Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 116150 |
| ensemblid | ENSG00000153989.8 |
| hgncid | 21042 |
| symbol | NUS1 |
| name | NUS1 dehydrodolichyl diphosphate synthase subunit |
| refseq_nuc | NM_138459.5 |
| refseq_prot | NP_612468.1 |
| ensembl_nuc | ENST00000368494.4 |
| ensembl_prot | ENSP00000357480.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 117675469 |
| end | 117710727 |
| strand | + |
| ver | v1.2 |
| region | chr6:117675469-117710727 |
| region5000 | chr6:117670469-117715727 |
| regionname0 | NUS1_chr6_117675469_117710727 |
| regionname5000 | NUS1_chr6_117670469_117715727 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 293 | 420 | 96 | 68 | 194 | 16 | 44 | 153 | NUS1_chr6_117670469_117715727 | NUS1 | MTGLY others(288): Show |
chr6 | 117670469 | 117715727 |
| a0002 | 0/0 | 293 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | NUS1_chr6_117670469_117715727 | NUS1 | MTGLY others(288): Show |
chr6 | 117670469 | 117715727 |
| a0003 | 0/0 | 293 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NUS1_chr6_117670469_117715727 | NUS1 | MTGLY others(288): Show |
chr6 | 117670469 | 117715727 |
| a0004 | 0/0 | 293 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | MTGLY others(288): Show |
chr6 | 117670469 | 117715727 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 879 | 398 | 78 | 68 | 190 | 16 | 44 | NUS1_chr6_117670469_117715727 | NUS1 | ATGAC others(874): Show |
chr6 | 117670469 | 117715727 | ||
| a0001c0002 | 0/0 | 879 | 18 | 18 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | ATGAC others(874): Show |
chr6 | 117670469 | 117715727 | ||
| a0001c0004 | 0/0 | 879 | 4 | 0 | 0 | 4 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | ATGAC others(874): Show |
chr6 | 117670469 | 117715727 | ||
| a0002c0003 | 0/0 | 879 | 5 | 0 | 0 | 5 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | ATGAC others(874): Show |
chr6 | 117670469 | 117715727 | ||
| a0003c0005 | 0/0 | 879 | 3 | 0 | 0 | 3 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | ATGAC others(874): Show |
chr6 | 117670469 | 117715727 | ||
| a0004c0006 | 0/0 | 879 | 2 | 0 | 2 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | ATGAC others(874): Show |
chr6 | 117670469 | 117715727 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4796 | 213 | 36 | 44 | 102 | 11 | 20 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0002 | 0/1 | 4797 | 64 | 5 | 10 | 36 | 2 | 10 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4792): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0003 | 0/0 | 4797 | 46 | 15 | 2 | 29 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4792): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0004 | 0/0 | 4795 | 25 | 5 | 6 | 8 | 2 | 4 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4790): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0005 | 0/0 | 4797 | 9 | 1 | 0 | 1 | 1 | 6 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4792): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0006 | 0/0 | 4796 | 6 | 6 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0007 | 0/0 | 4794 | 5 | 0 | 4 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4789): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0008 | 0/0 | 4797 | 4 | 4 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4792): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0009 | 0/0 | 4797 | 4 | 0 | 0 | 3 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4792): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0010 | 0/0 | 4796 | 3 | 0 | 0 | 3 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0012 | 0/0 | 4796 | 3 | 3 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0013 | 0/0 | 4796 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0014 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0016 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4662): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0017 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0018 | 0/0 | 4796 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0019 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0020 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0021 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0022 | 0/0 | 4795 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4790): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0024 | 0/0 | 4797 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4792): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0025 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0026 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0027 | 0/0 | 4797 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4792): Show |
chr6 | 117670469 | 117715727 |
| a0001c0001t0028 | 1/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0001c0002t0004 | 0/0 | 4795 | 14 | 14 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4790): Show |
chr6 | 117670469 | 117715727 |
| a0001c0002t0011 | 0/0 | 4795 | 3 | 3 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4790): Show |
chr6 | 117670469 | 117715727 |
| a0001c0002t0015 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4790): Show |
chr6 | 117670469 | 117715727 |
| a0001c0004t0001 | 0/0 | 4796 | 4 | 0 | 0 | 4 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0002c0003t0001 | 0/0 | 4796 | 4 | 0 | 0 | 4 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| a0002c0003t0023 | 0/0 | 4797 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4792): Show |
chr6 | 117670469 | 117715727 |
| a0003c0005t0002 | 0/0 | 4797 | 3 | 0 | 0 | 3 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4792): Show |
chr6 | 117670469 | 117715727 |
| a0004c0006t0001 | 0/0 | 4796 | 2 | 0 | 2 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | GTACT others(4791): Show |
chr6 | 117670469 | 117715727 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 1 | 4 | 14 | 1 | 3 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 1 | 0 | 3 | 3 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0015 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0021 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0005 | 0/0 | 9 | 0 | 0 | 6 | 1 | 2 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0007 | 0/0 | 7 | 1 | 1 | 1 | 0 | 4 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0002 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0022 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0005g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0007g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0008g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0009g0029 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0009g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0010g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0012g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0012g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0013g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0014g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0014g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0016g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0018g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0019g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0021g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0022g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0024g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0025g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0026g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0027g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0001t0028g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0011g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0002t0015g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0004t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0002c0003t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0002c0003t0023g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0003c0005t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0003c0005t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0003c0005t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| a0004c0006t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0153 | EUR | FIN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0257 | EUR | FIN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00597 | hp2 | a0001 | c0001 | t0010 | g0122 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00733 | hp2 | a0001 | c0001 | t0018 | g0006 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0058 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0022 | EUR | IBS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0249 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01943 | hp1 | a0004 | c0006 | t0001 | g0001 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01952 | hp2 | a0004 | c0006 | t0001 | g0001 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01981 | hp2 | a0001 | c0001 | t0022 | g0065 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01993 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02027 | hp1 | a0001 | c0001 | t0027 | g0226 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0246 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0020 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0029 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02132 | hp1 | a0001 | c0004 | t0001 | g0194 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02135 | hp2 | a0001 | c0001 | t0009 | g0029 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CDX | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | CDX | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0251 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02451 | hp2 | a0001 | c0002 | t0004 | g0055 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02572 | hp1 | a0001 | c0001 | t0014 | g0134 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0039 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0138 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0129 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0156 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0141 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0032 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02723 | hp1 | a0001 | c0002 | t0015 | g0244 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0024 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02809 | hp1 | a0001 | c0002 | t0011 | g0025 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02895 | hp2 | a0001 | c0002 | t0011 | g0025 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02896 | hp1 | a0001 | c0002 | t0004 | g0028 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0245 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02976 | hp1 | a0001 | c0002 | t0011 | g0025 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02976 | hp2 | a0001 | c0001 | t0026 | g0196 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0054 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0055 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0250 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0247 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0024 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0039 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0028 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0067 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0054 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0146 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03831 | hp1 | a0001 | c0001 | t0009 | g0029 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03834 | hp2 | a0001 | c0001 | t0024 | g0043 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03942 | hp1 | a0001 | c0001 | t0020 | g0001 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03942 | hp2 | a0001 | c0001 | t0019 | g0094 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0024 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0155 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0139 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0032 | AFR | YRI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0028 | AFR | YRI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | YRI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0157 | AFR | YRI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18944 | hp2 | a0001 | c0001 | t0025 | g0216 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18945 | hp2 | a0001 | c0004 | t0001 | g0046 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18953 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18960 | hp2 | a0001 | c0001 | t0013 | g0208 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18964 | hp1 | a0001 | c0001 | t0009 | g0261 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18964 | hp2 | a0001 | c0001 | t0010 | g0038 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18966 | hp1 | a0001 | c0001 | t0016 | g0060 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18966 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18973 | hp2 | a0001 | c0001 | t0021 | g0040 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18987 | hp2 | a0003 | c0005 | t0002 | g0184 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19007 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0248 | AFR | LWK | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | LWK | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | LWK | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19054 | hp2 | a0001 | c0001 | t0007 | g0062 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19074 | hp2 | a0001 | c0004 | t0001 | g0046 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19077 | hp2 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19078 | hp1 | a0003 | c0005 | t0002 | g0051 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19079 | hp1 | a0003 | c0005 | t0002 | g0069 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19082 | hp1 | a0001 | c0004 | t0001 | g0195 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19087 | hp1 | a0001 | c0001 | t0010 | g0038 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0158 | AFR | ASW | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ASW | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0161 | EUR | TSI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | GIH | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0131 | AFR | MSL | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | USA | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | USA | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA18955 | hp2 | a0002 | c0003 | t0023 | g0037 | EAS | JPT | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | USA | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | USA | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0259 | REF | REF | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0028 | g0188 | REF | REF | NUS1_chr6_117670469_117715727 | NUS1 | chr6 | 117670469 | 117715727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:117675867 | G | C | 1 | a0004 | 2 | HG01943.hp1 HG01952.hp2 |
