Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 120406 |
| ensemblid | ENSG00000204361.10 |
| hgncid | 26331 |
| symbol | NXPE2 |
| name | neurexophilin and PC-esterase domain family member 2 |
| refseq_nuc | NM_182495.6 |
| refseq_prot | NP_872301.2 |
| ensembl_nuc | ENST00000389586.6 |
| ensembl_prot | ENSP00000374237.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 114678527 |
| end | 114707069 |
| strand | + |
| ver | v1.2 |
| region | chr11:114678527-114707069 |
| region5000 | chr11:114673527-114712069 |
| regionname0 | NXPE2_chr11_114678527_114707069 |
| regionname5000 | NXPE2_chr11_114673527_114712069 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 559 | 230 | 72 | 39 | 91 | 9 | 18 | 69 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0002 | 0/0 | 559 | 121 | 13 | 26 | 61 | 4 | 17 | 47 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0003 | 0/1 | 559 | 54 | 0 | 5 | 43 | 1 | 4 | 39 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0004 | 0/0 | 559 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0005 | 0/0 | 559 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0006 | 0/0 | 559 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0007 | 0/0 | 559 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0008 | 0/0 | 559 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0009 | 0/0 | 559 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0010 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0011 | 0/0 | 559 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| a0012 | 0/0 | 514 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(509): Show |
chr11 | 114673527 | 114712069 |
| a0013 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | MVEKI others(554): Show |
chr11 | 114673527 | 114712069 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1677 | 161 | 45 | 32 | 69 | 4 | 11 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0001c0003 | 1/0 | 1677 | 64 | 22 | 7 | 22 | 5 | 7 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0001c0006 | 0/0 | 1677 | 4 | 4 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0001c0014 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0002c0002 | 0/0 | 1677 | 115 | 11 | 25 | 58 | 4 | 17 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0002c0008 | 0/0 | 1677 | 3 | 1 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0002c0013 | 0/0 | 1677 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0002c0018 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0002c0019 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0003c0004 | 0/1 | 1677 | 54 | 0 | 5 | 43 | 1 | 4 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0004c0005 | 0/0 | 1677 | 8 | 6 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0005c0007 | 0/0 | 1677 | 3 | 0 | 0 | 0 | 0 | 3 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0006c0010 | 0/0 | 1677 | 2 | 0 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0007c0011 | 0/0 | 1677 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0008c0009 | 0/0 | 1677 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0009c0012 | 0/0 | 1677 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0010c0020 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0011c0016 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0012c0017 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 | ||
| a0013c0015 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | ATGGT others(1672): Show |
chr11 | 114673527 | 114712069 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1868 | 160 | 44 | 32 | 69 | 4 | 11 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0001c0001t0004 | 0/0 | 1868 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0001c0003t0001 | 1/0 | 1868 | 64 | 22 | 7 | 22 | 5 | 7 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0001c0006t0001 | 0/0 | 1868 | 4 | 4 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0001c0014t0001 | 0/0 | 1868 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0002c0002t0001 | 0/0 | 1868 | 114 | 10 | 25 | 58 | 4 | 17 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0002c0002t0002 | 0/0 | 1868 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0002c0008t0001 | 0/0 | 1868 | 3 | 1 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0002c0013t0001 | 0/0 | 1868 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0002c0018t0001 | 0/0 | 1868 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0002c0019t0001 | 0/0 | 1868 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0003c0004t0001 | 0/1 | 1868 | 54 | 0 | 5 | 43 | 1 | 4 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0004c0005t0001 | 0/0 | 1868 | 8 | 6 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0005c0007t0001 | 0/0 | 1868 | 3 | 0 | 0 | 0 | 0 | 3 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0006c0010t0002 | 0/0 | 1868 | 2 | 0 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0007c0011t0001 | 0/0 | 1868 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0008c0009t0001 | 0/0 | 1868 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0009c0012t0001 | 0/0 | 1868 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0010c0020t0001 | 0/0 | 1868 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0011c0016t0001 | 0/0 | 1868 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0012c0017t0003 | 0/0 | 1868 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| a0013c0015t0001 | 0/0 | 1868 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | AATCA others(1863): Show |
chr11 | 114673527 | 114712069 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 64 | 5 | 14 | 37 | 4 | 4 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0009 | 0/0 | 7 | 2 | 4 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0022 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0005 | 0/0 | 11 | 2 | 1 | 6 | 0 | 2 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0008 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0016 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0025 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0006t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0006t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0001c0014t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0002 | 0/0 | 33 | 3 | 0 | 30 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0006 | 0/0 | 9 | 0 | 6 | 0 | 0 | 3 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0011 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0048 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0008t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0008t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0013t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0018t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0002c0019t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0003 | 0/0 | 28 | 0 | 0 | 28 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0004 | 0/0 | 13 | 0 | 4 | 6 | 1 | 2 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0003c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0004c0005t0001g0012 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0004c0005t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0004c0005t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0005c0007t0001g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0006c0010t0002g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0007c0011t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0008c0009t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0009c0012t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0009c0012t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0010c0020t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0011c0016t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0012c0017t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| a0013c0015t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0048 | EUR | GBR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0034 | EUR | FIN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00423 | hp1 | a0010 | c0020 | t0001 | g0039 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00544 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00621 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00642 | hp2 | a0002 | c0013 | t0001 | g0035 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0058 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00738 | hp2 | a0006 | c0010 | t0002 | g0055 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG00741 | hp2 | a0003 | c0004 | t0001 | g0004 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01099 | hp2 | a0006 | c0010 | t0002 | g0055 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01109 | hp2 | a0004 | c0005 | t0001 | g0012 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01192 | hp2 | a0003 | c0004 | t0001 | g0083 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01257 | hp2 | a0003 | c0004 | t0001 | g0004 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01258 | hp2 | a0003 | c0004 | t0001 | g0004 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0150 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0016 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0049 | EUR | IBS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0035 | EUR | IBS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0051 | EUR | IBS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01516 | hp2 | a0003 | c0004 | t0001 | g0004 | EUR | IBS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0051 | EUR | IBS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0049 | EUR | IBS | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02004 | hp2 | a0003 | c0004 | t0001 | g0004 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02027 | hp2 | a0003 | c0004 | t0001 | g0080 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02040 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02132 | hp2 | a0002 | c0008 | t0001 | g0052 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02135 | hp2 | a0007 | c0011 | t0001 | g0001 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02165 | hp1 | a0002 | c0008 | t0001 | g0052 | EAS | CDX | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02280 | hp2 | a0008 | c0009 | t0001 | g0026 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0154 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02523 | hp2 | a0002 | c0019 | t0001 | g0037 | EAS | KHV | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02572 | hp2 | a0001 | c0006 | t0001 | g0054 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0147 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02647 | hp1 | a0001 | c0014 | t0001 | g0167 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02698 | hp2 | a0005 | c0007 | t0001 | g0004 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0158 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0162 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0103 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02886 | hp1 | a0011 | c0016 | t0001 | g0010 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02895 | hp2 | a0004 | c0005 | t0001 | g0012 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02897 | hp1 | a0004 | c0005 | t0001 | g0012 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0159 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03130 | hp2 | a0004 | c0005 | t0001 | g0012 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03209 | hp1 | a0004 | c0005 | t0001 | g0036 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0170 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03486 | hp2 | a0004 | c0005 | t0001 | g0036 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0156 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0164 | AFR | ESN | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03579 | hp2 | a0001 | c0006 | t0001 | g0054 | AFR | MSL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0105 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03688 | hp1 | a0003 | c0004 | t0001 | g0057 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03688 | hp2 | a0005 | c0007 | t0001 | g0004 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0016 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03831 | hp2 | a0003 | c0004 | t0001 | g0004 | SAS | BEB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03927 | hp2 | a0003 | c0004 | t0001 | g0004 | SAS | BEB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | BEB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0157 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | BEB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04184 | hp2 | a0003 | c0004 | t0001 | g0075 | SAS | BEB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0108 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0059 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0016 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0024 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG04228 | hp2 | a0005 | c0007 | t0001 | g0004 | SAS | STU | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0153 | AFR | YRI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18522 | hp2 | a0001 | c0006 | t0001 | g0169 | AFR | YRI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | CHB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | CHB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18906 | hp2 | a0008 | c0009 | t0001 | g0026 | AFR | YRI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18939 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18940 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18945 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18947 | hp2 | a0003 | c0004 | t0001 | g0077 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18948 | hp2 | a0003 | c0004 | t0001 | g0032 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18953 | hp1 | a0003 | c0004 | t0001 | g0079 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18956 | hp2 | a0003 | c0004 | t0001 | g0084 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18961 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18967 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18969 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18970 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18972 | hp1 | a0009 | c0012 | t0001 | g0099 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18977 | hp2 | a0012 | c0017 | t0003 | g0123 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18983 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18985 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18986 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18988 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18993 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18995 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18998 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18999 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19000 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19001 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19001 | hp2 | a0013 | c0015 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19002 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19003 | hp2 | a0007 | c0011 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19006 | hp2 | a0003 | c0004 | t0001 | g0076 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19010 | hp1 | a0003 | c0004 | t0001 | g0078 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19011 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | LWK | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | LWK | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | LWK | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0062 | AFR | LWK | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19054 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19057 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19060 | hp1 | a0003 | c0004 | t0001 | g0081 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19062 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19072 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19074 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19076 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19080 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19081 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19083 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19084 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19086 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19087 | hp1 | a0009 | c0012 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19087 | hp2 | a0003 | c0004 | t0001 | g0032 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19091 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19240 | hp1 | a0004 | c0005 | t0001 | g0111 | AFR | YRI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | YRI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0050 | EUR | TSI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0011 | EUR | TSI | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | GIH | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0050 | SAS | GIH | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG01123 | hp2 | a0004 | c0005 | t0001 | g0012 | AMR | CLM | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0161 | AFR | ACB | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | USA | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | USA | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0163 | AFR | USA | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA20300 | hp2 | a0002 | c0018 | t0001 | g0043 | AFR | USA | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA21309 | hp1 | a0002 | c0008 | t0001 | g0056 | AFR | LWK | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| homoSapiens | chm13v2 | a0003 | c0004 | t0001 | g0082 | REF | REF | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0152 | REF | REF | NXPE2_chr11_114673527_114712069 | NXPE2 | chr11 | 114673527 | 114712069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:114698184 | T | C | 1 | a0005 | 3 | HG02698.hp2 HG03688.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.272T>C | p.Leu91Pro | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 321/1868 | 272/1680 | 91/559 | chr11 | 114698184 | |||
| chr11:114698220 | T | C | 2 | a0003 a0005 |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
missense_variant | MODERATE | c.308T>C | p.Val103Ala | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 357/1868 | 308/1680 | 103/559 | chr11 | 114698220 | |||
| chr11:114698364 | G | A | 1 | a0013 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.452G>A | p.Arg151Lys | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 501/1868 | 452/1680 | 151/559 | chr11 | 114698364 | |||
| chr11:114698480 | T | C | 1 | a0011 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.568T>C | p.Ser190Pro | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 617/1868 | 568/1680 | 190/559 | chr11 | 114698480 | |||
| chr11:114698651 | G | T | 1 | a0010 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.739G>T | p.Asp247Tyr | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 788/1868 | 739/1680 | 247/559 | chr11 | 114698651 | |||
| chr11:114704032 | T | C | 1 | a0008 | 2 | HG02280.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.908T>C | p.Ile303Thr | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/6 | 957/1868 | 908/1680 | 303/559 | chr11 | 114704032 | |||
| chr11:114705904 | A | T | 3 | a0002 a0009 a0010 |
124 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(121): Show |
missense_variant | MODERATE | c.1052A>T | p.Asn351Ile | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 5/6 | 1101/1868 | 1052/1680 | 351/559 | chr11 | 114705904 | |||
| chr11:114705961 | A | G | 1 | a0009 | 2 | NA18972.hp1 NA19087.hp1 |
missense_variant | MODERATE | c.1109A>G | p.His370Arg | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 5/6 | 1158/1868 | 1109/1680 | 370/559 | chr11 | 114705961 | |||
| chr11:114706485 | A | C | 1 | a0007 | 2 | HG02135.hp2 NA19003.hp2 |
missense_variant | MODERATE | c.1235A>C | p.Lys412Thr | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 6/6 | 1284/1868 | 1235/1680 | 412/559 | chr11 | 114706485 | |||
| chr11:114706734 | T | C | 1 | a0006 | 2 | HG00738.hp2 HG01099.hp2 |
missense_variant | MODERATE | c.1484T>C | p.Ile495Thr | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 6/6 | 1533/1868 | 1484/1680 | 495/559 | chr11 | 114706734 | |||
| chr11:114706793 | A | T | 1 | a0012 | 1 | NA18977.hp2 | stop_gained | HIGH | c.1543A>T | p.Arg515* | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 6/6 | 1592/1868 | 1543/1680 | 515/559 | chr11 | 114706793 | |||
| chr11:114706796 | G | T | 1 | a0004 | 8 | HG01109.hp2 HG01123.hp2 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.1546G>T | p.Asp516Tyr | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 6/6 | 1595/1868 | 1546/1680 | 516/559 | chr11 | 114706796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:114698050 | G | A | 1 | a0002c0013 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.138G>A | p.Ser46Ser | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 187/1868 | 138/1680 | 46/559 | chr11 | 114698050 | |||
| chr11:114698218 | T | C | 2 | a0001c0006 a0001c0014 |
5 | HG02572.hp2 HG02647.hp1 HG03486.hp1 others(2): Show |
synonymous_variant | LOW | c.306T>C | p.His102His | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 355/1868 | 306/1680 | 102/559 | chr11 | 114698218 | |||
| chr11:114698332 | A | G | 14 | a0001c0001 a0001c0006 a0002c0002 others(11): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
synonymous_variant | LOW | c.420A>G | p.Gly140Gly | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 469/1868 | 420/1680 | 140/559 | chr11 | 114698332 | |||
| chr11:114698590 | T | C | 2 | a0001c0006 a0001c0014 |
5 | HG02572.hp2 HG02647.hp1 HG03486.hp1 others(2): Show |
synonymous_variant | LOW | c.678T>C | p.Asn226Asn | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 727/1868 | 678/1680 | 226/559 | chr11 | 114698590 | |||
| chr11:114698665 | A | G | 1 | a0002c0019 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.753A>G | p.Glu251Glu | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/6 | 802/1868 | 753/1680 | 251/559 | chr11 | 114698665 | |||
| chr11:114706849 | T | C | 1 | a0002c0018 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.1599T>C | p.Ile533Ile | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 6/6 | 1648/1868 | 1599/1680 | 533/559 | chr11 | 114706849 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:114706957 | C | G | 1 | a0001c0001t0004 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27C>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 6/6 | 27 | chr11 | 114706957 | ||||||
| chr11:114706987 | C | T | 2 | a0002c0002t0002 a0006c0010t0002 |
3 | HG00738.hp2 HG01099.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*57C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 6/6 | 57 | chr11 | 114706987 | ||||||
| chr11:114707049 | T | A | 1 | a0012c0017t0003 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119T>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 6/6 | 119 | chr11 | 114707049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:114678653 | G | A | 1 | a0002c0008t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.26+52G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114678653 | |||||||
| chr11:114678694 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 |
6 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+93C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114678694 | |||||||
| chr11:114678846 | G | A | 1 | a0003c0004t0001g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.26+245G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114678846 | |||||||
