Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64744 |
| ensemblid | ENSG00000084070.12 |
| hgncid | 25082 |
| symbol | SMAP2 |
| name | small ArfGAP2 |
| refseq_nuc | NM_022733.3 |
| refseq_prot | NP_073570.1 |
| ensembl_nuc | ENST00000372718.8 |
| ensembl_prot | ENSP00000361803.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 40373727 |
| end | 40423322 |
| strand | + |
| ver | v1.2 |
| region | chr1:40373727-40423322 |
| region5000 | chr1:40368727-40428322 |
| regionname0 | SMAP2_chr1_40373727_40423322 |
| regionname5000 | SMAP2_chr1_40368727_40428322 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 429 | 394 | 88 | 60 | 188 | 16 | 40 | 146 | SMAP2_chr1_40368727_40428322 | SMAP2 | MTGKS others(424): Show |
chr1 | 40368727 | 40428322 |
| a0002 | 0/0 | 429 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | MTGKS others(424): Show |
chr1 | 40368727 | 40428322 |
| a0003 | 0/0 | 429 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | MTGKS others(424): Show |
chr1 | 40368727 | 40428322 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1287 | 363 | 79 | 53 | 183 | 12 | 35 | SMAP2_chr1_40368727_40428322 | SMAP2 | ATGAC others(1282): Show |
chr1 | 40368727 | 40428322 | ||
| a0001c0002 | 1/0 | 1287 | 18 | 0 | 4 | 5 | 4 | 4 | SMAP2_chr1_40368727_40428322 | SMAP2 | ATGAC others(1282): Show |
chr1 | 40368727 | 40428322 | ||
| a0001c0003 | 0/0 | 1287 | 10 | 8 | 2 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | ATGAC others(1282): Show |
chr1 | 40368727 | 40428322 | ||
| a0001c0005 | 0/0 | 1287 | 3 | 1 | 1 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | ATGAC others(1282): Show |
chr1 | 40368727 | 40428322 | ||
| a0002c0004 | 0/0 | 1287 | 4 | 4 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | ATGAC others(1282): Show |
chr1 | 40368727 | 40428322 | ||
| a0003c0006 | 0/0 | 1287 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | ATGAC others(1282): Show |
chr1 | 40368727 | 40428322 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2905 | 344 | 72 | 52 | 173 | 11 | 35 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| a0001c0001t0002 | 0/0 | 2905 | 7 | 0 | 1 | 6 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| a0001c0001t0003 | 0/0 | 2904 | 4 | 4 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2899): Show |
chr1 | 40368727 | 40428322 |
| a0001c0001t0005 | 0/0 | 2905 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| a0001c0001t0006 | 0/0 | 2905 | 3 | 3 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| a0001c0001t0007 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| a0001c0001t0008 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| a0001c0002t0001 | 1/0 | 2905 | 18 | 0 | 4 | 5 | 4 | 4 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| a0001c0003t0001 | 0/0 | 2905 | 10 | 8 | 2 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| a0001c0005t0001 | 0/0 | 2905 | 3 | 1 | 1 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| a0002c0004t0004 | 0/0 | 2907 | 4 | 4 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2902): Show |
chr1 | 40368727 | 40428322 |
| a0003c0006t0001 | 0/0 | 2905 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | GGAGG others(2900): Show |
chr1 | 40368727 | 40428322 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0006 | 0/0 | 5 | 2 | 1 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0009 | 0/0 | 5 | 3 | 1 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0005g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0006g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0043 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0005t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0001c0005t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0002c0004t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0002c0004t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0002c0004t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0003c0006t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| a0003c0006t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0298 | EUR | GBR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0243 | EUR | FIN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00323 | hp2 | a0001 | c0001 | t0008 | g0297 | EUR | FIN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0103 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0214 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0104 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01433 | hp1 | a0001 | c0005 | t0001 | g0099 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0040 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0040 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0100 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01891 | hp1 | a0002 | c0004 | t0004 | g0026 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0098 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0101 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02622 | hp2 | a0002 | c0004 | t0004 | g0160 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0248 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03017 | hp1 | a0001 | c0005 | t0001 | g0097 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0091 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0215 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03579 | hp1 | a0002 | c0004 | t0004 | g0161 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0092 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18997 | hp1 | a0003 | c0006 | t0001 | g0285 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19085 | hp1 | a0003 | c0006 | t0001 | g0284 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA19240 | hp2 | a0002 | c0004 | t0004 | g0026 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ASW | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0216 | EUR | TSI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | GIH | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | GIH | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0102 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | USA | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | USA | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0123 | REF | REF | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0043 | REF | REF | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40416797 | G | A | 1 | a0002 | 4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.865G>A | p.Ala289Thr | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/10 | 1259/2905 | 865/1290 | 289/429 | chr1 | 40416797 | |||
| chr1:40416951 | T | C | 1 | a0003 | 2 | NA18997.hp1 NA19085.hp1 |
missense_variant | MODERATE | c.1019T>C | p.Met340Thr | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/10 | 1413/2905 | 1019/1290 | 340/429 | chr1 | 40416951 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40415369 | C | G | 5 | a0001c0001 a0001c0003 a0001c0005 others(2): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
synonymous_variant | LOW | c.669C>G | p.Ser223Ser | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/10 | 1063/2905 | 669/1290 | 223/429 | chr1 | 40415369 | |||
| chr1:40417075 | G | A | 1 | a0001c0005 | 3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
synonymous_variant | LOW | c.1143G>A | p.Gln381Gln | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/10 | 1537/2905 | 1143/1290 | 381/429 | chr1 | 40417075 | |||
| chr1:40417081 | A | G | 1 | a0001c0003 | 10 | HG01069.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
synonymous_variant | LOW | c.1149A>G | p.Gln383Gln | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/10 | 1543/2905 | 1149/1290 | 383/429 | chr1 | 40417081 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40373862 | G | A | 1 | a0001c0001t0005 | 3 | HG00438.hp2 NA18940.hp2 NA18984.hp2 |
5_prime_UTR_variant | MODIFIER | c.-259G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/10 | 259 | chr1 | 40373862 | ||||||
| chr1:40374049 | C | A | 1 | a0001c0001t0002 | 7 | HG00423.hp2 HG01928.hp1 NA18945.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-72C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/10 | 72 | chr1 | 40374049 | ||||||
| chr1:40422897 | A | AGT | 1 | a0002c0004t0004 | 4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*809_*810dupGT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 811 | INFO_REALIGN_3_PRIME | chr1 | 40422897 | |||||
| chr1:40422926 | C | T | 1 | a0001c0001t0006 | 3 | HG01884.hp2 HG02559.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*825C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 825 | chr1 | 40422926 | ||||||
| chr1:40422935 | C | T | 1 | a0001c0001t0008 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*834C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 834 | chr1 | 40422935 | ||||||
| chr1:40423038 | AT | A | 1 | a0001c0001t0003 | 4 | HG02630.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*938delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 938 | chr1 | 40423038 | ||||||
| chr1:40423162 | G | A | 2 | a0001c0001t0007 a0002c0004t0004 |
5 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1061G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 1061 | chr1 | 40423162 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40374227 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01167.hp1 | splice_region_variant&intron_variant | LOW | c.103+4G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374227 | |||||||
| chr1:40374392 | G | T | 1 | a0001c0001t0001g0304 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.103+169G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374392 | |||||||
| chr1:40374516 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.103+293T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374516 | |||||||
| chr1:40374556 | C | G | 1 | a0001c0001t0001g0303 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.103+333C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374556 | |||||||
| chr1:40374577 | T | TTGCG | 55 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.103+373_103+376dup others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374577 | ||||||
| chr1:40374596 | C | CGTGCGT | 6 | a0001c0001t0001g0035 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
7 | HG00642.hp1 HG01123.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+376_103+377ins others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374596 | ||||||
| chr1:40374596 | CGT | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(52): Show |
79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.103+401_103+402del others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374596 | ||||||
| chr1:40374596 | CGTGT | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
6 | HG02109.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+399_103+402del others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374596 | ||||||
| chr1:40374598 | T | TGC | 97 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(94): Show |
121 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.103+376_103+377ins others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374598 | ||||||
| chr1:40374599 | G | GCGTGTT | 18 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0171 others(15): Show |
21 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.103+376_103+377ins others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374599 | |||||||
| chr1:40374600 | T | C | 32 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(29): Show |
37 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.103+377T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374600 | |||||||
| chr1:40374602 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(51): Show |
78 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.103+379T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374602 | |||||||
| chr1:40374604 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG02109.hp1 HG04184.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+381T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374604 | |||||||
| chr1:40374620 | T | TGA | 6 | a0001c0002t0001g0040 a0001c0002t0001g0213 a0001c0002t0001g0214 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+398_103+399ins others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374620 | ||||||
| chr1:40374622 | T | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(48): Show |
64 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.103+399T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374622 | |||||||
| chr1:40374622 | T | TGA | 1 | a0001c0001t0006g0015 | 3 | HG01884.hp2 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.103+400_103+401ins others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374622 | ||||||
| chr1:40374622 | T | TGAGA | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.103+400_103+401ins others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374622 | ||||||
