Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 152519 |
| ensemblid | ENSG00000163293.12 |
| hgncid | 27194 |
| symbol | NIPAL1 |
| name | NIPA like domain containing 1 |
| refseq_nuc | NM_207330.3 |
| refseq_prot | NP_997213.1 |
| ensembl_nuc | ENST00000295461.10 |
| ensembl_prot | ENSP00000295461.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 48016772 |
| end | 48040173 |
| strand | + |
| ver | v1.2 |
| region | chr4:48016772-48040173 |
| region5000 | chr4:48011772-48045173 |
| regionname0 | NIPAL1_chr4_48016772_48040173 |
| regionname5000 | NIPAL1_chr4_48011772_48045173 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 410 | 324 | 80 | 55 | 137 | 13 | 37 | 105 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | MGAQV others(405): Show |
chr4 | 48011772 | 48045173 |
| a0002 | 0/0 | 410 | 85 | 13 | 17 | 43 | 3 | 9 | 37 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | MGAQV others(405): Show |
chr4 | 48011772 | 48045173 |
| a0003 | 0/0 | 410 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | MGAQV others(405): Show |
chr4 | 48011772 | 48045173 |
| a0004 | 0/0 | 410 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | MGAQV others(405): Show |
chr4 | 48011772 | 48045173 |
| a0005 | 0/0 | 410 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | MGAQV others(405): Show |
chr4 | 48011772 | 48045173 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1230 | 315 | 77 | 55 | 132 | 13 | 36 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | ATGGG others(1225): Show |
chr4 | 48011772 | 48045173 | ||
| a0001c0003 | 0/0 | 1230 | 5 | 0 | 0 | 5 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | ATGGG others(1225): Show |
chr4 | 48011772 | 48045173 | ||
| a0001c0005 | 0/0 | 1230 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | ATGGG others(1225): Show |
chr4 | 48011772 | 48045173 | ||
| a0001c0006 | 0/0 | 1230 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | ATGGG others(1225): Show |
chr4 | 48011772 | 48045173 | ||
| a0002c0002 | 0/0 | 1230 | 84 | 13 | 17 | 42 | 3 | 9 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | ATGGG others(1225): Show |
chr4 | 48011772 | 48045173 | ||
| a0002c0007 | 0/0 | 1230 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | ATGGG others(1225): Show |
chr4 | 48011772 | 48045173 | ||
| a0003c0004 | 0/0 | 1230 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | ATGGG others(1225): Show |
chr4 | 48011772 | 48045173 | ||
| a0004c0008 | 0/0 | 1230 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | ATGGG others(1225): Show |
chr4 | 48011772 | 48045173 | ||
| a0005c0009 | 0/0 | 1230 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | ATGGG others(1225): Show |
chr4 | 48011772 | 48045173 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5302 | 98 | 19 | 8 | 56 | 0 | 15 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0003 | 0/0 | 5302 | 68 | 16 | 26 | 13 | 5 | 8 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0004 | 0/1 | 5302 | 49 | 3 | 7 | 31 | 3 | 4 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0005 | 0/0 | 5302 | 35 | 0 | 11 | 13 | 5 | 6 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0006 | 1/0 | 5302 | 18 | 16 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0007 | 0/0 | 5303 | 10 | 9 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5298): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0008 | 0/0 | 5302 | 9 | 0 | 0 | 9 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0009 | 0/0 | 5305 | 7 | 6 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5300): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0010 | 0/0 | 5302 | 4 | 0 | 0 | 3 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0011 | 0/0 | 5302 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0013 | 0/0 | 5302 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0015 | 0/0 | 5302 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0016 | 0/0 | 5303 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5298): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0017 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0018 | 0/0 | 5303 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5298): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0019 | 0/0 | 5302 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0020 | 0/0 | 5303 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5298): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0021 | 0/0 | 5301 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5296): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0022 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0001t0024 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5298): Show |
chr4 | 48011772 | 48045173 |
| a0001c0003t0001 | 0/0 | 5302 | 5 | 0 | 0 | 5 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0005t0003 | 0/0 | 5302 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0001c0006t0005 | 0/0 | 5302 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0002c0002t0002 | 0/0 | 5302 | 77 | 12 | 14 | 39 | 3 | 9 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0002c0002t0012 | 0/0 | 5303 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5298): Show |
chr4 | 48011772 | 48045173 |
| a0002c0002t0014 | 0/0 | 5302 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0002c0002t0023 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0002c0007t0002 | 0/0 | 5302 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0003c0004t0001 | 0/0 | 5302 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0004c0008t0001 | 0/0 | 5302 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| a0005c0009t0003 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | GCGGG others(5297): Show |
chr4 | 48011772 | 48045173 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 65 | 14 | 5 | 41 | 0 | 5 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0004 | 0/0 | 28 | 2 | 16 | 0 | 4 | 6 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0007 | 0/0 | 17 | 1 | 4 | 11 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0002 | 0/0 | 33 | 0 | 6 | 23 | 1 | 3 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0014 | 0/1 | 4 | 1 | 1 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0005g0005 | 0/0 | 20 | 0 | 6 | 9 | 1 | 4 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0005g0011 | 0/0 | 8 | 0 | 4 | 0 | 4 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0005g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0006g0006 | 1/0 | 18 | 16 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0007g0010 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0008g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0009g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0010g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0011g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0013g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0015g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0016g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0017g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0018g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0019g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0021g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0022g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0001t0024g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0003t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0005t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0005t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0005t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0001c0006t0005g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0003 | 0/0 | 25 | 0 | 0 | 25 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0008 | 0/0 | 15 | 1 | 6 | 1 | 3 | 4 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0009 | 0/0 | 15 | 6 | 4 | 0 | 0 | 5 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0012g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0014g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0014g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0002t0023g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0002c0007t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0003c0004t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0004c0008t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| a0005c0009t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | GBR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0005 | EUR | GBR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0094 | EUR | FIN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0039 | EUR | FIN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0011 | EUR | FIN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00408 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00642 | hp2 | a0001 | c0001 | t0009 | g0013 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | CHS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01167 | hp1 | a0002 | c0002 | t0012 | g0003 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01169 | hp2 | a0002 | c0002 | t0012 | g0003 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0011 | EUR | IBS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0076 | EUR | IBS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0011 | EUR | IBS | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0037 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01981 | hp1 | a0002 | c0002 | t0012 | g0003 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02071 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02129 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0015 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PEL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0015 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02615 | hp2 | a0001 | c0005 | t0003 | g0073 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02630 | hp1 | a0001 | c0001 | t0022 | g0060 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02717 | hp1 | a0001 | c0005 | t0003 | g0083 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0036 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0043 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02809 | hp1 | a0001 | c0005 | t0003 | g0082 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02965 | hp2 | a0001 | c0001 | t0017 | g0006 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02970 | hp2 | a0001 | c0001 | t0016 | g0026 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03017 | hp1 | a0001 | c0006 | t0005 | g0005 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03098 | hp2 | a0001 | c0001 | t0013 | g0015 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03130 | hp2 | a0001 | c0001 | t0024 | g0010 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03239 | hp1 | a0001 | c0001 | t0021 | g0040 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0050 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | ESN | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0045 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03831 | hp2 | a0001 | c0001 | t0020 | g0002 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04184 | hp1 | a0001 | c0001 | t0010 | g0001 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | BEB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0009 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | STU | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18747 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | CHB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | YRI | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18945 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18949 | hp2 | a0001 | c0001 | t0018 | g0090 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18963 | hp2 | a0002 | c0007 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18969 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18971 | hp2 | a0001 | c0001 | t0019 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18973 | hp2 | a0002 | c0002 | t0014 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18979 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18984 | hp1 | a0002 | c0002 | t0014 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18987 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18989 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18992 | hp2 | a0001 | c0001 | t0011 | g0069 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19001 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19004 | hp2 | a0001 | c0001 | t0015 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19006 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19007 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | LWK | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | LWK | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0085 | AFR | LWK | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | LWK | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19056 | hp1 | a0004 | c0008 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19064 | hp2 | a0001 | c0001 | t0015 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19075 | hp2 | a0002 | c0002 | t0014 | g0048 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19077 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | YRI | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA19240 | hp2 | a0005 | c0009 | t0003 | g0074 | AFR | YRI | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ASW | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0072 | AFR | ASW | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0011 | EUR | TSI | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | GIH | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | GIH | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | ACB | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | USA | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0026 | AFR | USA | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | USA | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | USA | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA21309 | hp1 | a0002 | c0002 | t0023 | g0034 | AFR | LWK | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | LWK | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0014 | REF | REF | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0006 | REF | REF | NIPAL1_chr4_48011772_48045173 | NIPAL1 | chr4 | 48011772 | 48045173 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48025112 | T | C | 1 | a0003 | 3 | NA18969.hp2 NA18979.hp2 NA19007.hp2 |