| chr11:114678850 | A | ATG | 4 | a0002c0002t0001g0006 a0002c0002t0001g0058 a0002c0002t0001g0059 others(1): Show |
12 | HG00733.hp2 HG01192.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.26+263_26+264dupGT | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 114678850 | ||||||
| chr11:114679149 | T | C | 3 | a0001c0003t0001g0061 a0001c0003t0001g0062 a0008c0009t0001g0026 |
4 | HG02280.hp2 HG02630.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-508T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114679149 | |||||||
| chr11:114679205 | A | G | 1 | a0006c0010t0002g0055 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.27-452A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114679205 | |||||||
| chr11:114679247 | CGT | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(144): Show |
357 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.27-393_27-392delGT | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 114679247 | ||||||
| chr11:114679319 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
19 | HG00642.hp1 HG01099.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-338G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114679319 | |||||||
| chr11:114679422 | G | T | 11 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0024 others(8): Show |
28 | HG00140.hp1 HG00733.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.27-235G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114679422 | |||||||
| chr11:114679492 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.27-165G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114679492 | |||||||
| chr11:114679508 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
19 | HG00642.hp1 HG01099.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-149G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114679508 | |||||||
| chr11:114679598 | C | T | 11 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0024 others(8): Show |
28 | HG00140.hp1 HG00733.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.27-59C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114679598 | |||||||
| chr11:114679599 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-58G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114679599 | |||||||
| chr11:114679612 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(144): Show |
357 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.27-45A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 1/5 | chr11 | 114679612 | |||||||
| chr11:114679801 | C | T | 1 | a0002c0002t0001g0143 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.132+39C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114679801 | |||||||
| chr11:114679954 | G | T | 4 | a0001c0006t0001g0054 a0001c0006t0001g0169 a0001c0006t0001g0170 others(1): Show |
5 | HG02572.hp2 HG03486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+192G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114679954 | |||||||
| chr11:114680012 | A | G | 1 | a0001c0001t0001g0046 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.132+250A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114680012 | |||||||
| chr11:114680038 | G | A | 15 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 others(12): Show |
35 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.132+276G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114680038 | |||||||
| chr11:114680297 | T | G | 1 | a0001c0003t0001g0149 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.132+535T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114680297 | |||||||
| chr11:114680406 | G | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0072 |
5 | HG02257.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+644G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114680406 | |||||||
| chr11:114680422 | A | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
120 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.132+660A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114680422 | |||||||
| chr11:114680544 | C | G | 1 | a0001c0001t0001g0046 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.132+782C>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114680544 | |||||||
| chr11:114680643 | TC | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0072 |
5 | HG02257.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+882delC | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114680643 | |||||||
| chr11:114680902 | A | C | 1 | a0004c0005t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.132+1140A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114680902 | |||||||
| chr11:114680942 | C | T | 1 | a0001c0006t0001g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.132+1180C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114680942 | |||||||
| chr11:114681290 | C | T | 1 | a0002c0002t0001g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.132+1528C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114681290 | |||||||
| chr11:114681293 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.132+1531G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114681293 | |||||||
| chr11:114681451 | C | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02559.hp1 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1689C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114681451 | |||||||
| chr11:114681472 | A | G | 70 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(67): Show |
138 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.132+1710A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114681472 | |||||||
| chr11:114681555 | C | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 others(11): Show |
34 | HG00140.hp1 HG00733.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.132+1793C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114681555 | |||||||
| chr11:114681969 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.132+2207A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114681969 | |||||||
| chr11:114682012 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.132+2250T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682012 | |||||||
| chr11:114682066 | A | G | 2 | a0001c0001t0001g0072 a0001c0014t0001g0167 |
2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.132+2304A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682066 | |||||||
| chr11:114682074 | G | A | 1 | a0002c0002t0001g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.132+2312G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682074 | |||||||
| chr11:114682117 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.132+2355A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682117 | |||||||
| chr11:114682155 | A | G | 1 | a0001c0003t0001g0166 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.132+2393A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682155 | |||||||
| chr11:114682196 | G | A | 1 | a0001c0003t0001g0150 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.132+2434G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682196 | |||||||
| chr11:114682217 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.132+2455G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682217 | |||||||
| chr11:114682356 | C | T | 1 | a0002c0002t0001g0109 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.132+2594C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682356 | |||||||
| chr11:114682429 | G | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0074 |
3 | HG02615.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.132+2667G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682429 | |||||||
| chr11:114682478 | G | T | 1 | a0003c0004t0001g0084 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.132+2716G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682478 | |||||||
| chr11:114682731 | A | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(65): Show |
136 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.132+2969A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682731 | |||||||
| chr11:114682780 | A | G | 2 | a0002c0002t0001g0043 a0002c0018t0001g0043 |
2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.132+3018A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682780 | |||||||
| chr11:114682848 | GA | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(65): Show |
134 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.132+3097delA | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114682848 | ||||||
| chr11:114682864 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02559.hp1 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+3102T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114682864 | |||||||
| chr11:114683051 | A | G | 1 | a0003c0004t0001g0083 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.132+3289A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683051 | |||||||
| chr11:114683061 | G | A | 1 | a0002c0002t0001g0086 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.132+3299G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683061 | |||||||
| chr11:114683090 | G | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0087 a0001c0001t0001g0171 others(13): Show |
36 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.132+3328G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683090 | |||||||
| chr11:114683272 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.132+3510G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683272 | |||||||
| chr11:114683425 | G | GTT | 17 | a0001c0001t0001g0139 a0001c0006t0001g0054 a0001c0006t0001g0170 others(14): Show |
60 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.132+3676_132+3677d others(4): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114683425 | ||||||
| chr11:114683490 | G | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(10): Show |
20 | HG00642.hp1 HG01099.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.132+3728G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683490 | |||||||
| chr11:114683507 | G | A | 1 | a0003c0004t0001g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.132+3745G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683507 | |||||||
| chr11:114683561 | C | T | 3 | a0001c0006t0001g0054 a0001c0006t0001g0169 a0001c0006t0001g0170 |
4 | HG02572.hp2 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+3799C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683561 | |||||||
| chr11:114683607 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.132+3845C>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683607 | |||||||
| chr11:114683653 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.132+3891T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683653 | |||||||
| chr11:114683683 | G | A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0108 |
3 | HG00323.hp1 HG02148.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.132+3921G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683683 | |||||||
| chr11:114683817 | T | C | 1 | a0001c0003t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.132+4055T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683817 | |||||||
| chr11:114683932 | AGTTACAT | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.132+4178_132+4184d others(9): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114683932 | ||||||
| chr11:114683983 | T | C | 2 | a0001c0003t0001g0062 a0008c0009t0001g0026 |
3 | HG02280.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.132+4221T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114683983 | |||||||
| chr11:114684003 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
362 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.132+4241A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684003 | |||||||
