Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4678 |
| ensemblid | ENSG00000132780.17 |
| hgncid | 7644 |
| symbol | NASP |
| name | nuclear autoantigenic sperm protein |
| refseq_nuc | NM_002482.4 |
| refseq_prot | NP_002473.2 |
| ensembl_nuc | ENST00000350030.8 |
| ensembl_prot | ENSP00000255120.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 45584041 |
| end | 45618893 |
| strand | + |
| ver | v1.2 |
| region | chr1:45584041-45618893 |
| region5000 | chr1:45579041-45623893 |
| regionname0 | NASP_chr1_45584041_45618893 |
| regionname5000 | NASP_chr1_45579041_45623893 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 788 | 281 | 66 | 67 | 108 | 8 | 30 | 74 | NASP_chr1_45579041_45623893 | NASP | MAMES others(783): Show |
chr1 | 45579041 | 45623893 |
| a0002 | 0/0 | 788 | 12 | 0 | 0 | 12 | 0 | 0 | 12 | NASP_chr1_45579041_45623893 | NASP | MAMES others(783): Show |
chr1 | 45579041 | 45623893 |
| a0003 | 0/0 | 788 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | MAMES others(783): Show |
chr1 | 45579041 | 45623893 |
| a0004 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | MAMES others(783): Show |
chr1 | 45579041 | 45623893 |
| a0005 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | MAMES others(783): Show |
chr1 | 45579041 | 45623893 |
| a0006 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | MAMES others(783): Show |
chr1 | 45579041 | 45623893 |
| a0007 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | MAMES others(783): Show |
chr1 | 45579041 | 45623893 |
| a0008 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | MAMES others(783): Show |
chr1 | 45579041 | 45623893 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2364 | 147 | 39 | 27 | 60 | 4 | 17 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0001c0002 | 1/0 | 2364 | 102 | 21 | 29 | 42 | 1 | 8 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0001c0003 | 0/1 | 2364 | 24 | 4 | 11 | 0 | 3 | 5 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0001c0005 | 0/0 | 2364 | 3 | 0 | 0 | 3 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0001c0007 | 0/0 | 2364 | 2 | 0 | 0 | 2 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0001c0008 | 0/0 | 2364 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0001c0010 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0002c0004 | 0/0 | 2364 | 12 | 0 | 0 | 12 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0003c0006 | 0/0 | 2364 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0004c0013 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0005c0011 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0006c0009 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0007c0012 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 | ||
| a0008c0014 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | ATGGC others(2359): Show |
chr1 | 45579041 | 45623893 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3225 | 140 | 32 | 27 | 60 | 4 | 17 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0001t0003 | 0/0 | 3225 | 5 | 5 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0001t0004 | 0/0 | 3225 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0002t0001 | 1/0 | 3225 | 100 | 20 | 28 | 42 | 1 | 8 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0002t0005 | 0/0 | 3225 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0002t0006 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0003t0001 | 0/0 | 3225 | 2 | 1 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0003t0002 | 0/1 | 3225 | 22 | 3 | 10 | 0 | 3 | 5 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0005t0001 | 0/0 | 3225 | 3 | 0 | 0 | 3 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0007t0001 | 0/0 | 3225 | 2 | 0 | 0 | 2 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0008t0002 | 0/0 | 3225 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0001c0010t0001 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0002c0004t0001 | 0/0 | 3225 | 12 | 0 | 0 | 12 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0003c0006t0001 | 0/0 | 3225 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0004c0013t0001 | 0/0 | 3225 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0005c0011t0001 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0006c0009t0001 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0007c0012t0001 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| a0008c0014t0001 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | CTCTA others(3220): Show |
chr1 | 45579041 | 45623893 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0002t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0007t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0007t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0008t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0008t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0001c0010t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0002c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0003c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0003c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0004c0013t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0005c0011t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0006c0009t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0007c0012t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| a0008c0014t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0006 | EUR | GBR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0147 | EUR | FIN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0152 | EUR | FIN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00544 | hp1 | a0001 | c0007 | t0001 | g0278 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00673 | hp2 | a0001 | c0005 | t0001 | g0251 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0145 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0139 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0154 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01099 | hp1 | a0001 | c0003 | t0002 | g0138 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0214 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0153 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0146 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0131 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01257 | hp1 | a0001 | c0003 | t0002 | g0140 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0143 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0232 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0279 | EUR | IBS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0285 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0157 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0282 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0284 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02148 | hp2 | a0004 | c0013 | t0001 | g0239 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | CDX | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0188 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0205 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0238 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02293 | hp2 | a0001 | c0002 | t0005 | g0281 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0160 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0130 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0156 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02683 | hp2 | a0001 | c0003 | t0002 | g0155 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02717 | hp2 | a0003 | c0006 | t0001 | g0275 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0151 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0142 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02922 | hp1 | a0001 | c0008 | t0002 | g0149 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0290 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0144 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0141 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03139 | hp1 | a0005 | c0011 | t0001 | g0166 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0249 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0273 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0006 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0215 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0250 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0286 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | STU | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18944 | hp1 | a0002 | c0004 | t0001 | g0173 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18959 | hp1 | a0006 | c0009 | t0001 | g0248 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18959 | hp2 | a0001 | c0007 | t0001 | g0277 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18968 | hp1 | a0002 | c0004 | t0001 | g0177 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18969 | hp2 | a0002 | c0004 | t0001 | g0183 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18971 | hp2 | a0002 | c0004 | t0001 | g0180 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18974 | hp1 | a0002 | c0004 | t0001 | g0175 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18979 | hp2 | a0001 | c0005 | t0001 | g0222 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18984 | hp2 | a0002 | c0004 | t0001 | g0179 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18986 | hp2 | a0002 | c0004 | t0001 | g0181 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18987 | hp1 | a0001 | c0005 | t0001 | g0267 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19000 | hp2 | a0002 | c0004 | t0001 | g0184 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19002 | hp2 | a0007 | c0012 | t0001 | g0291 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19006 | hp1 | a0001 | c0010 | t0001 | g0110 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19006 | hp2 | a0002 | c0004 | t0001 | g0174 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19007 | hp1 | a0002 | c0004 | t0001 | g0176 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | LWK | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | LWK | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19043 | hp2 | a0008 | c0014 | t0001 | g0272 | AFR | LWK | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19067 | hp2 | a0002 | c0004 | t0001 | g0182 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19084 | hp1 | a0002 | c0004 | t0001 | g0178 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19240 | hp1 | a0003 | c0006 | t0001 | g0276 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | ASW | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02486 | hp2 | a0001 | c0008 | t0002 | g0150 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| HG06807 | hp2 | a0001 | c0002 | t0006 | g0274 | AFR | USA | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0148 | REF | REF | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0203 | REF | REF | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:45584177 | G | C | 1 | a0002 | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
missense_variant | MODERATE | c.31G>C | p.Val11Leu | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/15 | 137/3225 | 31/2367 | 11/788 | chr1 | 45584177 | |||
| chr1:45607518 | C | G | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.607C>G | p.Leu203Val | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 713/3225 | 607/2367 | 203/788 | chr1 | 45607518 | |||
| chr1:45607814 | C | A | 1 | a0006 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.903C>A | p.Asp301Glu | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1009/3225 | 903/2367 | 301/788 | chr1 | 45607814 | |||
| chr1:45607845 | G | A | 1 | a0007 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.934G>A | p.Asp312Asn | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1040/3225 | 934/2367 | 312/788 | chr1 | 45607845 | |||
| chr1:45615137 | C | G | 1 | a0004 | 1 | HG02148.hp2 | missense_variant | MODERATE | c.1791C>G | p.Asn597Lys | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 10/15 | 1897/3225 | 1791/2367 | 597/788 | chr1 | 45615137 | |||
| chr1:45616389 | C | G | 1 | a0005 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.2075C>G | p.Ser692Cys | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 12/15 | 2181/3225 | 2075/2367 | 692/788 | chr1 | 45616389 | |||
| chr1:45617554 | C | T | 1 | a0003 | 2 | HG02717.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.2249C>T | p.Pro750Leu | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 14/15 | 2355/3225 | 2249/2367 | 750/788 | chr1 | 45617554 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:45607496 | A | C | 1 | a0001c0008 | 2 | HG02486.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.585A>C | p.Pro195Pro | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 691/3225 | 585/2367 | 195/788 | chr1 | 45607496 | |||
| chr1:45607817 | G | A | 3 | a0001c0001 a0001c0010 a0005c0011 |
149 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
synonymous_variant | LOW | c.906G>A | p.Pro302Pro | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1012/3225 | 906/2367 | 302/788 | chr1 | 45607817 | |||
| chr1:45607925 | A | G | 2 | a0001c0007 a0002c0004 |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
synonymous_variant | LOW | c.1014A>G | p.Val338Val | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1120/3225 | 1014/2367 | 338/788 | chr1 | 45607925 | |||
| chr1:45608084 | T | C | 1 | a0001c0010 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.1173T>C | p.Pro391Pro | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1279/3225 | 1173/2367 | 391/788 | chr1 | 45608084 | |||
| chr1:45613182 | A | G | 5 | a0001c0001 a0001c0003 a0001c0008 others(2): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
