Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9489 |
| ensemblid | ENSG00000087157.19 |
| hgncid | 30029 |
| symbol | PGS1 |
| name | phosphatidylglycerophosphate synthase 1 |
| refseq_nuc | NM_024419.5 |
| refseq_prot | NP_077733.3 |
| ensembl_nuc | ENST00000262764.11 |
| ensembl_prot | ENSP00000262764.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 78378649 |
| end | 78424659 |
| strand | + |
| ver | v1.2 |
| region | chr17:78378649-78424659 |
| region5000 | chr17:78373649-78429659 |
| regionname0 | PGS1_chr17_78378649_78424659 |
| regionname5000 | PGS1_chr17_78373649_78429659 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 556 | 389 | 87 | 76 | 164 | 16 | 44 | 127 | PGS1_chr17_78373649_78429659 | PGS1 | MAVAA others(551): Show |
chr17 | 78373649 | 78429659 |
| a0002 | 0/0 | 556 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | MAVAA others(551): Show |
chr17 | 78373649 | 78429659 |
| a0003 | 0/0 | 556 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PGS1_chr17_78373649_78429659 | PGS1 | MAVAA others(551): Show |
chr17 | 78373649 | 78429659 |
| a0004 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | MAVAA others(551): Show |
chr17 | 78373649 | 78429659 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1668 | 198 | 44 | 36 | 80 | 11 | 27 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0001c0002 | 1/1 | 1668 | 168 | 28 | 36 | 80 | 5 | 17 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0001c0003 | 0/0 | 1668 | 15 | 13 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0001c0006 | 0/0 | 1668 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0001c0007 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0001c0008 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0001c0010 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0001c0011 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0001c0012 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0001c0013 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0002c0004 | 0/0 | 1668 | 5 | 5 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0003c0005 | 0/0 | 1668 | 3 | 0 | 0 | 3 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 | ||
| a0004c0009 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | ATGGC others(1663): Show |
chr17 | 78373649 | 78429659 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2297 | 177 | 36 | 33 | 75 | 7 | 26 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0001t0002 | 0/0 | 2301 | 10 | 3 | 3 | 0 | 4 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2296): Show |
chr17 | 78373649 | 78429659 |
| a0001c0001t0003 | 0/0 | 2297 | 3 | 3 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0001t0004 | 0/0 | 2294 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2289): Show |
chr17 | 78373649 | 78429659 |
| a0001c0001t0005 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0001t0006 | 0/0 | 2297 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0001t0009 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0001t0010 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0001t0012 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0001t0015 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0002t0001 | 0/1 | 2297 | 135 | 19 | 25 | 74 | 3 | 13 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0002t0002 | 0/0 | 2301 | 21 | 5 | 7 | 3 | 2 | 4 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2296): Show |
chr17 | 78373649 | 78429659 |
| a0001c0002t0003 | 1/0 | 2297 | 4 | 3 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0002t0004 | 0/0 | 2294 | 3 | 0 | 0 | 3 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2289): Show |
chr17 | 78373649 | 78429659 |
| a0001c0002t0005 | 0/0 | 2297 | 2 | 1 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0002t0007 | 0/0 | 2297 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0002t0013 | 0/0 | 2297 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0003t0001 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0003t0002 | 0/0 | 2301 | 12 | 11 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2296): Show |
chr17 | 78373649 | 78429659 |
| a0001c0003t0008 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0003t0016 | 0/0 | 2301 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2296): Show |
chr17 | 78373649 | 78429659 |
| a0001c0006t0001 | 0/0 | 2297 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0007t0006 | 0/0 | 2297 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0008t0001 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0010t0001 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0011t0002 | 0/0 | 2301 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2296): Show |
chr17 | 78373649 | 78429659 |
| a0001c0012t0008 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0001c0013t0011 | 0/0 | 2297 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0002c0004t0001 | 0/0 | 2297 | 5 | 5 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0003c0005t0001 | 0/0 | 2297 | 3 | 0 | 0 | 3 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2292): Show |
chr17 | 78373649 | 78429659 |
| a0004c0009t0014 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | GGAAG others(2389): Show |
chr17 | 78373649 | 78429659 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0002g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0009g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0010g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0012g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0001t0015g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0030 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0003g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0007g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0002t0013g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0003t0016g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0006t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0006t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0007t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0008t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0010t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0011t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0012t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0001c0013t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0002c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0003c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0003c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0003c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| a0004c0009t0014g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0165 | EUR | GBR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | GBR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | GBR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0167 | EUR | GBR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | FIN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0155 | EUR | FIN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00423 | hp2 | a0001 | c0010 | t0001 | g0227 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0070 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00741 | hp1 | a0001 | c0007 | t0006 | g0170 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0369 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01106 | hp1 | a0001 | c0003 | t0016 | g0076 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0368 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01109 | hp1 | a0001 | c0002 | t0007 | g0017 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01169 | hp2 | a0001 | c0002 | t0013 | g0001 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0084 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | PUR | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01256 | hp1 | a0001 | c0011 | t0002 | g0315 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0367 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0191 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01952 | hp1 | a0001 | c0002 | t0007 | g0112 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0370 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0351 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02040 | hp2 | a0004 | c0009 | t0014 | g0145 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0183 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02129 | hp1 | a0001 | c0002 | t0004 | g0173 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | CDX | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0375 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0077 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0331 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | KHV | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0194 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02647 | hp2 | a0001 | c0013 | t0011 | g0187 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0080 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0081 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0087 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0374 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0184 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02886 | hp2 | a0001 | c0003 | t0008 | g0018 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0114 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0340 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0181 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0182 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0179 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03209 | hp2 | a0001 | c0003 | t0002 | g0178 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0185 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0177 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03486 | hp2 | a0002 | c0004 | t0001 | g0193 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0164 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0200 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0099 | AFR | ESN | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0195 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0002 | AFR | GWD | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03579 | hp1 | a0001 | c0012 | t0008 | g0188 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0363 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0224 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0362 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0118 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0175 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0291 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | BEB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0209 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0078 | SAS | STU | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0343 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CHB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | CHB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | CHB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0075 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18939 | hp1 | a0001 | c0001 | t0010 | g0348 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18940 | hp1 | a0001 | c0006 | t0001 | g0295 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18948 | hp2 | a0001 | c0002 | t0004 | g0138 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18964 | hp1 | a0003 | c0005 | t0001 | g0135 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18971 | hp2 | a0001 | c0008 | t0001 | g0009 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18980 | hp1 | a0003 | c0005 | t0001 | g0130 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18995 | hp2 | a0001 | c0001 | t0015 | g0300 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19000 | hp2 | a0003 | c0005 | t0001 | g0137 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19001 | hp2 | a0001 | c0001 | t0009 | g0366 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19012 | hp1 | a0001 | c0002 | t0004 | g0124 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0339 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19057 | hp2 | a0001 | c0006 | t0001 | g0261 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20129 | hp1 | a0002 | c0004 | t0001 | g0190 | AFR | ASW | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ASW | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0067 | EUR | TSI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | TSI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0203 | EUR | TSI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | TSI | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | GIH | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG01123 | hp2 | a0001 | c0003 | t0002 | g0026 | AMR | CLM | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0089 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0176 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0180 | AFR | MSL | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | USA | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | USA | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | USA | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | USA | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | LWK | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0030 | REF | REF | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0088 | REF | REF | PGS1_chr17_78373649_78429659 | PGS1 | chr17 | 78373649 | 78429659 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78403688 | A | T | 1 | a0004 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1001A>T | p.Gln334Leu | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/10 | 1018/2297 | 1001/1671 | 334/556 | chr17 | 78403688 | |||