| chr1:40374622 | TGTGA | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0218 |
4 | HG02165.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+401_103+404del others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374622 | ||||||
| chr1:40374624 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
239 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.103+401T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374624 | |||||||
| chr1:40374624 | T | TGA | 6 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0298 others(3): Show |
11 | HG00099.hp2 HG00323.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.103+418_103+419dup others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374624 | ||||||
| chr1:40374624 | T | TGAGA | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG01243.hp1 HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.103+416_103+419dup others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374624 | ||||||
| chr1:40374624 | TGA | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0237 others(3): Show |
15 | HG00544.hp2 HG00735.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.103+418_103+419del others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374624 | ||||||
| chr1:40374626 | A | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0301 others(1): Show |
5 | HG01175.hp2 HG02056.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+403A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374626 | |||||||
| chr1:40374677 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.103+454G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374677 | |||||||
| chr1:40374681 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
255 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.103+458A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374681 | |||||||
| chr1:40374801 | C | A | 1 | a0001c0001t0001g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+578C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374801 | |||||||
| chr1:40375184 | C | A | 19 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0154 others(16): Show |
22 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.103+961C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375184 | |||||||
| chr1:40375334 | C | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
5 | HG01175.hp2 HG02683.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+1111C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375334 | |||||||
| chr1:40375377 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.103+1154T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375377 | |||||||
| chr1:40375419 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+1196C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375419 | |||||||
| chr1:40375477 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+1254G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375477 | |||||||
| chr1:40375567 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.103+1344T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375567 | |||||||
| chr1:40375582 | C | A | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1359C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375582 | |||||||
| chr1:40375593 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1370A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375593 | |||||||
| chr1:40375826 | A | AC | 39 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0049 others(36): Show |
41 | HG00408.hp1 HG00558.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.103+1614dupC | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40375826 | ||||||
| chr1:40375826 | AC | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
133 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.103+1614delC | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40375826 | ||||||
| chr1:40375826 | ACC | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.103+1613_103+1614d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40375826 | ||||||
| chr1:40375837 | C | A | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1614C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375837 | |||||||
| chr1:40375838 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1615A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375838 | |||||||
| chr1:40375942 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1719A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375942 | |||||||
| chr1:40375943 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1720T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375943 | |||||||
| chr1:40375982 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0122 |
2 | HG00323.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.103+1759G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375982 | |||||||
| chr1:40376010 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.103+1787G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376010 | |||||||
| chr1:40376019 | C | T | 19 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0154 others(16): Show |
22 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.103+1796C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376019 | |||||||
| chr1:40376099 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.103+1876C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376099 | |||||||
| chr1:40376102 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0296 |
3 | HG00408.hp1 NA18967.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.103+1879C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376102 | |||||||
| chr1:40376197 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.103+1974C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376197 | |||||||
| chr1:40376238 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0106 others(1): Show |
7 | HG02622.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+2015A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376238 | |||||||
| chr1:40376242 | T | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(51): Show |
69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.103+2019T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376242 | |||||||
| chr1:40376261 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.103+2038G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376261 | |||||||
| chr1:40376675 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+2452G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376675 | |||||||
| chr1:40376692 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.103+2469A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376692 | |||||||
| chr1:40376816 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+2593G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376816 | |||||||
| chr1:40376818 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+2595G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376818 | |||||||
| chr1:40376827 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.103+2604C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376827 | |||||||
| chr1:40376828 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.103+2605A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376828 | |||||||
| chr1:40376860 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0153 |
2 | NA18975.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.103+2637A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376860 | |||||||
| chr1:40376892 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+2669A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376892 | |||||||
| chr1:40376928 | T | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0254 a0001c0001t0001g0279 |
9 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.103+2705T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376928 | |||||||
| chr1:40376942 | T | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+2719T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376942 | |||||||
| chr1:40376944 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.103+2721C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376944 | |||||||
| chr1:40377226 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.103+3003C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377226 | |||||||
| chr1:40377227 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+3004G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377227 | |||||||
| chr1:40377253 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.103+3030G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377253 | |||||||
| chr1:40377261 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0188 others(6): Show |
18 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.103+3038G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377261 | |||||||
| chr1:40377433 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+3210T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377433 | |||||||
| chr1:40377599 | G | T | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+3376G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377599 | |||||||
| chr1:40377660 | G | A | 1 | a0001c0001t0008g0297 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.103+3437G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377660 | |||||||
| chr1:40378087 | A | T | 1 | a0001c0001t0001g0233 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.103+3864A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378087 | |||||||
| chr1:40378134 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.103+3911T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378134 | |||||||
| chr1:40378147 | C | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(67): Show |
88 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.103+3924C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378147 | |||||||
| chr1:40378296 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.103+4073C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378296 | |||||||
| chr1:40378344 | T | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+4121T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378344 | |||||||
| chr1:40378364 | A | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.103+4141A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378364 | |||||||
| chr1:40378407 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+4184A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378407 | |||||||
| chr1:40378453 | A | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
8 | NA18941.hp2 NA18970.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+4230A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378453 | |||||||
| chr1:40378727 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.103+4504C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378727 | |||||||
| chr1:40378730 | T | G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0042 others(12): Show |
31 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+4507T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378730 | |||||||
| chr1:40378939 | C | T | 1 | a0001c0005t0001g0099 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.103+4716C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378939 | |||||||
| chr1:40378962 | ATTTCT | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(35): Show |
50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.103+4758_103+4762d others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40378962 | ||||||
| chr1:40378981 | CT | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
132 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.103+4773delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40378981 | ||||||
| chr1:40379030 | C | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(51): Show |
69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.103+4807C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379030 | |||||||
| chr1:40379098 | G | C | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+4875G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379098 | |||||||
| chr1:40379099 | C | G | 1 | a0001c0001t0001g0242 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+4876C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379099 | |||||||
| chr1:40379449 | T | C | 4 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 others(1): Show |
5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+5226T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379449 | |||||||
| chr1:40379524 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.103+5301C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379524 | |||||||
| chr1:40379555 | C | CT | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(51): Show |