| chr11:114684179 | G | A | 1 | a0002c0002t0001g0088 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.132+4417G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684179 | |||||||
| chr11:114684182 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.132+4420C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684182 | |||||||
| chr11:114684198 | C | T | 2 | a0001c0003t0001g0164 a0002c0002t0001g0107 |
2 | HG03491.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.132+4436C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684198 | |||||||
| chr11:114684376 | G | A | 3 | a0001c0001t0001g0046 a0001c0003t0001g0062 a0008c0009t0001g0026 |
5 | HG02280.hp2 HG02976.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+4614G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684376 | |||||||
| chr11:114684467 | G | A | 1 | a0001c0003t0001g0168 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.132+4705G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684467 | |||||||
| chr11:114684486 | A | G | 1 | a0002c0002t0001g0048 | 2 | HG00140.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.132+4724A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684486 | |||||||
| chr11:114684713 | A | T | 1 | a0002c0002t0001g0106 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.132+4951A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684713 | |||||||
| chr11:114684819 | T | C | 1 | a0002c0008t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+5057T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684819 | |||||||
| chr11:114684942 | T | C | 69 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(66): Show |
137 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.132+5180T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684942 | |||||||
| chr11:114684990 | G | T | 1 | a0001c0001t0001g0023 | 3 | HG02040.hp2 HG02523.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.132+5228G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114684990 | |||||||
| chr11:114685002 | C | A | 1 | a0002c0002t0001g0089 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.132+5240C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685002 | |||||||
| chr11:114685057 | G | C | 2 | a0002c0002t0001g0112 a0002c0002t0001g0145 |
2 | HG00738.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.132+5295G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685057 | |||||||
| chr11:114685086 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.132+5324A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685086 | |||||||
| chr11:114685109 | A | T | 1 | a0002c0002t0001g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.132+5347A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685109 | |||||||
| chr11:114685248 | G | A | 3 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 |
6 | HG01515.hp1 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+5486G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685248 | |||||||
| chr11:114685506 | C | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(62): Show |
131 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.132+5744C>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685506 | |||||||
| chr11:114685692 | C | A | 16 | a0001c0001t0001g0017 a0001c0001t0001g0087 a0001c0001t0001g0171 others(13): Show |
36 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.132+5930C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685692 | |||||||
| chr11:114685816 | C | A | 1 | a0002c0008t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+6054C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685816 | |||||||
| chr11:114685874 | C | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0021 others(43): Show |
125 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.132+6112C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685874 | |||||||
| chr11:114685949 | T | G | 2 | a0002c0002t0001g0035 a0002c0013t0001g0035 |
2 | HG00642.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.132+6187T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114685949 | |||||||
| chr11:114686098 | T | C | 1 | a0001c0003t0001g0049 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.132+6336T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114686098 | |||||||
| chr11:114686237 | C | A | 1 | a0001c0003t0001g0168 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.132+6475C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114686237 | |||||||
| chr11:114686313 | T | C | 2 | a0002c0002t0001g0013 a0002c0002t0001g0090 |
5 | HG01433.hp2 HG01981.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+6551T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114686313 | |||||||
| chr11:114686325 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
362 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.132+6563G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114686325 | |||||||
| chr11:114686500 | T | C | 2 | a0002c0002t0001g0043 a0002c0018t0001g0043 |
2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.132+6738T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114686500 | |||||||
| chr11:114686546 | C | T | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.132+6784C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114686546 | |||||||
| chr11:114686677 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.132+6915A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114686677 | |||||||
| chr11:114686738 | G | C | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.132+6976G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114686738 | |||||||
| chr11:114686841 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.132+7079G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114686841 | |||||||
| chr11:114687077 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.132+7315G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687077 | |||||||
| chr11:114687303 | G | A | 4 | a0002c0002t0001g0006 a0002c0002t0001g0058 a0002c0002t0001g0059 others(1): Show |
12 | HG00733.hp2 HG01192.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+7541G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687303 | |||||||
| chr11:114687366 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.132+7604C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687366 | |||||||
| chr11:114687537 | T | G | 1 | a0002c0002t0001g0091 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.132+7775T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687537 | |||||||
| chr11:114687565 | C | A | 1 | a0002c0002t0001g0089 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.132+7803C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687565 | |||||||
| chr11:114687769 | C | G | 1 | a0002c0002t0001g0089 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.132+8007C>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687769 | |||||||
| chr11:114687806 | T | C | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.132+8044T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687806 | |||||||
| chr11:114687855 | T | TG | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.132+8093_132+8094i others(3): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687855 | |||||||
| chr11:114687930 | C | T | 67 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(64): Show |
135 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.132+8168C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687930 | |||||||
| chr11:114687956 | C | G | 58 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(55): Show |
117 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.132+8194C>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114687956 | |||||||
| chr11:114688005 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.132+8243G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688005 | |||||||
| chr11:114688056 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.132+8294A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688056 | |||||||
| chr11:114688157 | G | A | 1 | a0002c0008t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+8395G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688157 | |||||||
| chr11:114688234 | C | T | 67 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(64): Show |
135 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.132+8472C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688234 | |||||||
| chr11:114688329 | A | G | 2 | a0002c0002t0001g0112 a0002c0002t0001g0145 |
2 | HG00738.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.132+8567A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688329 | |||||||
| chr11:114688407 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.132+8645A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688407 | |||||||
| chr11:114688410 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.132+8648C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688410 | |||||||
| chr11:114688434 | G | C | 1 | a0002c0002t0001g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.132+8672G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688434 | |||||||
| chr11:114688455 | T | G | 1 | a0003c0004t0001g0078 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.132+8693T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688455 | |||||||
| chr11:114688638 | T | G | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.132+8876T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688638 | |||||||
| chr11:114688660 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0092 a0002c0002t0001g0093 |
6 | HG00639.hp1 HG01074.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+8898G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688660 | |||||||
| chr11:114688747 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0085 |
5 | HG02055.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+8985A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688747 | |||||||
| chr11:114688777 | T | C | 1 | a0001c0003t0001g0150 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.132+9015T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688777 | |||||||
| chr11:114688967 | T | G | 1 | a0002c0002t0001g0059 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.133-9078T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114688967 | |||||||
| chr11:114689148 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.133-8897G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114689148 | |||||||
| chr11:114689626 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0004g0028 |
2 | HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.133-8419C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114689626 | |||||||
| chr11:114689915 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
362 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.133-8130T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114689915 | |||||||
| chr11:114689927 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.133-8118C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114689927 | |||||||
| chr11:114690084 | G | A | 15 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 others(12): Show |
35 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.133-7961G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690084 | |||||||
| chr11:114690178 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.133-7867A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690178 | |||||||
| chr11:114690245 | A | G | 1 | a0002c0008t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.133-7800A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690245 | |||||||
| chr11:114690256 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
362 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.133-7789T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690256 | |||||||
| chr11:114690360 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-7685G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690360 | |||||||