| chr17:78404024 | T | G | 1 | a0002 | 5 | HG01884.hp2 HG02630.hp1 HG03486.hp2 others(2): Show |
missense_variant | MODERATE | c.1337T>G | p.Leu446Arg | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/10 | 1354/2297 | 1337/1671 | 446/556 | chr17 | 78404024 | |||
| chr17:78414896 | G | T | 1 | a0003 | 3 | NA18964.hp1 NA18980.hp1 NA19000.hp2 |
missense_variant | MODERATE | c.1420G>T | p.Ala474Ser | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/10 | 1437/2297 | 1420/1671 | 474/556 | chr17 | 78414896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78378756 | C | T | 2 | a0001c0012 a0001c0013 |
2 | HG02647.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.91C>T | p.Leu31Leu | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/10 | 108/2297 | 91/1671 | 31/556 | chr17 | 78378756 | |||
| chr17:78399349 | C | T | 6 | a0001c0001 a0001c0003 a0001c0006 others(3): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
splice_region_variant&synonymous_variant | LOW | c.513C>T | p.Gly171Gly | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/10 | 530/2297 | 513/1671 | 171/556 | chr17 | 78399349 | |||
| chr17:78399427 | G | A | 1 | a0001c0007 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.591G>A | p.Thr197Thr | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/10 | 608/2297 | 591/1671 | 197/556 | chr17 | 78399427 | |||
| chr17:78400764 | G | A | 1 | a0001c0010 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.789G>A | p.Thr263Thr | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/10 | 806/2297 | 789/1671 | 263/556 | chr17 | 78400764 | |||
| chr17:78403746 | G | A | 1 | a0001c0003 | 15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
synonymous_variant | LOW | c.1059G>A | p.Pro353Pro | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/10 | 1076/2297 | 1059/1671 | 353/556 | chr17 | 78403746 | |||
| chr17:78404082 | C | T | 1 | a0001c0011 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1395C>T | p.His465His | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/10 | 1412/2297 | 1395/1671 | 465/556 | chr17 | 78404082 | |||
| chr17:78419621 | C | T | 1 | a0001c0006 | 2 | NA18940.hp1 NA19057.hp2 |
synonymous_variant | LOW | c.1627C>T | p.Leu543Leu | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/10 | 1644/2297 | 1627/1671 | 543/556 | chr17 | 78419621 | |||
| chr17:78419647 | G | C | 1 | a0001c0008 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1653G>C | p.Leu551Leu | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/10 | 1670/2297 | 1653/1671 | 551/556 | chr17 | 78419647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78424112 | G | A | 2 | a0001c0001t0009 a0001c0001t0010 |
2 | NA18939.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4447 | chr17 | 78424112 | ||||||
| chr17:78424137 | G | A | 1 | a0001c0013t0011 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4472 | chr17 | 78424137 | ||||||
| chr17:78424292 | G | A | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(21): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*242G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4627 | chr17 | 78424292 | ||||||
| chr17:78424307 | C | A | 2 | a0001c0001t0006 a0001c0007t0006 |
2 | HG00741.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*257C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4642 | chr17 | 78424307 | ||||||
| chr17:78424312 | G | A | 5 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(2): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*262G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4647 | chr17 | 78424312 | ||||||
| chr17:78424356 | T | A | 5 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(2): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*306T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4691 | chr17 | 78424356 | ||||||
| chr17:78424410 | T | TTTTCAGA others(90): Show |
1 | a0004c0009t0014 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*362_*458dupTTCAGA others(91): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4844 | INFO_REALIGN_3_PRIME | chr17 | 78424410 | |||||
| chr17:78424414 | C | T | 2 | a0001c0003t0008 a0001c0012t0008 |
2 | HG02886.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*364C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4749 | chr17 | 78424414 | ||||||
| chr17:78424432 | C | T | 1 | a0001c0002t0007 | 2 | HG01109.hp1 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*382C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4767 | chr17 | 78424432 | ||||||
| chr17:78424436 | A | G | 1 | a0001c0001t0015 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*386A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4771 | chr17 | 78424436 | ||||||
| chr17:78424502 | G | A | 2 | a0001c0001t0005 a0001c0002t0005 |
3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*452G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4837 | chr17 | 78424502 | ||||||
| chr17:78424525 | C | A | 1 | a0001c0001t0009 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*475C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4860 | chr17 | 78424525 | ||||||
| chr17:78424526 | A | G | 1 | a0001c0002t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*476A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4861 | chr17 | 78424526 | ||||||
| chr17:78424561 | A | ATTAT | 5 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(2): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*513_*514insATTT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4899 | INFO_REALIGN_3_PRIME | chr17 | 78424561 | |||||
| chr17:78424582 | A | G | 1 | a0001c0003t0016 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*532A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4917 | chr17 | 78424582 | ||||||
| chr17:78424610 | GTTT | G | 2 | a0001c0001t0004 a0001c0002t0004 |
5 | HG02040.hp1 HG02129.hp1 NA18948.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*563_*565delTTT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4948 | INFO_REALIGN_3_PRIME | chr17 | 78424610 | |||||
| chr17:78424617 | T | G | 1 | a0001c0001t0012 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*567T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 10/10 | 4952 | chr17 | 78424617 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78378882 | C | T | 1 | a0001c0001t0001g0375 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143+74C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78378882 | |||||||
| chr17:78378897 | C | G | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.143+89C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78378897 | |||||||
| chr17:78379014 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(124): Show |
137 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.143+206A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379014 | |||||||
| chr17:78379049 | C | G | 1 | a0001c0002t0001g0329 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.143+241C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379049 | |||||||
| chr17:78379266 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.143+458G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379266 | |||||||
| chr17:78379271 | T | C | 1 | a0001c0002t0007g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.143+463T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379271 | |||||||
| chr17:78379445 | G | A | 1 | a0001c0003t0008g0018 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.143+637G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379445 | |||||||
| chr17:78379657 | C | T | 1 | a0001c0001t0001g0374 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.143+849C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379657 | |||||||
| chr17:78379842 | T | A | 6 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(3): Show |
6 | NA18612.hp1 NA18941.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.143+1034T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379842 | |||||||
| chr17:78379875 | C | CT | 46 | a0001c0001t0001g0016 a0001c0001t0001g0327 a0001c0001t0001g0328 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.143+1077dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78379875 | ||||||
| chr17:78379976 | C | T | 3 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0326 |
3 | HG02148.hp1 NA18966.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.143+1168C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78379976 | |||||||
| chr17:78380027 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143+1219C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380027 | |||||||
| chr17:78380155 | C | T | 20 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(17): Show |
20 | HG00558.hp2 HG01069.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.143+1347C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380155 | |||||||
| chr17:78380173 | G | T | 1 | a0001c0002t0002g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.143+1365G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380173 | |||||||
| chr17:78380230 | C | T | 3 | a0001c0001t0001g0371 a0001c0001t0001g0372 a0001c0001t0001g0373 |
3 | NA18984.hp1 NA18990.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.143+1422C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380230 | |||||||
| chr17:78380270 | A | G | 22 | a0001c0002t0001g0186 a0001c0002t0001g0192 a0001c0002t0002g0189 others(19): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.143+1462A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380270 | |||||||
| chr17:78380444 | T | C | 48 | a0001c0001t0001g0016 a0001c0001t0001g0327 a0001c0001t0001g0328 others(45): Show |
49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.143+1636T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380444 | |||||||
| chr17:78380468 | T | C | 1 | a0001c0002t0001g0025 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.143+1660T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380468 | |||||||
| chr17:78380576 | C | A | 22 | a0001c0002t0001g0186 a0001c0002t0001g0192 a0001c0002t0002g0189 others(19): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.143+1768C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380576 | |||||||
| chr17:78380637 | AT | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG01891.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.143+1832delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78380637 | ||||||
| chr17:78380728 | A | G | 1 | a0001c0002t0001g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.143+1920A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380728 | |||||||
| chr17:78380861 | T | C | 1 | a0001c0003t0002g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.143+2053T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380861 | |||||||
| chr17:78380937 | G | A | 1 | a0001c0002t0001g0027 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.143+2129G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78380937 | |||||||
| chr17:78381020 | A | G | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.143+2212A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381020 | |||||||
| chr17:78381082 | A | T | 8 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(5): Show |
8 | HG00738.hp2 HG01943.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.143+2274A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381082 | |||||||
| chr17:78381344 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.143+2536G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381344 | |||||||
| chr17:78381377 | A | G | 138 | a0001c0001t0001g0016 a0001c0001t0001g0152 a0001c0001t0001g0327 others(135): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.143+2569A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381377 | |||||||
| chr17:78381401 | T | G | 222 | a0001c0001t0001g0016 a0001c0001t0001g0069 a0001c0001t0001g0152 others(219): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.143+2593T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381401 | |||||||
| chr17:78381408 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.143+2600G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381408 | |||||||
| chr17:78381416 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.143+2608T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381416 | |||||||
| chr17:78381421 | G | T | 1 | a0001c0011t0002g0315 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.143+2613G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381421 | |||||||
| chr17:78381476 | C | T | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.143+2668C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381476 | |||||||
| chr17:78381586 | A | T | 1 | a0002c0004t0001g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.143+2778A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381586 | |||||||
| chr17:78381592 | C | T | 44 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0335 others(41): Show |
44 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.143+2784C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381592 | |||||||
| chr17:78381821 | T | C | 1 | a0001c0002t0001g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.143+3013T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381821 | |||||||