synonymous_variant | LOW | c.1440A>G | p.Ser480Ser | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/15 | 1546/3225 | 1440/2367 | 480/788 | chr1 | 45613182 | |||
| chr1:45613212 | C | T | 5 | a0001c0001 a0001c0003 a0001c0008 others(2): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
synonymous_variant | LOW | c.1470C>T | p.Thr490Thr | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/15 | 1576/3225 | 1470/2367 | 490/788 | chr1 | 45613212 | |||
| chr1:45614326 | C | T | 1 | a0001c0005 | 3 | HG00673.hp2 NA18979.hp2 NA18987.hp1 |
synonymous_variant | LOW | c.1626C>T | p.Ala542Ala | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/15 | 1732/3225 | 1626/2367 | 542/788 | chr1 | 45614326 | |||
| chr1:45616658 | C | T | 1 | a0002c0004 | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
synonymous_variant | LOW | c.2112C>T | p.Ser704Ser | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/15 | 2218/3225 | 2112/2367 | 704/788 | chr1 | 45616658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:45584086 | A | C | 1 | a0001c0002t0006 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/15 | 61 | chr1 | 45584086 | ||||||
| chr1:45618370 | T | C | 1 | a0001c0002t0005 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*229T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 15/15 | 229 | chr1 | 45618370 | ||||||
| chr1:45618412 | T | C | 1 | a0001c0001t0003 | 5 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*271T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 15/15 | 271 | chr1 | 45618412 | ||||||
| chr1:45618599 | C | T | 1 | a0001c0001t0004 | 2 | HG03453.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*458C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 15/15 | 458 | chr1 | 45618599 | ||||||
| chr1:45618711 | G | T | 2 | a0001c0003t0002 a0001c0008t0002 |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 15/15 | 570 | chr1 | 45618711 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:45584229 | A | C | 1 | a0001c0002t0001g0292 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.59+24A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584229 | |||||||
| chr1:45584267 | G | T | 1 | a0007c0012t0001g0291 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.59+62G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584267 | |||||||
| chr1:45584332 | TTCGG | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.59+128_59+131delTC others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584332 | |||||||
| chr1:45584422 | C | T | 1 | a0001c0002t0001g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.59+217C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584422 | |||||||
| chr1:45584462 | T | A | 1 | a0001c0001t0003g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59+257T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584462 | |||||||
| chr1:45584473 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59+268C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584473 | |||||||
| chr1:45584597 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 |
3 | NA18963.hp1 NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.59+392C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584597 | |||||||
| chr1:45584605 | A | G | 4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
4 | HG03490.hp1 HG03654.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+400A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584605 | |||||||
| chr1:45584779 | C | G | 9 | a0001c0002t0001g0280 a0001c0002t0001g0282 a0001c0002t0001g0283 others(6): Show |
9 | HG01099.hp2 HG01109.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+574C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584779 | |||||||
| chr1:45584795 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.59+590C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584795 | |||||||
| chr1:45584889 | G | T | 23 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0003t0002g0006 others(20): Show |
24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.59+684G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584889 | |||||||
| chr1:45584929 | G | A | 2 | a0001c0001t0001g0167 a0005c0011t0001g0166 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.59+724G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584929 | |||||||
| chr1:45585084 | G | T | 1 | a0001c0002t0001g0279 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.59+879G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585084 | |||||||
| chr1:45585159 | T | C | 5 | a0001c0002t0001g0168 a0001c0002t0001g0169 a0001c0002t0001g0170 others(2): Show |
5 | NA18962.hp2 NA18977.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+954T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585159 | |||||||
| chr1:45585262 | T | A | 1 | a0001c0001t0001g0011 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.59+1057T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585262 | |||||||
| chr1:45585349 | A | G | 1 | a0001c0003t0002g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.59+1144A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585349 | |||||||
| chr1:45585381 | G | A | 3 | a0001c0003t0002g0138 a0001c0003t0002g0139 a0001c0003t0002g0140 |
3 | HG00735.hp2 HG01099.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.59+1176G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585381 | |||||||
| chr1:45585474 | A | G | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.59+1269A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585474 | |||||||
| chr1:45585744 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG01081.hp1 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.59+1539C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585744 | |||||||
| chr1:45585803 | T | C | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+1598T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585803 | |||||||
| chr1:45585885 | C | T | 4 | a0001c0001t0001g0167 a0003c0006t0001g0275 a0003c0006t0001g0276 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+1680C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585885 | |||||||
| chr1:45585947 | T | G | 1 | a0001c0002t0001g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59+1742T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585947 | |||||||
| chr1:45586043 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.59+1838G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586043 | |||||||
| chr1:45586069 | T | C | 2 | a0001c0002t0001g0186 a0001c0002t0001g0187 |
2 | NA19009.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.59+1864T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586069 | |||||||
| chr1:45586239 | C | CGT | 19 | a0001c0002t0001g0168 a0001c0002t0001g0169 a0001c0002t0001g0233 others(16): Show |
19 | HG01099.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.59+2078_59+2079dup others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | C | CGTGT | 16 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0172 others(13): Show |
16 | HG00408.hp1 HG00673.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.59+2076_59+2079dup others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | C | CGTGTGT | 6 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(3): Show |
6 | HG00544.hp2 HG01346.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.59+2074_59+2079dup others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | C | CGTGTGTG others(1): Show |
5 | a0001c0002t0001g0266 a0001c0002t0001g0268 a0001c0002t0001g0269 others(2): Show |
5 | HG02040.hp1 NA18522.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+2072_59+2079dup others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | C | CGTGTGTG others(3): Show |
1 | a0001c0002t0001g0271 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.59+2070_59+2079dup others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | C | CGTGTGTG others(7): Show |
2 | a0001c0002t0001g0273 a0008c0014t0001g0272 |
2 | HG03490.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.59+2066_59+2079dup others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | C | CGTGTGTG others(9): Show |
1 | a0001c0002t0006g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59+2064_59+2079dup others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | C | CGTGTGTG others(29): Show |
1 | a0003c0006t0001g0276 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.59+2044_59+2079dup others(36): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | CGT | C | 10 | a0001c0002t0001g0186 a0001c0002t0001g0193 a0001c0002t0001g0194 others(7): Show |
10 | HG01975.hp1 HG01975.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2078_59+2079del others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | CGTGT | C | 5 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0190 others(2): Show |
5 | HG01891.hp1 HG01981.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+2076_59+2079del others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | CGTGTGTG others(9): Show |
C | 3 | a0001c0003t0002g0151 a0001c0003t0002g0152 a0001c0003t0002g0160 |
3 | HG00323.hp2 HG02602.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.59+2064_59+2079del others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586239 | CGTGTGTG others(11): Show |
C | 11 | a0001c0003t0002g0006 a0001c0003t0002g0138 a0001c0003t0002g0141 others(8): Show |
12 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.59+2062_59+2079del others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | ||||||
| chr1:45586261 | TGTGTGTG others(16): Show |
T | 1 | a0001c0001t0001g0159 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.59+2080_59+2102del others(23): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586261 | ||||||
| chr1:45586263 | TGTGTGTG others(14): Show |
T | 1 | a0001c0001t0001g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.59+2080_59+2100del others(21): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586263 | ||||||
| chr1:45586264 | GTGTGTGT others(15): Show |
G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0001g0126 |
3 | HG02486.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.59+2060_59+2081del others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586264 | |||||||
| chr1:45586264 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0001g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.59+2060_59+2083del others(24): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586264 | |||||||
| chr1:45586266 | GTGTGTGT others(25): Show |
G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0105 a0001c0001t0001g0108 |
3 | NA18979.hp1 NA18986.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.59+2062_59+2093del others(32): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586266 | |||||||
| chr1:45586267 | TGTGTGTG others(10): Show |
T | 1 | a0001c0003t0002g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.59+2080_59+2096del others(17): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586267 | ||||||
| chr1:45586268 | GTGTGTGT others(11): Show |
G | 5 | a0001c0003t0002g0139 a0001c0003t0002g0140 a0001c0003t0002g0155 others(2): Show |
5 | HG00735.hp2 HG01257.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+2064_59+2081del others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586268 | |||||||
| chr1:45586270 | GTGTGTGT others(9): Show |
G | 2 | a0001c0003t0001g0130 a0001c0003t0001g0131 |
2 | HG01243.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.59+2066_59+2081del others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586270 | |||||||
| chr1:45586271 | TGTGTGTG others(6): Show |
T | 2 | a0001c0002t0001g0279 a0001c0003t0002g0153 |
2 | HG01167.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.59+2080_59+2092del others(13): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586271 | ||||||
| chr1:45586272 | GTGTGTGT others(7): Show |
G | 3 | a0001c0002t0001g0221 a0001c0002t0001g0225 a0001c0003t0002g0214 |
3 | HG01106.hp1 HG01192.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.59+2068_59+2081del others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586272 | |||||||
| chr1:45586272 | GTGTGTGT others(19): Show |
G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG00280.hp2 NA18963.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+2068_59+2093del others(26): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586272 | |||||||
| chr1:45586273 | TGTGTGTG others(4): Show |
T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0028 others(4): Show |
7 | HG01109.hp1 HG01123.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.59+2080_59+2090del others(11): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586273 | ||||||
| chr1:45586274 | GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.59+2070_59+2087del others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586274 | |||||||
| chr1:45586275 | TGTGTGTG others(2): Show |
T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0025 others(19): Show |
22 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.59+2080_59+2088del others(9): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586275 | ||||||
| chr1:45586276 | GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0001g0087 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.59+2072_59+2093del others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586276 | |||||||
| chr1:45586277 | TGTGTGTG | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(13): Show |
16 | HG01069.hp2 HG01167.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.59+2080_59+2086del others(7): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586277 | ||||||
| chr1:45586278 | GTGTGTGG others(13): Show |
G | 1 | a0001c0001t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59+2074_59+2093del others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586278 | |||||||
| chr1:45586279 | T | TG | 3 | a0001c0002t0001g0290 a0002c0004t0001g0177 a0002c0004t0001g0180 |
