
| chr16:67867440 | A | G | 83 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0010 others(80): Show |
102 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.100-900A>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67867440 | |||||||
| chr16:67868167 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0029 others(28): Show |
39 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.100-173G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67868167 | |||||||
| chr16:67868280 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0044 others(5): Show |
12 | HG00738.hp2 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-60G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 2/4 | chr16 | 67868280 | |||||||
| chr16:67868423 | A | T | 83 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0010 others(80): Show |
102 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.171+12A>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 3/4 | chr16 | 67868423 | |||||||
| chr16:67868466 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172-35C>G | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 3/4 | chr16 | 67868466 | |||||||
| chr16:67868756 | G | A | 3 | a0001c0001t0002g0151 a0001c0001t0003g0026 a0001c0001t0003g0149 |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+157G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67868756 | |||||||
| chr16:67869084 | CT | C | 72 | a0001c0001t0001g0053 a0001c0001t0001g0089 a0001c0001t0001g0126 others(69): Show |
88 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.270+502delT | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 67869084 | ||||||
| chr16:67869084 | CTT | C | 15 | a0001c0001t0002g0075 a0001c0001t0003g0027 a0001c0001t0003g0028 others(12): Show |
18 | HG01109.hp1 HG01884.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.270+501_270+502del others(2): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 67869084 | ||||||
| chr16:67869336 | C | T | 5 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0144 others(2): Show |
6 | HG00438.hp1 NA18940.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+737C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67869336 | |||||||
| chr16:67869393 | C | T | 2 | a0001c0001t0002g0179 a0001c0001t0004g0178 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.270+794C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67869393 | |||||||
| chr16:67869445 | G | GACCCCCC others(7): Show |
1 | a0001c0001t0001g0091 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.270+847_270+860dup others(14): Show |
NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 67869445 | ||||||
| chr16:67869524 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.270+925G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67869524 | |||||||
| chr16:67869699 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.270+1100C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67869699 | |||||||
| chr16:67869903 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.271-897C>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67869903 | |||||||
| chr16:67869982 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.271-818T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67869982 | |||||||
| chr16:67870387 | A | T | 1 | a0001c0001t0002g0182 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.271-413A>T | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67870387 | |||||||
| chr16:67870507 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0096 |
2 | NA18957.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.271-293G>A | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67870507 | |||||||
| chr16:67870554 | T | C | 1 | a0001c0001t0003g0027 | 2 | HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.271-246T>C | NUTF2 | ENSG00000102898.13 | transcript | ENST00000219169.9 | protein_coding | 4/4 | chr16 | 67870554 |