Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100131211 |
| ensemblid | ENSG00000189362.12 |
| hgncid | 33700 |
| symbol | NEMP2 |
| name | nuclear envelope integral membrane protein 2 |
| refseq_nuc | NM_001142645.2 |
| refseq_prot | NP_001136117.1 |
| ensembl_nuc | ENST00000409150.8 |
| ensembl_prot | ENSP00000386292.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 190504338 |
| end | 190534722 |
| strand | - |
| ver | v1.2 |
| region | chr2:190504338-190534722 |
| region5000 | chr2:190499338-190539722 |
| regionname0 | NEMP2_chr2_190504338_190534722 |
| regionname5000 | NEMP2_chr2_190499338_190539722 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 417 | 341 | 83 | 63 | 151 | 11 | 31 | 119 | NEMP2_chr2_190499338_190539722 | NEMP2 | MGPRQ others(412): Show |
chr2 | 190499338 | 190539722 |
| a0002 | 0/0 | 417 | 60 | 6 | 9 | 37 | 1 | 7 | 33 | NEMP2_chr2_190499338_190539722 | NEMP2 | MRPRQ others(412): Show |
chr2 | 190499338 | 190539722 |
| a0003 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | MGPRQ others(412): Show |
chr2 | 190499338 | 190539722 |
| a0004 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | MGPRQ others(412): Show |
chr2 | 190499338 | 190539722 |
| a0005 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | MPPPP others(412): Show |
chr2 | 190499338 | 190539722 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1251 | 196 | 24 | 50 | 96 | 6 | 19 | NEMP2_chr2_190499338_190539722 | NEMP2 | ATGGG others(1246): Show |
chr2 | 190499338 | 190539722 | ||
| a0001c0002 | 1/0 | 1251 | 140 | 59 | 12 | 55 | 5 | 8 | NEMP2_chr2_190499338_190539722 | NEMP2 | ATGGG others(1246): Show |
chr2 | 190499338 | 190539722 | ||
| a0001c0005 | 0/0 | 1251 | 5 | 0 | 1 | 0 | 0 | 4 | NEMP2_chr2_190499338_190539722 | NEMP2 | ATGGG others(1246): Show |
chr2 | 190499338 | 190539722 | ||
| a0002c0003 | 0/0 | 1251 | 55 | 1 | 9 | 37 | 1 | 7 | NEMP2_chr2_190499338_190539722 | NEMP2 | ATGCG others(1246): Show |
chr2 | 190499338 | 190539722 | ||
| a0002c0004 | 0/0 | 1251 | 5 | 5 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ATGCG others(1246): Show |
chr2 | 190499338 | 190539722 | ||
| a0003c0007 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ATGGG others(1246): Show |
chr2 | 190499338 | 190539722 | ||
| a0004c0008 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ATGGG others(1246): Show |
chr2 | 190499338 | 190539722 | ||
| a0005c0006 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ATGCC others(1246): Show |
chr2 | 190499338 | 190539722 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6174 | 106 | 18 | 32 | 49 | 0 | 6 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0001t0003 | 0/0 | 6174 | 49 | 0 | 16 | 18 | 4 | 11 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0001t0006 | 0/0 | 6174 | 25 | 0 | 2 | 21 | 2 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0001t0007 | 0/0 | 6174 | 6 | 0 | 0 | 6 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0001t0010 | 0/0 | 6174 | 3 | 3 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0001t0015 | 0/0 | 6174 | 2 | 0 | 0 | 0 | 0 | 2 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0001t0016 | 0/0 | 6174 | 2 | 2 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0001t0025 | 0/0 | 6174 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0001t0026 | 0/0 | 6174 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0001t0028 | 0/0 | 6174 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0002 | 0/0 | 6174 | 87 | 22 | 8 | 52 | 3 | 2 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0005 | 0/0 | 6174 | 35 | 24 | 4 | 1 | 2 | 4 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0008 | 0/0 | 6178 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6173): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0011 | 0/0 | 6174 | 2 | 2 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0012 | 0/0 | 6174 | 2 | 2 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0014 | 0/0 | 6174 | 2 | 2 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0017 | 0/0 | 6174 | 2 | 2 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0018 | 0/0 | 6174 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0019 | 0/0 | 6174 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0020 | 0/0 | 6174 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0021 | 0/0 | 6174 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0023 | 0/0 | 6174 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0024 | 1/0 | 6172 | 1 | 0 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6167): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0027 | 0/0 | 6174 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0029 | 0/0 | 6174 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0002t0030 | 0/0 | 6174 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0001c0005t0008 | 0/0 | 6178 | 3 | 0 | 1 | 0 | 0 | 2 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6173): Show |
chr2 | 190499338 | 190539722 |
| a0001c0005t0013 | 0/0 | 6178 | 2 | 0 | 0 | 0 | 0 | 2 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6173): Show |
chr2 | 190499338 | 190539722 |
| a0002c0003t0004 | 0/0 | 6174 | 47 | 1 | 4 | 36 | 0 | 6 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0002c0003t0009 | 0/0 | 6174 | 4 | 0 | 4 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0002c0003t0018 | 0/0 | 6174 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0002c0003t0031 | 0/0 | 6174 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0002c0003t0032 | 0/0 | 6174 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0002c0003t0033 | 0/0 | 6174 | 1 | 0 | 0 | 0 | 1 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0002c0004t0001 | 0/0 | 6174 | 5 | 5 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0003c0007t0022 | 0/0 | 6174 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0004c0008t0007 | 0/0 | 6174 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | ACTTC others(6169): Show |
chr2 | 190499338 | 190539722 |
| a0005c0006t0034 | 0/0 | 6174 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | GCAGC others(6169): Show |
chr2 | 190499338 | 190539722 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/1 | 33 | 0 | 7 | 23 | 0 | 2 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0006 | 0/0 | 11 | 0 | 4 | 7 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0008 | 0/0 | 9 | 0 | 8 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0026 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0027 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0003 | 0/0 | 22 | 0 | 6 | 5 | 3 | 8 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0025 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0006g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0006g0018 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0006g0019 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0006g0033 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0006g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0006g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0007g0024 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0010g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0015g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0016g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0016g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0025g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0026g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0001t0028g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0001 | 0/0 | 38 | 3 | 4 | 30 | 1 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0007 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0022 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0005 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0013 | 0/0 | 5 | 0 | 0 | 1 | 1 | 3 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0029 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0005g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0011g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0014g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0017g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0017g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0018g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0019g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0020g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0021g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0023g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0024g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0027g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0029g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0002t0030g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0005t0008g0028 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0001c0005t0013g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0004 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0009 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0009g0023 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0018g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0031g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0032g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0003t0033g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0002c0004t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0003c0007t0022g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0004c0008t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| a0005c0006t0034g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0003 | t0033 | g0096 | EUR | GBR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0039 | EUR | FIN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0120 