3 | HG02922.hp2 NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.59+2075dupG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586279 | ||||||
| chr1:45586279 | TGTGTG | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(12): Show |
15 | HG00408.hp2 HG00738.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.59+2080_59+2084del others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586279 | ||||||
| chr1:45586280 | GTGTGGTG others(11): Show |
G | 8 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0090 others(5): Show |
8 | HG01243.hp1 HG02647.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.59+2076_59+2093del others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586280 | |||||||
| chr1:45586281 | T | TGGTGTGT others(57): Show |
4 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0183 others(1): Show |
4 | NA18944.hp1 NA18969.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2077_59+2078ins others(64): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586281 | ||||||
| chr1:45586281 | TGTG | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(7): Show |
10 | HG02071.hp2 HG02135.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2080_59+2082del others(3): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586281 | ||||||
| chr1:45586281 | TGTGGTGT others(21): Show |
T | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.59+2080_59+2107del others(28): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586281 | ||||||
| chr1:45586282 | GTGGTGTG others(9): Show |
G | 6 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0085 others(3): Show |
6 | HG00642.hp1 HG00673.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.59+2078_59+2093del others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586282 | |||||||
| chr1:45586283 | TG | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(17): Show |
20 | HG01074.hp2 HG01081.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.59+2080delG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586283 | ||||||
| chr1:45586284 | G | GGT | 3 | a0001c0002t0001g0211 a0001c0002t0001g0212 a0001c0002t0001g0227 |
3 | HG01258.hp2 HG04204.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.59+2103_59+2104dup others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586284 | ||||||
| chr1:45586284 | G | GGTGTGTG others(60): Show |
1 | a0002c0004t0001g0181 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.59+2091_59+2092ins others(67): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586284 | ||||||
| chr1:45586284 | G | GT | 15 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(12): Show |
15 | HG00438.hp1 HG02004.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(1): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTCACCCA others(45): Show |
1 | a0001c0007t0001g0277 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(52): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGGTGTG others(62): Show |
3 | a0002c0004t0001g0175 a0002c0004t0001g0176 a0002c0004t0001g0178 |
3 | NA18974.hp1 NA19007.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(69): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0102 others(6): Show |
9 | HG00642.hp2 HG00735.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(3): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTCACC others(47): Show |
1 | a0001c0007t0001g0278 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(54): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGT | 10 | a0001c0001t0001g0005 a0001c0001t0001g0078 a0001c0001t0001g0083 others(7): Show |
10 | HG01928.hp1 HG02572.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGG others(66): Show |
1 | a0002c0004t0001g0182 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(73): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT | 3 | a0001c0001t0001g0082 a0001c0001t0001g0116 a0001c0001t0001g0289 |
3 | NA19043.hp1 NA19066.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(7): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT others(55): Show |
2 | a0002c0004t0001g0177 a0002c0004t0001g0180 |
2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(62): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT others(2): Show |
3 | a0001c0001t0001g0088 a0001c0001t0001g0100 a0001c0001t0003g0092 |
3 | HG00609.hp2 HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(9): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT others(55): Show |
1 | a0002c0004t0001g0179 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(62): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0001g0099 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(11): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT others(6): Show |
2 | a0001c0001t0003g0084 a0001c0002t0001g0200 |
2 | HG00609.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(13): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT others(8): Show |
1 | a0001c0002t0001g0219 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(15): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT others(10): Show |
1 | a0001c0010t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(17): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT others(14): Show |
1 | a0001c0001t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(21): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | G | GTGTGTGT others(24): Show |
1 | a0003c0006t0001g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(31): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | |||||||
| chr1:45586284 | GGTGTGTG others(7): Show |
G | 2 | a0001c0001t0001g0080 a0001c0001t0003g0007 |
2 | HG02572.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.59+2091_59+2104del others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586284 | ||||||
| chr1:45586286 | T | G | 1 | a0001c0002t0006g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59+2081T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586286 | |||||||
| chr1:45586297 | GT | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
84 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.59+2093delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586297 | |||||||
| chr1:45586298 | T | TG | 23 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0078 others(20): Show |
24 | HG00735.hp1 HG01928.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.59+2094dupG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586298 | ||||||
| chr1:45586306 | T | G | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.59+2101T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586306 | |||||||
| chr1:45586308 | TG | T | 3 | a0001c0001t0001g0167 a0001c0002t0001g0232 a0001c0002t0001g0259 |
3 | HG01433.hp1 HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.59+2105delG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586308 | ||||||
| chr1:45586518 | G | A | 1 | a0001c0002t0001g0170 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.59+2313G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586518 | |||||||
| chr1:45586548 | C | G | 2 | a0001c0001t0004g0133 a0001c0001t0004g0134 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.59+2343C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586548 | |||||||
| chr1:45586554 | G | A | 1 | a0001c0002t0006g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59+2349G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586554 | |||||||
| chr1:45586568 | C | T | 1 | a0001c0007t0001g0278 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.59+2363C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586568 | |||||||
| chr1:45586920 | A | C | 1 | a0001c0002t0001g0246 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.59+2715A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586920 | |||||||
| chr1:45586924 | C | G | 1 | a0001c0002t0001g0231 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.59+2719C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586924 | |||||||
| chr1:45587089 | C | A | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.59+2884C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587089 | |||||||
| chr1:45587177 | C | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.59+2972C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587177 | |||||||
| chr1:45587185 | G | GT | 16 | a0001c0001t0001g0076 a0001c0001t0001g0289 a0001c0002t0001g0230 others(13): Show |
16 | NA18944.hp1 NA18955.hp2 NA18968.hp1 others(13): Show |
intron_variant | MODIFIER | c.59+2989dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587185 | ||||||
| chr1:45587291 | A | G | 3 | a0001c0001t0001g0132 a0001c0003t0001g0130 a0001c0003t0001g0131 |
3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.59+3086A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587291 | |||||||
| chr1:45587425 | C | T | 3 | a0001c0001t0001g0132 a0001c0003t0001g0130 a0001c0003t0001g0131 |
3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.59+3220C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587425 | |||||||
| chr1:45587487 | C | A | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.59+3282C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587487 | |||||||
| chr1:45587661 | C | CATATATA others(11): Show |
1 | a0001c0001t0001g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.59+3466_59+3483dup others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | ||||||
| chr1:45587661 | C | CATATATA others(15): Show |
2 | a0001c0008t0002g0149 a0001c0008t0002g0150 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.59+3462_59+3483dup others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | ||||||
| chr1:45587661 | C | CATATATA others(19): Show |
1 | a0001c0002t0001g0285 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.59+3458_59+3483dup others(26): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | ||||||
| chr1:45587661 | C | CATATATA others(21): Show |
1 | a0001c0002t0001g0259 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(28): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | ||||||
| chr1:45587661 | CAT | C | 4 | a0001c0001t0004g0133 a0001c0001t0004g0134 a0001c0002t0001g0201 others(1): Show |
4 | HG02074.hp1 HG02083.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3482_59+3483del others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | ||||||
| chr1:45587661 | CATATATA others(1): Show |
C | 3 | a0001c0002t0001g0247 a0001c0007t0001g0277 a0001c0007t0001g0278 |
3 | HG00544.hp1 HG02300.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.59+3476_59+3483del others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | ||||||
| chr1:45587685 | T | A | 2 | a0001c0002t0001g0201 a0001c0002t0001g0202 |
2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.59+3480T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587685 | |||||||
| chr1:45587687 | T | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
13 | HG01074.hp2 HG01934.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+3482T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587687 | |||||||
| chr1:45587687 | T | TAA | 3 | a0001c0001t0001g0012 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG01928.hp1 HG03098.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.59+3483_59+3484dup others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATAA | 4 | a0001c0003t0002g0139 a0001c0003t0002g0140 a0001c0003t0002g0143 others(1): Show |
4 | HG00735.hp2 HG01257.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(3): Show |
12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(9): Show |
12 | HG00438.hp2 HG00733.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(5): Show |
26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
28 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(7): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
25 | HG00609.hp2 HG00642.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(15): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(9): Show |
16 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0043 others(13): Show |
18 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(11): Show |
30 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(27): Show |
30 | HG00323.hp2 HG00733.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(13): Show |
1 | a0001c0002t0001g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(12): Show |
1 | a0001c0002t0001g0172 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(19): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(13): Show |
13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0111 others(10): Show |
13 | HG02040.hp2 HG02647.hp2 HG03486.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(15): Show |
29 | a0001c0001t0001g0005 a0001c0001t0001g0056 a0001c0001t0001g0057 others(26): Show |
30 | HG00673.hp2 HG01106.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(17): Show |
21 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(18): Show |
21 | HG00408.hp1 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(24): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(19): Show |
25 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(22): Show |
25 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(26): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(21): Show |
22 | a0001c0001t0001g0064 a0001c0001t0001g0122 a0001c0001t0001g0123 others(19): Show |
22 | HG00609.hp1 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(28): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(22): Show |
1 | a0001c0002t0001g0225 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(29): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(23): Show |
20 | a0001c0001t0001g0011 a0001c0001t0001g0065 a0001c0001t0001g0066 others(17): Show |
20 | HG00408.hp2 HG01517.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(30): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(25): Show |
7 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(4): Show |