| chr11:114690410 | C | T | 2 | a0002c0002t0001g0104 a0002c0002t0001g0107 |
2 | HG02735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.133-7635C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690410 | |||||||
| chr11:114690437 | G | A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0108 |
3 | HG00323.hp1 HG02148.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.133-7608G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690437 | |||||||
| chr11:114690695 | T | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 |
6 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-7350T>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690695 | |||||||
| chr11:114690708 | C | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02559.hp1 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-7337C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690708 | |||||||
| chr11:114690709 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.133-7336G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690709 | |||||||
| chr11:114690868 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(176): Show |
425 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(422): Show |
intron_variant | MODIFIER | c.133-7177C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690868 | |||||||
| chr11:114690902 | C | A | 67 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(64): Show |
135 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.133-7143C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114690902 | |||||||
| chr11:114691002 | T | C | 1 | a0001c0001t0001g0021 | 3 | HG00438.hp2 NA18612.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.133-7043T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691002 | |||||||
| chr11:114691196 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.133-6849G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691196 | |||||||
| chr11:114691309 | T | A | 1 | a0001c0003t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.133-6736T>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691309 | |||||||
| chr11:114691411 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.133-6634A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691411 | |||||||
| chr11:114691445 | C | T | 26 | a0001c0003t0001g0005 a0001c0003t0001g0007 a0001c0003t0001g0008 others(23): Show |
61 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.133-6600C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691445 | |||||||
| chr11:114691511 | G | A | 1 | a0001c0003t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.133-6534G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691511 | |||||||
| chr11:114691512 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.133-6533G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691512 | |||||||
| chr11:114691517 | T | C | 4 | a0001c0006t0001g0054 a0001c0006t0001g0169 a0001c0006t0001g0170 others(1): Show |
5 | HG02572.hp2 HG03486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-6528T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691517 | |||||||
| chr11:114691546 | T | A | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-6499T>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691546 | |||||||
| chr11:114691577 | A | AG | 69 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(66): Show |
137 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.133-6467dupG | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114691577 | ||||||
| chr11:114691824 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(144): Show |
357 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.133-6221A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691824 | |||||||
| chr11:114691831 | TG | T | 27 | a0001c0003t0001g0005 a0001c0003t0001g0007 a0001c0003t0001g0008 others(24): Show |
62 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.133-6210delG | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114691831 | ||||||
| chr11:114691877 | C | T | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG01261.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.133-6168C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691877 | |||||||
| chr11:114691932 | T | C | 2 | a0004c0005t0001g0012 a0004c0005t0001g0111 |
6 | HG01109.hp2 HG01123.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-6113T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691932 | |||||||
| chr11:114691973 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 |
6 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-6072C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114691973 | |||||||
| chr11:114692182 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.133-5863C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114692182 | |||||||
| chr11:114692246 | T | C | 1 | a0002c0002t0001g0047 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.133-5799T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114692246 | |||||||
| chr11:114692304 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(175): Show |
424 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(421): Show |
intron_variant | MODIFIER | c.133-5741C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114692304 | |||||||
| chr11:114692321 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.133-5724G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114692321 | |||||||
| chr11:114692331 | A | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0130 others(3): Show |
11 | HG02055.hp2 HG02145.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.133-5714A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114692331 | |||||||
| chr11:114692520 | G | T | 3 | a0001c0006t0001g0054 a0001c0006t0001g0169 a0001c0006t0001g0170 |
4 | HG02572.hp2 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-5525G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114692520 | |||||||
| chr11:114692739 | G | A | 4 | a0001c0003t0001g0007 a0001c0003t0001g0155 a0001c0003t0001g0168 others(1): Show |
13 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-5306G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114692739 | |||||||
| chr11:114692909 | T | C | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-5136T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114692909 | |||||||
| chr11:114693088 | C | T | 1 | a0002c0002t0001g0109 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.133-4957C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114693088 | |||||||
| chr11:114693481 | G | A | 30 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0074 others(27): Show |
66 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.133-4564G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114693481 | |||||||
| chr11:114693484 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0072 |
5 | HG02257.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-4561C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114693484 | |||||||
| chr11:114693600 | C | G | 67 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(64): Show |
135 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.133-4445C>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114693600 | |||||||
| chr11:114693826 | A | G | 1 | a0001c0006t0001g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.133-4219A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114693826 | |||||||
| chr11:114694056 | C | T | 1 | a0002c0002t0001g0020 | 3 | HG00621.hp1 NA18943.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.133-3989C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694056 | |||||||
| chr11:114694183 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.133-3862T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694183 | |||||||
| chr11:114694199 | A | C | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-3846A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694199 | |||||||
| chr11:114694308 | A | G | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-3737A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694308 | |||||||
| chr11:114694392 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(74): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.133-3653A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694392 | |||||||
| chr11:114694613 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0085 |
5 | HG02055.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-3432A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694613 | |||||||
| chr11:114694700 | A | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(65): Show |
136 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.133-3345A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694700 | |||||||
| chr11:114694717 | G | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.133-3328G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694717 | |||||||
| chr11:114694808 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 |
6 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-3237C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694808 | |||||||
| chr11:114694846 | A | AT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.133-3191dupT | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114694846 | ||||||
| chr11:114694930 | ATAAC | A | 3 | a0001c0006t0001g0054 a0001c0006t0001g0169 a0001c0006t0001g0170 |
4 | HG02572.hp2 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-3111_133-3108d others(6): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114694930 | ||||||
| chr11:114694938 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.133-3107G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114694938 | |||||||
| chr11:114695156 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.133-2889T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695156 | |||||||
| chr11:114695188 | G | C | 4 | a0001c0006t0001g0054 a0001c0006t0001g0169 a0001c0006t0001g0170 others(1): Show |
5 | HG02572.hp2 HG03486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-2857G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695188 | |||||||
| chr11:114695271 | A | G | 1 | a0001c0003t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.133-2774A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695271 | |||||||
| chr11:114695280 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.133-2765G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695280 | |||||||
| chr11:114695288 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.133-2757A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695288 | |||||||
| chr11:114695309 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.133-2736C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695309 | |||||||
| chr11:114695325 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.133-2720T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695325 | |||||||
| chr11:114695407 | C | T | 1 | a0001c0001t0001g0041 | 2 | NA18959.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.133-2638C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695407 | |||||||
| chr11:114695715 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 others(11): Show |
34 | HG00140.hp1 HG00733.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.133-2330G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695715 | |||||||
| chr11:114695743 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.133-2302T>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695743 | |||||||
| chr11:114695830 | A | AAC | 40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0021 others(37): Show |
106 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.133-2179_133-2178d others(4): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACAC | 10 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0044 others(7): Show |