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00558 | hp1 | a0002 | c0003 | t0004 | g0009 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00609 | hp1 | a0002 | c0003 | t0004 | g0004 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0045 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00621 | hp1 | a0002 | c0003 | t0004 | g0100 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0018 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00735 | hp1 | a0002 | c0003 | t0004 | g0009 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01070 | hp2 | a0002 | c0003 | t0009 | g0023 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01071 | hp2 | a0002 | c0003 | t0009 | g0023 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01106 | hp1 | a0001 | c0005 | t0008 | g0028 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0033 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01192 | hp1 | a0001 | c0002 | t0005 | g0029 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01255 | hp2 | a0002 | c0003 | t0032 | g0095 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01256 | hp1 | a0002 | c0003 | t0009 | g0023 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01258 | hp2 | a0002 | c0003 | t0009 | g0023 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01261 | hp2 | a0001 | c0002 | t0005 | g0020 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01361 | hp2 | a0001 | c0002 | t0005 | g0069 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01496 | hp1 | a0002 | c0003 | t0004 | g0098 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01496 | hp2 | a0001 | c0002 | t0005 | g0068 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0033 | EUR | IBS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0033 | EUR | IBS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0115 | EUR | IBS | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01884 | hp1 | a0001 | c0002 | t0030 | g0160 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01891 | hp1 | a0002 | c0004 | t0001 | g0015 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01981 | hp1 | a0002 | c0003 | t0004 | g0009 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02055 | hp1 | a0001 | c0001 | t0025 | g0130 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02056 | hp2 | a0001 | c0002 | t0005 | g0013 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02074 | hp2 | a0002 | c0003 | t0004 | g0009 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0018 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0064 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | CDX | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02280 | hp1 | a0003 | c0007 | t0022 | g0060 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PEL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02451 | hp2 | a0002 | c0004 | t0001 | g0015 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02572 | hp2 | a0001 | c0002 | t0012 | g0057 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02602 | hp2 | a0002 | c0003 | t0004 | g0087 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02615 | hp2 | a0002 | c0004 | t0001 | g0015 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0151 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02683 | hp1 | a0001 | c0002 | t0005 | g0013 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02683 | hp2 | a0001 | c0005 | t0013 | g0035 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02698 | hp2 | a0001 | c0005 | t0008 | g0028 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02717 | hp2 | a0001 | c0002 | t0005 | g0012 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0039 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02735 | hp2 | a0002 | c0003 | t0004 | g0040 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02809 | hp1 | a0001 | c0002 | t0005 | g0020 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0084 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02818 | hp2 | a0001 | c0002 | t0012 | g0058 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02886 | hp1 | a0002 | c0003 | t0004 | g0088 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0020 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02895 | hp2 | a0001 | c0002 | t0011 | g0038 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02897 | hp1 | a0001 | c0002 | t0011 | g0038 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02897 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0085 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0078 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02976 | hp1 | a0001 | c0002 | t0005 | g0012 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03017 | hp1 | a0001 | c0002 | t0005 | g0066 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03017 | hp2 | a0002 | c0003 | t0018 | g0102 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03130 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0076 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03195 | hp2 | a0001 | c0002 | t0027 | g0124 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0063 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03453 | hp1 | a0001 | c0002 | t0014 | g0044 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0032 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03486 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0012 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0041 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03492 | hp1 | a0001 | c0001 | t0015 | g0041 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0012 | AFR | ESN | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03579 | hp1 | a0001 | c0002 | t0014 | g0044 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0020 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03654 | hp2 | a0002 | c0003 | t0004 | g0009 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03669 | hp1 | a0001 | c0002 | t0005 | g0013 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03688 | hp1 | a0002 | c0003 | t0004 | g0086 | SAS | STU | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | STU | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0075 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03710 | hp2 | a0001 | c0005 | t0013 | g0035 | SAS | PJL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03831 | hp1 | a0001 | c0002 | t0020 | g0081 | SAS | BEB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03831 | hp2 | a0002 | c0003 | t0004 | g0004 | SAS | BEB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03834 | hp2 | a0001 | c0005 | t0008 | g0028 | SAS | BEB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03942 | hp1 | a0001 | c0002 | t0018 | g0104 | SAS | BEB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | STU | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG04228 | hp1 | a0001 | c0002 | t0005 | g0013 | SAS | STU | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG04228 | hp2 | a0002 | c0003 | t0004 | g0040 | SAS | STU | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18522 | hp1 | a0001 | c0002 | t0017 | g0157 | AFR | YRI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18522 | hp2 | a0001 | c0002 | t0008 | g0059 | AFR | YRI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | CHB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18906 | hp1 | a0001 | c0002 | t0005 | g0065 | AFR | YRI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | YRI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18941 | hp2 | a0002 | c0003 | t0004 | g0092 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18942 | hp2 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18944 | hp1 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18948 | hp2 | a0001 | c0002 | t0019 | g0079 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0046 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18954 | hp2 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18956 | hp2 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18957 | hp2 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18960 | hp2 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18961 | hp2 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18962 | hp2 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18963 | hp2 | a0001 | c0001 | t0026 | g0108 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18964 | hp2 | a0002 | c0003 | t0004 | g0101 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18969 | hp2 | a0004 | c0008 | t0007 | g0113 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18971 | hp1 | a0002 | c0003 | t0004 | g0089 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18972 | hp1 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18974 | hp2 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18977 | hp2 | a0002 | c0003 | t0004 | g0097 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18978 | hp2 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18980 | hp1 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18983 | hp2 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0129 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18989 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18991 | hp1 | a0001 | c0001 | t0006 | g0046 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18993 | hp2 | a0001 | c0001 | t0028 | g0117 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18997 | hp2 | a0002 | c0003 | t0004 | g0093 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19000 | hp2 | a0002 | c0003 | t0031 | g0099 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19001 | hp2 | a0001 | c0001 | t0006 | g0128 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19002 | hp2 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19010 | hp1 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19010 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19011 | hp2 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | LWK | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | LWK | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19056 | hp1 | a0002 | c0003 | t0004 | g0091 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19056 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19059 | hp1 | a0002 | c0003 | t0004 | g0094 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19063 | hp2 | a0002 | c0003 | t0004 | g0009 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19065 | hp1 | a0005 | c0006 | t0034 | g0052 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19068 | hp1 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19074 | hp2 | a0002 | c0003 | t0004 | g0090 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19075 | hp1 | a0001 | c0001 | t0007 | g0112 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19077 | hp1 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19077 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19078 | hp2 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19081 | hp1 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19082 | hp1 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19083 | hp1 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19084 | hp2 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19090 | hp1 | a0001 | c0002 | t0021 | g0056 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19091 | hp2 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19240 | hp1 | a0002 | c0004 | t0001 | g0015 | AFR | YRI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ASW | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | ASW | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20752 | hp1 | a0001 | c0002 | t0005 | g0013 | EUR | TSI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0022 | EUR | TSI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20805 | hp2 | a0001 | c0002 | t0005 | g0067 | EUR | TSI | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | GIH | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | GIH | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01123 | hp1 | a0002 | c0003 | t0004 | g0009 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0077 | AMR | CLM | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02109 | hp1 | a0002 | c0004 | t0001 | g0015 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02109 | hp2 | a0001 | c0001 | t0016 | g0152 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02486 | hp2 | a0001 | c0002 | t0023 | g0061 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03471 | hp1 | a0001 | c0002 | t0017 | g0123 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG03471 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | MSL | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | USA | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| HG06807 | hp2 | a0001 | c0002 | t0029 | g0159 | AFR | USA | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA18955 | hp2 | a0002 | c0003 | t0004 | g0004 | EAS | JPT | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0012 | AFR | USA | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | LWK | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0024 | g0062 | REF | REF | NEMP2_chr2_190499338_190539722 | NEMP2 | chr2 | 190499338 | 190539722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190510487 | G | A | 1 | a0003 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1004C>T | p.Thr335Met | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 8/9 | 1071/6172 | 1004/1254 | 335/417 | chr2 | 190510487 | |||
| chr2:190514586 | T | C | 1 | a0004 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.820A>G | p.Met274Val | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/9 | 887/6172 | 820/1254 | 274/417 | chr2 | 190514586 | |||
| chr2:190534631 | A | G | 1 | a0005 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.25T>C | p.Trp9Arg | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 92/6172 | 25/1254 | 9/417 | chr2 | 190534631 | |||
| chr2:190534634 | A | C | 1 | a0005 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.22T>G | p.Trp8Gly | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 89/6172 | 22/1254 | 8/417 | chr2 | 190534634 | |||
| chr2:190534636 | C | T | 1 | a0005 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.20G>A | p.Arg7Gln | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 87/6172 | 20/1254 | 7/417 | chr2 | 190534636 | |||
| chr2:190534639 | C | G | 1 | a0005 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.17G>C | p.Gly6Ala | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 84/6172 | 17/1254 | 6/417 | chr2 | 190534639 | |||
| chr2:190534641 | T | G | 1 | a0005 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.15A>C | p.Gln5His | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 82/6172 | 15/1254 | 5/417 | chr2 | 190534641 | |||
| chr2:190534642 | T | G | 1 | a0005 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.14A>C | p.Gln5Pro | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 81/6172 | 14/1254 | 5/417 | chr2 | 190534642 | |||
| chr2:190534645 | C | G | 1 | a0005 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.11G>C | p.Arg4Pro | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 78/6172 | 11/1254 | 4/417 | chr2 | 190534645 | |||
| chr2:190534651 | C | G | 1 | a0005 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.5G>C | p.Gly2Ala | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 72/6172 | 5/1254 | 2/417 | chr2 | 190534651 | |||
| chr2:190534652 | C | G | 2 | a0002 a0005 |
61 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(58): Show |
missense_variant | MODERATE | c.4G>C | p.Gly2Arg | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 71/6172 | 4/1254 | 2/417 | chr2 | 190534652 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190514542 | G | A | 3 | a0001c0001 a0002c0004 a0004c0008 |
202 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(199): Show |
synonymous_variant | LOW | c.864C>T | p.Ala288Ala | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/9 | 931/6172 | 864/1254 | 288/417 | chr2 | 190514542 | |||
| chr2:190519052 | G | A | 1 | a0001c0005 | 5 | HG01106.hp1 HG02683.hp2 HG02698.hp2 others(2): Show |
synonymous_variant | LOW | c.345C>T | p.Asn115Asn | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 3/9 | 412/6172 | 345/1254 | 115/417 | chr2 | 190519052 | |||
| chr2:190534635 | C | G | 1 | a0005c0006 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.21G>C | p.Arg7Arg | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 88/6172 | 21/1254 | 7/417 | chr2 | 190534635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190504347 | A | G | 1 | a0003c0007t0022 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4842T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 4842 | chr2 | 190504347 | ||||||
| chr2:190504664 | A | G | 1 | a0001c0002t0029 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4525T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 4525 | chr2 | 190504664 | ||||||
| chr2:190505082 | G | T | 1 | a0001c0002t0027 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4107C>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 4107 | chr2 | 190505082 | ||||||
| chr2:190505126 | G | A | 6 | a0001c0002t0021 a0002c0003t0004 a0002c0003t0009 others(3): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*4063C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 4063 | chr2 | 190505126 | ||||||
| chr2:190505172 | T | C | 1 | a0002c0003t0033 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4017A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 4017 | chr2 | 190505172 | ||||||
| chr2:190505220 | A | G | 1 | a0002c0003t0032 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3969T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 3969 | chr2 | 190505220 | ||||||
| chr2:190505335 | T | G | 1 | a0001c0002t0019 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3854A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 3854 | chr2 | 190505335 | ||||||
| chr2:190505397 | G | A | 1 | a0001c0002t0027 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3792C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 3792 | chr2 | 190505397 | ||||||
| chr2:190505542 | A | G | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0015 others(3): Show |
60 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3647T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 3647 | chr2 | 190505542 | ||||||
| chr2:190505797 | G | T | 1 | a0001c0002t0017 | 2 | HG03471.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3392C>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 3392 | chr2 | 190505797 | ||||||
| chr2:190505884 | G | T | 1 | a0001c0001t0016 | 2 | HG02109.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3305C>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 3305 | chr2 | 190505884 | ||||||
| chr2:190505933 | T | C | 4 | a0001c0002t0014 a0001c0002t0017 a0001c0002t0027 others(1): Show |
6 | HG03195.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3256A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 3256 | chr2 | 190505933 | ||||||
| chr2:190505936 | A | G | 1 | a0001c0001t0026 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3253T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 3253 | chr2 | 190505936 | ||||||
| chr2:190506152 | C | G | 1 | a0001c0002t0011 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3037G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 3037 | chr2 | 190506152 | ||||||