70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.103+5356dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40379555 | ||||||
| chr1:40379555 | C | CTT | 6 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0209 others(3): Show |
7 | HG00639.hp2 HG01433.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+5355_103+5356d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40379555 | ||||||
| chr1:40379555 | CT | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(106): Show |
146 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.103+5356delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40379555 | ||||||
| chr1:40379555 | CTT | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0069 a0001c0001t0001g0070 others(7): Show |
11 | HG00597.hp1 HG01069.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.103+5355_103+5356d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40379555 | ||||||
| chr1:40379675 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.103+5452C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379675 | |||||||
| chr1:40379707 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.103+5484T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379707 | |||||||
| chr1:40379713 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.103+5490G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379713 | |||||||
| chr1:40380309 | T | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(51): Show |
69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.103+6086T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380309 | |||||||
| chr1:40380320 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.103+6097C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380320 | |||||||
| chr1:40380457 | A | C | 1 | a0001c0001t0001g0256 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.103+6234A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380457 | |||||||
| chr1:40380529 | C | CT | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
127 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.103+6317dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40380529 | ||||||
| chr1:40380529 | C | CTTTTTT | 46 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0034 others(43): Show |
66 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.103+6312_103+6317d others(8): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40380529 | ||||||
| chr1:40380529 | C | CTTTTTTT | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(145): Show |
190 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.103+6311_103+6317d others(9): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40380529 | ||||||
| chr1:40380560 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG00558.hp1 NA18942.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+6337C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380560 | |||||||
| chr1:40380572 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.103+6349C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380572 | |||||||
| chr1:40380693 | C | A | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0111 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+6470C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380693 | |||||||
| chr1:40380750 | G | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(45): Show |
62 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.103+6527G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380750 | |||||||
| chr1:40380813 | G | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0172 a0001c0001t0001g0173 others(5): Show |
9 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.103+6590G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380813 | |||||||
| chr1:40380934 | T | C | 1 | a0001c0001t0001g0014 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+6711T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380934 | |||||||
| chr1:40380985 | G | A | 27 | a0001c0001t0001g0041 a0001c0001t0001g0108 a0001c0001t0001g0109 others(24): Show |
31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+6762G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380985 | |||||||
| chr1:40381142 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.103+6919A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381142 | |||||||
| chr1:40381162 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.103+6939G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381162 | |||||||
| chr1:40381175 | C | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.103+6952C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381175 | |||||||
| chr1:40381383 | T | C | 2 | a0001c0003t0001g0100 a0001c0003t0001g0105 |
2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.103+7160T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381383 | |||||||
| chr1:40381559 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.103+7336G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381559 | |||||||
| chr1:40381740 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.103+7517A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381740 | |||||||
| chr1:40381819 | A | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.103+7596A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381819 | |||||||
| chr1:40381940 | CT | C | 27 | a0001c0001t0001g0041 a0001c0001t0001g0108 a0001c0001t0001g0109 others(24): Show |
31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+7719delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40381940 | ||||||
| chr1:40382150 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0188 others(6): Show |
18 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.103+7927T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382150 | |||||||
| chr1:40382197 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.103+7974C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382197 | |||||||
| chr1:40382762 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.103+8539T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382762 | |||||||
| chr1:40382769 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+8546T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382769 | |||||||
| chr1:40382914 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.103+8691G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382914 | |||||||
| chr1:40383149 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+8926G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383149 | |||||||
| chr1:40383158 | T | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(67): Show |
88 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.103+8935T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383158 | |||||||
| chr1:40383276 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.103+9053G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383276 | |||||||
| chr1:40383319 | G | GCTC | 4 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 others(1): Show |
5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+9099_103+9101d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40383319 | ||||||
| chr1:40383531 | G | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0188 others(6): Show |
18 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.103+9308G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383531 | |||||||
| chr1:40383703 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.103+9480G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383703 | |||||||
| chr1:40383759 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.103+9536A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383759 | |||||||
| chr1:40384007 | A | G | 1 | a0001c0001t0001g0014 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+9784A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384007 | |||||||
| chr1:40384105 | C | T | 1 | a0001c0005t0001g0098 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.103+9882C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384105 | |||||||
| chr1:40384339 | A | T | 26 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(23): Show |
31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+10116A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384339 | |||||||
| chr1:40384484 | T | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.103+10261T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384484 | |||||||
| chr1:40384534 | A | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02615.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.103+10311A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384534 | |||||||
| chr1:40384559 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0090 |
2 | NA18977.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.103+10336T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384559 | |||||||
| chr1:40384615 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.103+10392G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384615 | |||||||
| chr1:40384914 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0241 |
4 | HG02723.hp1 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+10691T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384914 | |||||||
| chr1:40384941 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.103+10718G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384941 | |||||||
| chr1:40385041 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+10818C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385041 | |||||||
| chr1:40385079 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0241 |
4 | HG02723.hp1 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+10856C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385079 | |||||||
| chr1:40385421 | T | A | 3 | a0001c0001t0001g0257 a0001c0001t0001g0259 a0001c0001t0001g0275 |
3 | HG01496.hp2 HG02074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.103+11198T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385421 | |||||||
| chr1:40385455 | G | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+11232G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385455 | |||||||
| chr1:40385697 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG00733.hp1 HG01099.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+11474C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385697 | |||||||
| chr1:40385874 | A | AT | 27 | a0001c0001t0001g0041 a0001c0001t0001g0108 a0001c0001t0001g0109 others(24): Show |
31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+11652dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40385874 | ||||||
| chr1:40386030 | G | A | 27 | a0001c0001t0001g0041 a0001c0001t0001g0108 a0001c0001t0001g0109 others(24): Show |
31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+11807G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386030 | |||||||
| chr1:40386042 | G | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+11819G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386042 | |||||||
| chr1:40386190 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.103+11967C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386190 | |||||||
| chr1:40386269 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0183 |
2 | HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.103+12046A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386269 | |||||||
| chr1:40386435 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.103+12212A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386435 | |||||||
| chr1:40386462 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.103+12239T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386462 | |||||||
| chr1:40386660 | GTTT | G | 26 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(23): Show |
31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+12439_103+1244 others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386660 | ||||||
| chr1:40386665 | C | G | 26 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(23): Show |
31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+12442C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386665 | |||||||
| chr1:40386668 | T | A | 26 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(23): Show |
31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+12445T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386668 | |||||||
| chr1:40386669 | C | T | 26 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(23): Show |
31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+12446C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386669 | |||||||
| chr1:40386676 | G | C | 1 | a0001c0001t0001g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+12453G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386676 | |||||||
| chr1:40386691 | G | C | 1 | a0001c0001t0001g0260 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.103+12468G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386691 | |||||||