7 | HG01975.hp2 HG02080.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(32): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(27): Show |
4 | a0001c0001t0001g0159 a0001c0002t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG01069.hp1 HG01361.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(34): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(28): Show |
1 | a0001c0002t0001g0257 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(35): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(29): Show |
2 | a0001c0001t0001g0073 a0002c0004t0001g0184 |
2 | NA18947.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(36): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(30): Show |
1 | a0001c0001t0001g0074 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(37): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(31): Show |
1 | a0001c0002t0001g0229 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(38): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587687 | T | TATATATA others(35): Show |
1 | a0001c0001t0001g0075 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(42): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | ||||||
| chr1:45587709 | G | A | 1 | a0001c0002t0001g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.59+3504G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587709 | |||||||
| chr1:45587840 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.60-3383C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587840 | |||||||
| chr1:45587841 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.60-3382C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587841 | |||||||
| chr1:45587855 | A | G | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-3368A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587855 | |||||||
| chr1:45587869 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.60-3354G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587869 | |||||||
| chr1:45587877 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.60-3346C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587877 | |||||||
| chr1:45587902 | C | T | 1 | a0001c0002t0001g0209 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.60-3321C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587902 | |||||||
| chr1:45587979 | G | A | 1 | a0001c0003t0002g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.60-3244G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587979 | |||||||
| chr1:45588011 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.60-3212G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588011 | |||||||
| chr1:45588076 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.60-3147C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588076 | |||||||
| chr1:45588357 | C | G | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-2866C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588357 | |||||||
| chr1:45588383 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.60-2840C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588383 | |||||||
| chr1:45588463 | T | A | 1 | a0001c0001t0003g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60-2760T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588463 | |||||||
| chr1:45588466 | C | T | 2 | a0001c0001t0001g0167 a0005c0011t0001g0166 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.60-2757C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588466 | |||||||
| chr1:45588665 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.60-2558C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588665 | |||||||
| chr1:45588668 | G | A | 1 | a0001c0003t0001g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60-2555G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588668 | |||||||
| chr1:45588814 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.60-2409A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588814 | |||||||
| chr1:45588957 | G | GTGTT | 15 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0190 others(12): Show |
15 | HG00733.hp1 HG01106.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.60-2242_60-2239dup others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | ||||||
| chr1:45588957 | G | GTGTTTGT others(5): Show |
4 | a0001c0002t0001g0195 a0001c0002t0001g0217 a0001c0002t0001g0218 others(1): Show |
4 | HG00738.hp2 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-2250_60-2239dup others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | ||||||
| chr1:45588957 | G | GTGTTTGT others(9): Show |
1 | a0001c0002t0001g0191 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.60-2254_60-2239dup others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | ||||||
| chr1:45588957 | GTGTT | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.60-2242_60-2239del others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | ||||||
| chr1:45588957 | GTGTTTGT others(1): Show |
G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0002t0001g0266 others(2): Show |
5 | HG00544.hp1 HG02040.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-2246_60-2239del others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | ||||||
| chr1:45589064 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.60-2159A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589064 | |||||||
| chr1:45589105 | G | A | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-2118G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589105 | |||||||
| chr1:45589320 | C | T | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.60-1903C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589320 | |||||||
| chr1:45589444 | G | A | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.60-1779G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589444 | |||||||
| chr1:45589514 | A | G | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.60-1709A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589514 | |||||||
| chr1:45589629 | G | T | 1 | a0001c0003t0002g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.60-1594G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589629 | |||||||
| chr1:45589889 | G | A | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-1334G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589889 | |||||||
| chr1:45589928 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.60-1295C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589928 | |||||||
| chr1:45589957 | A | G | 2 | a0001c0003t0002g0141 a0001c0003t0002g0142 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.60-1266A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589957 | |||||||
| chr1:45589998 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0035 |
3 | HG01081.hp2 HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-1225G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589998 | |||||||
| chr1:45590015 | T | C | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.60-1208T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590015 | |||||||
| chr1:45590022 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.60-1201C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590022 | |||||||
| chr1:45590099 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.60-1124T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590099 | |||||||
| chr1:45590180 | C | A | 1 | a0001c0002t0001g0230 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.60-1043C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590180 | |||||||
| chr1:45590186 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.60-1037A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590186 | |||||||
| chr1:45590318 | G | A | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.60-905G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590318 | |||||||
| chr1:45590359 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0118 |
2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.60-864C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590359 | |||||||
| chr1:45590371 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.60-852G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590371 | |||||||
| chr1:45590405 | A | G | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-818A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590405 | |||||||
| chr1:45590460 | A | G | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60-763A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590460 | |||||||
| chr1:45590473 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60-750C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590473 | |||||||
| chr1:45590480 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.60-743C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590480 | |||||||
| chr1:45590504 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0034 others(2): Show |
5 | HG01943.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-719C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590504 | |||||||
| chr1:45590528 | C | T | 3 | a0001c0001t0001g0132 a0001c0003t0001g0130 a0001c0003t0001g0131 |
3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.60-695C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590528 | |||||||
| chr1:45590549 | C | CA | 14 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0047 others(11): Show |
14 | HG00738.hp2 HG01346.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.60-656dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590549 | ||||||
| chr1:45590682 | C | CT | 34 | a0001c0001t0001g0053 a0001c0001t0001g0074 a0001c0001t0001g0077 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.60-520dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590682 | ||||||
| chr1:45590682 | C | CTT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.60-521_60-520dupTT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590682 | ||||||
| chr1:45590682 | C | CTTT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0054 others(9): Show |
12 | HG00673.hp1 HG00738.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.60-522_60-520dupTT others(1): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590682 | ||||||
| chr1:45590682 | CT | C | 42 | a0001c0001t0001g0132 a0001c0001t0001g0289 a0001c0002t0001g0185 others(39): Show |
42 | HG00438.hp2 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.60-520delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590682 | ||||||
| chr1:45590709 | G | A | 3 | a0001c0002t0001g0238 a0001c0002t0001g0249 a0001c0002t0001g0290 |
3 | HG02280.hp1 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.60-514G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590709 | |||||||
| chr1:45590744 | T | TA | 5 | a0001c0001t0001g0036 a0001c0001t0001g0054 a0001c0001t0001g0080 others(2): Show |
5 | HG00673.hp1 NA18945.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-472dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590744 | ||||||
| chr1:45590866 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0001g0125 others(1): Show |
4 | HG02486.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-357A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590866 | |||||||
| chr1:45591386 | G | A | 3 | a0001c0002t0001g0238 a0001c0002t0001g0249 a0001c0002t0001g0290 |
3 | HG02280.hp1 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.107+116G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591386 | |||||||
| chr1:45591470 | C | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01069.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.107+200C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591470 | |||||||
| chr1:45591472 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.107+202A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591472 | |||||||
| chr1:45591554 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0001g0125 others(1): Show |
4 | HG02486.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+284A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591554 | |||||||
| chr1:45591613 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.107+343T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591613 | |||||||
| chr1:45591730 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+460G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591730 | |||||||
| chr1:45591881 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+611T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591881 | |||||||
| chr1:45592048 | C | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+778C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592048 | |||||||
| chr1:45592054 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.107+784C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592054 | |||||||
| chr1:45592137 | A | C | 1 | a0001c0002t0001g0205 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.107+867A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592137 | |||||||
| chr1:45592145 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+875C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592145 | |||||||
| chr1:45592181 | C | T | 1 | a0005c0011t0001g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.107+911C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592181 | |||||||
| chr1:45592291 | T | A | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+1021T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592291 | |||||||
| chr1:45592571 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.107+1301A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592571 | |||||||
| chr1:45592605 | C | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.107+1335C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592605 | |||||||
| chr1:45592748 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+1478C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592748 | |||||||