| chr17:78381920 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG01891.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.143+3112G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381920 | |||||||
| chr17:78381921 | C | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00741.hp2 NA18983.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.143+3113C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381921 | |||||||
| chr17:78381966 | C | A | 11 | a0001c0003t0002g0176 a0001c0003t0002g0177 a0001c0003t0002g0178 others(8): Show |
11 | HG02055.hp1 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.143+3158C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78381966 | |||||||
| chr17:78382009 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.143+3201G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382009 | |||||||
| chr17:78382014 | A | G | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.143+3206A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382014 | |||||||
| chr17:78382117 | A | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0002t0001g0192 others(6): Show |
10 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+3309A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382117 | |||||||
| chr17:78382198 | A | G | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.143+3390A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382198 | |||||||
| chr17:78382213 | C | G | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.143+3405C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382213 | |||||||
| chr17:78382332 | G | A | 46 | a0001c0001t0001g0152 a0001c0002t0001g0007 a0001c0002t0001g0008 others(43): Show |
49 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.143+3524G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382332 | |||||||
| chr17:78382339 | C | T | 2 | a0001c0012t0008g0188 a0001c0013t0011g0187 |
2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.143+3531C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382339 | |||||||
| chr17:78382521 | G | C | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.143+3713G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382521 | |||||||
| chr17:78382522 | G | A | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.143+3714G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382522 | |||||||
| chr17:78382581 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.143+3773A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382581 | |||||||
| chr17:78382621 | C | T | 4 | a0001c0001t0001g0368 a0001c0001t0002g0367 a0001c0001t0002g0369 others(1): Show |
4 | HG01074.hp2 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+3813C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382621 | |||||||
| chr17:78382636 | G | GT | 95 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0069 others(92): Show |
99 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.143+3852dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78382636 | ||||||
| chr17:78382636 | G | GTT | 73 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(70): Show |
75 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.143+3851_143+3852d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78382636 | ||||||
| chr17:78382636 | G | GTTT | 18 | a0001c0001t0001g0152 a0001c0001t0001g0313 a0001c0002t0001g0010 others(15): Show |
19 | HG00673.hp1 HG01358.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.143+3850_143+3852d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78382636 | ||||||
| chr17:78382636 | G | T | 1 | a0001c0001t0009g0366 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.143+3828G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382636 | |||||||
| chr17:78382636 | GT | G | 26 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0314 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.143+3852delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78382636 | ||||||
| chr17:78382640 | T | G | 2 | a0001c0001t0001g0223 a0001c0001t0006g0224 |
2 | HG00733.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.143+3832T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382640 | |||||||
| chr17:78382642 | T | TG | 32 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0028 others(29): Show |
34 | HG00544.hp2 HG00609.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.143+3834_143+3835i others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382642 | |||||||
| chr17:78382703 | C | G | 2 | a0001c0002t0001g0056 a0001c0002t0001g0057 |
2 | HG00544.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.143+3895C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382703 | |||||||
| chr17:78382728 | C | T | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.143+3920C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382728 | |||||||
| chr17:78382745 | C | G | 1 | a0001c0002t0001g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.143+3937C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382745 | |||||||
| chr17:78382788 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
134 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.143+3980G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382788 | |||||||
| chr17:78382836 | G | A | 103 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0090 others(100): Show |
107 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.143+4028G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382836 | |||||||
| chr17:78382902 | C | T | 1 | a0001c0002t0002g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.143+4094C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382902 | |||||||
| chr17:78382934 | C | T | 72 | a0001c0001t0001g0152 a0001c0002t0001g0001 a0001c0002t0001g0007 others(69): Show |
77 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.143+4126C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78382934 | |||||||
| chr17:78383179 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143+4371G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383179 | |||||||
| chr17:78383251 | CT | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(123): Show |
136 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.143+4456delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78383251 | ||||||
| chr17:78383336 | C | A | 1 | a0001c0001t0001g0309 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.143+4528C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383336 | |||||||
| chr17:78383469 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.143+4661G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383469 | |||||||
| chr17:78383632 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.143+4824A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383632 | |||||||
| chr17:78383682 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.143+4874G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383682 | |||||||
| chr17:78383698 | A | G | 1 | a0001c0002t0002g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.143+4890A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383698 | |||||||
| chr17:78383788 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.143+4980C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383788 | |||||||
| chr17:78383857 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0327 a0001c0001t0001g0328 others(5): Show |
9 | HG01884.hp1 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.143+5049G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383857 | |||||||
| chr17:78383938 | C | G | 11 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(8): Show |
11 | HG02738.hp1 NA18960.hp1 NA18989.hp1 others(8): Show |
intron_variant | MODIFIER | c.143+5130C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383938 | |||||||
| chr17:78383968 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.143+5160A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383968 | |||||||
| chr17:78383970 | C | T | 2 | a0001c0012t0008g0188 a0001c0013t0011g0187 |
2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.143+5162C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78383970 | |||||||
| chr17:78384045 | G | A | 46 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(43): Show |
48 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.143+5237G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384045 | |||||||
| chr17:78384161 | G | A | 2 | a0001c0002t0001g0197 a0001c0002t0001g0198 |
2 | HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.143+5353G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384161 | |||||||
| chr17:78384321 | C | T | 1 | a0001c0002t0001g0055 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.143+5513C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384321 | |||||||
| chr17:78384656 | G | C | 1 | a0001c0001t0001g0342 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+5848G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384656 | |||||||
| chr17:78384656 | G | T | 1 | a0001c0001t0001g0305 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.143+5848G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384656 | |||||||
| chr17:78384713 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.143+5905C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384713 | |||||||
| chr17:78384765 | C | A | 1 | a0001c0002t0001g0156 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.143+5957C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384765 | |||||||
| chr17:78384861 | G | A | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.143+6053G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384861 | |||||||
| chr17:78384940 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
134 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.143+6132C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384940 | |||||||
| chr17:78384969 | G | A | 2 | a0001c0002t0001g0116 a0001c0002t0001g0143 |
2 | NA19004.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.143+6161G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78384969 | |||||||
| chr17:78385041 | C | T | 33 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(30): Show |
33 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.143+6233C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385041 | |||||||
| chr17:78385180 | G | A | 48 | a0001c0001t0001g0152 a0001c0002t0001g0007 a0001c0002t0001g0008 others(45): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.143+6372G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385180 | |||||||
| chr17:78385237 | A | G | 48 | a0001c0001t0001g0016 a0001c0001t0001g0327 a0001c0001t0001g0328 others(45): Show |
49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.143+6429A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385237 | |||||||
| chr17:78385278 | C | T | 1 | a0001c0002t0002g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.143+6470C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385278 | |||||||
| chr17:78385293 | A | AT | 31 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(28): Show |
31 | HG00558.hp2 HG00733.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.143+6498dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78385293 | ||||||
| chr17:78385322 | A | G | 1 | a0001c0002t0001g0054 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.143+6514A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385322 | |||||||
| chr17:78385335 | T | C | 48 | a0001c0001t0001g0016 a0001c0001t0001g0327 a0001c0001t0001g0328 others(45): Show |
49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.143+6527T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385335 | |||||||
| chr17:78385382 | G | A | 83 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(80): Show |
86 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.143+6574G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385382 | |||||||
| chr17:78385413 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.143+6605C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385413 | |||||||
| chr17:78385414 | G | A | 1 | a0001c0002t0001g0060 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.143+6606G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385414 | |||||||
| chr17:78385524 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.143+6716C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385524 | |||||||
| chr17:78385560 | A | T | 1 | a0001c0001t0001g0360 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.143+6752A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385560 | |||||||
| chr17:78385576 | G | C | 4 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0003g0339 others(1): Show |
4 | HG01884.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+6768G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385576 | |||||||
| chr17:78385662 | A | C | 48 | a0001c0001t0001g0016 a0001c0001t0001g0327 a0001c0001t0001g0328 others(45): Show |
49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.144-6814A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385662 | |||||||
| chr17:78385916 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.144-6560C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385916 | |||||||
| chr17:78385998 | C | T | 205 | a0001c0001t0001g0016 a0001c0001t0001g0152 a0001c0001t0001g0327 others(202): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.144-6478C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78385998 | |||||||