missense_variant | MODERATE | c.91T>C | p.Cys31Arg | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/6 | 159/5302 | 91/1233 | 31/410 | chr4 | 48025112 | |||
| chr4:48035909 | A | G | 1 | a0002 | 85 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(82): Show |
missense_variant | MODERATE | c.970A>G | p.Ile324Val | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1038/5302 | 970/1233 | 324/410 | chr4 | 48035909 | |||
| chr4:48036081 | A | G | 1 | a0005 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1142A>G | p.Asn381Ser | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1210/5302 | 1142/1233 | 381/410 | chr4 | 48036081 | |||
| chr4:48036143 | G | A | 1 | a0004 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.1204G>A | p.Val402Ile | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1272/5302 | 1204/1233 | 402/410 | chr4 | 48036143 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48025327 | T | C | 1 | a0001c0006 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.306T>C | p.Thr102Thr | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/6 | 374/5302 | 306/1233 | 102/410 | chr4 | 48025327 | |||
| chr4:48034954 | T | C | 1 | a0001c0005 | 3 | HG02615.hp2 HG02717.hp1 HG02809.hp1 |
synonymous_variant | LOW | c.535T>C | p.Leu179Leu | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 5/6 | 603/5302 | 535/1233 | 179/410 | chr4 | 48034954 | |||
| chr4:48035683 | G | A | 1 | a0002c0007 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.744G>A | p.Ala248Ala | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 812/5302 | 744/1233 | 248/410 | chr4 | 48035683 | |||
| chr4:48035950 | C | T | 1 | a0001c0003 | 5 | NA18961.hp1 NA18974.hp2 NA19011.hp1 others(2): Show |
synonymous_variant | LOW | c.1011C>T | p.Ile337Ile | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1079/5302 | 1011/1233 | 337/410 | chr4 | 48035950 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48036362 | C | T | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(20): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*190C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 190 | chr4 | 48036362 | ||||||
| chr4:48036567 | G | A | 6 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0015 others(3): Show |
62 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*395G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 395 | chr4 | 48036567 | ||||||
| chr4:48036699 | G | A | 11 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0013 others(8): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*527G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 527 | chr4 | 48036699 | ||||||
| chr4:48036826 | C | A | 2 | a0001c0001t0018 a0001c0001t0019 |
2 | NA18949.hp2 NA18971.hp2 |
3_prime_UTR_variant | MODIFIER | c.*654C>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 654 | chr4 | 48036826 | ||||||
| chr4:48036997 | A | G | 1 | a0002c0002t0014 | 3 | NA18973.hp2 NA18984.hp1 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*825A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 825 | chr4 | 48036997 | ||||||
| chr4:48037304 | A | C | 1 | a0002c0002t0023 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1132A>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1132 | chr4 | 48037304 | ||||||
| chr4:48037407 | G | GTTA | 1 | a0001c0001t0009 | 7 | HG00642.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1238_*1240dupATT | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1241 | INFO_REALIGN_3_PRIME | chr4 | 48037407 | |||||
| chr4:48037554 | G | A | 1 | a0001c0001t0016 | 2 | HG02970.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1382G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1382 | chr4 | 48037554 | ||||||
| chr4:48037561 | A | G | 2 | a0001c0001t0013 a0001c0001t0022 |
4 | HG02145.hp1 HG02451.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1389A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1389 | chr4 | 48037561 | ||||||
| chr4:48037653 | A | G | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(20): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*1481A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1481 | chr4 | 48037653 | ||||||
| chr4:48037885 | A | T | 11 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0013 others(8): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1713A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1713 | chr4 | 48037885 | ||||||
| chr4:48038081 | A | T | 1 | a0001c0001t0024 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1909A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1909 | chr4 | 48038081 | ||||||
| chr4:48038119 | A | G | 1 | a0001c0001t0022 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1947A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1947 | chr4 | 48038119 | ||||||
| chr4:48038166 | C | T | 1 | a0001c0001t0011 | 3 | NA18945.hp2 NA18992.hp2 NA19006.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1994C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 1994 | chr4 | 48038166 | ||||||
| chr4:48038325 | A | G | 1 | a0001c0001t0015 | 2 | NA19004.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2153A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 2153 | chr4 | 48038325 | ||||||
| chr4:48038774 | C | T | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(26): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
3_prime_UTR_variant | MODIFIER | c.*2602C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 2602 | chr4 | 48038774 | ||||||
| chr4:48038811 | TA | T | 3 | a0001c0001t0005 a0001c0001t0021 a0001c0006t0005 |
37 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2640delA | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 2640 | chr4 | 48038811 | ||||||
| chr4:48039021 | T | TA | 3 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0024 |
13 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2860dupA | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 2861 | INFO_REALIGN_3_PRIME | chr4 | 48039021 | |||||
| chr4:48039231 | A | T | 1 | a0001c0001t0008 | 9 | HG00408.hp2 HG02071.hp2 NA18747.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3059A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 3059 | chr4 | 48039231 | ||||||
| chr4:48039341 | C | CA | 5 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0020 others(2): Show |
41 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3183dupA | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 3184 | INFO_REALIGN_3_PRIME | chr4 | 48039341 | |||||
| chr4:48039531 | G | A | 1 | a0001c0001t0017 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3359G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 3359 | chr4 | 48039531 | ||||||
| chr4:48039778 | A | G | 1 | a0001c0001t0010 | 4 | HG02129.hp2 HG04184.hp1 NA19001.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3606A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 6/6 | 3606 | chr4 | 48039778 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48017154 | A | G | 1 | a0001c0001t0004g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.46+269A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48017154 | |||||||