missense_variant | MODERATE | c.197G>C | p.Arg66Pro | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/5 | 399/4796 | 197/882 | 66/293 | chr6 | 117675867 | |||
| chr6:117693149 | A | T | 1 | a0003 | 3 | NA18987.hp2 NA19078.hp1 NA19079.hp1 |
missense_variant | MODERATE | c.523A>T | p.Asn175Tyr | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 2/5 | 725/4796 | 523/882 | 175/293 | chr6 | 117693149 | |||
| chr6:117693163 | T | A | 1 | a0002 | 5 | HG02074.hp2 NA18953.hp2 NA18955.hp2 others(2): Show |
missense_variant | MODERATE | c.537T>A | p.Asp179Glu | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 2/5 | 739/4796 | 537/882 | 179/293 | chr6 | 117693163 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:117675733 | G | T | 1 | a0001c0004 | 4 | HG02132.hp1 NA18945.hp2 NA19074.hp2 others(1): Show |
synonymous_variant | LOW | c.63G>T | p.Thr21Thr | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/5 | 265/4796 | 63/882 | 21/293 | chr6 | 117675733 | |||
| chr6:117706982 | A | G | 1 | a0001c0002 | 18 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
synonymous_variant | LOW | c.849A>G | p.Gln283Gln | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 1051/4796 | 849/882 | 283/293 | chr6 | 117706982 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:117675486 | G | A | 1 | a0001c0001t0008 | 4 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-185G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/5 | 185 | chr6 | 117675486 | ||||||
| chr6:117675566 | G | A | 1 | a0001c0002t0015 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/5 | 105 | chr6 | 117675566 | ||||||
| chr6:117675655 | T | C | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(27): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
5_prime_UTR_variant | MODIFIER | c.-16T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/5 | 16 | chr6 | 117675655 | ||||||
| chr6:117675667 | G | A | 1 | a0001c0001t0010 | 3 | HG00597.hp2 NA18964.hp2 NA19087.hp1 |
5_prime_UTR_variant | MODIFIER | c.-4G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/5 | 4 | chr6 | 117675667 | ||||||
| chr6:117707033 | A | G | 1 | a0001c0001t0012 | 3 | HG02717.hp2 HG03579.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*18A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 18 | chr6 | 117707033 | ||||||
| chr6:117707035 | T | C | 1 | a0001c0001t0027 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 20 | chr6 | 117707035 | ||||||
| chr6:117707093 | A | G | 1 | a0001c0001t0009 | 4 | HG02080.hp1 HG02135.hp2 HG03831.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*78A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 78 | chr6 | 117707093 | ||||||
| chr6:117707502 | A | C | 1 | a0001c0002t0011 | 3 | HG02809.hp1 HG02895.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*487A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 487 | chr6 | 117707502 | ||||||
| chr6:117707506 | C | T | 2 | a0001c0001t0005 a0001c0001t0008 |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*491C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 491 | chr6 | 117707506 | ||||||
| chr6:117707675 | G | T | 1 | a0001c0001t0026 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*660G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 660 | chr6 | 117707675 | ||||||
| chr6:117708182 | C | T | 1 | a0001c0001t0014 | 2 | HG02572.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1167C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 1167 | chr6 | 117708182 | ||||||
| chr6:117708639 | C | T | 1 | a0001c0001t0025 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1624C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 1624 | chr6 | 117708639 | ||||||
| chr6:117708640 | G | A | 1 | a0001c0001t0013 | 2 | NA18960.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1625G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 1625 | chr6 | 117708640 | ||||||
| chr6:117708642 | C | CT | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(7): Show |
133 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1638dupT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 1639 | INFO_REALIGN_3_PRIME | chr6 | 117708642 | |||||
| chr6:117709011 | A | G | 1 | a0001c0001t0024 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1996A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 1996 | chr6 | 117709011 | ||||||
| chr6:117709075 | G | T | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(4): Show |
119 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*2060G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 2060 | chr6 | 117709075 | ||||||
| chr6:117709121 | TTCACCTG others(122): Show |
T | 1 | a0001c0001t0016 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107_*2235del | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 2107 | chr6 | 117709121 | ||||||
| chr6:117709155 | G | T | 1 | a0001c0001t0001 | 3 | HG02027.hp2 NA18977.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2140G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 2140 | chr6 | 117709155 | ||||||
| chr6:117709194 | G | A | 1 | a0001c0001t0001 | 3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2179G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 2179 | chr6 | 117709194 | ||||||
| chr6:117709287 | CTT | C | 2 | a0001c0001t0007 a0001c0001t0022 |
6 | HG01255.hp2 HG01952.hp1 HG01981.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2274_*2275delTT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 2274 | INFO_REALIGN_3_PRIME | chr6 | 117709287 | |||||
| chr6:117709442 | G | T | 2 | a0001c0001t0005 a0001c0001t0008 |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2427G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 2427 | chr6 | 117709442 | ||||||
| chr6:117709496 | A | G | 1 | a0001c0001t0020 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2481A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 2481 | chr6 | 117709496 | ||||||
| chr6:117710082 | C | T | 1 | a0001c0001t0005 | 9 | HG02698.hp1 HG02735.hp2 HG03239.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3067C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3067 | chr6 | 117710082 | ||||||
| chr6:117710108 | C | T | 1 | a0001c0001t0019 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3093C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3093 | chr6 | 117710108 | ||||||
| chr6:117710133 | G | A | 2 | a0001c0001t0005 a0001c0001t0008 |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3118G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3118 | chr6 | 117710133 | ||||||
| chr6:117710160 | A | T | 1 | a0001c0001t0018 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3145A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3145 | chr6 | 117710160 | ||||||
| chr6:117710173 | A | G | 1 | a0001c0001t0026 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3158A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3158 | chr6 | 117710173 | ||||||
| chr6:117710200 | A | G | 1 | a0001c0001t0024 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3185A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3185 | chr6 | 117710200 | ||||||
| chr6:117710244 | GT | G | 4 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0011 others(1): Show |
43 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3236delT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3236 | INFO_REALIGN_3_PRIME | chr6 | 117710244 | |||||
| chr6:117710361 | C | T | 1 | a0001c0001t0006 | 6 | HG02622.hp2 HG02647.hp2 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3346C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3346 | chr6 | 117710361 | ||||||
| chr6:117710453 | G | A | 1 | a0001c0001t0014 | 2 | HG02572.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3438G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3438 | chr6 | 117710453 | ||||||
| chr6:117710658 | T | C | 1 | a0001c0001t0017 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3643T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 5/5 | 3643 | chr6 | 117710658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:117676288 | A | AG | 16 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(13): Show |
31 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.415+203_415+204ins others(1): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117676288 | |||||||
| chr6:117676293 | C | T | 13 | a0001c0001t0002g0007 a0001c0001t0002g0056 a0001c0001t0002g0253 others(10): Show |
22 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.415+208C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117676293 | |||||||
| chr6:117676470 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.415+385A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117676470 | |||||||
| chr6:117676476 | G | A | 2 | a0001c0001t0012g0032 a0001c0001t0012g0067 |
3 | HG02717.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.415+391G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117676476 | |||||||
| chr6:117676570 | C | T | 11 | a0001c0002t0004g0028 a0001c0002t0004g0054 a0001c0002t0004g0055 others(8): Show |
15 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.415+485C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117676570 | |||||||
| chr6:117676807 | C | G | 1 | a0001c0001t0001g0053 | 2 | HG02071.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.415+722C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117676807 | |||||||
| chr6:117676844 | G | A | 3 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0002g0255 |
3 | HG02004.hp2 HG03654.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.415+759G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117676844 | |||||||
| chr6:117677012 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.415+927C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677012 | |||||||
| chr6:117677070 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.415+985T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677070 | |||||||
| chr6:117677127 | T | C | 1 | a0003c0005t0002g0069 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.415+1042T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677127 | |||||||
| chr6:117677159 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.415+1074G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677159 | |||||||
| chr6:117677300 | T | G | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+1215T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677300 | |||||||
| chr6:117677375 | A | G | 1 | a0001c0001t0003g0242 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.415+1290A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677375 | |||||||
| chr6:117677438 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(60): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.415+1353T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677438 | |||||||
| chr6:117677546 | A | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
16 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+1461A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677546 | |||||||
| chr6:117677555 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.415+1470T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677555 | |||||||