| chr1:45592753 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.107+1483G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592753 | |||||||
| chr1:45592754 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.107+1484A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592754 | |||||||
| chr1:45592853 | T | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0001g0125 others(1): Show |
4 | HG02486.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+1583T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592853 | |||||||
| chr1:45592883 | G | A | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+1613G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592883 | |||||||
| chr1:45592915 | A | C | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+1645A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592915 | |||||||
| chr1:45593086 | T | C | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+1816T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593086 | |||||||
| chr1:45593218 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+1948G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593218 | |||||||
| chr1:45593252 | G | A | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+1982G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593252 | |||||||
| chr1:45593462 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0135 others(2): Show |
5 | HG01081.hp1 HG01168.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+2192G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593462 | |||||||
| chr1:45593510 | G | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
11 | HG02083.hp1 HG02602.hp2 HG03834.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+2240G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593510 | |||||||
| chr1:45593533 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.107+2263C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593533 | |||||||
| chr1:45593535 | C | CA | 43 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0041 others(40): Show |
43 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.107+2285dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593535 | ||||||
| chr1:45593535 | C | CAA | 13 | a0001c0001t0001g0094 a0001c0001t0001g0125 a0001c0007t0001g0278 others(10): Show |
13 | HG00544.hp1 HG02486.hp1 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.107+2284_107+2285d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593535 | ||||||
| chr1:45593535 | CA | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0069 others(14): Show |
17 | HG00408.hp2 HG00733.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.107+2285delA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593535 | ||||||
| chr1:45593663 | CT | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0114 a0001c0001t0001g0119 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+2405delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593663 | ||||||
| chr1:45593684 | C | T | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+2414C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593684 | |||||||
| chr1:45593710 | T | C | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+2440T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593710 | |||||||
| chr1:45593855 | CA | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.107+2597delA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593855 | ||||||
| chr1:45593866 | AAT | A | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.107+2597_107+2598d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593866 | |||||||
| chr1:45593868 | T | A | 1 | a0001c0002t0001g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107+2598T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593868 | |||||||
| chr1:45593941 | A | G | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+2671A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593941 | |||||||
| chr1:45593996 | T | C | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+2726T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593996 | |||||||
| chr1:45594064 | C | T | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+2794C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594064 | |||||||
| chr1:45594163 | T | TA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.107+2899dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45594163 | ||||||
| chr1:45594174 | C | A | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+2904C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594174 | |||||||
| chr1:45594190 | G | T | 2 | a0001c0001t0004g0133 a0001c0001t0004g0134 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.107+2920G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594190 | |||||||
| chr1:45594201 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+2931C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594201 | |||||||
| chr1:45594258 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+2988G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594258 | |||||||
| chr1:45594265 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG01891.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.107+2995G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594265 | |||||||
| chr1:45594323 | C | CA | 7 | a0001c0002t0001g0187 a0001c0002t0001g0206 a0001c0002t0001g0233 others(4): Show |
7 | HG00544.hp1 HG01175.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+3065dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45594323 | ||||||
| chr1:45594568 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+3298G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594568 | |||||||
| chr1:45594936 | A | G | 1 | a0001c0002t0001g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.107+3666A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594936 | |||||||
| chr1:45594991 | C | T | 2 | a0001c0001t0001g0167 a0005c0011t0001g0166 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.107+3721C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594991 | |||||||
| chr1:45595002 | T | C | 1 | a0001c0002t0001g0287 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.107+3732T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595002 | |||||||
| chr1:45595090 | A | G | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.107+3820A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595090 | |||||||
| chr1:45595127 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.107+3858_107+3859i others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595127 | ||||||
| chr1:45595127 | TTTTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.107+3859_107+3868d others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595127 | ||||||
| chr1:45595127 | TTTTGTGT others(11): Show |
T | 1 | a0003c0006t0001g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.107+3859_107+3876d others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595127 | ||||||
| chr1:45595127 | TTTTGTGT others(15): Show |
T | 1 | a0003c0006t0001g0276 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107+3859_107+3880d others(24): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595127 | ||||||
| chr1:45595128 | TTTGTG | T | 3 | a0001c0001t0001g0009 a0001c0002t0001g0190 a0001c0002t0001g0246 |
3 | HG02055.hp2 NA19002.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.107+3860_107+3864d others(7): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595128 | ||||||
| chr1:45595129 | T | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0066 a0001c0001t0001g0073 others(4): Show |
7 | HG00280.hp1 HG02132.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+3859T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595129 | |||||||
| chr1:45595129 | T | TTG | 21 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0031 others(18): Show |
22 | HG00099.hp2 HG00408.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.107+3917_107+3918d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | T | TTGTG | 12 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0061 others(9): Show |
12 | HG00438.hp1 HG01099.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+3915_107+3918d others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | T | TTGTGTG | 14 | a0001c0001t0001g0025 a0001c0001t0001g0036 a0001c0001t0001g0044 others(11): Show |
14 | HG00323.hp1 HG01346.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.107+3913_107+3918d others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | T | TTGTGTGT others(1): Show |
11 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0085 others(8): Show |
11 | HG00673.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+3911_107+3918d others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | T | TTGTGTGT others(3): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0024 others(4): Show |
7 | HG01109.hp1 HG03486.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+3909_107+3918d others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | T | TTGTGTGT others(5): Show |
2 | a0001c0001t0001g0017 a0001c0002t0001g0263 |
2 | HG00544.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.107+3907_107+3918d others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.107+3905_107+3918d others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.107+3903_107+3918d others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTG | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(36): Show |
40 | HG00438.hp2 HG00609.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.107+3917_107+3918d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTG | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0027 others(29): Show |
32 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.107+3915_107+3918d others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTG | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(28): Show |
31 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.107+3913_107+3918d others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(1): Show |
T | 22 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0063 others(19): Show |
22 | HG00609.hp2 HG00733.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.107+3911_107+3918d others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(3): Show |
T | 20 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0040 others(17): Show |
20 | HG00642.hp1 HG01891.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.107+3909_107+3918d others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(5): Show |
T | 3 | a0001c0001t0001g0067 a0001c0007t0001g0277 a0002c0004t0001g0177 |
3 | HG03239.hp1 NA18959.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.107+3907_107+3918d others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(7): Show |
T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0111 a0001c0002t0001g0238 others(1): Show |
4 | HG02280.hp1 HG03942.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+3905_107+3918d others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(9): Show |
T | 3 | a0001c0001t0001g0089 a0001c0003t0002g0146 a0004c0013t0001g0239 |
3 | HG01192.hp1 HG02148.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.107+3903_107+3918d others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(11): Show |
T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0167 a0001c0002t0001g0269 |
3 | HG02258.hp2 HG02735.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.107+3901_107+3918d others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(13): Show |
T | 2 | a0001c0001t0001g0128 a0001c0002t0001g0250 |
2 | HG03710.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.107+3899_107+3918d others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(15): Show |
T | 3 | a0001c0002t0001g0226 a0001c0002t0001g0227 a0001c0002t0001g0252 |
3 | HG02451.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.107+3897_107+3918d others(24): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(19): Show |
T | 1 | a0001c0002t0001g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107+3893_107+3918d others(28): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595129 | TTGTGTGT others(31): Show |
T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG01891.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.107+3881_107+3918d others(40): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | ||||||
| chr1:45595234 | T | C | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.107+3964T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595234 | |||||||
| chr1:45595434 | T | C | 2 | a0001c0001t0004g0133 a0001c0001t0004g0134 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.107+4164T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595434 | |||||||
| chr1:45595452 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+4182A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595452 | |||||||
| chr1:45595639 | T | C | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+4369T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595639 | |||||||
| chr1:45595650 | A | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+4380A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595650 | |||||||
| chr1:45595850 | C | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+4580C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595850 | |||||||
| chr1:45595944 | T | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+4674T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595944 | |||||||
| chr1:45596155 | G | A | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+4885G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596155 | |||||||
| chr1:45596206 | G | C | 2 | a0001c0001t0001g0167 a0005c0011t0001g0166 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.107+4936G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596206 | |||||||