| chr2:190506315 | A | G | 15 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0011 others(12): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*2874T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 2874 | chr2 | 190506315 | ||||||
| chr2:190506401 | T | A | 1 | a0001c0001t0028 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2788A>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 2788 | chr2 | 190506401 | ||||||
| chr2:190506475 | T | G | 1 | a0001c0001t0015 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2714A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 2714 | chr2 | 190506475 | ||||||
| chr2:190506491 | T | C | 6 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0016 others(3): Show |
140 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*2698A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 2698 | chr2 | 190506491 | ||||||
| chr2:190506625 | A | G | 1 | a0001c0001t0026 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2564T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 2564 | chr2 | 190506625 | ||||||
| chr2:190506646 | T | C | 2 | a0001c0002t0017 a0001c0002t0029 |
3 | HG03471.hp1 HG06807.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2543A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 2543 | chr2 | 190506646 | ||||||
| chr2:190506677 | C | A | 6 | a0001c0002t0021 a0002c0003t0004 a0002c0003t0009 others(3): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2512G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 2512 | chr2 | 190506677 | ||||||
| chr2:190506923 | G | A | 6 | a0001c0002t0021 a0002c0003t0004 a0002c0003t0009 others(3): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2266C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 2266 | chr2 | 190506923 | ||||||
| chr2:190507103 | A | G | 1 | a0002c0003t0031 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2086T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 2086 | chr2 | 190507103 | ||||||
| chr2:190507254 | T | C | 1 | a0002c0003t0009 | 4 | HG01070.hp2 HG01071.hp2 HG01256.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1935A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 1935 | chr2 | 190507254 | ||||||
| chr2:190507333 | T | G | 2 | a0001c0002t0012 a0001c0002t0030 |
3 | HG01884.hp1 HG02572.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1856A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 1856 | chr2 | 190507333 | ||||||
| chr2:190507511 | T | A | 1 | a0001c0005t0013 | 2 | HG02683.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1678A>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 1678 | chr2 | 190507511 | ||||||
| chr2:190507727 | T | TATCA | 3 | a0001c0002t0008 a0001c0005t0008 a0001c0005t0013 |
6 | HG01106.hp1 HG02683.hp2 HG02698.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1458_*1461dupTGAT | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 1461 | chr2 | 190507727 | ||||||
| chr2:190507901 | A | G | 2 | a0001c0001t0007 a0004c0008t0007 |
7 | HG00544.hp1 NA18942.hp2 NA18944.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1288T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 1288 | chr2 | 190507901 | ||||||
| chr2:190507990 | A | G | 1 | a0001c0001t0025 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1199T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 1199 | chr2 | 190507990 | ||||||
| chr2:190508036 | T | G | 2 | a0001c0001t0007 a0004c0008t0007 |
7 | HG00544.hp1 NA18942.hp2 NA18944.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1153A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 1153 | chr2 | 190508036 | ||||||
| chr2:190508515 | C | CAT | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(34): Show |
403 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(400): Show |
3_prime_UTR_variant | MODIFIER | c.*673_*674insAT | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 673 | chr2 | 190508515 | ||||||
| chr2:190508620 | G | A | 1 | a0001c0002t0020 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 569 | chr2 | 190508620 | ||||||
| chr2:190508720 | G | A | 6 | a0001c0002t0021 a0002c0003t0004 a0002c0003t0009 others(3): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*469C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 469 | chr2 | 190508720 | ||||||
| chr2:190508752 | G | A | 6 | a0001c0002t0021 a0002c0003t0004 a0002c0003t0009 others(3): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*437C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 437 | chr2 | 190508752 | ||||||
| chr2:190508993 | C | T | 1 | a0001c0001t0006 | 25 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*196G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 196 | chr2 | 190508993 | ||||||
| chr2:190509049 | C | T | 32 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(29): Show |
364 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*140G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 9/9 | 140 | chr2 | 190509049 | ||||||
| chr2:190534656 | T | G | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 1 | chr2 | 190534656 | ||||||
| chr2:190534657 | T | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-2A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 2 | chr2 | 190534657 | ||||||
| chr2:190534663 | G | A | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-8C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 8 | chr2 | 190534663 | ||||||
| chr2:190534666 | G | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 11 | chr2 | 190534666 | ||||||
| chr2:190534671 | C | G | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 16 | chr2 | 190534671 | ||||||
| chr2:190534672 | T | A | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17A>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 17 | chr2 | 190534672 | ||||||
| chr2:190534676 | T | G | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-21A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 21 | chr2 | 190534676 | ||||||
| chr2:190534677 | G | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 22 | chr2 | 190534677 | ||||||
| chr2:190534680 | A | G | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 25 | chr2 | 190534680 | ||||||
| chr2:190534685 | A | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 30 | chr2 | 190534685 | ||||||
| chr2:190534688 | C | G | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 33 | chr2 | 190534688 | ||||||
| chr2:190534693 | G | T | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38C>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 38 | chr2 | 190534693 | ||||||
| chr2:190534707 | T | C | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(21): Show |
265 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
5_prime_UTR_variant | MODIFIER | c.-52A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 52 | chr2 | 190534707 | ||||||
| chr2:190534708 | G | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 53 | chr2 | 190534708 | ||||||
| chr2:190534710 | G | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-55C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | chr2 | 190534710 | |||||||
| chr2:190534711 | A | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 56 | chr2 | 190534711 | ||||||
| chr2:190534714 | A | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 59 | chr2 | 190534714 | ||||||
| chr2:190534719 | A | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-64T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | chr2 | 190534719 | |||||||
| chr2:190534720 | A | T | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-65T>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 65 | chr2 | 190534720 | ||||||
| chr2:190534722 | T | C | 1 | a0005c0006t0034 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/9 | 67 | chr2 | 190534722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190509317 | C | T | 29 | a0001c0002t0014g0044 a0001c0002t0017g0123 a0001c0002t0017g0157 others(26): Show |
62 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(59): Show |
splice_region_variant&intron_variant | LOW | c.1131-5G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 8/8 | chr2 | 190509317 | |||||||
| chr2:190509391 | T | C | 1 | a0003c0007t0022g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1131-79A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 8/8 | chr2 | 190509391 | |||||||
| chr2:190509707 | A | G | 4 | a0001c0002t0017g0123 a0001c0002t0017g0157 a0001c0002t0029g0159 others(1): Show |
4 | HG01884.hp1 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131-395T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 8/8 | chr2 | 190509707 | |||||||
| chr2:190510119 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1130+242C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 8/8 | chr2 | 190510119 | |||||||
| chr2:190510231 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1130+130G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 8/8 | chr2 | 190510231 | |||||||
| chr2:190510343 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0156 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1130+18G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 8/8 | chr2 | 190510343 | |||||||
| chr2:190510343 | C | G | 1 | a0001c0001t0003g0107 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1130+18G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 8/8 | chr2 | 190510343 | |||||||
| chr2:190510649 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(109): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.954-112C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190510649 | |||||||
| chr2:190510682 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.954-145G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190510682 | |||||||