| chr6:117677567 | T | C | 2 | a0001c0001t0012g0032 a0001c0001t0012g0067 |
3 | HG02717.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.415+1482T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117677567 | |||||||
| chr6:117678020 | C | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
10 | HG00408.hp1 NA18948.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.415+1935C>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117678020 | |||||||
| chr6:117678347 | T | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(45): Show |
74 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.415+2262T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117678347 | |||||||
| chr6:117678532 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(54): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.415+2447T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117678532 | |||||||
| chr6:117678650 | G | A | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+2565G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117678650 | |||||||
| chr6:117678677 | G | GT | 28 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0064 others(25): Show |
33 | HG00438.hp2 HG00733.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.415+2613dupT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117678677 | ||||||
| chr6:117678677 | GT | G | 76 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0021 others(73): Show |
102 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.415+2613delT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117678677 | ||||||
| chr6:117678677 | GTT | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(49): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.415+2612_415+2613d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117678677 | ||||||
| chr6:117678707 | G | T | 1 | a0001c0001t0004g0162 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.415+2622G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117678707 | |||||||
| chr6:117678825 | A | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.415+2740A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117678825 | |||||||
| chr6:117678973 | C | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
7 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.415+2888C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117678973 | |||||||
| chr6:117679053 | A | G | 6 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0130 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+2968A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679053 | |||||||
| chr6:117679205 | A | G | 1 | a0001c0001t0005g0161 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.415+3120A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679205 | |||||||
| chr6:117679267 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.415+3182G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679267 | |||||||
| chr6:117679300 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.415+3215G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679300 | |||||||
| chr6:117679501 | G | A | 2 | a0001c0001t0014g0134 a0001c0001t0014g0138 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.415+3416G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679501 | |||||||
| chr6:117679515 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.415+3430A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679515 | |||||||
| chr6:117679687 | A | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.415+3602A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679687 | |||||||
| chr6:117679687 | A | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0234 |
3 | HG02922.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.415+3602A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679687 | |||||||
| chr6:117679857 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.415+3772G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679857 | |||||||
| chr6:117679891 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01074.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.415+3806T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679891 | |||||||
| chr6:117679930 | A | T | 1 | a0001c0001t0004g0160 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.415+3845A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117679930 | |||||||
| chr6:117680138 | A | C | 2 | a0001c0001t0010g0038 a0001c0001t0010g0122 |
3 | HG00597.hp2 NA18964.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.415+4053A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680138 | |||||||
| chr6:117680145 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.415+4060G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680145 | |||||||
| chr6:117680148 | T | G | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+4063T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680148 | |||||||
| chr6:117680394 | C | T | 6 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0130 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+4309C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680394 | |||||||
| chr6:117680619 | A | G | 2 | a0001c0001t0003g0045 a0001c0001t0003g0192 |
3 | HG00609.hp1 HG02155.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.415+4534A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680619 | |||||||
| chr6:117680690 | C | T | 1 | a0001c0001t0006g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415+4605C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680690 | |||||||
| chr6:117680847 | G | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.415+4762G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680847 | |||||||
| chr6:117680850 | T | G | 3 | a0001c0004t0001g0046 a0001c0004t0001g0194 a0001c0004t0001g0195 |
4 | HG02132.hp1 NA18945.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+4765T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680850 | |||||||
| chr6:117680864 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0230 |
3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415+4779G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680864 | |||||||
| chr6:117680942 | C | T | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+4857C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680942 | |||||||
| chr6:117680963 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
16 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+4878G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117680963 | |||||||
| chr6:117681010 | C | A | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+4925C>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117681010 | |||||||
| chr6:117681172 | C | T | 23 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(20): Show |
25 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.415+5087C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117681172 | |||||||
| chr6:117681173 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(54): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.415+5088G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117681173 | |||||||
| chr6:117681204 | T | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
7 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.415+5119T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117681204 | |||||||
| chr6:117681411 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0230 |
3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415+5326C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117681411 | |||||||
| chr6:117681439 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.415+5354C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117681439 | |||||||
| chr6:117681732 | T | G | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+5647T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117681732 | |||||||
| chr6:117682034 | A | G | 6 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0130 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+5949A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682034 | |||||||
| chr6:117682122 | G | A | 1 | a0001c0001t0012g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.415+6037G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682122 | |||||||
| chr6:117682143 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0230 a0001c0001t0026g0196 |
4 | HG02055.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+6058G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682143 | |||||||
| chr6:117682153 | CCTAA | C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
7 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.415+6072_415+6075d others(6): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117682153 | ||||||
| chr6:117682206 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.415+6121C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682206 | |||||||
| chr6:117682257 | T | C | 1 | a0001c0001t0004g0162 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.415+6172T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682257 | |||||||
| chr6:117682367 | A | G | 6 | a0001c0001t0001g0050 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
7 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.415+6282A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682367 | |||||||
| chr6:117682381 | C | T | 1 | a0001c0001t0007g0062 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.415+6296C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682381 | |||||||
| chr6:117682397 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.415+6312T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682397 | |||||||
| chr6:117682416 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(61): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.415+6331A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682416 | |||||||
| chr6:117682427 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.415+6342C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682427 | |||||||
| chr6:117682629 | C | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.415+6544C>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682629 | |||||||
| chr6:117682658 | G | A | 4 | a0001c0001t0005g0139 a0001c0001t0005g0140 a0001c0001t0005g0141 others(1): Show |
4 | HG02698.hp1 HG04204.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+6573G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682658 | |||||||
| chr6:117682667 | G | T | 1 | a0001c0001t0003g0026 | 3 | NA18986.hp2 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.415+6582G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682667 | |||||||
| chr6:117682707 | C | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(45): Show |
75 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.415+6622C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682707 | |||||||
| chr6:117682787 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.415+6702G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682787 | |||||||
| chr6:117682804 | C | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(45): Show |
75 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.415+6719C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682804 | |||||||
| chr6:117682843 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.415+6758C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682843 | |||||||
| chr6:117682876 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.415+6791C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682876 | |||||||
| chr6:117682915 | T | C | 1 | a0001c0001t0001g0053 | 2 | HG02071.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.415+6830T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117682915 | |||||||
| chr6:117683165 | T | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(42): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.415+7080T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683165 | |||||||
| chr6:117683218 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.415+7133T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683218 | |||||||
| chr6:117683221 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.415+7136T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683221 | |||||||
| chr6:117683235 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.415+7150A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683235 | |||||||
| chr6:117683422 | A | G | 2 | a0001c0001t0012g0032 a0001c0001t0012g0067 |
3 | HG02717.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.415+7337A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683422 | |||||||
| chr6:117683440 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0230 |
3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415+7355A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683440 | |||||||
| chr6:117683446 | A | G | 10 | a0001c0002t0004g0028 a0001c0002t0004g0054 a0001c0002t0004g0055 others(7): Show |
14 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.415+7361A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683446 | |||||||
| chr6:117683467 | T | A | 25 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(22): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.415+7382T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683467 | |||||||