| chr1:40386710 | T | G | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(35): Show |
50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.103+12487T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386710 | |||||||
| chr1:40386716 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.103+12493T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386716 | |||||||
| chr1:40386740 | G | GT | 4 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0106 others(1): Show |
7 | HG02622.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+12525dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386740 | ||||||
| chr1:40386750 | AAAC | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
255 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.103+12537_103+1253 others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386750 | ||||||
| chr1:40386841 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0127 a0001c0001t0001g0128 |
4 | HG03491.hp2 HG03492.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+12618T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386841 | |||||||
| chr1:40386853 | C | CT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(110): Show |
151 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.103+12648dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386853 | ||||||
| chr1:40386853 | C | CTT | 7 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0089 others(4): Show |
12 | HG00099.hp2 HG01106.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.103+12647_103+1264 others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386853 | ||||||
| chr1:40386886 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0166 |
3 | HG01123.hp1 HG01256.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.103+12663T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386886 | |||||||
| chr1:40386892 | C | T | 19 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0154 others(16): Show |
22 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.103+12669C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386892 | |||||||
| chr1:40386977 | A | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | NA18943.hp2 NA18947.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.103+12754A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386977 | |||||||
| chr1:40387131 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+12908G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387131 | |||||||
| chr1:40387143 | A | T | 4 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 others(1): Show |
5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+12920A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387143 | |||||||
| chr1:40387149 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.103+12926G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387149 | |||||||
| chr1:40387172 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.103+12949T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387172 | |||||||
| chr1:40387240 | A | C | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.103+13017A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387240 | |||||||
| chr1:40387264 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.103+13041G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387264 | |||||||
| chr1:40387399 | T | G | 2 | a0001c0005t0001g0097 a0001c0005t0001g0099 |
2 | HG01433.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.103+13176T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387399 | |||||||
| chr1:40387411 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | NA18967.hp2 NA18968.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.103+13188G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387411 | |||||||
| chr1:40387418 | G | C | 1 | a0001c0001t0001g0261 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.103+13195G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387418 | |||||||
| chr1:40387522 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.103+13299A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387522 | |||||||
| chr1:40387611 | A | AG | 80 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(77): Show |
98 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.103+13391dupG | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40387611 | ||||||
| chr1:40387659 | G | A | 80 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(77): Show |
98 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.103+13436G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387659 | |||||||
| chr1:40387696 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0212 |
2 | NA18951.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.103+13473C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387696 | |||||||
| chr1:40387709 | C | T | 1 | a0001c0001t0001g0044 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.103+13486C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387709 | |||||||
| chr1:40387713 | C | T | 1 | a0001c0003t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103+13490C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387713 | |||||||
| chr1:40387753 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+13530G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387753 | |||||||
| chr1:40387817 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.103+13594C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387817 | |||||||
| chr1:40387910 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.103+13687C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387910 | |||||||
| chr1:40387920 | T | TG | 15 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0042 others(12): Show |
31 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+13700dupG | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40387920 | ||||||
| chr1:40387951 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.103+13728C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387951 | |||||||
| chr1:40388037 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.103+13814C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388037 | |||||||
| chr1:40388054 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.103+13831G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388054 | |||||||
| chr1:40388068 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+13845C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388068 | |||||||
| chr1:40388089 | C | T | 2 | a0001c0001t0001g0114 a0001c0003t0001g0151 |
2 | HG03540.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.103+13866C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388089 | |||||||
| chr1:40388137 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.103+13914A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388137 | |||||||
| chr1:40388220 | A | G | 4 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 others(1): Show |
5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+13997A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388220 | |||||||
| chr1:40388288 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103+14065T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388288 | |||||||
| chr1:40388371 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.103+14148C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388371 | |||||||
| chr1:40388458 | CGACACTC others(43): Show |
C | 1 | a0001c0001t0001g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103+14259_103+1430 others(54): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40388458 | ||||||
| chr1:40388562 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+14339C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388562 | |||||||
| chr1:40388612 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.103+14389G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388612 | |||||||
| chr1:40388663 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.103+14440C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388663 | |||||||
| chr1:40389059 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.103+14836G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389059 | |||||||
| chr1:40389070 | C | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+14847C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389070 | |||||||
| chr1:40389096 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+14873A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389096 | |||||||
| chr1:40389180 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.103+14957A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389180 | |||||||
| chr1:40389473 | G | GT | 81 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(78): Show |
99 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.103+15256dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40389473 | ||||||
| chr1:40389506 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.103+15283A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389506 | |||||||
| chr1:40389730 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.103+15507T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389730 | |||||||
| chr1:40389756 | G | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0094 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103+15533G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389756 | |||||||
| chr1:40389918 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(78): Show |
99 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.103+15695C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389918 | |||||||
| chr1:40389924 | C | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
5 | NA18943.hp2 NA18947.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+15701C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389924 | |||||||
| chr1:40389932 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(52): Show |
70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.103+15709C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389932 | |||||||
| chr1:40389983 | G | C | 1 | a0001c0001t0001g0304 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.103+15760G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389983 | |||||||
| chr1:40390019 | A | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(385): Show |
intron_variant | MODIFIER | c.103+15796A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40390019 | |||||||
| chr1:40390419 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.103+16196T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40390419 | |||||||
| chr1:40390974 | GA | G | 27 | a0001c0001t0001g0041 a0001c0001t0001g0108 a0001c0001t0001g0109 others(24): Show |
31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.104-15761delA | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40390974 | |||||||
| chr1:40391023 | G | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.104-15713G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391023 | |||||||
| chr1:40391038 | T | C | 2 | a0002c0004t0004g0160 a0002c0004t0004g0161 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.104-15698T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391038 | |||||||
| chr1:40391104 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(78): Show |
99 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.104-15632C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391104 | |||||||
| chr1:40391235 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.104-15501A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391235 | |||||||
| chr1:40391252 | A | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(385): Show |
intron_variant | MODIFIER | c.104-15484A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391252 | |||||||
| chr1:40391293 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.104-15443A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391293 | |||||||
| chr1:40391308 | T | C | 2 | a0002c0004t0004g0160 a0002c0004t0004g0161 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.104-15428T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391308 | |||||||
| chr1:40391691 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-15045T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391691 | |||||||
| chr1:40391858 | A | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.104-14878A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391858 | |||||||
| chr1:40391998 | A | G | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0111 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-14738A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391998 | |||||||
| chr1:40392026 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.104-14710T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392026 | |||||||
| chr1:40392080 | A | G | 4 | a0001c0001t0001g0066 a0001c0001t0001g0096 a0001c0001t0001g0165 others(1): Show |