| chr17:78386097 | A | G | 1 | a0001c0001t0001g0374 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.144-6379A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386097 | |||||||
| chr17:78386098 | C | T | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-6378C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386098 | |||||||
| chr17:78386125 | C | A | 9 | a0001c0002t0001g0186 a0001c0002t0001g0192 a0001c0002t0002g0189 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.144-6351C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386125 | |||||||
| chr17:78386179 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.144-6297G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386179 | |||||||
| chr17:78386215 | A | C | 65 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0069 others(62): Show |
68 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.144-6261A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386215 | |||||||
| chr17:78386283 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.144-6193G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386283 | |||||||
| chr17:78386380 | A | G | 1 | a0001c0003t0002g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.144-6096A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386380 | |||||||
| chr17:78386676 | A | T | 1 | a0001c0001t0001g0110 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144-5800A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386676 | |||||||
| chr17:78386710 | C | T | 155 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(152): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.144-5766C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386710 | |||||||
| chr17:78386869 | C | A | 16 | a0001c0002t0001g0001 a0001c0002t0001g0113 a0001c0002t0001g0155 others(13): Show |
18 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.144-5607C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386869 | |||||||
| chr17:78386972 | A | G | 6 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(3): Show |
6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-5504A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386972 | |||||||
| chr17:78386972 | ATGATGAT others(2): Show |
A | 32 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(29): Show |
32 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.144-5486_144-5478d others(11): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78386972 | ||||||
| chr17:78386975 | ATGATGG | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0360 others(2): Show |
6 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-5495_144-5490d others(8): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78386975 | ||||||
| chr17:78386978 | ATGG | A | 3 | a0001c0001t0001g0341 a0001c0001t0001g0358 a0001c0001t0001g0359 |
3 | HG02486.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.144-5495_144-5493d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78386978 | ||||||
| chr17:78386978 | ATGGTGAT others(5): Show |
A | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0374 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-5495_144-5484d others(14): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78386978 | ||||||
| chr17:78386990 | G | A | 40 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(37): Show |
41 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.144-5486G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78386990 | |||||||
| chr17:78387005 | A | G | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-5471A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387005 | |||||||
| chr17:78387008 | G | A | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-5468G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387008 | |||||||
| chr17:78387043 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.144-5433C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387043 | |||||||
| chr17:78387232 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG01891.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.144-5244G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387232 | |||||||
| chr17:78387238 | A | G | 45 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(42): Show |
46 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.144-5238A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387238 | |||||||
| chr17:78387252 | T | C | 45 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(42): Show |
46 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.144-5224T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387252 | |||||||
| chr17:78387257 | G | A | 1 | a0001c0003t0002g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.144-5219G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387257 | |||||||
| chr17:78387291 | A | G | 3 | a0001c0001t0002g0015 a0001c0001t0002g0270 a0001c0001t0002g0304 |
4 | HG00140.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-5185A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387291 | |||||||
| chr17:78387294 | G | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0341 others(2): Show |
6 | HG02145.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-5182G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387294 | |||||||
| chr17:78387297 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.144-5179C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387297 | |||||||
| chr17:78387303 | C | CT | 9 | a0001c0001t0009g0366 a0001c0002t0001g0071 a0001c0002t0001g0072 others(6): Show |
9 | HG01106.hp1 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.144-5161dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387303 | ||||||
| chr17:78387303 | C | CTT | 25 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0090 others(22): Show |
26 | HG01243.hp1 HG02129.hp1 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.144-5162_144-5161d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387303 | ||||||
| chr17:78387428 | TAGCTGGG | T | 47 | a0001c0001t0001g0016 a0001c0001t0001g0217 a0001c0001t0001g0333 others(44): Show |
48 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.144-5046_144-5040d others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387428 | ||||||
| chr17:78387526 | T | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0341 others(8): Show |
12 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.144-4950T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387526 | |||||||
| chr17:78387540 | A | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0294 |
3 | HG02602.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.144-4936A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387540 | |||||||
| chr17:78387550 | T | C | 1 | a0001c0002t0001g0028 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.144-4926T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387550 | |||||||
| chr17:78387590 | C | T | 137 | a0001c0001t0001g0250 a0001c0001t0001g0293 a0001c0001t0001g0333 others(134): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.144-4886C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387590 | |||||||
| chr17:78387598 | C | CT | 107 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0090 others(104): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.144-4859dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387598 | ||||||
| chr17:78387598 | C | CTT | 6 | a0001c0001t0001g0109 a0001c0002t0001g0027 a0001c0002t0001g0143 others(3): Show |
6 | HG00741.hp1 HG02015.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-4860_144-4859d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387598 | ||||||
| chr17:78387598 | CT | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(176): Show |
192 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.144-4859delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78387598 | ||||||
| chr17:78387631 | G | A | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.144-4845G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387631 | |||||||
| chr17:78387685 | G | A | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(346): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.144-4791G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387685 | |||||||
| chr17:78387726 | G | A | 11 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0338 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-4750G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387726 | |||||||
| chr17:78387751 | C | T | 3 | a0001c0001t0001g0346 a0001c0001t0001g0374 a0001c0001t0005g0340 |
3 | HG02818.hp1 HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.144-4725C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78387751 | |||||||
| chr17:78388052 | T | C | 1 | a0001c0001t0003g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.144-4424T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388052 | |||||||
| chr17:78388135 | G | A | 1 | a0001c0001t0002g0343 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144-4341G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388135 | |||||||
| chr17:78388139 | G | A | 45 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(42): Show |
46 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.144-4337G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388139 | |||||||
| chr17:78388173 | G | A | 1 | a0001c0003t0002g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.144-4303G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388173 | |||||||
| chr17:78388195 | G | A | 14 | a0001c0003t0001g0079 a0001c0003t0002g0026 a0001c0003t0002g0081 others(11): Show |
14 | HG01123.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-4281G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388195 | |||||||
| chr17:78388197 | G | C | 60 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(57): Show |
61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4279G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388197 | |||||||
| chr17:78388234 | T | C | 60 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(57): Show |
61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4242T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388234 | |||||||
| chr17:78388258 | C | T | 2 | a0001c0002t0001g0160 a0001c0002t0001g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.144-4218C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388258 | |||||||
| chr17:78388357 | C | T | 60 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(57): Show |
61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4119C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388357 | |||||||
| chr17:78388436 | G | T | 1 | a0001c0002t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.144-4040G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388436 | |||||||
| chr17:78388452 | A | G | 60 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(57): Show |
61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4024A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388452 | |||||||
| chr17:78388453 | T | C | 60 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(57): Show |
61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-4023T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388453 | |||||||
| chr17:78388456 | C | T | 1 | a0001c0002t0001g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.144-4020C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388456 | |||||||
| chr17:78388506 | T | A | 1 | a0001c0002t0001g0174 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.144-3970T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388506 | |||||||
| chr17:78388506 | T | TA | 60 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(57): Show |
61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-3970_144-3969i others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388506 | |||||||
| chr17:78388507 | T | A | 1 | a0001c0002t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.144-3969T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388507 | |||||||
| chr17:78388512 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144-3964T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388512 | |||||||
| chr17:78388513 | A | T | 1 | a0001c0001t0001g0110 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144-3963A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388513 | |||||||
| chr17:78388599 | G | A | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-3877G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388599 | |||||||
| chr17:78388662 | G | A | 14 | a0001c0003t0001g0079 a0001c0003t0002g0026 a0001c0003t0002g0081 others(11): Show |
14 | HG01123.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-3814G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388662 | |||||||
| chr17:78388760 | C | T | 14 | a0001c0003t0001g0079 a0001c0003t0002g0026 a0001c0003t0002g0081 others(11): Show |
14 | HG01123.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-3716C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388760 | |||||||
| chr17:78388816 | A | ACTGT | 60 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(57): Show |
61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-3658_144-3657i others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78388816 | ||||||
| chr17:78388940 | C | T | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-3536C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388940 | |||||||
| chr17:78388963 | T | C | 61 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(58): Show |
62 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.144-3513T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78388963 | |||||||