| chr6:117683470 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.415+7385C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683470 | |||||||
| chr6:117683595 | A | G | 1 | a0001c0001t0003g0190 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.415+7510A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683595 | |||||||
| chr6:117683625 | T | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
18 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.415+7540T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683625 | |||||||
| chr6:117683629 | T | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0230 |
3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415+7544T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683629 | |||||||
| chr6:117683651 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.415+7566T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683651 | |||||||
| chr6:117683654 | CTT | C | 25 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(22): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.415+7570_415+7571d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683654 | |||||||
| chr6:117683676 | T | C | 1 | a0001c0001t0012g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.415+7591T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683676 | |||||||
| chr6:117683758 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.415+7673A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683758 | |||||||
| chr6:117683867 | A | G | 3 | a0002c0003t0001g0020 a0002c0003t0001g0037 a0002c0003t0023g0037 |
5 | HG02074.hp2 NA18953.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+7782A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683867 | |||||||
| chr6:117683977 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0234 |
3 | HG02922.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.415+7892A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117683977 | |||||||
| chr6:117684007 | T | C | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.415+7922T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684007 | |||||||
| chr6:117684035 | T | G | 16 | a0001c0001t0001g0050 a0001c0001t0001g0220 a0001c0001t0001g0221 others(13): Show |
20 | HG00140.hp2 HG01069.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.415+7950T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684035 | |||||||
| chr6:117684129 | C | G | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+8044C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684129 | |||||||
| chr6:117684154 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(267): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.415+8069T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684154 | |||||||
| chr6:117684169 | A | G | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.415+8084A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684169 | |||||||
| chr6:117684208 | C | A | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.415+8123C>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684208 | |||||||
| chr6:117684328 | A | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(45): Show |
75 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.415+8243A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684328 | |||||||
| chr6:117684371 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
16 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+8286G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684371 | |||||||
| chr6:117684424 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0234 |
3 | HG02922.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.415+8339C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684424 | |||||||
| chr6:117684502 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0121 |
2 | HG02735.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.415+8417A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684502 | |||||||
| chr6:117684657 | C | T | 1 | a0001c0001t0026g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.416-8385C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684657 | |||||||
| chr6:117684684 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0126 others(2): Show |
13 | HG00280.hp1 HG00733.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.416-8358A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684684 | |||||||
| chr6:117684705 | G | C | 1 | a0001c0001t0004g0162 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.416-8337G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684705 | |||||||
| chr6:117684749 | T | C | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-8293T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684749 | |||||||
| chr6:117684905 | A | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(54): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.416-8137A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684905 | |||||||
| chr6:117684979 | A | C | 4 | a0001c0002t0004g0028 a0001c0002t0004g0055 a0001c0002t0004g0247 others(1): Show |
7 | HG02258.hp2 HG02451.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-8063A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117684979 | |||||||
| chr6:117685015 | C | T | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-8027C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685015 | |||||||
| chr6:117685141 | CA | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0233 a0001c0001t0025g0216 |
3 | HG00438.hp2 NA18944.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.416-7897delA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117685141 | ||||||
| chr6:117685173 | A | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0091 others(13): Show |
27 | HG00597.hp2 HG00741.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.416-7869A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685173 | |||||||
| chr6:117685180 | C | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0119 a0001c0001t0001g0124 |
3 | NA18959.hp1 NA18989.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.416-7862C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685180 | |||||||
| chr6:117685339 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.416-7703G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685339 | |||||||
| chr6:117685370 | T | A | 6 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0130 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-7672T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685370 | |||||||
| chr6:117685440 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.416-7602G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685440 | |||||||
| chr6:117685460 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.416-7582C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685460 | |||||||
| chr6:117685887 | A | G | 1 | a0001c0001t0003g0026 | 3 | NA18986.hp2 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.416-7155A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685887 | |||||||
| chr6:117685917 | G | A | 12 | a0001c0002t0004g0028 a0001c0002t0004g0054 a0001c0002t0004g0055 others(9): Show |
18 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.416-7125G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685917 | |||||||
| chr6:117685927 | A | G | 25 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(22): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.416-7115A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685927 | |||||||
| chr6:117685964 | T | TA | 11 | a0001c0001t0001g0050 a0001c0001t0001g0109 a0001c0001t0001g0220 others(8): Show |
12 | HG00140.hp2 HG01069.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-7064dupA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117685964 | ||||||
| chr6:117685964 | TA | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(33): Show |
46 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.416-7064delA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117685964 | ||||||
| chr6:117685987 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.416-7055C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685987 | |||||||
| chr6:117685991 | G | A | 1 | a0001c0001t0002g0163 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.416-7051G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117685991 | |||||||
| chr6:117686000 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
16 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-7042G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686000 | |||||||
| chr6:117686106 | A | G | 1 | a0001c0001t0005g0161 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.416-6936A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686106 | |||||||
| chr6:117686115 | G | A | 1 | a0001c0001t0003g0190 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.416-6927G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686115 | |||||||
| chr6:117686129 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.416-6913T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686129 | |||||||
| chr6:117686153 | C | G | 1 | a0001c0002t0004g0247 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.416-6889C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686153 | |||||||
| chr6:117686249 | G | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.416-6793G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686249 | |||||||
| chr6:117686254 | C | T | 3 | a0001c0004t0001g0046 a0001c0004t0001g0194 a0001c0004t0001g0195 |
4 | HG02132.hp1 NA18945.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-6788C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686254 | |||||||
| chr6:117686329 | A | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
16 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-6713A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686329 | |||||||
| chr6:117686437 | G | C | 2 | a0001c0001t0014g0134 a0001c0001t0014g0138 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.416-6605G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686437 | |||||||
| chr6:117686645 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02630.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-6397G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686645 | |||||||
| chr6:117686766 | A | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(35): Show |
65 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.416-6276A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686766 | |||||||
| chr6:117686825 | A | G | 1 | a0001c0002t0011g0025 | 3 | HG02809.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.416-6217A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686825 | |||||||
| chr6:117686845 | AGTGTGTA others(1): Show |
A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0107 a0001c0001t0004g0142 others(3): Show |
7 | HG01255.hp1 HG01358.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-6190_416-6183d others(10): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686845 | ||||||
| chr6:117686845 | AGTGTGTA others(3): Show |
A | 8 | a0001c0001t0001g0193 a0001c0001t0004g0152 a0001c0001t0004g0153 others(5): Show |
10 | HG00280.hp2 HG01071.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.416-6190_416-6181d others(12): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686845 | ||||||
| chr6:117686845 | AGTGTGTA others(11): Show |
A | 1 | a0001c0002t0004g0055 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.416-6190_416-6173d others(20): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686845 | ||||||
| chr6:117686846 | GTGTGTA | G | 3 | a0001c0002t0004g0245 a0001c0002t0004g0248 a0001c0002t0015g0244 |
3 | HG02723.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.416-6190_416-6185d others(8): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686846 | ||||||
| chr6:117686848 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.416-6194G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686848 | |||||||
| chr6:117686849 | T | A | 1 | a0001c0001t0003g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.416-6193T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686849 | |||||||
| chr6:117686852 | A | ATG | 14 | a0001c0001t0001g0050 a0001c0001t0001g0221 a0001c0001t0001g0223 others(11): Show |
15 | HG00408.hp2 HG01069.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.416-6144_416-6143d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686852 | ||||||
| chr6:117686852 | A | ATGTG | 2 | a0001c0001t0003g0010 a0001c0001t0003g0137 |
3 | HG02559.hp1 HG03098.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.416-6146_416-6143d others(6): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686852 | ||||||
| chr6:117686852 | ATG | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0053 others(18): Show |
26 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.416-6144_416-6143d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686852 | ||||||
| chr6:117686852 | ATGTG | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(37): Show |