| chr4:48017306 | G | A | 43 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0059 others(40): Show |
135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.46+421G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48017306 | |||||||
| chr4:48017493 | C | CTT | 89 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0059 others(86): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.46+609_46+610insTT | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48017493 | ||||||
| chr4:48017511 | A | G | 28 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0016g0026 others(25): Show |
89 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.46+626A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48017511 | |||||||
| chr4:48017609 | C | T | 11 | a0001c0001t0001g0019 a0001c0001t0005g0005 a0001c0001t0005g0011 others(8): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.46+724C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48017609 | |||||||
| chr4:48017642 | G | T | 11 | a0001c0001t0001g0019 a0001c0001t0005g0005 a0001c0001t0005g0011 others(8): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.46+757G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48017642 | |||||||
| chr4:48017842 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0059 others(88): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.46+957T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48017842 | |||||||
| chr4:48017852 | G | A | 1 | a0001c0001t0007g0072 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.46+967G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48017852 | |||||||
| chr4:48017863 | CAT | C | 2 | a0001c0001t0001g0071 a0001c0001t0013g0015 |
4 | HG02040.hp2 HG02145.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+995_46+996delAT | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48017863 | ||||||
| chr4:48017863 | CATAT | C | 43 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0059 others(40): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.46+993_46+996delAT others(2): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48017863 | ||||||
| chr4:48017863 | CATATAT | C | 46 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0003g0004 others(43): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.46+991_46+996delAT others(4): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48017863 | ||||||
| chr4:48017865 | T | C | 1 | a0001c0001t0001g0012 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.46+980T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48017865 | |||||||
| chr4:48017869 | T | C | 43 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0059 others(40): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.46+984T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48017869 | |||||||
| chr4:48018020 | A | C | 1 | a0001c0001t0005g0020 | 2 | NA18984.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.46+1135A>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48018020 | |||||||
| chr4:48018061 | A | T | 1 | a0001c0001t0004g0099 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.46+1176A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48018061 | |||||||
| chr4:48018252 | A | G | 1 | a0001c0001t0009g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.46+1367A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48018252 | |||||||
| chr4:48018285 | TGTAA | T | 11 | a0001c0001t0001g0019 a0001c0001t0005g0005 a0001c0001t0005g0011 others(8): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.46+1406_46+1409del others(4): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48018285 | ||||||
| chr4:48018495 | T | C | 1 | a0001c0005t0003g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.46+1610T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48018495 | |||||||
| chr4:48018500 | A | G | 11 | a0001c0001t0001g0019 a0001c0001t0005g0005 a0001c0001t0005g0011 others(8): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.46+1615A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48018500 | |||||||
| chr4:48018793 | C | A | 1 | a0005c0009t0003g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.46+1908C>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48018793 | |||||||
| chr4:48018915 | A | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0016 others(21): Show |
110 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.46+2030A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48018915 | |||||||
| chr4:48019186 | T | A | 9 | a0001c0001t0001g0077 a0001c0001t0003g0004 a0001c0001t0003g0030 others(6): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.46+2301T>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48019186 | |||||||
| chr4:48019202 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.46+2317C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48019202 | |||||||
| chr4:48019246 | C | T | 2 | a0001c0001t0013g0015 a0001c0001t0022g0060 |
4 | HG02145.hp1 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+2361C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48019246 | |||||||
| chr4:48019315 | T | C | 6 | a0001c0001t0003g0031 a0001c0001t0003g0084 a0001c0001t0003g0098 others(3): Show |
7 | HG02258.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+2430T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48019315 | |||||||
| chr4:48019522 | G | A | 3 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0004g0085 |
5 | HG01884.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+2637G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48019522 | |||||||
| chr4:48019629 | A | G | 1 | a0001c0001t0009g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.46+2744A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48019629 | |||||||
| chr4:48019826 | T | G | 1 | a0001c0001t0004g0086 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.46+2941T>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48019826 | |||||||
| chr4:48019908 | C | A | 31 | a0001c0001t0001g0055 a0001c0001t0003g0035 a0001c0001t0009g0013 others(28): Show |
94 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.46+3023C>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48019908 | |||||||
| chr4:48020074 | C | T | 1 | a0005c0009t0003g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.46+3189C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48020074 | |||||||
| chr4:48020223 | A | T | 4 | a0001c0001t0007g0010 a0001c0001t0007g0072 a0001c0001t0016g0026 others(1): Show |
13 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.46+3338A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48020223 | |||||||
| chr4:48020799 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.46+3914A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48020799 | |||||||
| chr4:48020810 | A | T | 1 | a0001c0001t0005g0045 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.46+3925A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48020810 | |||||||
| chr4:48020811 | A | G | 1 | a0001c0001t0004g0039 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.46+3926A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48020811 | |||||||