4 | NA18747.hp1 NA18995.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-14656A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392080 | |||||||
| chr1:40392390 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.104-14346C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392390 | |||||||
| chr1:40392447 | C | A | 2 | a0001c0002t0001g0213 a0001c0002t0001g0214 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.104-14289C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392447 | |||||||
| chr1:40392609 | AGCAGGGT others(202): Show |
A | 1 | a0001c0001t0001g0143 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.104-14124_104-1391 others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40392609 | ||||||
| chr1:40392772 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0020 |
2 | HG02155.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.104-13964A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392772 | |||||||
| chr1:40392836 | A | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0258 a0001c0001t0001g0272 others(1): Show |
4 | NA18941.hp1 NA18956.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-13900A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392836 | |||||||
| chr1:40392873 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0148 |
3 | NA18747.hp2 NA18957.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.104-13863G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392873 | |||||||
| chr1:40392884 | G | C | 1 | a0001c0001t0001g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.104-13852G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392884 | |||||||
| chr1:40392898 | G | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(80): Show |
101 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.104-13838G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392898 | |||||||
| chr1:40393011 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.104-13725G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393011 | |||||||
| chr1:40393101 | C | CA | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.104-13622dupA | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393101 | ||||||
| chr1:40393101 | C | CAA | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(37): Show |
54 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.104-13623_104-1362 others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393101 | ||||||
| chr1:40393204 | T | TAGTC | 83 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(80): Show |
101 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.104-13531_104-1352 others(8): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393204 | ||||||
| chr1:40393315 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-13421A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393315 | |||||||
| chr1:40393380 | C | T | 2 | a0002c0004t0004g0160 a0002c0004t0004g0161 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.104-13356C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393380 | |||||||
| chr1:40393407 | A | C | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.104-13329A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393407 | |||||||
| chr1:40393541 | C | CT | 7 | a0001c0001t0001g0014 a0001c0001t0001g0235 a0001c0002t0001g0017 others(4): Show |
11 | HG01943.hp2 HG02145.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.104-13173dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393541 | ||||||
| chr1:40393541 | CT | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.104-13173delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393541 | ||||||
| chr1:40393541 | CTT | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(101): Show |
136 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.104-13174_104-1317 others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393541 | ||||||
| chr1:40393563 | T | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(35): Show |
50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.104-13173T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393563 | |||||||
| chr1:40393864 | A | C | 4 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 others(1): Show |
5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-12872A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393864 | |||||||
| chr1:40393865 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0191 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.104-12871G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393865 | |||||||
| chr1:40394052 | C | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-12684C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394052 | |||||||
| chr1:40394110 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG00408.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.104-12626G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394110 | |||||||
| chr1:40394516 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.104-12220C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394516 | |||||||
| chr1:40394685 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.104-12051C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394685 | |||||||
| chr1:40394747 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-11989G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394747 | |||||||
| chr1:40394758 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.104-11978C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394758 | |||||||
| chr1:40394794 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.104-11942G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394794 | |||||||
| chr1:40394975 | C | T | 1 | a0001c0005t0001g0099 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.104-11761C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394975 | |||||||
| chr1:40395044 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.104-11692G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395044 | |||||||
| chr1:40395049 | A | G | 1 | a0001c0001t0001g0014 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.104-11687A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395049 | |||||||
| chr1:40395082 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.104-11654T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395082 | |||||||
| chr1:40395317 | G | A | 3 | a0001c0001t0001g0257 a0001c0001t0001g0259 a0001c0001t0001g0275 |
3 | HG01496.hp2 HG02074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.104-11419G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395317 | |||||||
| chr1:40395437 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0241 |
4 | HG02723.hp1 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-11299T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395437 | |||||||
| chr1:40395468 | G | A | 1 | a0001c0001t0001g0010 | 3 | NA18939.hp2 NA18980.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.104-11268G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395468 | |||||||
| chr1:40395520 | A | AAAT | 46 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(43): Show |
62 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.104-11195_104-1119 others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40395520 | ||||||
| chr1:40395577 | T | TACTAAAA others(14): Show |
290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.104-11157_104-1115 others(25): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40395577 | ||||||
| chr1:40395733 | G | T | 1 | a0002c0004t0004g0026 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-11003G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395733 | |||||||
| chr1:40395760 | A | C | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.104-10976A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395760 | |||||||
| chr1:40395970 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.104-10766G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395970 | |||||||
| chr1:40396077 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0033 others(41): Show |
65 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.104-10659G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396077 | |||||||
| chr1:40396117 | T | TCTTTCCG others(5): Show |
1 | a0001c0001t0001g0136 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10617_104-1061 others(16): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40396117 | ||||||
| chr1:40396121 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10615C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396121 | |||||||
| chr1:40396127 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10609T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396127 | |||||||
| chr1:40396128 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10608C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396128 | |||||||
| chr1:40396139 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10597C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396139 | |||||||
| chr1:40396142 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10594C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396142 | |||||||
| chr1:40396168 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-10568A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396168 | |||||||
| chr1:40396192 | G | A | 1 | a0001c0001t0006g0015 | 3 | HG01884.hp2 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.104-10544G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396192 | |||||||
| chr1:40396229 | A | G | 17 | a0001c0001t0001g0041 a0001c0001t0001g0148 a0001c0001t0001g0187 others(14): Show |
21 | HG00423.hp2 HG00438.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.104-10507A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396229 | |||||||
| chr1:40396467 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.104-10269T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396467 | |||||||
| chr1:40396589 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-10147A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396589 | |||||||
| chr1:40396825 | G | A | 5 | a0001c0001t0001g0255 a0001c0001t0001g0258 a0001c0001t0001g0272 others(2): Show |
5 | HG02056.hp2 NA18941.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-9911G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396825 | |||||||
| chr1:40396897 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.104-9839G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396897 | |||||||
| chr1:40396986 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0241 |
4 | HG02723.hp1 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-9750C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396986 | |||||||
| chr1:40397057 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-9679C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397057 | |||||||
| chr1:40397104 | G | A | 1 | a0001c0002t0001g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.104-9632G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397104 | |||||||
| chr1:40397159 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.104-9577G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397159 | |||||||
| chr1:40397229 | A | C | 1 | a0001c0001t0001g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-9507A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397229 | |||||||
| chr1:40397680 | CATTGCCT others(4): Show |
C | 1 | a0002c0004t0004g0160 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.104-9055_104-9045d others(13): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397680 | |||||||
| chr1:40397692 | G | T | 1 | a0002c0004t0004g0160 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.104-9044G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397692 | |||||||
| chr1:40397725 | G | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-9011G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397725 | |||||||
| chr1:40397913 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-8823G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397913 | |||||||
| chr1:40398094 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-8642A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398094 | |||||||
| chr1:40398095 | T | A | 1 | a0001c0005t0001g0097 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.104-8641T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398095 | |||||||
| chr1:40398332 | C | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-8404C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398332 | |||||||
| chr1:40398342 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.104-8394G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398342 | |||||||
| chr1:40398342 | G | GC | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
380 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(377): Show |
intron_variant | MODIFIER | c.104-8393dupC | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40398342 | ||||||