49 | HG00323.hp1 HG00438.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.416-6146_416-6143d others(6): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686852 | ||||||
| chr6:117686852 | ATGTGTG | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
114 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.416-6148_416-6143d others(8): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686852 | ||||||
| chr6:117686852 | ATGTGTGT others(1): Show |
A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(49): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.416-6150_416-6143d others(10): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686852 | ||||||
| chr6:117686852 | ATGTGTGT others(3): Show |
A | 28 | a0001c0001t0001g0047 a0001c0001t0001g0147 a0001c0001t0001g0159 others(25): Show |
32 | HG00738.hp2 HG01516.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.416-6152_416-6143d others(12): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686852 | ||||||
| chr6:117686852 | ATGTGTGT others(5): Show |
A | 3 | a0001c0001t0001g0048 a0001c0001t0004g0146 a0001c0001t0004g0162 |
3 | HG00639.hp1 HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.416-6154_416-6143d others(14): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686852 | ||||||
| chr6:117686852 | ATGTGTGT others(9): Show |
A | 2 | a0001c0001t0001g0023 a0001c0001t0004g0023 |
3 | HG02818.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.416-6158_416-6143d others(18): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117686852 | ||||||
| chr6:117686867 | T | C | 1 | a0001c0001t0002g0260 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.416-6175T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117686867 | |||||||
| chr6:117687050 | T | C | 1 | a0001c0001t0019g0094 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.416-5992T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687050 | |||||||
| chr6:117687100 | C | T | 37 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(34): Show |
47 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.416-5942C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687100 | |||||||
| chr6:117687320 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.416-5722T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687320 | |||||||
| chr6:117687326 | A | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0214 a0001c0001t0001g0232 |
4 | HG01167.hp2 HG01361.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-5716A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687326 | |||||||
| chr6:117687393 | C | T | 1 | a0001c0002t0011g0025 | 3 | HG02809.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.416-5649C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687393 | |||||||
| chr6:117687468 | T | G | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.416-5574T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687468 | |||||||
| chr6:117687489 | T | C | 9 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(6): Show |
11 | HG02630.hp1 HG02698.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-5553T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687489 | |||||||
| chr6:117687548 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.416-5494T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687548 | |||||||
| chr6:117687636 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(43): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.416-5406T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687636 | |||||||
| chr6:117687787 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.416-5255C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687787 | |||||||
| chr6:117687892 | A | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(42): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.416-5150A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687892 | |||||||
| chr6:117687942 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.416-5100C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117687942 | |||||||
| chr6:117688065 | A | T | 1 | a0001c0001t0004g0151 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.416-4977A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688065 | |||||||
| chr6:117688066 | T | A | 1 | a0001c0001t0004g0151 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.416-4976T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688066 | |||||||
| chr6:117688362 | G | T | 23 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(20): Show |
25 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.416-4680G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688362 | |||||||
| chr6:117688449 | CT | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(134): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.416-4580delT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117688449 | ||||||
| chr6:117688463 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.416-4579A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688463 | |||||||
| chr6:117688499 | A | G | 1 | a0001c0001t0003g0190 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.416-4543A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688499 | |||||||
| chr6:117688615 | T | C | 25 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(22): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.416-4427T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688615 | |||||||
| chr6:117688673 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.416-4369G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688673 | |||||||
| chr6:117688680 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.416-4362T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688680 | |||||||
| chr6:117688698 | C | T | 2 | a0001c0001t0012g0032 a0001c0001t0012g0067 |
3 | HG02717.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.416-4344C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688698 | |||||||
| chr6:117688770 | T | A | 1 | a0001c0001t0002g0164 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.416-4272T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688770 | |||||||
| chr6:117688781 | A | T | 1 | a0001c0001t0002g0164 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.416-4261A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117688781 | |||||||
| chr6:117689024 | T | C | 2 | a0001c0001t0002g0042 a0001c0001t0002g0165 |
3 | NA18954.hp2 NA18970.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.416-4018T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689024 | |||||||
| chr6:117689041 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.416-4001G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689041 | |||||||
| chr6:117689199 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.416-3843G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689199 | |||||||
| chr6:117689239 | T | G | 1 | a0001c0001t0002g0166 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.416-3803T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689239 | |||||||
| chr6:117689244 | T | G | 1 | a0001c0001t0006g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.416-3798T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689244 | |||||||
| chr6:117689251 | G | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.416-3791G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689251 | |||||||
| chr6:117689374 | C | T | 2 | a0001c0001t0014g0134 a0001c0001t0014g0138 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.416-3668C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689374 | |||||||
| chr6:117689539 | A | AT | 12 | a0001c0002t0004g0028 a0001c0002t0004g0054 a0001c0002t0004g0055 others(9): Show |
18 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.416-3494dupT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117689539 | ||||||
| chr6:117689544 | T | G | 1 | a0001c0001t0001g0057 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.416-3498T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689544 | |||||||
| chr6:117689561 | G | GT | 12 | a0001c0001t0002g0186 a0001c0001t0004g0151 a0001c0001t0005g0024 others(9): Show |
15 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.416-3472dupT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117689561 | ||||||
| chr6:117689562 | T | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
6 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-3480T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689562 | |||||||
| chr6:117689570 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG00140.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.416-3472T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689570 | |||||||
| chr6:117689780 | A | T | 1 | a0001c0001t0002g0164 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.416-3262A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117689780 | |||||||
| chr6:117690032 | A | T | 1 | a0001c0001t0002g0164 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.416-3010A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690032 | |||||||
| chr6:117690055 | T | C | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-2987T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690055 | |||||||
| chr6:117690160 | A | T | 1 | a0001c0001t0002g0164 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.416-2882A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690160 | |||||||
| chr6:117690248 | C | T | 1 | a0001c0001t0026g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.416-2794C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690248 | |||||||
| chr6:117690296 | A | G | 1 | a0001c0001t0005g0024 | 3 | HG02735.hp2 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.416-2746A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690296 | |||||||
| chr6:117690299 | C | T | 1 | a0001c0001t0003g0189 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.416-2743C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690299 | |||||||
| chr6:117690300 | G | A | 1 | a0001c0002t0004g0251 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.416-2742G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690300 | |||||||
| chr6:117690301 | TA | T | 37 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(34): Show |
47 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.416-2740delA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690301 | |||||||
| chr6:117690464 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.416-2578A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690464 | |||||||
| chr6:117690560 | C | T | 42 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0013 others(39): Show |
67 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.416-2482C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690560 | |||||||
| chr6:117690576 | C | T | 3 | a0001c0001t0002g0044 a0001c0001t0002g0185 a0001c0001t0002g0186 |
4 | NA18995.hp1 NA19059.hp2 NA19089.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-2466C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690576 | |||||||
| chr6:117690627 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0213 a0001c0001t0001g0230 others(1): Show |
5 | HG00609.hp2 HG02055.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-2415A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690627 | |||||||
| chr6:117690692 | A | C | 4 | a0001c0001t0002g0051 a0003c0005t0002g0051 a0003c0005t0002g0069 others(1): Show |
4 | NA18987.hp2 NA18999.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-2350A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690692 | |||||||
| chr6:117690767 | G | A | 2 | a0001c0001t0004g0152 a0001c0001t0004g0153 |
2 | HG00280.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.416-2275G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690767 | |||||||
| chr6:117690781 | G | A | 25 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(22): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.416-2261G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690781 | |||||||
| chr6:117690807 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(55): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.416-2235C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690807 | |||||||
| chr6:117690855 | T | C | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0234 |
3 | HG02922.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.416-2187T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690855 | |||||||
| chr6:117690902 | C | G | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-2140C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117690902 | |||||||
| chr6:117690979 | C | CA | 60 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0034 others(57): Show |
72 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.416-2041dupA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117690979 | ||||||
| chr6:117690979 | C | CAA | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(77): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.416-2042_416-2041d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117690979 | ||||||
| chr6:117690979 | C | CAAA | 8 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0111 others(5): Show |