18 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.133-2181_133-2178d others(6): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACACAC | 19 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0100 others(16): Show |
33 | HG00621.hp1 HG00733.hp2 HG02148.hp1 others(30): Show |
intron_variant | MODIFIER | c.133-2183_133-2178d others(8): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACACACA others(1): Show |
27 | a0001c0001t0001g0009 a0001c0001t0001g0087 a0001c0001t0001g0171 others(24): Show |
69 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.133-2185_133-2178d others(10): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACACACA others(3): Show |
13 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0006t0001g0169 others(10): Show |
17 | HG00323.hp1 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.133-2187_133-2178d others(12): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACACACA others(5): Show |
18 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0028 others(15): Show |
26 | HG01099.hp2 HG01109.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.133-2189_133-2178d others(14): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACACACA others(7): Show |
24 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0064 others(21): Show |
36 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.133-2191_133-2178d others(16): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACACACA others(9): Show |
10 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0006t0001g0054 others(7): Show |
12 | HG01109.hp1 HG01943.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-2193_133-2178d others(18): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACACACA others(11): Show |
9 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0041 others(6): Show |
14 | HG00140.hp1 HG00642.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.133-2195_133-2178d others(20): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACACACA others(13): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0002c0002t0001g0011 |
5 | HG01175.hp1 HG03239.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-2197_133-2178d others(22): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | AACACACA others(15): Show |
4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0002c0002t0001g0048 others(1): Show |
5 | HG02451.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-2199_133-2178d others(24): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | A | ACACACAC others(6): Show |
1 | a0002c0002t0001g0013 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.133-2215_133-2214i others(15): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695830 | |||||||
| chr11:114695830 | AAC | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0003t0001g0005 others(3): Show |
10 | HG00741.hp1 HG01169.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.133-2179_133-2178d others(4): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695830 | AACAC | A | 24 | a0001c0003t0001g0005 a0001c0003t0001g0007 a0001c0003t0001g0008 others(21): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.133-2181_133-2178d others(6): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114695830 | ||||||
| chr11:114695867 | A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0069 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.133-2178_133-2177i others(17): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695867 | |||||||
| chr11:114695950 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.133-2095G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114695950 | |||||||
| chr11:114696030 | A | G | 7 | a0001c0001t0001g0171 a0001c0003t0001g0008 a0001c0003t0001g0161 others(4): Show |
14 | HG02258.hp1 HG02559.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.133-2015A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696030 | |||||||
| chr11:114696195 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02559.hp1 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-1850G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696195 | |||||||
| chr11:114696230 | T | G | 2 | a0001c0003t0001g0156 a0001c0003t0001g0157 |
2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.133-1815T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696230 | |||||||
| chr11:114696331 | C | CA | 11 | a0001c0001t0001g0022 a0001c0001t0001g0118 a0001c0001t0001g0137 others(8): Show |
13 | HG01943.hp2 HG02258.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-1707dupA | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114696331 | ||||||
| chr11:114696337 | AACC | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 others(10): Show |
32 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.133-1706_133-1704d others(5): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114696337 | ||||||
| chr11:114696338 | AC | A | 2 | a0001c0003t0001g0062 a0008c0009t0001g0026 |
3 | HG02280.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.133-1705delC | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114696338 | ||||||
| chr11:114696338 | ACC | A | 2 | a0002c0002t0001g0047 a0002c0002t0001g0059 |
3 | HG01168.hp1 HG01169.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.133-1706_133-1705d others(4): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696338 | |||||||
| chr11:114696339 | C | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(149): Show |
375 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(372): Show |
intron_variant | MODIFIER | c.133-1706C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696339 | |||||||
| chr11:114696340 | C | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0118 a0001c0001t0001g0137 others(11): Show |
17 | HG01943.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.133-1705C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696340 | |||||||
| chr11:114696340 | CA | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0066 others(16): Show |
27 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.133-1686delA | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114696340 | ||||||
| chr11:114696341 | A | C | 1 | a0003c0004t0001g0076 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.133-1704A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696341 | |||||||
| chr11:114696342 | A | C | 4 | a0001c0003t0001g0062 a0002c0002t0001g0047 a0002c0002t0001g0059 others(1): Show |
6 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-1703A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696342 | |||||||
| chr11:114696343 | A | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 others(10): Show |
32 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.133-1702A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696343 | |||||||
| chr11:114696356 | A | AAAG | 11 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(8): Show |
53 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.133-1687_133-1686i others(5): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114696356 | ||||||
| chr11:114696356 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.133-1689A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696356 | |||||||
| chr11:114696360 | G | GA | 12 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(9): Show |
54 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.133-1682dupA | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 114696360 | ||||||
| chr11:114696504 | C | A | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-1541C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696504 | |||||||
| chr11:114696550 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.133-1495C>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696550 | |||||||
| chr11:114696677 | T | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 others(13): Show |
36 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.133-1368T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696677 | |||||||
| chr11:114696681 | G | A | 1 | a0002c0008t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.133-1364G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696681 | |||||||
| chr11:114696763 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(3): Show |
9 | HG02257.hp2 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.133-1282C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696763 | |||||||
| chr11:114696882 | C | T | 1 | a0002c0002t0001g0101 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.133-1163C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696882 | |||||||
| chr11:114696951 | A | T | 1 | a0001c0006t0001g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.133-1094A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114696951 | |||||||
| chr11:114697140 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.133-905C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114697140 | |||||||
| chr11:114697254 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.133-791C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114697254 | |||||||
| chr11:114697271 | A | G | 1 | a0001c0001t0001g0017 | 4 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-774A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114697271 | |||||||
| chr11:114697280 | A | G | 69 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(66): Show |
137 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.133-765A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114697280 | |||||||
| chr11:114697326 | G | T | 1 | a0002c0002t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.133-719G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114697326 | |||||||
| chr11:114697454 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.133-591G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114697454 | |||||||
| chr11:114697483 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.133-562A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114697483 | |||||||
| chr11:114697557 | G | A | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-488G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114697557 | |||||||
| chr11:114697983 | A | G | 1 | a0002c0002t0001g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.133-62A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 2/5 | chr11 | 114697983 | |||||||
| chr11:114698822 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.866+44C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114698822 | |||||||
| chr11:114698838 | A | G | 1 | a0002c0002t0001g0106 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.866+60A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114698838 | |||||||
| chr11:114698930 | T | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
6 | HG02559.hp1 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.866+152T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114698930 | |||||||
| chr11:114699156 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.866+378C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114699156 | |||||||
| chr11:114699405 | C | T | 1 | a0001c0003t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.866+627C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114699405 | |||||||
| chr11:114699467 | T | G | 77 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(74): Show |
154 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.866+689T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114699467 | |||||||
| chr11:114699491 | G | A | 2 | a0002c0002t0001g0018 a0002c0002t0001g0143 |
4 | NA18970.hp1 NA19003.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+713G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114699491 | |||||||
| chr11:114699586 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.866+808A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114699586 | |||||||
| chr11:114699654 | G | GTCCTATA others(3): Show |
2 | a0002c0002t0001g0112 a0002c0002t0001g0145 |