| chr1:45596304 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.107+5034C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596304 | |||||||
| chr1:45596376 | T | C | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+5106T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596376 | |||||||
| chr1:45596590 | C | T | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+5320C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596590 | |||||||
| chr1:45596741 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.107+5471C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596741 | |||||||
| chr1:45596745 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.107+5475A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596745 | |||||||
| chr1:45596771 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.108-5484C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596771 | |||||||
| chr1:45596847 | T | TG | 3 | a0001c0001t0001g0132 a0001c0003t0001g0130 a0001c0003t0001g0131 |
3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.108-5406dupG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45596847 | ||||||
| chr1:45596907 | T | C | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.108-5348T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596907 | |||||||
| chr1:45597237 | G | A | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-5018G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45597237 | |||||||
| chr1:45597281 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.108-4974T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45597281 | |||||||
| chr1:45597285 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0046 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.108-4970C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45597285 | |||||||
| chr1:45597298 | C | CTT | 111 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(108): Show |
111 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.108-4934_108-4933d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | ||||||
| chr1:45597298 | C | CTTT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
98 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.108-4935_108-4933d others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | ||||||
| chr1:45597298 | C | CTTTT | 35 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
36 | HG01346.hp2 HG01943.hp1 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.108-4936_108-4933d others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | ||||||
| chr1:45597298 | C | CTTTTT | 8 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0118 others(5): Show |
8 | HG02486.hp1 HG02622.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-4937_108-4933d others(7): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | ||||||
| chr1:45597298 | CT | C | 9 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(6): Show |
9 | NA18944.hp1 NA18969.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-4933delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | ||||||
| chr1:45597298 | CTTTTTTT others(1): Show |
C | 22 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0003t0002g0006 others(19): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.108-4940_108-4933d others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | ||||||
| chr1:45597786 | A | G | 1 | a0001c0003t0001g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108-4469A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45597786 | |||||||
| chr1:45598026 | T | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108-4229T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598026 | |||||||
| chr1:45598058 | A | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-4197A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598058 | |||||||
| chr1:45598163 | C | T | 3 | a0001c0002t0001g0168 a0001c0002t0001g0169 a0001c0002t0001g0171 |
3 | NA18977.hp2 NA18988.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.108-4092C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598163 | |||||||
| chr1:45598172 | C | CT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.108-4067dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45598172 | ||||||
| chr1:45598172 | C | CTT | 45 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0077 others(42): Show |
46 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.108-4068_108-4067d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45598172 | ||||||
| chr1:45598470 | T | C | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.108-3785T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598470 | |||||||
| chr1:45598490 | G | A | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.108-3765G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598490 | |||||||
| chr1:45599000 | G | A | 1 | a0001c0002t0001g0242 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.108-3255G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599000 | |||||||
| chr1:45599081 | G | A | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.108-3174G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599081 | |||||||
| chr1:45599090 | C | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-3165C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599090 | |||||||
| chr1:45599224 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0024 |
2 | HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.108-3031G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599224 | |||||||
| chr1:45599280 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.108-2975C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599280 | |||||||
| chr1:45599307 | C | G | 1 | a0001c0002t0001g0254 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.108-2948C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599307 | |||||||
| chr1:45599379 | C | T | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.108-2876C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599379 | |||||||
| chr1:45599568 | C | T | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.108-2687C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599568 | |||||||
| chr1:45599610 | A | T | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.108-2645A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599610 | |||||||
| chr1:45599619 | GGGTTTCA others(16): Show |
G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-2629_108-2607d others(25): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599619 | ||||||
| chr1:45599803 | C | T | 2 | a0003c0006t0001g0275 a0003c0006t0001g0276 |
2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2452C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599803 | |||||||
| chr1:45599820 | A | C | 3 | a0002c0004t0001g0174 a0002c0004t0001g0175 a0002c0004t0001g0176 |
3 | NA18974.hp1 NA19006.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.108-2435A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599820 | |||||||
| chr1:45599881 | A | G | 2 | a0001c0001t0001g0167 a0005c0011t0001g0166 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.108-2374A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599881 | |||||||
| chr1:45599951 | G | GTTTTTTT others(7): Show |
1 | a0005c0011t0001g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108-2303_108-2302i others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599951 | ||||||
| chr1:45599953 | A | AT | 43 | a0001c0001t0001g0046 a0001c0001t0001g0077 a0001c0001t0001g0119 others(40): Show |
43 | HG00408.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.108-2280dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | ||||||
| chr1:45599953 | A | ATT | 8 | a0001c0002t0001g0206 a0001c0002t0001g0220 a0001c0002t0001g0230 others(5): Show |
8 | HG00544.hp2 HG00673.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-2281_108-2280d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | ||||||
| chr1:45599953 | A | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0167 others(1): Show |
5 | HG02083.hp1 HG02258.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-2302A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599953 | |||||||
| chr1:45599953 | AT | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.108-2280delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | ||||||
| chr1:45599953 | ATT | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0089 others(4): Show |
7 | HG00642.hp1 HG01069.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-2281_108-2280d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | ||||||
| chr1:45599953 | ATTTT | A | 9 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0176 others(6): Show |
9 | NA18944.hp1 NA18969.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-2283_108-2280d others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | ||||||
| chr1:45600087 | A | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-2168A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600087 | |||||||
| chr1:45600203 | A | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-2052A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600203 | |||||||
| chr1:45600271 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG01891.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.108-1984T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600271 | |||||||
| chr1:45600281 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.108-1974C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600281 | |||||||
| chr1:45600326 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.108-1929T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600326 | |||||||
| chr1:45600369 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.108-1886T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600369 | |||||||
| chr1:45600618 | T | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-1637T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600618 | |||||||
| chr1:45600659 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.108-1596A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600659 | |||||||
| chr1:45600737 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.108-1518T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600737 | |||||||
| chr1:45600936 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.108-1319A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600936 | |||||||
| chr1:45601013 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0105 a0001c0001t0001g0108 |
3 | NA18979.hp1 NA18986.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.108-1242C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601013 | |||||||
| chr1:45601049 | A | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG01891.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.108-1206A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601049 | |||||||
| chr1:45601189 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.108-1066T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601189 | |||||||
| chr1:45601356 | A | G | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.108-899A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601356 | |||||||
| chr1:45601514 | A | G | 1 | a0001c0002t0001g0186 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.108-741A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601514 | |||||||
| chr1:45601591 | C | G | 3 | a0001c0002t0001g0185 a0001c0002t0001g0201 a0001c0002t0001g0202 |
3 | HG02015.hp2 HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.108-664C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601591 | |||||||
| chr1:45601597 | G | A | 25 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0004g0133 others(22): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.108-658G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601597 | |||||||
| chr1:45601678 | G | A | 1 | a0001c0002t0001g0205 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.108-577G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601678 | |||||||
| chr1:45601745 | A | AT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(117): Show |
124 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.108-482dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | ||||||
| chr1:45601745 | A | ATT | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(68): Show |
73 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.108-483_108-482dup others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | ||||||
| chr1:45601745 | A | ATTT | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0024 others(9): Show |
12 | HG01074.hp2 HG01109.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-484_108-482dup others(3): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | ||||||
| chr1:45601745 | A | ATTTT | 16 | a0001c0001t0004g0134 a0001c0002t0001g0188 a0001c0002t0001g0190 others(13): Show |
17 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.108-485_108-482dup others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | ||||||
| chr1:45601745 | A | ATTTTT | 6 | a0001c0001t0004g0133 a0001c0003t0002g0139 a0001c0003t0002g0146 others(3): Show |
6 | HG00735.hp2 HG01167.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-486_108-482dup others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | ||||||
| chr1:45601745 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01069.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.108-491_108-482dup others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | ||||||
| chr1:45601745 | AT | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0052 others(2): Show |
6 | HG02083.hp1 HG02886.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-482delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | ||||||
| chr1:45601745 | ATTTTTTT others(4): Show |
A | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-492_108-482del others(11): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | ||||||