| chr17:78388986 | TAAGTTGA others(2): Show |
T | 60 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(57): Show |
61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-3480_144-3472d others(11): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78388986 | ||||||
| chr17:78389053 | C | CT | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(118): Show |
131 | HG00423.hp2 HG00639.hp1 HG00733.hp1 others(128): Show |
intron_variant | MODIFIER | c.144-3401dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | ||||||
| chr17:78389053 | C | CTT | 31 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0098 others(28): Show |
33 | HG00140.hp1 HG00438.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.144-3402_144-3401d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | ||||||
| chr17:78389053 | C | CTTT | 16 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0280 others(13): Show |
16 | HG01123.hp2 HG01952.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.144-3403_144-3401d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | ||||||
| chr17:78389053 | C | CTTTTT | 29 | a0001c0001t0001g0333 a0001c0001t0001g0338 a0001c0001t0001g0342 others(26): Show |
29 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.144-3405_144-3401d others(7): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | ||||||
| chr17:78389053 | C | CTTTTTT | 9 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0337 others(6): Show |
9 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-3406_144-3401d others(8): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | ||||||
| chr17:78389053 | CT | C | 75 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(72): Show |
78 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.144-3401delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389053 | ||||||
| chr17:78389075 | T | G | 1 | a0001c0002t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.144-3401T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389075 | |||||||
| chr17:78389076 | G | C | 1 | a0001c0002t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.144-3400G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389076 | |||||||
| chr17:78389077 | C | G | 1 | a0001c0002t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.144-3399C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389077 | |||||||
| chr17:78389080 | G | T | 61 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(58): Show |
62 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.144-3396G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389080 | |||||||
| chr17:78389119 | A | AT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0090 others(18): Show |
22 | HG02129.hp1 HG02165.hp2 NA18941.hp1 others(19): Show |
intron_variant | MODIFIER | c.144-3356dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389119 | ||||||
| chr17:78389127 | A | G | 8 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0073 others(5): Show |
8 | HG01243.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.144-3349A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389127 | |||||||
| chr17:78389186 | C | T | 59 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(56): Show |
60 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.144-3290C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389186 | |||||||
| chr17:78389229 | T | C | 61 | a0001c0001t0001g0016 a0001c0001t0001g0229 a0001c0001t0001g0333 others(58): Show |
62 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.144-3247T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389229 | |||||||
| chr17:78389250 | C | A | 60 | a0001c0001t0001g0016 a0001c0001t0001g0229 a0001c0001t0001g0333 others(57): Show |
61 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.144-3226C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389250 | |||||||
| chr17:78389300 | C | T | 61 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(58): Show |
62 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.144-3176C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389300 | |||||||
| chr17:78389331 | G | A | 1 | a0001c0002t0001g0117 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.144-3145G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389331 | |||||||
| chr17:78389337 | G | A | 13 | a0001c0003t0001g0079 a0001c0003t0002g0081 a0001c0003t0002g0176 others(10): Show |
13 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.144-3139G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389337 | |||||||
| chr17:78389411 | T | C | 9 | a0001c0002t0001g0186 a0001c0002t0001g0192 a0001c0002t0002g0189 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.144-3065T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389411 | |||||||
| chr17:78389474 | C | T | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.144-3002C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389474 | |||||||
| chr17:78389501 | A | G | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.144-2975A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389501 | |||||||
| chr17:78389574 | GCCTCCCA others(6): Show |
G | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-2901_144-2889d others(15): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389574 | |||||||
| chr17:78389622 | C | CT | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.144-2845dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78389622 | ||||||
| chr17:78389622 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.144-2854C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389622 | |||||||
| chr17:78389636 | C | G | 1 | a0001c0001t0001g0278 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.144-2840C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389636 | |||||||
| chr17:78389642 | C | A | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.144-2834C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389642 | |||||||
| chr17:78389744 | G | A | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.144-2732G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389744 | |||||||
| chr17:78389804 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.144-2672C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389804 | |||||||
| chr17:78389891 | T | C | 1 | a0001c0003t0002g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.144-2585T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389891 | |||||||
| chr17:78389956 | A | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(205): Show |
220 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.144-2520A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389956 | |||||||
| chr17:78389978 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.144-2498G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389978 | |||||||
| chr17:78389986 | A | G | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.144-2490A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78389986 | |||||||
| chr17:78390008 | G | T | 1 | a0001c0001t0001g0289 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.144-2468G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390008 | |||||||
| chr17:78390062 | T | TCCCCCCG others(8): Show |
2 | a0001c0001t0001g0266 a0001c0011t0002g0315 |
2 | HG01256.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.144-2409_144-2408i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCCG others(9): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0251 |
2 | HG00438.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.144-2409_144-2408i others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(8): Show |
1 | a0001c0001t0001g0324 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.144-2403_144-2402i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(9): Show |
4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0253 others(1): Show |
4 | HG01099.hp1 HG02738.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-2403_144-2402i others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(6): Show |
1 | a0001c0001t0001g0110 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.144-2402_144-2401i others(15): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(9): Show |
1 | a0001c0001t0001g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.144-2402_144-2401i others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(7): Show |
51 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
58 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(8): Show |
76 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0092 others(73): Show |
80 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(13): Show |
1 | a0001c0001t0001g0109 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.144-2402_144-2401i others(22): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(9): Show |
14 | a0001c0001t0001g0101 a0001c0001t0001g0214 a0001c0001t0001g0217 others(11): Show |
14 | HG00639.hp1 HG00735.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(10): Show |
5 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0301 others(2): Show |
5 | HG01070.hp1 HG02451.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(19): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390062 | T | TCCCCCGC others(8): Show |
1 | a0001c0001t0001g0289 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.144-2404_144-2403i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390062 | ||||||
| chr17:78390067 | C | CGCCCCCG others(8): Show |
6 | a0001c0001t0001g0342 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG00609.hp1 HG01109.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390067 | ||||||
| chr17:78390067 | C | CGCCCCCG others(7): Show |
40 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(37): Show |
41 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.144-2402_144-2401i others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390067 | ||||||
| chr17:78390068 | G | A | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.144-2408G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390068 | |||||||
| chr17:78390148 | C | G | 6 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(3): Show |
6 | NA18612.hp1 NA18941.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-2328C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390148 | |||||||
| chr17:78390193 | C | A | 76 | a0001c0001t0001g0152 a0001c0002t0001g0001 a0001c0002t0001g0007 others(73): Show |
81 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.144-2283C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390193 | |||||||
| chr17:78390237 | C | A | 1 | a0001c0001t0003g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.144-2239C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390237 | |||||||
| chr17:78390254 | C | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(202): Show |
217 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.144-2222C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390254 | |||||||
| chr17:78390266 | A | G | 1 | a0003c0005t0001g0135 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.144-2210A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390266 | |||||||
| chr17:78390324 | GT | G | 9 | a0001c0001t0001g0360 a0001c0003t0002g0177 a0001c0003t0002g0178 others(6): Show |
9 | HG02630.hp2 HG02818.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-2151delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390324 | |||||||
| chr17:78390325 | T | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(141): Show |
155 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.144-2151T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390325 | |||||||
| chr17:78390325 | T | G | 40 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(37): Show |
41 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.144-2151T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390325 | |||||||
| chr17:78390325 | T | TG | 11 | a0001c0002t0001g0163 a0001c0002t0001g0186 a0001c0002t0001g0192 others(8): Show |
11 | HG01099.hp2 HG01175.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-2146dupG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390325 | ||||||
| chr17:78390326 | G | T | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.144-2150G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390326 | |||||||
| chr17:78390328 | GGGA | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(141): Show |
155 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.144-2144_144-2142d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78390328 | ||||||
| chr17:78390331 | A | G | 187 | a0001c0001t0001g0016 a0001c0001t0001g0152 a0001c0001t0001g0336 others(184): Show |
195 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.144-2145A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390331 | |||||||
| chr17:78390332 | GGAA | G | 41 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(38): Show |
42 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.144-2143_144-2141d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390332 | |||||||
| chr17:78390335 | A | G | 5 | a0001c0001t0001g0336 a0001c0001t0001g0359 a0001c0001t0001g0362 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-2141A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390335 | |||||||
| chr17:78390368 | C | T | 2 | a0001c0002t0001g0160 a0001c0002t0001g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.144-2108C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390368 | |||||||