8 | HG00639.hp1 HG01361.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-2043_416-2041d others(5): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117690979 | ||||||
| chr6:117690979 | CA | C | 5 | a0001c0001t0001g0030 a0001c0001t0002g0164 a0001c0001t0002g0183 others(2): Show |
6 | HG00323.hp2 HG02976.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-2041delA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117690979 | ||||||
| chr6:117691179 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.416-1863C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691179 | |||||||
| chr6:117691548 | C | T | 1 | a0001c0001t0026g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.416-1494C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691548 | |||||||
| chr6:117691552 | G | GAT | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0088 |
3 | HG00642.hp2 HG01081.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.416-1486_416-1485d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691552 | ||||||
| chr6:117691552 | G | GATAGATA others(3): Show |
1 | a0001c0001t0001g0086 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.416-1487_416-1486i others(12): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691552 | ||||||
| chr6:117691552 | G | GATAGATA others(5): Show |
1 | a0001c0001t0001g0033 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.416-1487_416-1486i others(14): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691552 | ||||||
| chr6:117691552 | G | GATATAT | 3 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0089 |
3 | HG01261.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.416-1485_416-1484i others(8): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691552 | ||||||
| chr6:117691552 | G | GATATATA others(1): Show |
4 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0080 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-1485_416-1484i others(10): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691552 | ||||||
| chr6:117691552 | G | GATATATA others(5): Show |
3 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.416-1485_416-1484i others(14): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691552 | ||||||
| chr6:117691552 | G | GATATATA others(7): Show |
3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0084 |
3 | HG00323.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.416-1485_416-1484i others(16): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691552 | ||||||
| chr6:117691553 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0004g0023 |
3 | HG02818.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.416-1489A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691553 | |||||||
| chr6:117691558 | G | GAT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0049 others(23): Show |
34 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.416-1456_416-1455d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | G | GATAT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(6): Show |
9 | HG00438.hp2 HG01167.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-1458_416-1455d others(6): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | G | GATATAT | 3 | a0001c0001t0001g0003 a0001c0001t0001g0217 a0001c0001t0025g0216 |
4 | NA18944.hp2 NA18977.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-1460_416-1455d others(8): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | G | GATATATA others(1): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0052 |
3 | HG02080.hp2 HG02129.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.416-1462_416-1455d others(10): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | G | GATATATA others(3): Show |
2 | a0001c0001t0001g0236 a0001c0001t0001g0238 |
2 | NA18981.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.416-1464_416-1455d others(12): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | G | GATATATA others(5): Show |
3 | a0001c0001t0001g0017 a0001c0001t0001g0237 a0001c0001t0001g0241 |
3 | HG00438.hp1 HG03654.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.416-1466_416-1455d others(14): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | G | GATATATA others(7): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0053 a0001c0001t0001g0070 others(2): Show |
6 | HG00735.hp1 HG01243.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-1468_416-1455d others(16): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | G | GATATATA others(9): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0240 |
2 | HG03831.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.416-1470_416-1455d others(18): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | G | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0034 others(19): Show |
24 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.416-1484G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691558 | |||||||
| chr6:117691558 | GAT | G | 34 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(31): Show |
57 | HG00140.hp2 HG00408.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.416-1456_416-1455d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | GATAT | G | 62 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0193 others(59): Show |
80 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.416-1458_416-1455d others(6): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | GATATAT | G | 31 | a0001c0001t0001g0035 a0001c0001t0001g0220 a0001c0001t0002g0013 others(28): Show |
45 | HG00140.hp1 HG01891.hp1 HG02055.hp1 others(42): Show |
intron_variant | MODIFIER | c.416-1460_416-1455d others(8): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691558 | GATATATA others(1): Show |
G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(59): Show |
118 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.416-1462_416-1455d others(10): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691558 | ||||||
| chr6:117691568 | T | G | 1 | a0001c0001t0002g0174 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.416-1474T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691568 | |||||||
| chr6:117691574 | T | G | 1 | a0001c0001t0003g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.416-1468T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691574 | |||||||
| chr6:117691588 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.416-1454G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691588 | |||||||
| chr6:117691597 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.416-1445A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691597 | |||||||
| chr6:117691687 | ATATT | A | 10 | a0001c0002t0004g0028 a0001c0002t0004g0054 a0001c0002t0004g0055 others(7): Show |
14 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.416-1352_416-1349d others(6): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117691687 | ||||||
| chr6:117691741 | C | A | 1 | a0001c0001t0007g0058 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.416-1301C>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691741 | |||||||
| chr6:117691871 | G | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
6 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-1171G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117691871 | |||||||
| chr6:117692533 | T | A | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.416-509T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117692533 | |||||||
| chr6:117692708 | A | C | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.416-334A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117692708 | |||||||
| chr6:117692711 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.416-331A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117692711 | |||||||
| chr6:117692831 | C | T | 25 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(22): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.416-211C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | chr6 | 117692831 | |||||||
| chr6:117692838 | C | CT | 6 | a0001c0002t0004g0054 a0001c0002t0004g0246 a0001c0002t0004g0247 others(3): Show |
7 | HG01891.hp1 HG02055.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-196dupT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 117692838 | ||||||
| chr6:117693236 | T | A | 1 | a0001c0001t0004g0152 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.541+69T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 2/4 | chr6 | 117693236 | |||||||
| chr6:117693350 | A | G | 1 | a0001c0002t0011g0025 | 3 | HG02809.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.541+183A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 2/4 | chr6 | 117693350 | |||||||
| chr6:117693448 | A | C | 1 | a0001c0001t0005g0141 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.541+281A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 2/4 | chr6 | 117693448 | |||||||
| chr6:117693768 | G | T | 1 | a0001c0001t0003g0173 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.542-263G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 2/4 | chr6 | 117693768 | |||||||
| chr6:117693826 | A | G | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.542-205A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 2/4 | chr6 | 117693826 | |||||||
| chr6:117693958 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0237 others(3): Show |
9 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.542-73T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 2/4 | chr6 | 117693958 | |||||||
| chr6:117694300 | G | A | 2 | a0001c0001t0012g0032 a0001c0001t0012g0067 |
3 | HG02717.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.691+120G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117694300 | |||||||
| chr6:117694597 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.691+417T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117694597 | |||||||
| chr6:117694691 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0172 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.691+511C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117694691 | |||||||
| chr6:117695026 | C | G | 1 | a0001c0002t0004g0246 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.691+846C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695026 | |||||||
| chr6:117695124 | G | A | 1 | a0001c0001t0026g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.691+944G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695124 | |||||||
| chr6:117695136 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(42): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.691+956G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695136 | |||||||
| chr6:117695149 | G | T | 1 | a0001c0001t0026g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.691+969G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695149 | |||||||
| chr6:117695180 | T | C | 1 | a0001c0002t0011g0025 | 3 | HG02809.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.691+1000T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695180 | |||||||
| chr6:117695193 | C | CA | 14 | a0001c0001t0001g0050 a0001c0001t0001g0221 a0001c0001t0001g0223 others(11): Show |
15 | HG00741.hp2 HG01069.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.691+1041dupA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117695193 | ||||||
| chr6:117695193 | CA | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.691+1041delA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117695193 | ||||||
| chr6:117695193 | CAA | C | 25 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(22): Show |
29 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.691+1040_691+1041d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117695193 | ||||||
| chr6:117695210 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0234 |
3 | HG02922.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.691+1030A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695210 | |||||||
| chr6:117695218 | A | AG | 6 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0130 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.691+1038_691+1039i others(3): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695218 | |||||||
| chr6:117695299 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.691+1119C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695299 | |||||||
| chr6:117695350 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(55): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.691+1170T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695350 | |||||||
| chr6:117695404 | G | T | 1 | a0001c0001t0001g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.691+1224G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695404 | |||||||
| chr6:117695405 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.691+1225C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695405 | |||||||
| chr6:117695496 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.691+1316G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695496 | |||||||
| chr6:117695611 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.691+1431A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695611 | |||||||
| chr6:117695673 | C | T | 7 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