| chr1:40398412 | A | AC | 93 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.104-8324_104-8323i others(3): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398412 | |||||||
| chr1:40398420 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.104-8316G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398420 | |||||||
| chr1:40398517 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-8219G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398517 | |||||||
| chr1:40398596 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.104-8140T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398596 | |||||||
| chr1:40398624 | G | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-8112G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398624 | |||||||
| chr1:40398837 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.104-7899G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398837 | |||||||
| chr1:40398862 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.104-7874A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398862 | |||||||
| chr1:40398872 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.104-7864G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398872 | |||||||
| chr1:40398986 | T | C | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.104-7750T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398986 | |||||||
| chr1:40399184 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.104-7552G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399184 | |||||||
| chr1:40399205 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.104-7531T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399205 | |||||||
| chr1:40399310 | A | AT | 7 | a0001c0002t0001g0040 a0001c0002t0001g0214 a0001c0002t0001g0216 others(4): Show |
8 | HG00735.hp1 HG01169.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-7405dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | ||||||
| chr1:40399310 | A | ATT | 5 | a0001c0001t0001g0014 a0001c0005t0001g0097 a0001c0005t0001g0098 others(2): Show |
8 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-7406_104-7405d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | ||||||
| chr1:40399310 | A | ATTT | 21 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0027 others(18): Show |
37 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.104-7407_104-7405d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | ||||||
| chr1:40399310 | A | ATTTT | 127 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.104-7408_104-7405d others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | ||||||
| chr1:40399310 | A | ATTTTT | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
96 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.104-7409_104-7405d others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | ||||||
| chr1:40399310 | A | ATTTTTT | 22 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0051 others(19): Show |
25 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.104-7410_104-7405d others(8): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | ||||||
| chr1:40399319 | T | TTTA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0070 others(2): Show |
8 | HG02080.hp2 HG02155.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-7415_104-7414i others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399319 | ||||||
| chr1:40399320 | T | TTA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
44 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.104-7415_104-7414i others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399320 | ||||||
| chr1:40399325 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-7411T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399325 | |||||||
| chr1:40399326 | T | A | 1 | a0001c0001t0001g0079 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.104-7410T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399326 | |||||||
| chr1:40399332 | G | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-7404G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399332 | |||||||
| chr1:40399400 | T | C | 1 | a0001c0002t0001g0248 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.104-7336T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399400 | |||||||
| chr1:40399450 | G | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0085 a0001c0001t0001g0087 |
3 | HG01891.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.104-7286G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399450 | |||||||
| chr1:40399498 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.104-7238T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399498 | |||||||
| chr1:40399629 | C | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-7107C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399629 | |||||||
| chr1:40399656 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-7080C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399656 | |||||||
| chr1:40399701 | CA | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(165): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.104-7022delA | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399701 | ||||||
| chr1:40399709 | AAAAAAG | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(79): Show |
100 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.104-7022_104-7017d others(8): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399709 | ||||||
| chr1:40399772 | T | TA | 37 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(34): Show |
54 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.104-6955dupA | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399772 | ||||||
| chr1:40399796 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.104-6940G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399796 | |||||||
| chr1:40399940 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0208 |
2 | NA18940.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.104-6796G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399940 | |||||||
| chr1:40399961 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0033 others(41): Show |
65 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.104-6775G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399961 | |||||||
| chr1:40400034 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.104-6702G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400034 | |||||||
| chr1:40400036 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.104-6700G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400036 | |||||||
| chr1:40400129 | G | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0042 others(12): Show |
31 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.104-6607G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400129 | |||||||
| chr1:40400296 | A | G | 1 | a0001c0002t0001g0247 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.104-6440A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400296 | |||||||
| chr1:40400379 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-6357A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400379 | |||||||
| chr1:40400616 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0033 others(75): Show |
104 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.104-6120C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400616 | |||||||
| chr1:40400649 | TGAA | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0218 others(4): Show |
16 | HG00544.hp2 HG00735.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.104-6083_104-6081d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40400649 | ||||||
| chr1:40400818 | CTGG | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(374): Show |
intron_variant | MODIFIER | c.104-5911_104-5909d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40400818 | ||||||
| chr1:40400862 | C | T | 6 | a0001c0002t0001g0040 a0001c0002t0001g0213 a0001c0002t0001g0214 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-5874C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400862 | |||||||
| chr1:40401127 | A | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(20): Show |
36 | HG00408.hp1 HG00639.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.104-5609A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401127 | |||||||
| chr1:40401129 | C | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(20): Show |
36 | HG00408.hp1 HG00639.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.104-5607C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401129 | |||||||
| chr1:40401130 | G | A | 1 | a0001c0003t0001g0102 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.104-5606G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401130 | |||||||
| chr1:40401146 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
264 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.104-5590T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401146 | |||||||
| chr1:40401179 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(195): Show |
262 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.104-5557C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401179 | |||||||
| chr1:40401186 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(328): Show |
intron_variant | MODIFIER | c.104-5550T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401186 | |||||||
| chr1:40401254 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0166 |
3 | HG01123.hp1 HG01256.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.104-5482T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401254 | |||||||
| chr1:40401273 | A | G | 4 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 others(1): Show |
5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-5463A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401273 | |||||||
| chr1:40401365 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.104-5371A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401365 | |||||||
| chr1:40401490 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.104-5246C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401490 | |||||||
| chr1:40402129 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(50): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.104-4607A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402129 | |||||||
| chr1:40402301 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.104-4435G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402301 | |||||||
| chr1:40402460 | T | G | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.104-4276T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402460 | |||||||
| chr1:40402461 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.104-4275T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402461 | |||||||
| chr1:40402613 | C | T | 1 | a0001c0002t0001g0040 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.104-4123C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402613 | |||||||
| chr1:40402669 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-4067A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402669 | |||||||
| chr1:40402744 | G | A | 4 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 others(1): Show |
5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-3992G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402744 | |||||||
| chr1:40402870 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.104-3866C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402870 | |||||||
| chr1:40403229 | A | C | 1 | a0001c0001t0001g0133 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.104-3507A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403229 | |||||||
| chr1:40403276 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0042 others(12): Show |
31 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.104-3460C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403276 | |||||||
| chr1:40403282 | C | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.104-3454C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403282 | |||||||
| chr1:40403373 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.104-3363C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403373 | |||||||
| chr1:40403412 | C | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.104-3324C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403412 | |||||||
| chr1:40403454 | A | C | 2 | a0002c0004t0004g0160 a0002c0004t0004g0161 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.104-3282A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403454 | |||||||
| chr1:40403461 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0206 |
3 | HG02602.hp2 NA18985.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.104-3275C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403461 | |||||||
| chr1:40403600 | A | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0042 others(15): Show |