| chr4:48020828 | G | C | 1 | a0002c0002t0002g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46+3943G>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48020828 | |||||||
| chr4:48021131 | C | T | 1 | a0001c0001t0013g0015 | 3 | HG02145.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.47-3937C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021131 | |||||||
| chr4:48021307 | A | AGATG | 42 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(39): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.47-3761_47-3760ins others(4): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021307 | |||||||
| chr4:48021309 | A | T | 42 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(39): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.47-3759A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021309 | |||||||
| chr4:48021310 | G | T | 42 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(39): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.47-3758G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021310 | |||||||
| chr4:48021312 | C | CCG | 42 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(39): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.47-3755_47-3754ins others(2): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48021312 | ||||||
| chr4:48021314 | C | A | 42 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(39): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.47-3754C>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021314 | |||||||
| chr4:48021329 | C | T | 46 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0003g0004 others(43): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.47-3739C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021329 | |||||||
| chr4:48021369 | A | G | 1 | a0001c0001t0004g0097 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.47-3699A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021369 | |||||||
| chr4:48021556 | G | A | 90 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0077 others(87): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.47-3512G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021556 | |||||||
| chr4:48021752 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0022g0060 |
4 | HG02145.hp1 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-3316G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021752 | |||||||
| chr4:48021873 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0022g0060 |
4 | HG02145.hp1 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-3195G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021873 | |||||||
| chr4:48021889 | GTA | G | 89 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0077 others(86): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.47-3165_47-3164del others(2): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48021889 | ||||||
| chr4:48021978 | G | T | 1 | a0001c0001t0003g0096 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.47-3090G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48021978 | |||||||
| chr4:48022192 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.47-2876G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48022192 | |||||||
| chr4:48022363 | T | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(39): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.47-2705T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48022363 | |||||||
| chr4:48022548 | T | C | 90 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0077 others(87): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.47-2520T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48022548 | |||||||
| chr4:48022648 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.47-2420G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48022648 | |||||||
| chr4:48022820 | C | CA | 47 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0003g0004 others(44): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.47-2239dupA | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48022820 | ||||||
| chr4:48022859 | A | G | 1 | a0002c0002t0002g0025 | 2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.47-2209A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48022859 | |||||||
| chr4:48022883 | G | A | 11 | a0001c0001t0001g0019 a0001c0001t0005g0005 a0001c0001t0005g0011 others(8): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.47-2185G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48022883 | |||||||
| chr4:48022998 | G | A | 1 | a0002c0002t0002g0049 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.47-2070G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48022998 | |||||||
| chr4:48023073 | G | GTTTTGT | 5 | a0001c0001t0003g0018 a0001c0001t0003g0095 a0001c0001t0013g0015 others(2): Show |
9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.47-1976_47-1971dup others(6): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48023073 | ||||||
| chr4:48023078 | G | T | 42 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(39): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.47-1990G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48023078 | |||||||
| chr4:48023189 | G | T | 16 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0039 others(13): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.47-1879G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48023189 | |||||||
| chr4:48023281 | C | T | 44 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(41): Show |
137 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.47-1787C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48023281 | |||||||
| chr4:48023457 | G | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0068 |
4 | HG02602.hp1 HG02735.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-1611G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48023457 | |||||||
| chr4:48023684 | G | A | 1 | a0001c0001t0004g0089 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.47-1384G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48023684 | |||||||
| chr4:48023852 | C | T | 90 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0077 others(87): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.47-1216C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48023852 | |||||||
| chr4:48023975 | CT | C | 61 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0061 others(58): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.47-1074delT | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48023975 | ||||||
| chr4:48023975 | CTT | C | 25 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0075 others(22): Show |
78 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.47-1075_47-1074del others(2): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48023975 | ||||||
| chr4:48024024 | G | A | 2 | a0001c0001t0013g0015 a0001c0001t0022g0060 |
4 | HG02145.hp1 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-1044G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024024 | |||||||
| chr4:48024047 | C | G | 30 | a0001c0001t0001g0055 a0001c0001t0003g0035 a0001c0001t0009g0013 others(27): Show |