| chr2:190510706 | A | C | 6 | a0001c0002t0014g0044 a0001c0002t0017g0123 a0001c0002t0017g0157 others(3): Show |
7 | HG01884.hp1 HG03195.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.954-169T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190510706 | |||||||
| chr2:190510752 | T | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(109): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.954-215A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190510752 | |||||||
| chr2:190510854 | C | A | 2 | a0002c0003t0004g0014 a0002c0003t0004g0089 |
6 | NA18960.hp2 NA18961.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.954-317G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190510854 | |||||||
| chr2:190510859 | C | T | 6 | a0001c0001t0006g0017 a0001c0001t0006g0019 a0001c0001t0006g0045 others(3): Show |
16 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.954-322G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190510859 | |||||||
| chr2:190510924 | G | A | 2 | a0001c0001t0001g0132 a0002c0004t0001g0015 |
6 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.954-387C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190510924 | |||||||
| chr2:190511083 | C | A | 1 | a0001c0001t0003g0111 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.954-546G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190511083 | |||||||
| chr2:190511287 | G | A | 1 | a0001c0002t0002g0082 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.954-750C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190511287 | |||||||
| chr2:190511551 | T | A | 1 | a0001c0002t0002g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.954-1014A>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190511551 | |||||||
| chr2:190511553 | A | AT | 5 | a0001c0001t0001g0048 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG00741.hp2 HG01978.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.954-1017dupA | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190511553 | |||||||
| chr2:190511553 | AT | A | 25 | a0001c0001t0001g0133 a0001c0001t0001g0139 a0001c0001t0006g0127 others(22): Show |
51 | HG01106.hp1 HG01168.hp1 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.954-1017delA | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190511553 | |||||||
| chr2:190511553 | ATTT | A | 20 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0009 others(17): Show |
52 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.954-1019_954-1017d others(5): Show |
NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190511553 | |||||||
| chr2:190511849 | C | T | 33 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0010 others(30): Show |
98 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.954-1312G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190511849 | |||||||
| chr2:190512083 | CCTT | C | 2 | a0001c0002t0014g0044 a0001c0002t0027g0124 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.954-1549_954-1547d others(5): Show |
NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190512083 | |||||||
| chr2:190512190 | T | A | 1 | a0001c0002t0012g0058 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.954-1653A>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190512190 | |||||||
| chr2:190512358 | C | T | 1 | a0001c0002t0002g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.954-1821G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190512358 | |||||||
| chr2:190512465 | G | A | 23 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0009 others(20): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.954-1928C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190512465 | |||||||
| chr2:190512825 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.953+1628C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190512825 | |||||||
| chr2:190512846 | G | A | 3 | a0001c0001t0006g0019 a0001c0001t0006g0128 a0001c0001t0006g0129 |
7 | HG00621.hp2 NA18970.hp1 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.953+1607C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190512846 | |||||||
| chr2:190513014 | C | T | 1 | a0001c0002t0002g0080 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.953+1439G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190513014 | |||||||
| chr2:190513057 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.953+1396A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190513057 | |||||||
| chr2:190513067 | T | C | 1 | a0001c0002t0027g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.953+1386A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190513067 | |||||||
| chr2:190513289 | A | G | 2 | a0001c0002t0012g0057 a0001c0002t0012g0058 |
2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.953+1164T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190513289 | |||||||
| chr2:190513311 | T | C | 23 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0009 others(20): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.953+1142A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190513311 | |||||||
| chr2:190513325 | A | G | 1 | a0001c0002t0027g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.953+1128T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190513325 | |||||||
| chr2:190513444 | C | T | 35 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0010 others(32): Show |
101 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.953+1009G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190513444 | |||||||
| chr2:190513449 | T | C | 1 | a0001c0002t0005g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.953+1004A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190513449 | |||||||
| chr2:190513788 | A | T | 1 | a0002c0003t0004g0101 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.953+665T>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190513788 | |||||||
| chr2:190514197 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0135 |
10 | HG01257.hp1 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.953+256C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 7/8 | chr2 | 190514197 | |||||||
| chr2:190514739 | C | A | 1 | a0001c0002t0002g0055 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.728-61G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190514739 | |||||||
| chr2:190514866 | C | T | 1 | a0002c0003t0004g0040 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.728-188G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190514866 | |||||||
| chr2:190515056 | G | C | 1 | a0001c0001t0001g0026 | 4 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-378C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190515056 | |||||||
| chr2:190515148 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0156 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.728-470C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190515148 | |||||||
| chr2:190515159 | G | A | 1 | a0001c0001t0010g0032 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.728-481C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190515159 | |||||||
| chr2:190515328 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0115 |
2 | HG01517.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.728-650C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190515328 | |||||||
| chr2:190515720 | G | T | 3 | a0001c0002t0002g0021 a0001c0002t0002g0072 a0001c0002t0002g0078 |
6 | HG02145.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.727+550C>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190515720 | |||||||
| chr2:190515938 | C | G | 1 | a0001c0001t0001g0016 | 5 | HG02257.hp2 HG02559.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.727+332G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190515938 | |||||||
| chr2:190516005 | GACAA | G | 9 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0090 others(6): Show |
22 | HG00609.hp1 HG00621.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.727+261_727+264del others(4): Show |
NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190516005 | |||||||
| chr2:190516260 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.727+10T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 6/8 | chr2 | 190516260 | |||||||
| chr2:190516828 | C | T | 1 | a0001c0002t0029g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.613-444G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190516828 | |||||||
| chr2:190516996 | C | T | 1 | a0001c0001t0006g0045 | 2 | HG00423.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.612+524G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190516996 | |||||||
| chr2:190517090 | C | CA | 4 | a0001c0002t0002g0030 a0001c0002t0014g0044 a0001c0002t0027g0124 others(1): Show |
7 | HG03195.hp2 HG03453.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+429dupT | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517090 | |||||||
| chr2:190517090 | CA | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(53): Show |
145 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(142): Show |
intron_variant | MODIFIER | c.612+429delT | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517090 | |||||||
| chr2:190517090 | CAA | C | 29 | a0001c0001t0001g0047 a0001c0001t0001g0109 a0001c0001t0001g0139 others(26): Show |
63 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.612+428_612+429del others(2): Show |
NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517090 | |||||||
| chr2:190517106 | A | T | 2 | a0001c0001t0016g0151 a0001c0001t0016g0152 |
2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.612+414T>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517106 | |||||||
| chr2:190517112 | G | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(31): Show |