| chr17:78390497 | G | T | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-1979G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390497 | |||||||
| chr17:78390516 | C | G | 2 | a0001c0001t0001g0344 a0001c0001t0001g0346 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.144-1960C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390516 | |||||||
| chr17:78390625 | G | A | 3 | a0001c0002t0001g0115 a0001c0002t0001g0136 a0001c0002t0001g0144 |
3 | NA18946.hp2 NA18961.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.144-1851G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390625 | |||||||
| chr17:78390678 | C | G | 1 | a0001c0001t0001g0244 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.144-1798C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390678 | |||||||
| chr17:78390703 | G | C | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA18982.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.144-1773G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390703 | |||||||
| chr17:78390728 | C | T | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.144-1748C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390728 | |||||||
| chr17:78390802 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.144-1674C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390802 | |||||||
| chr17:78390817 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.144-1659C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390817 | |||||||
| chr17:78390834 | C | T | 43 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(40): Show |
44 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.144-1642C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390834 | |||||||
| chr17:78390837 | T | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.144-1639T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390837 | |||||||
| chr17:78390903 | A | T | 72 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(69): Show |
75 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.144-1573A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78390903 | |||||||
| chr17:78391022 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.144-1454T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391022 | |||||||
| chr17:78391163 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.144-1313A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391163 | |||||||
| chr17:78391193 | A | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(181): Show |
195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.144-1283A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391193 | |||||||
| chr17:78391241 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.144-1235C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391241 | |||||||
| chr17:78391282 | G | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(135): Show |
148 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.144-1194G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391282 | |||||||
| chr17:78391295 | C | T | 43 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(40): Show |
44 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.144-1181C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391295 | |||||||
| chr17:78391563 | C | T | 1 | a0001c0002t0001g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.144-913C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391563 | |||||||
| chr17:78391611 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.144-865G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391611 | |||||||
| chr17:78391897 | T | C | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.144-579T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391897 | |||||||
| chr17:78391913 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.144-563C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78391913 | |||||||
| chr17:78391961 | GGTGCTTC others(8): Show |
G | 1 | a0001c0001t0001g0303 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.144-513_144-499del others(15): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr17 | 78391961 | ||||||
| chr17:78392054 | C | T | 1 | a0001c0002t0001g0046 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.144-422C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392054 | |||||||
| chr17:78392121 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(189): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.144-355A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392121 | |||||||
| chr17:78392164 | G | A | 15 | a0001c0003t0001g0079 a0001c0003t0002g0026 a0001c0003t0002g0081 others(12): Show |
15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.144-312G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392164 | |||||||
| chr17:78392246 | C | T | 1 | a0001c0002t0001g0156 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.144-230C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392246 | |||||||
| chr17:78392262 | T | C | 5 | a0001c0001t0001g0213 a0001c0001t0001g0230 a0001c0001t0001g0235 others(2): Show |
5 | HG00735.hp1 HG01099.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-214T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392262 | |||||||
| chr17:78392401 | A | G | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.144-75A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392401 | |||||||
| chr17:78392421 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.144-55G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 1/9 | chr17 | 78392421 | |||||||
| chr17:78392755 | T | C | 11 | a0001c0003t0002g0176 a0001c0003t0002g0177 a0001c0003t0002g0178 others(8): Show |
11 | HG02055.hp1 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.333+90T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78392755 | |||||||
| chr17:78392970 | A | T | 2 | a0001c0002t0001g0160 a0001c0002t0001g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.333+305A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78392970 | |||||||
| chr17:78393039 | C | T | 46 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+374C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393039 | |||||||
| chr17:78393047 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.333+382G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393047 | |||||||
| chr17:78393063 | C | CT | 10 | a0001c0001t0001g0098 a0001c0001t0001g0282 a0001c0002t0001g0111 others(7): Show |
10 | HG01109.hp1 HG01952.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+413dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78393063 | ||||||
| chr17:78393063 | CT | C | 47 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0333 others(44): Show |
48 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.333+413delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78393063 | ||||||
| chr17:78393083 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.333+418T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393083 | |||||||
| chr17:78393095 | C | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(180): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.333+430C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393095 | |||||||
| chr17:78393125 | A | G | 6 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(3): Show |
6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+460A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393125 | |||||||
| chr17:78393146 | C | T | 1 | a0001c0001t0015g0300 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.333+481C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393146 | |||||||
| chr17:78393209 | T | C | 372 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(369): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.333+544T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393209 | |||||||
| chr17:78393247 | A | T | 3 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0066 |
3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+582A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393247 | |||||||
| chr17:78393248 | G | A | 3 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0066 |
3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+583G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393248 | |||||||
| chr17:78393249 | ATGGGG | A | 3 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0066 |
3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+586_333+590del others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78393249 | ||||||
| chr17:78393255 | T | C | 3 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0066 |
3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+590T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393255 | |||||||
| chr17:78393256 | T | A | 3 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0066 |
3 | NA18612.hp2 NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.333+591T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393256 | |||||||
| chr17:78393281 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.333+616C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393281 | |||||||
| chr17:78393331 | A | G | 1 | a0001c0002t0002g0070 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.333+666A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393331 | |||||||
| chr17:78393446 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.333+781G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393446 | |||||||
| chr17:78393457 | T | A | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.333+792T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393457 | |||||||
| chr17:78393536 | C | T | 2 | a0001c0002t0005g0077 a0001c0002t0005g0084 |
2 | HG01243.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.333+871C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393536 | |||||||
| chr17:78393955 | C | T | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.333+1290C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393955 | |||||||
| chr17:78393999 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.333+1334C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78393999 | |||||||
| chr17:78394116 | A | G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0069 others(59): Show |
65 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.333+1451A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394116 | |||||||
| chr17:78394158 | C | T | 1 | a0001c0001t0002g0369 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.333+1493C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394158 | |||||||
| chr17:78394170 | TC | T | 106 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0093 others(103): Show |
107 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.333+1508delC | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78394170 | ||||||
| chr17:78394170 | TCC | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
186 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.333+1507_333+1508d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr17 | 78394170 | ||||||
| chr17:78394171 | C | CA | 4 | a0001c0001t0001g0016 a0001c0002t0001g0086 a0001c0002t0001g0111 others(1): Show |
5 | HG01261.hp2 HG01952.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+1506_333+1507i others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394171 | |||||||
| chr17:78394171 | CCCA | C | 67 | a0001c0001t0001g0358 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.333+1507_333+1509d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394171 | |||||||
| chr17:78394172 | C | A | 29 | a0001c0001t0001g0016 a0001c0001t0001g0106 a0001c0001t0001g0336 others(26): Show |
30 | HG01106.hp1 HG01106.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.333+1507C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394172 | |||||||
| chr17:78394173 | C | A | 135 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0092 others(132): Show |
137 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.333+1508C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394173 | |||||||
| chr17:78394218 | G | A | 1 | a0001c0002t0001g0329 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.333+1553G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394218 | |||||||
| chr17:78394651 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.334-1657G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394651 | |||||||
| chr17:78394746 | G | T | 1 | a0001c0001t0001g0355 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.334-1562G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394746 | |||||||
| chr17:78394782 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-1526C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394782 | |||||||
| chr17:78394924 | C | T | 72 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(69): Show |
75 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.334-1384C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394924 | |||||||
| chr17:78394993 | G | A | 6 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(3): Show |
6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-1315G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78394993 | |||||||
| chr17:78395051 | AT | A | 74 | a0001c0001t0001g0152 a0001c0002t0001g0001 a0001c0002t0001g0007 others(71): Show |
79 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.334-1256delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395051 | |||||||
| chr17:78395069 | G | A | 14 | a0001c0003t0001g0079 a0001c0003t0002g0026 a0001c0003t0002g0081 others(11): Show |