7 | HG01891.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.691+1493C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695673 | |||||||
| chr6:117695724 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.691+1544T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695724 | |||||||
| chr6:117695850 | A | G | 1 | a0001c0001t0002g0263 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.691+1670A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695850 | |||||||
| chr6:117695919 | A | C | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02630.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+1739A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695919 | |||||||
| chr6:117695963 | G | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.691+1783G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117695963 | |||||||
| chr6:117696003 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(62): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.691+1823T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696003 | |||||||
| chr6:117696153 | T | C | 1 | a0001c0001t0002g0056 | 2 | HG01099.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.691+1973T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696153 | |||||||
| chr6:117696161 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.691+1981A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696161 | |||||||
| chr6:117696237 | G | T | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.691+2057G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696237 | |||||||
| chr6:117696267 | T | C | 1 | a0001c0001t0004g0153 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.691+2087T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696267 | |||||||
| chr6:117696374 | C | G | 1 | a0001c0001t0002g0181 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.691+2194C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696374 | |||||||
| chr6:117696642 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0230 a0001c0001t0026g0196 |
4 | HG02055.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.691+2462A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696642 | |||||||
| chr6:117696741 | T | C | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.691+2561T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696741 | |||||||
| chr6:117696842 | C | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0230 a0001c0001t0012g0032 others(2): Show |
7 | HG02055.hp2 HG02717.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.691+2662C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696842 | |||||||
| chr6:117696870 | C | A | 2 | a0001c0001t0014g0134 a0001c0001t0014g0138 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.691+2690C>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696870 | |||||||
| chr6:117696940 | A | G | 11 | a0001c0002t0004g0028 a0001c0002t0004g0054 a0001c0002t0004g0055 others(8): Show |
15 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.691+2760A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117696940 | |||||||
| chr6:117697005 | A | C | 9 | a0001c0001t0004g0040 a0001c0001t0004g0135 a0001c0001t0004g0144 others(6): Show |
9 | HG02083.hp2 HG02165.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.691+2825A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697005 | |||||||
| chr6:117697119 | T | A | 1 | a0001c0001t0008g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.691+2939T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697119 | |||||||
| chr6:117697191 | A | T | 4 | a0001c0001t0002g0051 a0003c0005t0002g0051 a0003c0005t0002g0069 others(1): Show |
4 | NA18987.hp2 NA18999.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+3011A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697191 | |||||||
| chr6:117697216 | C | T | 2 | a0001c0001t0014g0134 a0001c0001t0014g0138 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.691+3036C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697216 | |||||||
| chr6:117697287 | A | G | 1 | a0001c0001t0004g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.691+3107A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697287 | |||||||
| chr6:117697478 | C | T | 37 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(34): Show |
47 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.691+3298C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697478 | |||||||
| chr6:117697526 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.691+3346A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697526 | |||||||
| chr6:117697679 | GAA | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
16 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.691+3501_691+3502d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117697679 | ||||||
| chr6:117697717 | G | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
6 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+3537G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697717 | |||||||
| chr6:117697840 | A | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
6 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+3660A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697840 | |||||||
| chr6:117697899 | A | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0172 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.691+3719A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697899 | |||||||
| chr6:117697952 | C | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0233 a0001c0001t0025g0216 |
3 | HG00438.hp2 NA18944.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.691+3772C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697952 | |||||||
| chr6:117697986 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.691+3806A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117697986 | |||||||
| chr6:117698015 | A | G | 25 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(22): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.691+3835A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698015 | |||||||
| chr6:117698024 | C | T | 1 | a0001c0002t0011g0025 | 3 | HG02809.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.691+3844C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698024 | |||||||
| chr6:117698362 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.691+4182C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698362 | |||||||
| chr6:117698384 | A | G | 1 | a0001c0001t0004g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.691+4204A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698384 | |||||||
| chr6:117698516 | G | A | 1 | a0001c0001t0014g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.691+4336G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698516 | |||||||
| chr6:117698527 | GAA | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(42): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.691+4350_691+4351d others(4): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117698527 | ||||||
| chr6:117698608 | A | G | 2 | a0002c0003t0001g0037 a0002c0003t0023g0037 |
2 | NA18953.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.691+4428A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698608 | |||||||
| chr6:117698632 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.691+4452C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698632 | |||||||
| chr6:117698670 | T | C | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(18): Show |
23 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.691+4490T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698670 | |||||||
| chr6:117698813 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(46): Show |
76 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.691+4633C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698813 | |||||||
| chr6:117698820 | C | T | 1 | a0001c0001t0001g0015 | 4 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+4640C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698820 | |||||||
| chr6:117698882 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.691+4702A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698882 | |||||||
| chr6:117698939 | T | G | 15 | a0001c0001t0001g0050 a0001c0001t0001g0221 a0001c0001t0001g0222 others(12): Show |
19 | HG00140.hp2 HG01069.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.692-4666T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117698939 | |||||||
| chr6:117699000 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(42): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.692-4605C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699000 | |||||||
| chr6:117699102 | T | A | 25 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(22): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.692-4503T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699102 | |||||||
| chr6:117699115 | A | G | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.692-4490A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699115 | |||||||
| chr6:117699138 | C | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(13): Show |
31 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.692-4467C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699138 | |||||||
| chr6:117699174 | G | GA | 10 | a0001c0002t0004g0028 a0001c0002t0004g0054 a0001c0002t0004g0055 others(7): Show |
14 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.692-4427dupA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117699174 | ||||||
| chr6:117699258 | G | A | 25 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(22): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.692-4347G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699258 | |||||||
| chr6:117699396 | G | C | 2 | a0001c0001t0002g0136 a0001c0001t0002g0172 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.692-4209G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699396 | |||||||
| chr6:117699512 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0237 others(3): Show |
9 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.692-4093A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699512 | |||||||
| chr6:117699563 | G | C | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.692-4042G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699563 | |||||||
| chr6:117699580 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.692-4025C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699580 | |||||||
| chr6:117699654 | G | A | 2 | a0001c0001t0002g0136 a0001c0001t0002g0172 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.692-3951G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699654 | |||||||
| chr6:117699674 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0230 |
3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.692-3931A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699674 | |||||||
| chr6:117699696 | G | A | 1 | a0001c0001t0016g0060 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.692-3909G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699696 | |||||||
| chr6:117699819 | T | TAGACAAT others(4): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0066 |
5 | HG00423.hp2 HG02056.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.692-3768_692-3758d others(13): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117699819 | ||||||
| chr6:117699819 | TAGACAAT others(4): Show |
T | 3 | a0001c0001t0001g0193 a0001c0001t0004g0039 a0001c0001t0004g0146 |
4 | HG02602.hp1 HG03491.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.692-3768_692-3758d others(13): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117699819 | ||||||
| chr6:117699952 | G | A | 1 | a0001c0001t0005g0139 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.692-3653G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117699952 | |||||||
| chr6:117700053 | A | G | 1 | a0001c0001t0026g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.692-3552A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117700053 | |||||||
| chr6:117700102 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.692-3503A>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117700102 | |||||||
| chr6:117700340 | G | A | 1 | a0001c0001t0001g0047 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.692-3265G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117700340 | |||||||
| chr6:117700372 | A | G | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0100 others(2): Show |
5 | HG01074.hp2 HG01081.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.692-3233A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117700372 | |||||||
| chr6:117700408 | A | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
6 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-3197A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117700408 | |||||||
| chr6:117700412 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.692-3193G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117700412 | |||||||
| chr6:117700659 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(62): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.692-2946A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117700659 | |||||||