93 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.612+408C>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517112 | |||||||
| chr2:190517190 | A | G | 1 | a0001c0002t0030g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.612+330T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517190 | |||||||
| chr2:190517199 | A | C | 1 | a0001c0002t0002g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.612+321T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517199 | |||||||
| chr2:190517280 | C | T | 23 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0009 others(20): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.612+240G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517280 | |||||||
| chr2:190517296 | T | C | 2 | a0001c0001t0003g0025 a0001c0001t0003g0103 |
5 | HG00735.hp2 HG01070.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.612+224A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517296 | |||||||
| chr2:190517431 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.612+89A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517431 | |||||||
| chr2:190517490 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.612+30A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 5/8 | chr2 | 190517490 | |||||||
| chr2:190517782 | T | C | 4 | a0001c0002t0017g0123 a0001c0002t0017g0157 a0001c0002t0029g0159 others(1): Show |
4 | HG01884.hp1 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.519-169A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 4/8 | chr2 | 190517782 | |||||||
| chr2:190518058 | T | C | 1 | a0001c0002t0005g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.519-445A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 4/8 | chr2 | 190518058 | |||||||
| chr2:190518310 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.518+426G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 4/8 | chr2 | 190518310 | |||||||
| chr2:190518389 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00642.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.518+347C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 4/8 | chr2 | 190518389 | |||||||
| chr2:190518607 | C | T | 1 | a0002c0003t0004g0091 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.518+129G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 4/8 | chr2 | 190518607 | |||||||
| chr2:190518622 | A | G | 33 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0010 others(30): Show |
98 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.518+114T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 4/8 | chr2 | 190518622 | |||||||
| chr2:190519198 | C | G | 23 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0009 others(20): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.214-15G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190519198 | |||||||
| chr2:190519367 | A | T | 1 | a0001c0001t0015g0041 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.214-184T>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190519367 | |||||||
| chr2:190519671 | C | T | 2 | a0001c0002t0029g0159 a0001c0002t0030g0160 |
2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214-488G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190519671 | |||||||
| chr2:190519718 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.214-535A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190519718 | |||||||
| chr2:190519831 | C | T | 1 | a0001c0001t0010g0032 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.214-648G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190519831 | |||||||
| chr2:190519837 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.214-654C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190519837 | |||||||
| chr2:190519930 | T | C | 1 | a0001c0002t0005g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214-747A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190519930 | |||||||
| chr2:190520002 | C | A | 1 | a0001c0002t0017g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.214-819G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190520002 | |||||||
| chr2:190520053 | G | A | 1 | a0001c0002t0005g0065 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.214-870C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190520053 | |||||||
| chr2:190520080 | A | T | 2 | a0001c0001t0003g0106 a0001c0001t0015g0041 |
3 | HG02083.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.214-897T>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190520080 | |||||||
| chr2:190520198 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(48): Show |
138 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.214-1015C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190520198 | |||||||
| chr2:190520339 | G | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(109): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.214-1156C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190520339 | |||||||
| chr2:190520428 | T | G | 1 | a0001c0001t0010g0032 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.214-1245A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190520428 | |||||||
| chr2:190520465 | A | C | 1 | a0002c0003t0004g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.214-1282T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190520465 | |||||||
| chr2:190520532 | C | A | 6 | a0001c0002t0014g0044 a0001c0002t0017g0123 a0001c0002t0017g0157 others(3): Show |
7 | HG01884.hp1 HG03195.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-1349G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190520532 | |||||||
| chr2:190521087 | T | C | 1 | a0001c0002t0002g0083 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.214-1904A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190521087 | |||||||
| chr2:190521432 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(78): Show |
202 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.214-2249C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190521432 | |||||||
| chr2:190521786 | A | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18940.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.214-2603T>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190521786 | |||||||
| chr2:190521852 | T | C | 1 | a0002c0003t0004g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.214-2669A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190521852 | |||||||
| chr2:190521868 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(78): Show |
202 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.214-2685G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190521868 | |||||||
| chr2:190521878 | C | T | 1 | a0001c0002t0002g0076 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.214-2695G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190521878 | |||||||
| chr2:190522353 | T | G | 33 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0010 others(30): Show |
98 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.213+2910A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190522353 | |||||||
| chr2:190522431 | T | C | 1 | a0001c0002t0005g0012 | 5 | HG02717.hp2 HG02976.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+2832A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190522431 | |||||||
| chr2:190522484 | T | C | 1 | a0001c0001t0003g0116 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.213+2779A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190522484 | |||||||
| chr2:190522536 | A | G | 4 | a0001c0002t0017g0123 a0001c0002t0017g0157 a0001c0002t0029g0159 others(1): Show |
4 | HG01884.hp1 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+2727T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190522536 | |||||||
| chr2:190522620 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.213+2643G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190522620 | |||||||
| chr2:190522755 | C | T | 1 | a0001c0002t0002g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.213+2508G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190522755 | |||||||
| chr2:190522886 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
209 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.213+2377T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190522886 | |||||||
| chr2:190523132 | A | G | 30 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0010 others(27): Show |
92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.213+2131T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190523132 | |||||||
| chr2:190523465 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.213+1798G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190523465 | |||||||
| chr2:190523494 | G | A | 3 | a0001c0002t0002g0007 a0001c0002t0002g0084 a0001c0002t0002g0085 |
11 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+1769C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190523494 | |||||||
| chr2:190523618 | GT | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0016 others(105): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.213+1644delA | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190523618 | |||||||
| chr2:190523709 | C | T | 1 | a0002c0003t0004g0090 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.213+1554G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190523709 | |||||||
| chr2:190523716 | G | A | 1 | a0001c0002t0002g0039 | 2 | HG00323.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.213+1547C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190523716 | |||||||
| chr2:190523808 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.213+1455C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190523808 | |||||||