34 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.104-3136A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403600 | |||||||
| chr1:40403713 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0102 a0001c0003t0001g0105 |
3 | HG01884.hp1 HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.104-3023G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403713 | |||||||
| chr1:40403884 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104-2852A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403884 | |||||||
| chr1:40403916 | T | C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0172 a0001c0001t0001g0173 others(5): Show |
9 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-2820T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403916 | |||||||
| chr1:40404046 | C | CTTGCCTT others(9): Show |
1 | a0001c0001t0001g0201 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.104-2690_104-2689i others(18): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404046 | |||||||
| chr1:40404047 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.104-2689A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404047 | |||||||
| chr1:40404088 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0171 others(2): Show |
8 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-2648A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404088 | |||||||
| chr1:40404473 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0080 a0001c0001t0001g0089 |
3 | NA18984.hp1 NA19002.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.104-2263T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404473 | |||||||
| chr1:40404791 | CAT | C | 3 | a0002c0004t0004g0026 a0002c0004t0004g0160 a0002c0004t0004g0161 |
4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-1944_104-1943d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404791 | |||||||
| chr1:40404873 | C | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(37): Show |
52 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.104-1863C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404873 | |||||||
| chr1:40405102 | TAC | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(79): Show |
100 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.104-1632_104-1631d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40405102 | ||||||
| chr1:40405573 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(35): Show |
50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.104-1163C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40405573 | |||||||
| chr1:40405631 | A | G | 27 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0108 others(24): Show |
32 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.104-1105A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40405631 | |||||||
| chr1:40405745 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.104-991A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40405745 | |||||||
| chr1:40405825 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
380 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(377): Show |
intron_variant | MODIFIER | c.104-911A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40405825 | |||||||
| chr1:40406449 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.104-287G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40406449 | |||||||
| chr1:40406523 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.104-213G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40406523 | |||||||
| chr1:40406684 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0033 others(37): Show |
60 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.104-52G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40406684 | |||||||
| chr1:40406937 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0265 |
2 | NA18955.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.237+68A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40406937 | |||||||
| chr1:40406951 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(110): Show |
158 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.237+82C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40406951 | |||||||
| chr1:40406968 | G | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0272 a0001c0001t0001g0294 |
3 | NA18956.hp1 NA19000.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.237+99G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40406968 | |||||||
| chr1:40407034 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.237+165A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407034 | |||||||
| chr1:40407067 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.237+198C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407067 | |||||||
| chr1:40407092 | C | T | 3 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 |
3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.237+223C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407092 | |||||||
| chr1:40407319 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.237+450C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407319 | |||||||
| chr1:40407521 | A | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0180 a0001c0001t0001g0183 |
3 | HG03195.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.237+652A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407521 | |||||||
| chr1:40407538 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237+669A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407538 | |||||||
| chr1:40407749 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.237+880G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407749 | |||||||
| chr1:40407788 | TATC | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02615.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-861_238-859del others(3): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 40407788 | ||||||
| chr1:40407993 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0171 others(2): Show |
8 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-660G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407993 | |||||||
| chr1:40408126 | A | G | 1 | a0001c0001t0006g0015 | 3 | HG01884.hp2 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.238-527A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40408126 | |||||||
| chr1:40408337 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.238-316T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40408337 | |||||||
| chr1:40408916 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.323+178G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40408916 | |||||||
| chr1:40409017 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.323+279A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409017 | |||||||
| chr1:40409076 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.323+338C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409076 | |||||||
| chr1:40409272 | T | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
8 | NA18941.hp2 NA18970.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-485T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409272 | |||||||
| chr1:40409312 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.324-445T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409312 | |||||||
| chr1:40409382 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.324-375A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409382 | |||||||
| chr1:40409550 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.324-207A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409550 | |||||||
| chr1:40410072 | A | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0266 a0001c0001t0001g0287 |
3 | HG00558.hp2 NA18612.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.402+237A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410072 | |||||||
| chr1:40410109 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0153 |
2 | NA18975.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.402+274G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410109 | |||||||
| chr1:40410152 | C | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.402+317C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410152 | |||||||
| chr1:40410162 | C | T | 3 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 |
3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.402+327C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410162 | |||||||
| chr1:40410441 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0023 others(72): Show |
101 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.402+606A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410441 | |||||||
| chr1:40410612 | C | G | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(35): Show |
50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.402+777C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410612 | |||||||
| chr1:40410682 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.402+847A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410682 | |||||||
| chr1:40410783 | C | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
49 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.402+948C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410783 | |||||||
| chr1:40410829 | T | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.402+994T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410829 | |||||||
| chr1:40411329 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.402+1494G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411329 | |||||||
| chr1:40411368 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(19): Show |
38 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.402+1533C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411368 | |||||||
| chr1:40411439 | GC | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0071 |
4 | NA18960.hp1 NA18974.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-1576delC | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411439 | |||||||
| chr1:40411442 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.403-1574A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411442 | |||||||
| chr1:40411446 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.403-1570G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411446 | |||||||
| chr1:40411514 | T | G | 1 | a0001c0001t0001g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.403-1502T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411514 | |||||||
| chr1:40411540 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.403-1476G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411540 | |||||||
| chr1:40411599 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(69): Show |
90 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.403-1417G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411599 | |||||||
| chr1:40411764 | TGTC | T | 4 | a0001c0001t0001g0264 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-1249_403-1247d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 40411764 | ||||||
| chr1:40411794 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.403-1222G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411794 | |||||||
| chr1:40411809 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.403-1207G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411809 | |||||||
| chr1:40411911 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0096 a0001c0001t0001g0288 |
3 | NA18995.hp1 NA19058.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.403-1105C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411911 | |||||||
| chr1:40411972 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(31): Show |
50 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.403-1044G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411972 | |||||||
| chr1:40412192 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.403-824G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40412192 | |||||||
| chr1:40412224 | G | A | 6 | a0001c0002t0001g0040 a0001c0002t0001g0213 a0001c0002t0001g0214 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.403-792G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40412224 | |||||||
| chr1:40412820 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.403-196C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40412820 | |||||||
| chr1:40412836 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.403-180C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40412836 | |||||||
| chr1:40413137 | C | T | 27 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0108 others(24): Show |
32 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.489+35C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413137 | |||||||
| chr1:40413239 | C | G | 1 | a0001c0003t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.489+137C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413239 | |||||||