92 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.47-1021C>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024047 | |||||||
| chr4:48024074 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.47-994G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024074 | |||||||
| chr4:48024078 | T | A | 1 | a0001c0001t0018g0090 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.47-990T>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024078 | |||||||
| chr4:48024165 | G | T | 1 | a0001c0001t0005g0044 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.47-903G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024165 | |||||||
| chr4:48024262 | A | G | 1 | a0001c0001t0001g0016 | 3 | HG01069.hp1 HG01071.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.47-806A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024262 | |||||||
| chr4:48024303 | C | T | 1 | a0002c0002t0002g0057 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.47-765C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024303 | |||||||
| chr4:48024331 | TGCAGTGG others(7): Show |
T | 44 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(41): Show |
137 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.47-732_47-719delTG others(12): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48024331 | ||||||
| chr4:48024391 | T | A | 90 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0077 others(87): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.47-677T>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024391 | |||||||
| chr4:48024530 | C | G | 3 | a0001c0005t0003g0073 a0001c0005t0003g0082 a0001c0005t0003g0083 |
3 | HG02615.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.47-538C>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024530 | |||||||
| chr4:48024543 | A | C | 44 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0003g0035 others(41): Show |
137 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.47-525A>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024543 | |||||||
| chr4:48024724 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.47-344A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024724 | |||||||
| chr4:48024730 | C | T | 17 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0039 others(14): Show |
60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.47-338C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024730 | |||||||
| chr4:48024731 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.47-337G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024731 | |||||||
| chr4:48024799 | G | T | 11 | a0001c0001t0001g0019 a0001c0001t0005g0005 a0001c0001t0005g0011 others(8): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.47-269G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | chr4 | 48024799 | |||||||
| chr4:48024811 | AG | A | 27 | a0001c0001t0003g0018 a0001c0001t0003g0032 a0001c0001t0003g0033 others(24): Show |
83 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.47-252delG | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 48024811 | ||||||
| chr4:48025660 | G | C | 1 | a0001c0001t0001g0063 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.313+326G>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48025660 | |||||||
| chr4:48025904 | G | T | 1 | a0002c0002t0002g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.313+570G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48025904 | |||||||
| chr4:48025914 | A | G | 6 | a0001c0001t0003g0031 a0001c0001t0003g0084 a0001c0001t0003g0098 others(3): Show |
7 | HG02258.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.313+580A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48025914 | |||||||
| chr4:48025918 | C | A | 1 | a0002c0002t0002g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.313+584C>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48025918 | |||||||
| chr4:48025918 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.313+584C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48025918 | |||||||
| chr4:48025919 | G | A | 5 | a0001c0001t0003g0035 a0001c0001t0009g0013 a0001c0001t0009g0036 others(2): Show |
8 | HG00642.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.313+585G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48025919 | |||||||
| chr4:48025932 | C | T | 46 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0003g0004 others(43): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.313+598C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48025932 | |||||||
| chr4:48026026 | C | T | 1 | a0001c0001t0004g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.313+692C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026026 | |||||||
| chr4:48026080 | G | A | 43 | a0001c0001t0001g0019 a0001c0001t0003g0035 a0001c0001t0005g0005 others(40): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.313+746G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026080 | |||||||
| chr4:48026113 | G | C | 89 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0088 others(86): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.313+779G>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026113 | |||||||
| chr4:48026374 | A | C | 1 | a0001c0001t0004g0086 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.313+1040A>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026374 | |||||||
| chr4:48026425 | G | A | 43 | a0001c0001t0001g0019 a0001c0001t0003g0035 a0001c0001t0005g0005 others(40): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.313+1091G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026425 | |||||||
| chr4:48026435 | G | A | 1 | a0002c0002t0002g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.313+1101G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026435 | |||||||
| chr4:48026720 | AT | A | 5 | a0001c0001t0001g0028 a0001c0001t0003g0035 a0001c0001t0009g0036 others(2): Show |
6 | HG01891.hp1 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+1402delT | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 48026720 | ||||||
| chr4:48026721 | T | TA | 13 | a0001c0001t0001g0019 a0001c0001t0005g0005 a0001c0001t0005g0011 others(10): Show |
43 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.313+1387_313+1388i others(3): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026721 | |||||||
| chr4:48026722 | T | A | 84 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0088 others(81): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.313+1388T>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026722 | |||||||
| chr4:48026723 | T | A | 75 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0003g0004 others(72): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.313+1389T>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026723 | |||||||
| chr4:48026724 | T | A | 5 | a0001c0001t0003g0035 a0001c0001t0009g0036 a0001c0001t0009g0037 others(2): Show |
5 | HG01891.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+1390T>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026724 | |||||||
| chr4:48026725 | T | A | 1 | a0002c0002t0002g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.313+1391T>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026725 | |||||||