2 | HG00738.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.866+878_866+887dup others(10): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114699654 | ||||||
| chr11:114699686 | C | T | 70 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(67): Show |
145 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.866+908C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114699686 | |||||||
| chr11:114699796 | AT | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(154): Show |
376 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(373): Show |
intron_variant | MODIFIER | c.866+1033delT | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114699796 | ||||||
| chr11:114699824 | C | T | 1 | a0001c0001t0001g0017 | 4 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+1046C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114699824 | |||||||
| chr11:114699832 | C | T | 1 | a0002c0002t0001g0040 | 2 | NA18956.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.866+1054C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114699832 | |||||||
| chr11:114700008 | G | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0019 others(81): Show |
224 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.866+1230G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700008 | |||||||
| chr11:114700009 | G | C | 1 | a0003c0004t0001g0081 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.866+1231G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700009 | |||||||
| chr11:114700129 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0069 |
2 | HG01168.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.866+1351T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700129 | |||||||
| chr11:114700214 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 |
6 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.866+1436C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700214 | |||||||
| chr11:114700288 | C | A | 10 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0047 others(7): Show |
25 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.866+1510C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700288 | |||||||
| chr11:114700522 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(158): Show |
380 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(377): Show |
intron_variant | MODIFIER | c.866+1744G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700522 | |||||||
| chr11:114700582 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.866+1804T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700582 | |||||||
| chr11:114700597 | C | T | 8 | a0001c0001t0001g0045 a0001c0001t0001g0144 a0001c0003t0001g0008 others(5): Show |
16 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.866+1819C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700597 | |||||||
| chr11:114700690 | A | C | 7 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0072 others(4): Show |
14 | HG01109.hp2 HG01123.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.866+1912A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700690 | |||||||
| chr11:114700694 | T | C | 1 | a0001c0003t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.866+1916T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700694 | |||||||
| chr11:114700760 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.866+1982T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700760 | |||||||
| chr11:114700823 | A | G | 1 | a0001c0003t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.866+2045A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700823 | |||||||
| chr11:114700846 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.866+2068G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700846 | |||||||
| chr11:114700856 | T | C | 70 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(67): Show |
145 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.866+2078T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700856 | |||||||
| chr11:114700931 | T | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0033 others(7): Show |
19 | HG01109.hp2 HG01123.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.866+2153T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700931 | |||||||
| chr11:114700940 | A | T | 1 | a0001c0003t0001g0053 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.866+2162A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114700940 | |||||||
| chr11:114701043 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.866+2265G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114701043 | |||||||
| chr11:114701077 | G | T | 12 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0047 others(9): Show |
27 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.866+2299G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114701077 | |||||||
| chr11:114701184 | T | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0069 |
2 | HG01168.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.866+2406T>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114701184 | |||||||
| chr11:114701253 | G | A | 14 | a0003c0004t0001g0003 a0003c0004t0001g0004 a0003c0004t0001g0032 others(11): Show |
56 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.866+2475G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114701253 | |||||||
| chr11:114701632 | C | T | 1 | a0002c0002t0001g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.867-2359C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114701632 | |||||||
| chr11:114701638 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.867-2353C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114701638 | |||||||
| chr11:114701734 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.867-2257G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114701734 | |||||||
| chr11:114701875 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.867-2116G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114701875 | |||||||
| chr11:114702043 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.867-1948A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702043 | |||||||
| chr11:114702092 | C | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 |
6 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.867-1899C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702092 | |||||||
| chr11:114702095 | C | T | 79 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(76): Show |
158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.867-1896C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702095 | |||||||
| chr11:114702122 | C | A | 6 | a0001c0001t0001g0095 a0001c0003t0001g0061 a0001c0006t0001g0054 others(3): Show |
7 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.867-1869C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702122 | |||||||
| chr11:114702305 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0021 others(46): Show |
133 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.867-1686A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702305 | |||||||
| chr11:114702345 | TC | T | 73 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(70): Show |
151 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.867-1645delC | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702345 | |||||||
| chr11:114702356 | C | G | 1 | a0001c0003t0001g0150 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.867-1635C>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702356 | |||||||
| chr11:114702494 | G | A | 79 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(76): Show |
158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.867-1497G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702494 | |||||||
| chr11:114702542 | A | G | 79 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(76): Show |
158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.867-1449A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702542 | |||||||
| chr11:114702550 | A | C | 79 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(76): Show |
158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.867-1441A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702550 | |||||||
| chr11:114702616 | T | C | 1 | a0006c0010t0002g0055 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.867-1375T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702616 | |||||||
| chr11:114702700 | A | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
5 | HG02559.hp1 HG02615.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.867-1291A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702700 | |||||||
| chr11:114702713 | C | T | 1 | a0002c0002t0001g0097 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.867-1278C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702713 | |||||||
| chr11:114702838 | A | T | 13 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0047 others(10): Show |
28 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.867-1153A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702838 | |||||||
| chr11:114702904 | A | C | 1 | a0001c0003t0001g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.867-1087A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702904 | |||||||
| chr11:114702984 | C | T | 6 | a0001c0001t0001g0095 a0001c0006t0001g0054 a0001c0006t0001g0169 others(3): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.867-1007C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702984 | |||||||
| chr11:114702985 | G | A | 2 | a0001c0003t0001g0007 a0001c0003t0001g0155 |
10 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.867-1006G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114702985 | |||||||
| chr11:114703015 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.867-976G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703015 | |||||||
| chr11:114703188 | T | G | 1 | a0001c0003t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.867-803T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703188 | |||||||
| chr11:114703198 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0021 others(51): Show |
139 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.867-793C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703198 | |||||||
| chr11:114703319 | A | G | 1 | a0001c0003t0001g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.867-672A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703319 | |||||||
| chr11:114703365 | C | A | 1 | a0001c0003t0001g0151 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.867-626C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703365 | |||||||
| chr11:114703380 | G | A | 1 | a0001c0003t0001g0164 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.867-611G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703380 | |||||||
| chr11:114703486 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.867-505C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703486 | |||||||
| chr11:114703532 | G | A | 1 | a0001c0003t0001g0155 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.867-459G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703532 | |||||||
| chr11:114703653 | C | CATAG | 4 | a0001c0003t0001g0025 a0001c0003t0001g0158 a0001c0003t0001g0165 others(1): Show |
6 | HG01081.hp2 HG02717.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.867-295_867-292dup others(4): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703653 | ||||||
| chr11:114703653 | CATAG | C | 3 | a0001c0003t0001g0050 a0001c0003t0001g0157 a0001c0003t0001g0160 |
4 | HG04115.hp2 NA19086.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-295_867-292del others(4): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703653 | ||||||
| chr11:114703653 | CATAGATA others(1): Show |
C | 4 | a0001c0003t0001g0016 a0001c0003t0001g0049 a0001c0003t0001g0051 others(1): Show |
9 | HG00741.hp1 HG01358.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.867-299_867-292del others(8): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703653 | ||||||