14 | HG01123.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-1239G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395069 | |||||||
| chr17:78395188 | G | A | 2 | a0001c0002t0002g0200 a0001c0002t0002g0201 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.334-1120G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395188 | |||||||
| chr17:78395238 | A | G | 1 | a0001c0002t0001g0174 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.334-1070A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395238 | |||||||
| chr17:78395293 | A | G | 4 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(1): Show |
4 | HG02723.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1015A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395293 | |||||||
| chr17:78395305 | A | T | 49 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0025 others(46): Show |
52 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.334-1003A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395305 | |||||||
| chr17:78395373 | T | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(201): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.334-935T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395373 | |||||||
| chr17:78395572 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(156): Show |
170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.334-736C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395572 | |||||||
| chr17:78395583 | A | G | 372 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(369): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.334-725A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395583 | |||||||
| chr17:78395792 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0271 |
2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.334-516G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395792 | |||||||
| chr17:78395888 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.334-420G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395888 | |||||||
| chr17:78395894 | A | G | 2 | a0001c0012t0008g0188 a0001c0013t0011g0187 |
2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.334-414A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395894 | |||||||
| chr17:78395952 | C | G | 5 | a0001c0002t0001g0113 a0001c0002t0001g0166 a0001c0002t0001g0167 others(2): Show |
5 | HG00140.hp2 HG00741.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-356C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395952 | |||||||
| chr17:78395998 | C | T | 1 | a0001c0002t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.334-310C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78395998 | |||||||
| chr17:78396063 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(152): Show |
166 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.334-245G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78396063 | |||||||
| chr17:78396107 | G | A | 1 | a0001c0003t0002g0183 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.334-201G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78396107 | |||||||
| chr17:78396211 | C | T | 1 | a0001c0002t0002g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.334-97C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 2/9 | chr17 | 78396211 | |||||||
| chr17:78396444 | A | T | 5 | a0001c0002t0001g0113 a0001c0002t0001g0166 a0001c0002t0001g0167 others(2): Show |
5 | HG00140.hp2 HG00741.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+59A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396444 | |||||||
| chr17:78396675 | C | G | 73 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(70): Show |
76 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.411+290C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396675 | |||||||
| chr17:78396885 | T | C | 9 | a0001c0002t0001g0186 a0001c0002t0001g0192 a0001c0002t0002g0189 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.411+500T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396885 | |||||||
| chr17:78396946 | T | C | 1 | a0001c0003t0016g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.411+561T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396946 | |||||||
| chr17:78396949 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.411+564T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396949 | |||||||
| chr17:78396996 | CGGACCTG others(6): Show |
C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.411+612_411+624del others(13): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78396996 | |||||||
| chr17:78397167 | G | T | 3 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 |
3 | HG02922.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.411+782G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397167 | |||||||
| chr17:78397289 | A | ACAGACGG others(97): Show |
75 | a0001c0001t0001g0152 a0001c0002t0001g0001 a0001c0002t0001g0007 others(72): Show |
80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.411+905_412-859dup others(104): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397289 | ||||||
| chr17:78397291 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.411+906A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397291 | |||||||
| chr17:78397291 | A | GGACGGGC others(97): Show |
1 | a0001c0002t0004g0173 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.411+905_411+906ins others(104): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397291 | |||||||
| chr17:78397307 | CAG | C | 3 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 |
3 | HG02922.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.411+925_411+926del others(2): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397307 | ||||||
| chr17:78397332 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.412-920G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397332 | |||||||
| chr17:78397441 | C | CT | 13 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0134 others(10): Show |
14 | HG00408.hp2 HG00558.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.412-799dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397441 | ||||||
| chr17:78397458 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.412-794C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397458 | |||||||
| chr17:78397589 | A | AC | 48 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(45): Show |
49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.412-656dupC | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397589 | ||||||
| chr17:78397589 | A | ACCC | 55 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0069 others(52): Show |
58 | HG00140.hp1 HG00423.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.412-658_412-656dup others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397589 | ||||||
| chr17:78397589 | A | ACCCC | 21 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0109 others(18): Show |
21 | HG00438.hp1 HG01106.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.412-659_412-656dup others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397589 | ||||||
| chr17:78397594 | C | CCCG | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(79): Show |
90 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.412-656_412-655ins others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr17 | 78397594 | ||||||
| chr17:78397655 | AAAC | A | 48 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0025 others(45): Show |
51 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.412-596_412-594del others(3): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397655 | |||||||
| chr17:78397663 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.412-589G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397663 | |||||||
| chr17:78397681 | C | T | 8 | a0001c0001t0001g0335 a0001c0001t0001g0352 a0001c0001t0001g0353 others(5): Show |
8 | HG00099.hp2 HG01074.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-571C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397681 | |||||||
| chr17:78397704 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.412-548G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397704 | |||||||
| chr17:78397815 | C | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.412-437C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397815 | |||||||
| chr17:78397894 | G | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.412-358G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397894 | |||||||
| chr17:78397932 | G | T | 2 | a0001c0002t0001g0157 a0001c0002t0001g0158 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.412-320G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397932 | |||||||
| chr17:78397960 | C | T | 1 | a0001c0012t0008g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.412-292C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397960 | |||||||
| chr17:78397961 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.412-291G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397961 | |||||||
| chr17:78397994 | A | G | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.412-258A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78397994 | |||||||
| chr17:78398078 | A | G | 16 | a0001c0001t0001g0338 a0001c0003t0001g0079 a0001c0003t0002g0026 others(13): Show |
16 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.412-174A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398078 | |||||||
| chr17:78398096 | A | G | 3 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0326 |
3 | HG02148.hp1 NA18966.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.412-156A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398096 | |||||||
| chr17:78398114 | T | C | 75 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(72): Show |
80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.412-138T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398114 | |||||||
| chr17:78398124 | G | T | 6 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0347 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-128G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398124 | |||||||
| chr17:78398199 | A | G | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.412-53A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398199 | |||||||
| chr17:78398232 | T | C | 1 | a0001c0003t0002g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.412-20T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 3/9 | chr17 | 78398232 | |||||||
| chr17:78398368 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.511+17C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398368 | |||||||
| chr17:78398445 | T | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.511+94T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398445 | |||||||
| chr17:78398514 | T | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.511+163T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398514 | |||||||
| chr17:78398583 | G | C | 1 | a0001c0001t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.511+232G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398583 | |||||||
| chr17:78398640 | C | T | 1 | a0001c0002t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511+289C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398640 | |||||||
| chr17:78398888 | G | C | 3 | a0001c0002t0001g0007 a0001c0002t0001g0085 a0001c0002t0001g0120 |
4 | HG02132.hp1 NA18983.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.512-460G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398888 | |||||||
| chr17:78398957 | A | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.512-391A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78398957 | |||||||
| chr17:78399088 | T | C | 72 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(69): Show |
75 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.512-260T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399088 | |||||||
| chr17:78399116 | G | A | 6 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(3): Show |
6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.512-232G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399116 | |||||||
| chr17:78399284 | C | T | 1 | a0001c0001t0004g0351 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.512-64C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399284 | |||||||
| chr17:78399289 | T | C | 1 | a0001c0002t0001g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.512-59T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399289 | |||||||
| chr17:78399327 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.512-21G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399327 | |||||||
| chr17:78399340 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
splice_region_variant&intron_variant | LOW | c.512-8G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 4/9 | chr17 | 78399340 | |||||||
| chr17:78399553 | C | T | 72 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(69): Show |
75 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.701+16C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399553 | |||||||
| chr17:78399568 | C | T | 1 | a0001c0002t0001g0025 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.701+31C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399568 | |||||||
| chr17:78399669 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.701+132C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399669 | |||||||
| chr17:78399672 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.701+135G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399672 | |||||||