| chr2:190523957 | T | A | 2 | a0001c0002t0012g0057 a0001c0002t0012g0058 |
2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.213+1306A>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190523957 | |||||||
| chr2:190523993 | C | T | 1 | a0001c0002t0002g0036 | 2 | NA19004.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.213+1270G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190523993 | |||||||
| chr2:190524151 | A | C | 1 | a0002c0003t0004g0089 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.213+1112T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190524151 | |||||||
| chr2:190524249 | A | C | 1 | a0001c0001t0003g0105 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.213+1014T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190524249 | |||||||
| chr2:190524276 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.213+987T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190524276 | |||||||
| chr2:190524322 | T | C | 2 | a0001c0001t0016g0151 a0001c0001t0016g0152 |
2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.213+941A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190524322 | |||||||
| chr2:190524550 | G | A | 3 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0018g0104 |
3 | HG01496.hp2 HG03942.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.213+713C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190524550 | |||||||
| chr2:190524562 | C | G | 1 | a0001c0002t0014g0044 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.213+701G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190524562 | |||||||
| chr2:190524710 | T | C | 1 | a0002c0003t0031g0099 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.213+553A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190524710 | |||||||
| chr2:190524895 | C | T | 1 | a0001c0002t0029g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.213+368G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190524895 | |||||||
| chr2:190524929 | T | C | 4 | a0001c0002t0017g0123 a0001c0002t0017g0157 a0001c0002t0029g0159 others(1): Show |
4 | HG01884.hp1 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+334A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190524929 | |||||||
| chr2:190525048 | G | A | 1 | a0001c0002t0002g0022 | 4 | HG00741.hp1 HG01074.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+215C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190525048 | |||||||
| chr2:190525127 | T | C | 23 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0009 others(20): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.213+136A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190525127 | |||||||
| chr2:190525174 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.213+89A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 2/8 | chr2 | 190525174 | |||||||
| chr2:190525400 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(109): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.98-22C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190525400 | |||||||
| chr2:190525773 | T | C | 1 | a0001c0002t0027g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.98-395A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190525773 | |||||||
| chr2:190525776 | T | C | 1 | a0001c0001t0010g0032 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.98-398A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190525776 | |||||||
| chr2:190526047 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.98-669T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190526047 | |||||||
| chr2:190526065 | C | A | 2 | a0001c0002t0014g0044 a0001c0002t0027g0124 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.98-687G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190526065 | |||||||
| chr2:190526571 | G | A | 3 | a0001c0001t0003g0031 a0001c0001t0003g0118 a0001c0001t0028g0117 |
5 | NA18947.hp1 NA18966.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-1193C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190526571 | |||||||
| chr2:190526620 | T | C | 1 | a0002c0003t0004g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.98-1242A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190526620 | |||||||
| chr2:190526643 | T | C | 1 | a0002c0003t0018g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.98-1265A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190526643 | |||||||
| chr2:190526673 | T | C | 23 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0009 others(20): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.98-1295A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190526673 | |||||||
| chr2:190526682 | C | A | 1 | a0001c0002t0014g0044 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.98-1304G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190526682 | |||||||
| chr2:190527169 | G | C | 2 | a0001c0002t0014g0044 a0001c0002t0027g0124 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.98-1791C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190527169 | |||||||
| chr2:190527390 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.98-2012C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190527390 | |||||||
| chr2:190527845 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.98-2467T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190527845 | |||||||
| chr2:190528302 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0134 |
7 | HG02258.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-2924A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190528302 | |||||||
| chr2:190528387 | C | T | 1 | a0001c0002t0002g0075 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.98-3009G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190528387 | |||||||
| chr2:190528466 | C | G | 6 | a0001c0002t0002g0010 a0001c0002t0002g0053 a0001c0002t0002g0054 others(3): Show |
11 | HG00408.hp1 HG00423.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-3088G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190528466 | |||||||
| chr2:190528539 | A | G | 1 | a0001c0002t0002g0073 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.98-3161T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190528539 | |||||||
| chr2:190528566 | G | T | 2 | a0001c0001t0006g0033 a0001c0001t0006g0127 |
4 | HG01168.hp1 HG01169.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-3188C>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190528566 | |||||||
| chr2:190528692 | T | C | 1 | a0001c0002t0005g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.98-3314A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190528692 | |||||||
| chr2:190528720 | G | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(31): Show |
93 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.98-3342C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190528720 | |||||||
| chr2:190528756 | A | G | 1 | a0002c0003t0004g0088 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.98-3378T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190528756 | |||||||
| chr2:190528967 | C | A | 1 | a0001c0002t0005g0029 | 3 | HG01192.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.98-3589G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190528967 | |||||||
| chr2:190529061 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(78): Show |
202 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.98-3683C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529061 | |||||||
| chr2:190529093 | G | A | 22 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0009 others(19): Show |
54 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.98-3715C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529093 | |||||||
| chr2:190529395 | C | A | 1 | a0001c0001t0003g0119 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.98-4017G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529395 | |||||||
| chr2:190529398 | A | G | 28 | a0001c0001t0001g0109 a0001c0001t0003g0003 a0001c0001t0003g0025 others(25): Show |
60 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.98-4020T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529398 | |||||||
| chr2:190529484 | C | A | 29 | a0001c0001t0001g0109 a0001c0001t0003g0003 a0001c0001t0003g0025 others(26): Show |
63 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.98-4106G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529484 | |||||||
| chr2:190529608 | T | G | 6 | a0001c0002t0014g0044 a0001c0002t0017g0123 a0001c0002t0017g0157 others(3): Show |
7 | HG01884.hp1 HG03195.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-4230A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529608 | |||||||
| chr2:190529857 | T | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(49): Show |
139 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(136): Show |
intron_variant | MODIFIER | c.98-4479A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529857 | |||||||
| chr2:190529930 | C | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(31): Show |
93 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.98-4552G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529930 | |||||||
| chr2:190529963 | G | A | 1 | a0001c0001t0007g0120 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.98-4585C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529963 | |||||||
| chr2:190529989 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(85): Show |
210 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.97+4570T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529989 | |||||||
| chr2:190529996 | A | G | 2 | a0002c0003t0004g0086 a0002c0003t0004g0087 |
2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.97+4563T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190529996 | |||||||