| chr6:117700966 | G | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(45): Show |
75 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.692-2639G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117700966 | |||||||
| chr6:117701004 | CA | C | 38 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0193 others(35): Show |
48 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.692-2590delA | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117701004 | ||||||
| chr6:117701025 | A | AT | 27 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0052 others(24): Show |
36 | HG00140.hp2 HG00438.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.692-2567dupT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117701025 | ||||||
| chr6:117701071 | A | C | 2 | a0001c0001t0012g0032 a0001c0001t0012g0067 |
3 | HG02717.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.692-2534A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701071 | |||||||
| chr6:117701245 | C | CT | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(42): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.692-2343dupT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117701245 | ||||||
| chr6:117701245 | CT | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(61): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.692-2343delT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117701245 | ||||||
| chr6:117701268 | G | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0027 a0001c0001t0002g0176 others(1): Show |
10 | NA18942.hp2 NA18944.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.692-2337G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701268 | |||||||
| chr6:117701393 | C | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
16 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.692-2212C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701393 | |||||||
| chr6:117701399 | C | T | 1 | a0001c0002t0004g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.692-2206C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701399 | |||||||
| chr6:117701400 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(15): Show |
33 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.692-2205G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701400 | |||||||
| chr6:117701402 | G | A | 2 | a0001c0001t0014g0134 a0001c0001t0014g0138 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.692-2203G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701402 | |||||||
| chr6:117701405 | T | C | 1 | a0001c0002t0004g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.692-2200T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701405 | |||||||
| chr6:117701420 | A | G | 1 | a0001c0001t0003g0227 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.692-2185A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701420 | |||||||
| chr6:117701480 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
16 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.692-2125G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701480 | |||||||
| chr6:117701540 | G | T | 7 | a0001c0001t0002g0042 a0001c0001t0002g0044 a0001c0001t0002g0165 others(4): Show |
9 | HG02523.hp1 NA18954.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.692-2065G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701540 | |||||||
| chr6:117701799 | C | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.692-1806C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117701799 | |||||||
| chr6:117701862 | A | AT | 26 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0052 others(23): Show |
35 | HG00140.hp2 HG00438.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.692-1737dupT | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117701862 | ||||||
| chr6:117702008 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0114 |
7 | HG00741.hp1 HG01496.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.692-1597T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117702008 | |||||||
| chr6:117702129 | A | ATTTCCTG others(26): Show |
1 | a0001c0001t0001g0112 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.692-1453_692-1452i others(35): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117702129 | ||||||
| chr6:117702153 | T | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(55): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.692-1452T>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117702153 | |||||||
| chr6:117702237 | C | T | 4 | a0001c0001t0002g0043 a0001c0001t0002g0191 a0001c0001t0002g0228 others(1): Show |
4 | HG00735.hp2 HG01258.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.692-1368C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117702237 | |||||||
| chr6:117702245 | T | C | 1 | a0001c0001t0026g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.692-1360T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117702245 | |||||||
| chr6:117702477 | G | T | 1 | a0001c0001t0004g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.692-1128G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117702477 | |||||||
| chr6:117702534 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.692-1071G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117702534 | |||||||
| chr6:117702754 | C | T | 2 | a0001c0001t0012g0032 a0001c0001t0012g0067 |
3 | HG02717.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.692-851C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117702754 | |||||||
| chr6:117702971 | C | T | 1 | a0001c0001t0002g0042 | 2 | NA18970.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.692-634C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117702971 | |||||||
| chr6:117703068 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.692-537T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117703068 | |||||||
| chr6:117703193 | G | T | 1 | a0001c0001t0002g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.692-412G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117703193 | |||||||
| chr6:117703351 | C | G | 1 | a0001c0001t0022g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.692-254C>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | chr6 | 117703351 | |||||||
| chr6:117703542 | CTGTG | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0230 |
3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.692-50_692-47delTG others(2): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 117703542 | ||||||
| chr6:117704269 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.791+565A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704269 | |||||||
| chr6:117704431 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.791+727G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704431 | |||||||
| chr6:117704462 | G | A | 1 | a0001c0002t0015g0244 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.791+758G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704462 | |||||||
| chr6:117704468 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.791+764A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704468 | |||||||
| chr6:117704480 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.791+776T>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704480 | |||||||
| chr6:117704492 | A | C | 1 | a0001c0001t0008g0041 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.791+788A>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704492 | |||||||
| chr6:117704617 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0230 |
3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.791+913A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704617 | |||||||
| chr6:117704618 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.791+914G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704618 | |||||||
| chr6:117704727 | C | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0159 a0001c0001t0001g0221 others(3): Show |
7 | HG00140.hp2 HG01069.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.791+1023C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704727 | |||||||
| chr6:117704880 | T | A | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.791+1176T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704880 | |||||||
| chr6:117704963 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(118): Show |
200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.791+1259C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117704963 | |||||||
| chr6:117705122 | C | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
16 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.791+1418C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705122 | |||||||
| chr6:117705196 | C | A | 2 | a0001c0001t0006g0130 a0001c0001t0006g0132 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.791+1492C>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705196 | |||||||
| chr6:117705293 | G | A | 7 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG00323.hp1 HG00642.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.791+1589G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705293 | |||||||
| chr6:117705486 | C | T | 2 | a0001c0001t0012g0032 a0001c0001t0012g0067 |
3 | HG02717.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.792-1439C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705486 | |||||||
| chr6:117705494 | G | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(14): Show |
32 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.792-1431G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705494 | |||||||
| chr6:117705514 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.792-1411A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705514 | |||||||
| chr6:117705531 | A | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0053 others(9): Show |
19 | HG00438.hp1 HG00735.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.792-1394A>G | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705531 | |||||||
| chr6:117705576 | C | T | 69 | a0001c0001t0001g0068 a0001c0001t0002g0005 a0001c0001t0002g0007 others(66): Show |
119 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.792-1349C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705576 | |||||||
| chr6:117705607 | G | A | 4 | a0001c0001t0005g0139 a0001c0001t0005g0140 a0001c0001t0005g0141 others(1): Show |
4 | HG02698.hp1 HG04204.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-1318G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705607 | |||||||
| chr6:117705609 | T | A | 4 | a0001c0001t0005g0139 a0001c0001t0005g0140 a0001c0001t0005g0141 others(1): Show |
4 | HG02698.hp1 HG04204.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-1316T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705609 | |||||||
| chr6:117705637 | G | C | 6 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0187 others(3): Show |
15 | HG00741.hp2 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.792-1288G>C | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117705637 | |||||||
| chr6:117706185 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.792-740T>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117706185 | |||||||
| chr6:117706311 | T | TTTGGATG others(11): Show |
1 | a0001c0001t0002g0164 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.792-612_792-595dup others(18): Show |
NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 117706311 | ||||||
| chr6:117706333 | C | T | 10 | a0001c0001t0005g0024 a0001c0001t0005g0139 a0001c0001t0005g0140 others(7): Show |
13 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.792-592C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117706333 | |||||||
| chr6:117706461 | C | T | 1 | a0001c0004t0001g0195 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.792-464C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117706461 | |||||||
| chr6:117706497 | C | T | 1 | a0001c0001t0003g0189 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.792-428C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117706497 | |||||||
| chr6:117706667 | C | T | 68 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0013 others(65): Show |
118 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.792-258C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117706667 | |||||||
| chr6:117706668 | G | A | 1 | a0001c0001t0004g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.792-257G>A | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117706668 | |||||||
| chr6:117706785 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0230 |
3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.792-140C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117706785 | |||||||
| chr6:117706786 | G | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0230 |
3 | HG02055.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.792-139G>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117706786 | |||||||
| chr6:117706908 | C | T | 1 | a0001c0001t0003g0170 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.792-17C>T | NUS1 | ENSG00000153989.8 | transcript | ENST00000368494.4 | protein_coding | 4/4 | chr6 | 117706908 |