| chr11:114703653 | CATAGATA others(5): Show |
C | 1 | a0001c0003t0001g0151 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.867-303_867-292del others(12): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703653 | ||||||
| chr11:114703660 | AGATAGAT others(32): Show |
A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0171 a0001c0001t0001g0172 |
6 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.867-312_867-274del others(39): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703660 | ||||||
| chr11:114703668 | AGATAGAT others(24): Show |
A | 2 | a0001c0001t0001g0113 a0001c0006t0001g0169 |
2 | HG02074.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.867-304_867-274del others(31): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703668 | ||||||
| chr11:114703672 | AGATAGAT others(20): Show |
A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0073 a0001c0001t0001g0095 others(6): Show |
11 | HG00738.hp2 HG01099.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.867-300_867-274del others(27): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703672 | ||||||
| chr11:114703676 | AGATAGAT others(16): Show |
A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0023 others(16): Show |
32 | HG00140.hp2 HG00558.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.867-296_867-274del others(23): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703676 | ||||||
| chr11:114703677 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.867-314G>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703677 | |||||||
| chr11:114703680 | AGATAGAT others(12): Show |
A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0021 others(48): Show |
117 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.867-292_867-274del others(19): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703680 | ||||||
| chr11:114703683 | TAGATAGA others(28): Show |
T | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.867-304_867-270del others(35): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703683 | ||||||
| chr11:114703684 | AGATAGAT others(8): Show |
A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0021 others(28): Show |
74 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.867-291_867-277del others(15): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703684 | ||||||
| chr11:114703686 | A | G | 1 | a0002c0002t0001g0143 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.867-305A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703686 | |||||||
| chr11:114703687 | TAGATAGA others(24): Show |
T | 1 | a0002c0002t0001g0107 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.867-300_867-270del others(31): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703687 | ||||||
| chr11:114703688 | AGATAGAT others(4): Show |
A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0068 others(11): Show |
19 | HG01192.hp2 HG01975.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.867-291_867-281del others(11): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703688 | ||||||
| chr11:114703691 | TAGATAGA others(20): Show |
T | 7 | a0001c0001t0001g0009 a0002c0002t0001g0002 a0002c0002t0001g0034 others(4): Show |
10 | HG00323.hp1 HG02148.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.867-296_867-270del others(27): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703691 | ||||||
| chr11:114703692 | AGATAGAT | A | 2 | a0002c0002t0001g0047 a0010c0020t0001g0039 |
3 | HG00423.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.867-291_867-285del others(7): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703692 | ||||||
| chr11:114703695 | TAGATGAT others(16): Show |
T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0069 others(24): Show |
56 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.867-292_867-270del others(23): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703695 | ||||||
| chr11:114703699 | TGATAGAT others(12): Show |
T | 28 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(25): Show |
47 | HG00642.hp2 HG00673.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.867-291_867-273del others(19): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703699 | |||||||
| chr11:114703711 | A | G | 1 | a0001c0001t0001g0046 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.867-280A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703711 | |||||||
| chr11:114703714 | T | C | 16 | a0001c0003t0001g0153 a0003c0004t0001g0003 a0003c0004t0001g0004 others(13): Show |
59 | HG00544.hp2 HG00621.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.867-277T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703714 | |||||||
| chr11:114703726 | C | T | 1 | a0001c0003t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.867-265C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703726 | |||||||
| chr11:114703726 | CAGAT | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0003t0001g0168 others(5): Show |
9 | HG00423.hp1 HG01993.hp1 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.867-252_867-249del others(4): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 114703726 | ||||||
| chr11:114703730 | T | C | 62 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(59): Show |
133 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.867-261T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703730 | |||||||
| chr11:114703766 | G | A | 5 | a0001c0001t0001g0095 a0001c0006t0001g0054 a0001c0006t0001g0169 others(2): Show |
6 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.867-225G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703766 | |||||||
| chr11:114703770 | G | A | 5 | a0001c0001t0001g0095 a0001c0006t0001g0054 a0001c0006t0001g0169 others(2): Show |
6 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.867-221G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703770 | |||||||
| chr11:114703876 | C | A | 5 | a0001c0001t0001g0095 a0001c0006t0001g0054 a0001c0006t0001g0169 others(2): Show |
6 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.867-115C>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 3/5 | chr11 | 114703876 | |||||||
| chr11:114704097 | C | T | 64 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(61): Show |
127 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.928+45C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114704097 | |||||||
| chr11:114704098 | G | A | 1 | a0006c0010t0002g0055 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.928+46G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114704098 | |||||||
| chr11:114704265 | A | T | 73 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(70): Show |
151 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.928+213A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114704265 | |||||||
| chr11:114704331 | T | TG | 79 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(76): Show |
158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.928+279_928+280ins others(1): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114704331 | |||||||
| chr11:114704347 | G | A | 1 | a0006c0010t0002g0055 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.928+295G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114704347 | |||||||
| chr11:114704483 | A | C | 1 | a0001c0003t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.928+431A>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114704483 | |||||||
| chr11:114704495 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0065 |
3 | HG01943.hp1 HG01975.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.928+443T>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114704495 | |||||||
| chr11:114704768 | T | C | 84 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0027 others(81): Show |
191 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.928+716T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114704768 | |||||||
| chr11:114704788 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.928+736C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114704788 | |||||||
| chr11:114705051 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.929-730T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705051 | |||||||
| chr11:114705182 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.929-599G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705182 | |||||||
| chr11:114705272 | A | T | 11 | a0002c0002t0001g0013 a0002c0002t0001g0035 a0002c0002t0001g0037 others(8): Show |
14 | HG00642.hp2 HG01106.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-509A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705272 | |||||||
| chr11:114705443 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.929-338T>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705443 | |||||||
| chr11:114705564 | G | A | 1 | a0001c0003t0001g0061 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.929-217G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705564 | |||||||
| chr11:114705564 | G | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0085 |
5 | HG02055.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.929-217G>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705564 | |||||||
| chr11:114705583 | A | G | 67 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0067 others(64): Show |
142 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.929-198A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705583 | |||||||
| chr11:114705628 | A | G | 1 | a0002c0002t0001g0096 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.929-153A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705628 | |||||||
| chr11:114705656 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(158): Show |
380 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(377): Show |
intron_variant | MODIFIER | c.929-125A>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705656 | |||||||
| chr11:114705687 | G | A | 1 | a0001c0003t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.929-94G>A | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705687 | |||||||
| chr11:114705733 | T | C | 1 | a0001c0003t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.929-48T>C | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 4/5 | chr11 | 114705733 | |||||||
| chr11:114706082 | A | T | 1 | a0012c0017t0003g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1144+86A>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 5/5 | chr11 | 114706082 | |||||||
| chr11:114706085 | A | ATTTAT | 80 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(77): Show |
187 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.1144+119_1144+123d others(7): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 114706085 | ||||||
| chr11:114706085 | A | ATTTATTT others(3): Show |
5 | a0001c0003t0001g0151 a0002c0002t0001g0015 a0002c0002t0001g0039 others(2): Show |
8 | HG00423.hp1 HG02074.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144+114_1144+123d others(12): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 114706085 | ||||||
| chr11:114706085 | ATTTATTT others(3): Show |
A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0095 a0001c0006t0001g0054 others(2): Show |
7 | HG01106.hp1 HG01123.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144+114_1144+123d others(12): Show |
NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 114706085 | ||||||
| chr11:114706319 | T | G | 1 | a0006c0010t0002g0055 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1145-76T>G | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 5/5 | chr11 | 114706319 | |||||||
| chr11:114706351 | C | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0046 others(8): Show |
17 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1145-44C>T | NXPE2 | ENSG00000204361.10 | transcript | ENST00000389586.6 | protein_coding | 5/5 | chr11 | 114706351 |