| chr1:40413265 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.489+163G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413265 | |||||||
| chr1:40413265 | GT | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+165delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 40413265 | ||||||
| chr1:40413278 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.489+176G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413278 | |||||||
| chr1:40413303 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0110 others(4): Show |
9 | HG00639.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+201C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413303 | |||||||
| chr1:40413325 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.489+223T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413325 | |||||||
| chr1:40413582 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.489+480G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413582 | |||||||
| chr1:40413843 | C | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-316C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413843 | |||||||
| chr1:40413890 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.490-269G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413890 | |||||||
| chr1:40413962 | C | G | 1 | a0001c0001t0001g0016 | 3 | NA18941.hp2 NA18970.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.490-197C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413962 | |||||||
| chr1:40413964 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.490-195T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413964 | |||||||
| chr1:40414108 | A | G | 4 | a0001c0001t0001g0282 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG00733.hp1 HG01099.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-51A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40414108 | |||||||
| chr1:40414136 | G | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(35): Show |
50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.490-23G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40414136 | |||||||
| chr1:40414136 | G | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(335): Show |
intron_variant | MODIFIER | c.490-23G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40414136 | |||||||
| chr1:40414280 | T | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(110): Show |
158 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.571+40T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414280 | |||||||
| chr1:40414404 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.571+164G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414404 | |||||||
| chr1:40414434 | G | A | 3 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 |
3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.571+194G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414434 | |||||||
| chr1:40414528 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.571+288C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414528 | |||||||
| chr1:40414840 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.572-432T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414840 | |||||||
| chr1:40414887 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.572-385G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414887 | |||||||
| chr1:40414985 | A | G | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(19): Show |
26 | HG00639.hp2 HG02055.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.572-287A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414985 | |||||||
| chr1:40414990 | C | T | 2 | a0001c0003t0001g0103 a0001c0003t0001g0104 |
2 | HG01069.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.572-282C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414990 | |||||||
| chr1:40415013 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(69): Show |
90 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.572-259C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40415013 | |||||||
| chr1:40415076 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.572-196T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40415076 | |||||||
| chr1:40415132 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(39): Show |
56 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.572-140C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40415132 | |||||||
| chr1:40415517 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.681+136A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415517 | |||||||
| chr1:40415575 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(79): Show |
100 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.681+194A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415575 | |||||||
| chr1:40415657 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.681+276T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415657 | |||||||
| chr1:40415661 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.681+280T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415661 | |||||||
| chr1:40415674 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0110 others(4): Show |
9 | HG00639.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.681+293A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415674 | |||||||
| chr1:40415723 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | NA18957.hp2 NA18991.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.681+342C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415723 | |||||||
| chr1:40415775 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.681+394A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415775 | |||||||
| chr1:40415955 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
49 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.682-221G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415955 | |||||||
| chr1:40416168 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
49 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(46): Show |
splice_region_variant&intron_variant | LOW | c.682-8G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40416168 | |||||||
| chr1:40416360 | A | G | 3 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 |
3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.847+19A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 8/9 | chr1 | 40416360 | |||||||
| chr1:40417228 | C | CT | 65 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
86 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1164+151dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 40417228 | ||||||
| chr1:40417423 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(35): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1164+327C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417423 | |||||||
| chr1:40417460 | A | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0033 others(37): Show |
60 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1164+364A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417460 | |||||||
| chr1:40417509 | AAG | A | 3 | a0002c0004t0004g0026 a0002c0004t0004g0160 a0002c0004t0004g0161 |
4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+417_1164+418d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 40417509 | ||||||
| chr1:40417559 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0140 |
2 | NA18947.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1164+463C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417559 | |||||||
| chr1:40417572 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1164+476A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417572 | |||||||
| chr1:40417593 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1164+497C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417593 | |||||||
| chr1:40417594 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.1164+498A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417594 | |||||||
| chr1:40417692 | C | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02615.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1164+596C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417692 | |||||||
| chr1:40417712 | C | T | 3 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 |
3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1164+616C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417712 | |||||||
| chr1:40417851 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(35): Show |
50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1164+755C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417851 | |||||||
| chr1:40418616 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0218 others(5): Show |
17 | HG00544.hp2 HG00735.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1164+1520A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40418616 | |||||||
| chr1:40419017 | G | C | 1 | a0001c0001t0001g0274 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1164+1921G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419017 | |||||||
| chr1:40419026 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1164+1930C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419026 | |||||||
| chr1:40419041 | A | T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1164+1945A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419041 | |||||||
| chr1:40419280 | CT | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
267 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.1164+2202delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 40419280 | ||||||
| chr1:40419280 | CTT | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0238 a0001c0001t0001g0258 others(4): Show |
8 | HG01515.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1164+2201_1164+220 others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 40419280 | ||||||
| chr1:40419285 | T | A | 3 | a0002c0004t0004g0026 a0002c0004t0004g0160 a0002c0004t0004g0161 |
4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+2189T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419285 | |||||||
| chr1:40419334 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1164+2238G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419334 | |||||||
| chr1:40419624 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1165-2352A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419624 | |||||||
| chr1:40420082 | C | T | 3 | a0001c0005t0001g0097 a0001c0005t0001g0098 a0001c0005t0001g0099 |
3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1165-1894C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420082 | |||||||
| chr1:40420160 | A | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(81): Show |
102 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1165-1816A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420160 | |||||||
| chr1:40420460 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1165-1516C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420460 | |||||||
| chr1:40420631 | G | A | 1 | a0001c0002t0001g0247 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1165-1345G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420631 | |||||||
| chr1:40420819 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1165-1157T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420819 | |||||||
| chr1:40420925 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1165-1051A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420925 | |||||||
| chr1:40420943 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1165-1033T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420943 | |||||||
| chr1:40420985 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0191 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1165-991C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420985 | |||||||
| chr1:40420991 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1165-985T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420991 | |||||||
| chr1:40421367 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0106 |
3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1165-609C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40421367 | |||||||
| chr1:40421511 | T | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0171 others(1): Show |
7 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165-465T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40421511 | |||||||
| chr1:40421701 | A | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0171 others(2): Show |
8 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165-275A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40421701 | |||||||
| chr1:40421717 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0131 |
2 | NA18988.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1165-259G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40421717 |