| chr4:48026759 | G | A | 1 | a0001c0001t0021g0040 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.313+1425G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026759 | |||||||
| chr4:48026762 | A | G | 11 | a0001c0001t0001g0019 a0001c0001t0005g0005 a0001c0001t0005g0011 others(8): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.313+1428A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026762 | |||||||
| chr4:48026772 | A | G | 43 | a0001c0001t0001g0019 a0001c0001t0003g0035 a0001c0001t0005g0005 others(40): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.313+1438A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026772 | |||||||
| chr4:48026816 | T | A | 2 | a0001c0001t0003g0030 a0001c0001t0003g0075 |
3 | HG00735.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.313+1482T>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026816 | |||||||
| chr4:48026906 | C | T | 19 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0003g0004 others(16): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.313+1572C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026906 | |||||||
| chr4:48026960 | C | T | 43 | a0001c0001t0001g0019 a0001c0001t0003g0035 a0001c0001t0005g0005 others(40): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.313+1626C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026960 | |||||||
| chr4:48026967 | C | A | 2 | a0001c0001t0004g0091 a0001c0001t0004g0092 |
2 | NA18992.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.313+1633C>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48026967 | |||||||
| chr4:48027010 | G | A | 1 | a0001c0001t0009g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.313+1676G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48027010 | |||||||
| chr4:48027035 | A | T | 1 | a0001c0001t0001g0017 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.313+1701A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48027035 | |||||||
| chr4:48027101 | T | C | 18 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0039 others(15): Show |
61 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.313+1767T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48027101 | |||||||
| chr4:48027623 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.313+2289T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48027623 | |||||||
| chr4:48028019 | T | C | 43 | a0001c0001t0001g0019 a0001c0001t0003g0035 a0001c0001t0005g0005 others(40): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.314-2101T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028019 | |||||||
| chr4:48028041 | A | C | 2 | a0001c0001t0003g0032 a0001c0001t0003g0033 |
4 | HG01884.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-2079A>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028041 | |||||||
| chr4:48028049 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.314-2071T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028049 | |||||||
| chr4:48028272 | G | C | 42 | a0001c0001t0001g0019 a0001c0001t0003g0035 a0001c0001t0005g0005 others(39): Show |
135 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.314-1848G>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028272 | |||||||
| chr4:48028272 | G | T | 1 | a0001c0001t0005g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.314-1848G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028272 | |||||||
| chr4:48028318 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.314-1802G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028318 | |||||||
| chr4:48028394 | C | T | 2 | a0002c0002t0002g0054 a0002c0002t0002g0057 |
2 | NA18950.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.314-1726C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028394 | |||||||
| chr4:48028412 | A | G | 1 | a0002c0002t0002g0053 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.314-1708A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028412 | |||||||
| chr4:48028467 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA19000.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.314-1653A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028467 | |||||||
| chr4:48028556 | A | G | 1 | a0001c0005t0003g0083 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.314-1564A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028556 | |||||||
| chr4:48028738 | C | G | 3 | a0001c0001t0003g0031 a0001c0001t0003g0084 a0001c0001t0003g0098 |
4 | HG02258.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-1382C>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028738 | |||||||
| chr4:48028739 | C | G | 46 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0003g0004 others(43): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.314-1381C>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028739 | |||||||
| chr4:48028793 | G | A | 25 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(22): Show |
85 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.314-1327G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028793 | |||||||
| chr4:48028855 | C | T | 1 | a0001c0001t0004g0093 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.314-1265C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028855 | |||||||
| chr4:48028886 | G | C | 11 | a0001c0001t0001g0019 a0001c0001t0005g0005 a0001c0001t0005g0011 others(8): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.314-1234G>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028886 | |||||||
| chr4:48028957 | C | A | 9 | a0001c0001t0003g0018 a0001c0001t0003g0032 a0001c0001t0003g0033 others(6): Show |
22 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.314-1163C>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028957 | |||||||
| chr4:48028993 | C | T | 2 | a0001c0001t0013g0015 a0001c0001t0022g0060 |
4 | HG02145.hp1 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1127C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028993 | |||||||
| chr4:48028994 | G | A | 5 | a0001c0001t0003g0035 a0001c0001t0009g0013 a0001c0001t0009g0036 others(2): Show |
8 | HG00642.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.314-1126G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48028994 | |||||||
| chr4:48029152 | C | G | 30 | a0001c0001t0003g0035 a0001c0001t0009g0013 a0001c0001t0009g0036 others(27): Show |
93 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.314-968C>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48029152 | |||||||
| chr4:48029170 | G | A | 15 | a0002c0002t0002g0003 a0002c0002t0002g0021 a0002c0002t0002g0022 others(12): Show |
45 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.314-950G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48029170 | |||||||
| chr4:48029482 | G | A | 43 | a0001c0001t0001g0019 a0001c0001t0003g0035 a0001c0001t0005g0005 others(40): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.314-638G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48029482 | |||||||
| chr4:48029619 | A | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0003g0004 others(10): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.314-501A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48029619 | |||||||