| chr2:190530027 | G | A | 4 | a0001c0002t0017g0123 a0001c0002t0017g0157 a0001c0002t0029g0159 others(1): Show |
4 | HG01884.hp1 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+4532C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530027 | |||||||
| chr2:190530030 | C | G | 1 | a0001c0002t0002g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97+4529G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530030 | |||||||
| chr2:190530263 | C | T | 1 | a0001c0002t0002g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97+4296G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530263 | |||||||
| chr2:190530301 | C | T | 33 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0010 others(30): Show |
98 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.97+4258G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530301 | |||||||
| chr2:190530585 | AGATTG | A | 1 | a0001c0001t0001g0034 | 3 | HG00673.hp2 NA18955.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.97+3969_97+3973del others(5): Show |
NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530585 | |||||||
| chr2:190530663 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.97+3896C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530663 | |||||||
| chr2:190530699 | C | G | 1 | a0001c0001t0010g0032 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.97+3860G>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530699 | |||||||
| chr2:190530804 | T | A | 1 | a0001c0001t0006g0046 | 2 | NA18954.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.97+3755A>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530804 | |||||||
| chr2:190530834 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0135 |
10 | HG01257.hp1 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+3725G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530834 | |||||||
| chr2:190530894 | A | C | 1 | a0003c0007t0022g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.97+3665T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530894 | |||||||
| chr2:190530902 | G | A | 2 | a0002c0003t0004g0011 a0002c0003t0004g0101 |
7 | NA18954.hp2 NA18964.hp2 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+3657C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530902 | |||||||
| chr2:190530920 | T | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(49): Show |
139 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(136): Show |
intron_variant | MODIFIER | c.97+3639A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190530920 | |||||||
| chr2:190531334 | C | T | 1 | a0001c0002t0002g0070 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.97+3225G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190531334 | |||||||
| chr2:190531376 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0161 |
3 | HG00639.hp2 HG01109.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.97+3183G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190531376 | |||||||
| chr2:190531462 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(78): Show |
202 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.97+3097C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190531462 | |||||||
| chr2:190531530 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(109): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.97+3029A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190531530 | |||||||
| chr2:190531741 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.97+2818C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190531741 | |||||||
| chr2:190531979 | G | GA | 34 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(31): Show |
93 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.97+2579dupT | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190531979 | |||||||
| chr2:190532036 | C | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
365 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(362): Show |
intron_variant | MODIFIER | c.97+2523G>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190532036 | |||||||
| chr2:190532096 | G | A | 6 | a0001c0002t0005g0013 a0001c0002t0005g0066 a0001c0002t0005g0067 others(3): Show |
10 | HG01361.hp2 HG01496.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+2463C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190532096 | |||||||
| chr2:190532334 | A | G | 1 | a0001c0001t0001g0026 | 4 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+2225T>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190532334 | |||||||
| chr2:190532449 | C | T | 1 | a0001c0002t0012g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.97+2110G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190532449 | |||||||
| chr2:190532844 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.97+1715G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190532844 | |||||||
| chr2:190533277 | C | T | 23 | a0001c0002t0021g0056 a0002c0003t0004g0004 a0002c0003t0004g0009 others(20): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.97+1282G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190533277 | |||||||
| chr2:190533285 | G | C | 1 | a0001c0001t0003g0043 | 2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.97+1274C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190533285 | |||||||
| chr2:190533310 | G | A | 2 | a0001c0002t0014g0044 a0001c0002t0027g0124 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.97+1249C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190533310 | |||||||
| chr2:190533627 | A | C | 33 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0010 others(30): Show |
98 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.97+932T>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190533627 | |||||||
| chr2:190533774 | G | GA | 53 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
140 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(137): Show |
intron_variant | MODIFIER | c.97+784dupT | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190533774 | |||||||
| chr2:190533802 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.97+757C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190533802 | |||||||
| chr2:190533819 | G | A | 30 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0010 others(27): Show |
92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.97+740C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190533819 | |||||||
| chr2:190533878 | T | A | 3 | a0001c0002t0017g0157 a0001c0002t0029g0159 a0001c0002t0030g0160 |
3 | HG01884.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.97+681A>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190533878 | |||||||
| chr2:190534057 | A | ACAGC | 114 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.97+501_97+502insGC others(2): Show |
NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534057 | |||||||
| chr2:190534112 | C | T | 31 | a0001c0001t0001g0109 a0001c0001t0003g0003 a0001c0001t0003g0025 others(28): Show |
65 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.97+447G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534112 | |||||||
| chr2:190534121 | T | G | 1 | a0001c0001t0001g0050 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.97+438A>C | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534121 | |||||||
| chr2:190534208 | G | A | 1 | a0001c0001t0003g0122 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.97+351C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534208 | |||||||
| chr2:190534287 | T | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
140 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(137): Show |
intron_variant | MODIFIER | c.97+272A>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534287 | |||||||
| chr2:190534292 | A | T | 3 | a0001c0002t0002g0053 a0001c0002t0002g0054 a0001c0002t0002g0055 |
3 | HG00423.hp2 HG02165.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.97+267T>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534292 | |||||||
| chr2:190534356 | C | T | 29 | a0001c0001t0001g0109 a0001c0001t0003g0003 a0001c0001t0003g0025 others(26): Show |
61 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.97+203G>A | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534356 | |||||||
| chr2:190534402 | G | C | 24 | a0002c0003t0004g0004 a0002c0003t0004g0009 a0002c0003t0004g0011 others(21): Show |
60 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.97+157C>G | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534402 | |||||||
| chr2:190534430 | G | A | 24 | a0002c0003t0004g0004 a0002c0003t0004g0009 a0002c0003t0004g0011 others(21): Show |
60 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.97+129C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534430 | |||||||
| chr2:190534453 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.97+106C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534453 | |||||||
| chr2:190534475 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
136 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.97+84C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534475 | |||||||
| chr2:190534511 | G | A | 2 | a0001c0002t0029g0159 a0001c0002t0030g0160 |
2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97+48C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534511 | |||||||
| chr2:190534532 | G | GCGC | 2 | a0001c0001t0001g0051 a0001c0001t0001g0161 |
3 | HG00639.hp2 HG01109.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.97+24_97+26dupGCG | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534532 | |||||||
| chr2:190534547 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.97+12C>T | NEMP2 | ENSG00000189362.12 | transcript | ENST00000409150.8 | protein_coding | 1/8 | chr2 | 190534547 |