| chr1:45601778 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.108-477T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601778 | |||||||
| chr1:45601878 | C | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-377C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601878 | |||||||
| chr1:45601879 | C | T | 1 | a0001c0002t0001g0205 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.108-376C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601879 | |||||||
| chr1:45601975 | A | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-280A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601975 | |||||||
| chr1:45602030 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.108-225G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45602030 | |||||||
| chr1:45602208 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108-47A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45602208 | |||||||
| chr1:45602643 | C | A | 1 | a0001c0002t0001g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.218+278C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602643 | |||||||
| chr1:45602725 | G | A | 2 | a0001c0001t0004g0133 a0001c0001t0004g0134 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.218+360G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602725 | |||||||
| chr1:45602748 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.218+383G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602748 | |||||||
| chr1:45602872 | C | T | 1 | a0002c0004t0001g0184 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.218+507C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602872 | |||||||
| chr1:45602947 | T | A | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.218+582T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602947 | |||||||
| chr1:45603070 | C | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01069.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.218+705C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603070 | |||||||
| chr1:45603205 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.218+840C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603205 | |||||||
| chr1:45603423 | G | A | 1 | a0001c0002t0001g0218 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.218+1058G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603423 | |||||||
| chr1:45603605 | A | AT | 18 | a0001c0001t0001g0101 a0001c0001t0001g0126 a0001c0001t0001g0137 others(15): Show |
18 | HG00544.hp1 HG00642.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+1260dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 45603605 | ||||||
| chr1:45603605 | A | ATT | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(122): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.218+1259_218+1260d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 45603605 | ||||||
| chr1:45603605 | A | ATTT | 38 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(35): Show |
39 | HG02083.hp1 HG02109.hp1 HG02148.hp1 others(36): Show |
intron_variant | MODIFIER | c.218+1258_218+1260d others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 45603605 | ||||||
| chr1:45603640 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.218+1275G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603640 | |||||||
| chr1:45603720 | C | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-1216C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603720 | |||||||
| chr1:45603860 | C | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-1076C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603860 | |||||||
| chr1:45603940 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.219-996G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603940 | |||||||
| chr1:45604282 | C | T | 2 | a0003c0006t0001g0275 a0003c0006t0001g0276 |
2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.219-654C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604282 | |||||||
| chr1:45604534 | G | A | 1 | a0001c0002t0001g0280 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.219-402G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604534 | |||||||
| chr1:45604565 | A | T | 1 | a0001c0002t0001g0288 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.219-371A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604565 | |||||||
| chr1:45604575 | A | G | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.219-361A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604575 | |||||||
| chr1:45604748 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.219-188A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604748 | |||||||
| chr1:45604898 | A | G | 2 | a0001c0002t0001g0194 a0001c0003t0002g0143 |
2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.219-38A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604898 | |||||||
| chr1:45605166 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.299+150C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605166 | |||||||
| chr1:45605525 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.299+509C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605525 | |||||||
| chr1:45605651 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.299+635A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605651 | |||||||
| chr1:45605749 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.299+733A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605749 | |||||||
| chr1:45605774 | G | GT | 16 | a0001c0002t0001g0172 a0001c0002t0001g0187 a0001c0002t0001g0230 others(13): Show |
16 | NA18944.hp1 NA18966.hp2 NA18968.hp1 others(13): Show |
intron_variant | MODIFIER | c.300-689dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 45605774 | ||||||
| chr1:45605774 | GT | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.300-689delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 45605774 | ||||||
| chr1:45605791 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0031 |
2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.300-691T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605791 | |||||||
| chr1:45605793 | T | A | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.300-689T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605793 | |||||||
| chr1:45605833 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.300-649A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605833 | |||||||
| chr1:45605883 | T | C | 31 | a0001c0002t0001g0172 a0001c0002t0001g0185 a0001c0002t0001g0194 others(28): Show |
31 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.300-599T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605883 | |||||||
| chr1:45605912 | G | A | 1 | a0001c0002t0001g0246 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.300-570G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605912 | |||||||
| chr1:45606007 | C | T | 25 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0004g0133 others(22): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.300-475C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606007 | |||||||
| chr1:45606055 | C | T | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.300-427C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606055 | |||||||
| chr1:45606136 | T | C | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.300-346T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606136 | |||||||
| chr1:45606168 | C | G | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-314C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606168 | |||||||
| chr1:45606339 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.300-143C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606339 | |||||||
| chr1:45606712 | G | T | 3 | a0001c0002t0001g0226 a0001c0002t0001g0227 a0001c0002t0001g0252 |
3 | HG02451.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.409+121G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606712 | |||||||
| chr1:45606713 | C | T | 3 | a0001c0002t0001g0226 a0001c0002t0001g0227 a0001c0002t0001g0252 |
3 | HG02451.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.409+122C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606713 | |||||||
| chr1:45606718 | A | C | 1 | a0001c0002t0001g0212 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.409+127A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606718 | |||||||
| chr1:45606818 | T | C | 1 | a0002c0004t0001g0179 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.409+227T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606818 | |||||||
| chr1:45606890 | G | A | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.409+299G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606890 | |||||||
| chr1:45606936 | T | G | 1 | a0001c0001t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.409+345T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606936 | |||||||
| chr1:45606965 | T | C | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.410-356T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606965 | |||||||
| chr1:45607047 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01069.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.410-274T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607047 | |||||||
| chr1:45607098 | A | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.410-223A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607098 | |||||||
| chr1:45607106 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.410-215T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607106 | |||||||
| chr1:45607215 | G | C | 4 | a0001c0002t0001g0197 a0001c0002t0001g0199 a0001c0002t0001g0200 others(1): Show |
4 | HG00438.hp2 HG00609.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-106G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607215 | |||||||
| chr1:45607283 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.410-38G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607283 | |||||||
| chr1:45608381 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1426+44G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45608381 | |||||||
| chr1:45608457 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1426+120G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45608457 | |||||||
| chr1:45608961 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1426+624C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45608961 | |||||||
| chr1:45608995 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1426+658A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45608995 | |||||||
| chr1:45609218 | T | C | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1426+881T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609218 | |||||||
| chr1:45609435 | T | C | 1 | a0001c0003t0002g0006 | 2 | HG00099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1426+1098T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609435 | |||||||
| chr1:45609499 | A | AAAAC | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1426+1174_1426+117 others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45609499 | ||||||
| chr1:45609511 | C | CAAACAAA others(1): Show |
14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426+1177_1426+117 others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45609511 | ||||||
| chr1:45609628 | C | G | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426+1291C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609628 | |||||||
| chr1:45609732 | A | G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0034 others(2): Show |
5 | HG01943.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1426+1395A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609732 | |||||||
| chr1:45609875 | T | G | 1 | a0001c0003t0002g0143 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1426+1538T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609875 | |||||||
| chr1:45609892 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1426+1555C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609892 | |||||||
| chr1:45609937 | C | T | 35 | a0001c0002t0001g0172 a0001c0002t0001g0193 a0001c0002t0001g0194 others(32): Show |
35 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1426+1600C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609937 | |||||||
| chr1:45609966 | C | T | 36 | a0001c0002t0001g0172 a0001c0002t0001g0193 a0001c0002t0001g0194 others(33): Show |
36 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1426+1629C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609966 | |||||||
| chr1:45610060 | G | A | 14 | a0001c0007t0001g0277 a0001c0007t0001g0278 a0002c0004t0001g0173 others(11): Show |
14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426+1723G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610060 | |||||||
| chr1:45610111 | A | C | 2 | a0001c0001t0004g0133 a0001c0001t0004g0134 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1426+1774A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610111 | |||||||
| chr1:45610124 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1426+1787G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610124 | |||||||
| chr1:45610127 | A | G | 24 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0003t0002g0006 others(21): Show |
25 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1426+1790A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610127 | |||||||
| chr1:45610190 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1426+1853C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610190 | |||||||
| chr1:45610349 | G | T | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1426+2012G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610349 | |||||||
| chr1:45610386 | C | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1426+2049C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610386 | |||||||
| chr1:45610619 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1426+2282A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610619 | |||||||