| chr4:48029883 | C | T | 89 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0088 others(86): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.314-237C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | chr4 | 48029883 | |||||||
| chr4:48029885 | GA | G | 43 | a0001c0001t0001g0019 a0001c0001t0003g0035 a0001c0001t0005g0005 others(40): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.314-228delA | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 48029885 | ||||||
| chr4:48030339 | A | G | 43 | a0001c0001t0001g0019 a0001c0001t0003g0035 a0001c0001t0005g0005 others(40): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.370+163A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48030339 | |||||||
| chr4:48030496 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.370+320T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48030496 | |||||||
| chr4:48030521 | A | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0016 others(111): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.370+345A>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48030521 | |||||||
| chr4:48030694 | T | C | 10 | a0001c0001t0005g0005 a0001c0001t0005g0011 a0001c0001t0005g0020 others(7): Show |
37 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.370+518T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48030694 | |||||||
| chr4:48031054 | G | T | 2 | a0002c0002t0002g0052 a0005c0009t0003g0074 |
2 | NA18991.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.370+878G>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031054 | |||||||
| chr4:48031087 | T | G | 26 | a0001c0001t0003g0031 a0001c0001t0003g0035 a0001c0001t0003g0084 others(23): Show |
70 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.370+911T>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031087 | |||||||
| chr4:48031212 | A | C | 1 | a0001c0001t0003g0079 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.370+1036A>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031212 | |||||||
| chr4:48031221 | C | T | 50 | a0001c0001t0001g0012 a0001c0001t0003g0004 a0001c0001t0003g0007 others(47): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.370+1045C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031221 | |||||||
| chr4:48031253 | C | T | 1 | a0001c0001t0003g0033 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.370+1077C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031253 | |||||||
| chr4:48031266 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.370+1090T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031266 | |||||||
| chr4:48031565 | G | A | 87 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0018 others(84): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.370+1389G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031565 | |||||||
| chr4:48031588 | T | C | 2 | a0001c0001t0003g0018 a0001c0001t0003g0095 |
4 | HG02109.hp2 HG02145.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-1405T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031588 | |||||||
| chr4:48031626 | G | C | 2 | a0001c0001t0003g0032 a0001c0001t0003g0033 |
4 | HG01884.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-1367G>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031626 | |||||||
| chr4:48031637 | A | C | 1 | a0001c0001t0003g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.371-1356A>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031637 | |||||||
| chr4:48031824 | C | T | 9 | a0001c0001t0003g0018 a0001c0001t0003g0032 a0001c0001t0003g0033 others(6): Show |
22 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.371-1169C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031824 | |||||||
| chr4:48031951 | C | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0053 |
3 | NA18972.hp2 NA18977.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.371-1042C>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031951 | |||||||
| chr4:48031958 | C | T | 1 | a0005c0009t0003g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.371-1035C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48031958 | |||||||
| chr4:48032224 | T | C | 2 | a0001c0001t0005g0011 a0001c0001t0021g0040 |
9 | HG00323.hp2 HG01109.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.371-769T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48032224 | |||||||
| chr4:48032414 | A | G | 1 | a0002c0002t0002g0024 | 2 | HG00735.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.371-579A>G | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48032414 | |||||||
| chr4:48032471 | T | C | 29 | a0001c0001t0009g0013 a0001c0001t0009g0036 a0001c0001t0009g0037 others(26): Show |
92 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.371-522T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48032471 | |||||||
| chr4:48032688 | TAG | T | 4 | a0001c0001t0009g0013 a0001c0001t0009g0036 a0001c0001t0009g0037 others(1): Show |
7 | HG00642.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.371-302_371-301del others(2): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 48032688 | ||||||
| chr4:48032867 | C | T | 19 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0039 others(16): Show |
62 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.371-126C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 3/5 | chr4 | 48032867 | |||||||
| chr4:48033485 | A | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0042 |
3 | NA18984.hp2 NA19009.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.461+402A>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 4/5 | chr4 | 48033485 | |||||||
| chr4:48033529 | C | T | 87 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0018 others(84): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.461+446C>T | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 4/5 | chr4 | 48033529 | |||||||
| chr4:48033629 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0095 a0005c0009t0003g0074 |
5 | HG02109.hp2 HG02145.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.461+546T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 4/5 | chr4 | 48033629 | |||||||
| chr4:48033663 | T | C | 1 | a0002c0002t0002g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.461+580T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 4/5 | chr4 | 48033663 | |||||||
| chr4:48034319 | A | AT | 18 | a0001c0001t0004g0002 a0001c0001t0004g0014 a0001c0001t0004g0039 others(15): Show |
61 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.462-553dupT | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 48034319 | ||||||
| chr4:48034694 | G | A | 87 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0018 others(84): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.462-187G>A | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 4/5 | chr4 | 48034694 | |||||||
| chr4:48034720 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0095 a0005c0009t0003g0074 |
5 | HG02109.hp2 HG02145.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.462-161T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 4/5 | chr4 | 48034720 | |||||||
| chr4:48035463 | T | C | 1 | a0001c0001t0005g0041 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.623-99T>C | NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 5/5 | chr4 | 48035463 |