| chr1:45610826 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1427-2343C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610826 | |||||||
| chr1:45610850 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1427-2319G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610850 | |||||||
| chr1:45611063 | C | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1427-2106C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611063 | |||||||
| chr1:45611232 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1427-1937T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611232 | |||||||
| chr1:45611456 | C | CT | 38 | a0001c0001t0001g0076 a0001c0002t0001g0171 a0001c0002t0001g0172 others(35): Show |
38 | HG00544.hp1 HG00609.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1427-1685dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | ||||||
| chr1:45611456 | C | CTT | 12 | a0001c0001t0001g0128 a0001c0002t0001g0192 a0001c0002t0001g0197 others(9): Show |
12 | HG00438.hp2 HG00733.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1427-1686_1427-168 others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | ||||||
| chr1:45611456 | CT | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(39): Show |
43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1427-1685delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | ||||||
| chr1:45611456 | CTT | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1427-1686_1427-168 others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | ||||||
| chr1:45611456 | CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0114 a0001c0001t0001g0119 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1427-1693_1427-168 others(13): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | ||||||
| chr1:45611456 | CTTTTTTT others(3): Show |
C | 10 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0176 others(7): Show |
10 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.1427-1694_1427-168 others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | ||||||
| chr1:45611456 | CTTTTTTT others(393): Show |
C | 1 | a0001c0002t0001g0228 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1427-1691_1427-129 others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | ||||||
| chr1:45611555 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0119 a0001c0001t0001g0124 |
3 | HG01243.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1427-1614C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611555 | |||||||
| chr1:45611581 | C | T | 2 | a0001c0002t0001g0260 a0008c0014t0001g0272 |
2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1427-1588C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611581 | |||||||
| chr1:45611591 | C | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1427-1578C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611591 | |||||||
| chr1:45611666 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1427-1503C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611666 | |||||||
| chr1:45611756 | G | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1427-1413G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611756 | |||||||
| chr1:45611855 | C | CT | 24 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0034 others(21): Show |
24 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1427-1292dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611855 | ||||||
| chr1:45611855 | CT | C | 6 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0003t0002g0144 others(3): Show |
6 | HG01168.hp2 HG01192.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1427-1292delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611855 | ||||||
| chr1:45611855 | CTT | C | 12 | a0001c0001t0001g0167 a0002c0004t0001g0173 a0002c0004t0001g0174 others(9): Show |
12 | HG02258.hp2 NA18944.hp1 NA18968.hp1 others(9): Show |
intron_variant | MODIFIER | c.1427-1293_1427-129 others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611855 | ||||||
| chr1:45611877 | TG | T | 4 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0003c0006t0001g0275 others(1): Show |
4 | HG02280.hp2 HG02717.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1427-1291delG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611877 | |||||||
| chr1:45611878 | G | T | 105 | a0001c0002t0001g0033 a0001c0002t0001g0045 a0001c0002t0001g0168 others(102): Show |
105 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1427-1291G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611878 | |||||||
| chr1:45611883 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1427-1286G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611883 | |||||||
| chr1:45612043 | G | GT | 20 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0002t0001g0204 others(17): Show |
20 | HG00544.hp1 HG01074.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.1427-1115dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45612043 | ||||||
| chr1:45612054 | T | A | 1 | a0001c0002t0001g0266 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1427-1115T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612054 | |||||||
| chr1:45612061 | G | A | 1 | a0002c0004t0001g0182 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1427-1108G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612061 | |||||||
| chr1:45612427 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1427-742C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612427 | |||||||
| chr1:45612519 | T | A | 11 | a0001c0002t0001g0191 a0001c0002t0001g0195 a0001c0002t0001g0207 others(8): Show |
11 | HG00733.hp1 HG00738.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1427-650T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612519 | |||||||
| chr1:45612770 | A | G | 1 | a0001c0002t0001g0262 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1427-399A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612770 | |||||||
| chr1:45612858 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1427-311A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612858 | |||||||
| chr1:45612892 | T | C | 2 | a0003c0006t0001g0275 a0003c0006t0001g0276 |
2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1427-277T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612892 | |||||||
| chr1:45612958 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1427-211A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612958 | |||||||
| chr1:45613013 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1427-156A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45613013 | |||||||
| chr1:45613125 | C | T | 3 | a0001c0001t0001g0132 a0001c0003t0001g0130 a0001c0003t0001g0131 |
3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1427-44C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45613125 | |||||||
| chr1:45613443 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0119 a0001c0001t0001g0124 |
3 | HG01243.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1506+195C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | chr1 | 45613443 | |||||||
| chr1:45613719 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1507-377T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | chr1 | 45613719 | |||||||
| chr1:45613821 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1507-275A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | chr1 | 45613821 | |||||||
| chr1:45613908 | AT | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1507-185delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 45613908 | ||||||
| chr1:45614068 | A | G | 2 | a0001c0001t0001g0167 a0005c0011t0001g0166 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1507-28A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | chr1 | 45614068 | |||||||
| chr1:45614388 | ACT | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0068 |
3 | HG02015.hp1 HG02135.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1666+26_1666+27del others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 45614388 | ||||||
| chr1:45614475 | C | T | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1666+109C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614475 | |||||||
| chr1:45614548 | GT | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1666+190delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 45614548 | ||||||
| chr1:45614595 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1666+229A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614595 | |||||||
| chr1:45614628 | A | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1666+262A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614628 | |||||||
| chr1:45614639 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0119 a0001c0001t0001g0124 |
3 | HG01243.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1666+273A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614639 | |||||||
| chr1:45614694 | A | G | 1 | a0001c0005t0001g0267 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1667-319A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614694 | |||||||
| chr1:45614696 | G | A | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1667-317G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614696 | |||||||
| chr1:45614696 | G | C | 1 | a0001c0005t0001g0267 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1667-317G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614696 | |||||||
| chr1:45614843 | G | T | 1 | a0001c0005t0001g0267 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1667-170G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614843 | |||||||
| chr1:45614858 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1667-155T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614858 | |||||||
| chr1:45615216 | G | A | 1 | a0001c0002t0001g0245 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1855+15G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 10/14 | chr1 | 45615216 | |||||||
| chr1:45615275 | A | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1856-30A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 10/14 | chr1 | 45615275 | |||||||
| chr1:45615289 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1856-16A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 10/14 | chr1 | 45615289 | |||||||
| chr1:45615492 | G | C | 2 | a0001c0007t0001g0277 a0001c0007t0001g0278 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.2022+21G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615492 | |||||||
| chr1:45615551 | A | T | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.2022+80A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615551 | |||||||
| chr1:45615610 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.2022+139T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615610 | |||||||
| chr1:45615750 | C | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.2022+279C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615750 | |||||||
| chr1:45615808 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2022+337A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615808 | |||||||
| chr1:45615811 | C | T | 5 | a0001c0002t0001g0197 a0001c0002t0001g0199 a0001c0002t0001g0200 others(2): Show |
5 | HG00438.hp2 HG00609.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.2022+340C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615811 | |||||||
| chr1:45615926 | G | A | 1 | a0001c0003t0002g0153 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2023-411G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615926 | |||||||
| chr1:45616018 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2023-319G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616018 | |||||||
| chr1:45616059 | A | G | 12 | a0002c0004t0001g0173 a0002c0004t0001g0174 a0002c0004t0001g0175 others(9): Show |
12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.2023-278A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616059 | |||||||
| chr1:45616109 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2023-228G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616109 | |||||||
| chr1:45616268 | T | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.2023-69T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616268 | |||||||
| chr1:45616288 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.2023-49C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616288 | |||||||
| chr1:45616605 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2080-21A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 12/14 | chr1 | 45616605 | |||||||
| chr1:45616759 | C | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.2157+56C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/14 | chr1 | 45616759 | |||||||
| chr1:45617284 | A | G | 1 | a0001c0002t0005g0281 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2158-179A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/14 | chr1 | 45617284 | |||||||
| chr1:45617293 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.2158-170C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/14 | chr1 | 45617293 | |||||||
| chr1:45617352 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2158-111T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/14 | chr1 | 45617352 | |||||||
| chr1:45617654 | C | T | 1 | a0001c0003t0002g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2286+63C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 14/14 | chr1 | 45617654 | |||||||
| chr1:45617872 | T | G | 1 | a0001c0003t0002g0147 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2287-189T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 14/14 | chr1 | 45617872 | |||||||
| chr1:45618034 | C | G | 22 | a0001c0003t0002g0006 a0001c0003t0002g0138 a0001c0003t0002g0139 others(19): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2287-27C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 14/14 | chr1 | 45618034 |