| chr17:78399763 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701+226G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399763 | |||||||
| chr17:78399772 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0101 others(1): Show |
4 | NA18960.hp2 NA18963.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+235G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399772 | |||||||
| chr17:78399775 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.701+238A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399775 | |||||||
| chr17:78399795 | C | T | 1 | a0001c0002t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.701+258C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399795 | |||||||
| chr17:78399899 | C | G | 1 | a0001c0001t0001g0107 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.701+362C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399899 | |||||||
| chr17:78399953 | C | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0266 |
2 | NA18963.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.701+416C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78399953 | |||||||
| chr17:78400083 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.701+546G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400083 | |||||||
| chr17:78400095 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.701+558C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400095 | |||||||
| chr17:78400107 | C | T | 81 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(78): Show |
84 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.701+570C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400107 | |||||||
| chr17:78400239 | G | T | 1 | a0001c0001t0001g0253 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.702-438G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400239 | |||||||
| chr17:78400244 | G | T | 1 | a0001c0001t0009g0366 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.702-433G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400244 | |||||||
| chr17:78400245 | T | G | 1 | a0001c0001t0009g0366 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.702-432T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400245 | |||||||
| chr17:78400246 | G | T | 1 | a0001c0001t0009g0366 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.702-431G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400246 | |||||||
| chr17:78400277 | C | T | 1 | a0001c0003t0002g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.702-400C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400277 | |||||||
| chr17:78400293 | G | T | 1 | a0001c0001t0009g0366 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.702-384G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400293 | |||||||
| chr17:78400382 | C | CA | 68 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 others(65): Show |
71 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.702-282dupA | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 78400382 | ||||||
| chr17:78400382 | C | CAA | 7 | a0001c0002t0001g0033 a0001c0002t0001g0053 a0001c0002t0001g0060 others(4): Show |
7 | HG00408.hp1 HG02523.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.702-283_702-282dup others(2): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 78400382 | ||||||
| chr17:78400447 | C | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.702-230C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400447 | |||||||
| chr17:78400529 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.702-148G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400529 | |||||||
| chr17:78400543 | G | C | 1 | a0001c0002t0001g0034 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.702-134G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 5/9 | chr17 | 78400543 | |||||||
| chr17:78400881 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0299 |
2 | NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.880+26T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78400881 | |||||||
| chr17:78400882 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+27A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78400882 | |||||||
| chr17:78401047 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+192A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401047 | |||||||
| chr17:78401052 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+197A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401052 | |||||||
| chr17:78401095 | G | A | 80 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.880+240G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401095 | |||||||
| chr17:78401138 | A | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+283A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401138 | |||||||
| chr17:78401211 | A | T | 3 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0326 |
3 | HG02148.hp1 NA18966.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.880+356A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401211 | |||||||
| chr17:78401228 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+373C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401228 | |||||||
| chr17:78401253 | A | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+398A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401253 | |||||||
| chr17:78401262 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.880+407G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401262 | |||||||
| chr17:78401333 | T | G | 4 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(1): Show |
4 | HG02723.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.880+478T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401333 | |||||||
| chr17:78401389 | C | T | 3 | a0001c0002t0001g0060 a0001c0002t0001g0063 a0001c0002t0001g0068 |
3 | NA18959.hp1 NA18985.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.880+534C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401389 | |||||||
| chr17:78401702 | G | T | 1 | a0002c0004t0001g0194 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.880+847G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401702 | |||||||
| chr17:78401731 | G | A | 1 | a0001c0002t0001g0031 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.880+876G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401731 | |||||||
| chr17:78401749 | T | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+894T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401749 | |||||||
| chr17:78401787 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.880+932G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401787 | |||||||
| chr17:78401814 | A | T | 2 | a0001c0002t0002g0200 a0001c0002t0002g0201 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.880+959A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401814 | |||||||
| chr17:78401869 | TG | T | 22 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(19): Show |
22 | HG00558.hp2 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.880+1015delG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401869 | |||||||
| chr17:78401912 | C | T | 4 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(1): Show |
4 | HG02723.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.880+1057C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401912 | |||||||
| chr17:78401977 | C | A | 1 | a0001c0001t0002g0263 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.880+1122C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401977 | |||||||
| chr17:78401977 | C | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.880+1122C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78401977 | |||||||
| chr17:78402020 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1165A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402020 | |||||||
| chr17:78402043 | GTGT | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1189_880+1191d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402043 | |||||||
| chr17:78402049 | G | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1194G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402049 | |||||||
| chr17:78402051 | AG | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1199delG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402051 | ||||||
| chr17:78402076 | G | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.880+1221G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402076 | |||||||
| chr17:78402187 | G | T | 1 | a0001c0001t0001g0353 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.880+1332G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402187 | |||||||
| chr17:78402223 | G | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
156 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.881-1345G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402223 | |||||||
| chr17:78402323 | G | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.881-1245G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402323 | |||||||
| chr17:78402373 | A | T | 1 | a0001c0001t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.881-1195A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402373 | |||||||
| chr17:78402397 | CATATATA others(1): Show |
C | 3 | a0001c0002t0001g0066 a0001c0002t0002g0067 a0001c0002t0002g0078 |
3 | HG04228.hp2 NA19074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.881-1147_881-1140d others(10): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402397 | ||||||
| chr17:78402397 | CATATATA others(3): Show |
C | 70 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(67): Show |
73 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.881-1149_881-1140d others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402397 | ||||||
| chr17:78402397 | CATATATA others(5): Show |
C | 3 | a0001c0002t0001g0116 a0001c0002t0001g0143 a0001c0002t0001g0153 |
3 | HG00673.hp1 NA19004.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.881-1151_881-1140d others(14): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402397 | ||||||
| chr17:78402411 | TATATATA others(11): Show |
T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(141): Show |
155 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.881-1155_881-1138d others(20): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402411 | ||||||
| chr17:78402411 | TATATATA others(13): Show |
T | 48 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(45): Show |
49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.881-1155_881-1136d others(22): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402411 | ||||||
| chr17:78402413 | TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0277 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.881-1153_881-1138d others(18): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402413 | ||||||
| chr17:78402413 | TATATATA others(11): Show |
T | 14 | a0001c0003t0001g0079 a0001c0003t0002g0026 a0001c0003t0002g0081 others(11): Show |
14 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.881-1153_881-1136d others(20): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402413 | ||||||
| chr17:78402415 | TATATATA others(7): Show |
T | 1 | a0001c0002t0001g0007 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.881-1151_881-1138d others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402415 | ||||||
| chr17:78402417 | TATATATA others(5): Show |
T | 81 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(78): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.881-1149_881-1138d others(14): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402417 | ||||||
| chr17:78402419 | TATATATA others(3): Show |
T | 8 | a0001c0002t0001g0140 a0001c0002t0001g0157 a0001c0002t0001g0158 others(5): Show |
8 | HG01175.hp1 HG02723.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.881-1147_881-1138d others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 78402419 | ||||||
| chr17:78402427 | T | C | 5 | a0001c0002t0001g0020 a0001c0002t0001g0024 a0001c0002t0001g0045 others(2): Show |
5 | HG00738.hp1 HG04228.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-1141T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402427 | |||||||
| chr17:78402429 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.881-1139C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402429 | |||||||
| chr17:78402436 | A | G | 1 | a0001c0002t0002g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.881-1132A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402436 | |||||||
| chr17:78402506 | G | A | 1 | a0001c0001t0001g0346 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.881-1062G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402506 | |||||||
| chr17:78402555 | C | T | 3 | a0001c0002t0001g0113 a0001c0002t0001g0167 a0001c0002t0001g0171 |
3 | HG00140.hp2 HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.881-1013C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402555 | |||||||
| chr17:78402748 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.881-820C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402748 | |||||||
| chr17:78402813 | T | C | 23 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(20): Show |
23 | HG00558.hp2 HG00733.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.881-755T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402813 | |||||||
| chr17:78402996 | C | T | 3 | a0001c0001t0002g0015 a0001c0001t0002g0270 a0001c0001t0002g0304 |
4 | HG00140.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.881-572C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78402996 | |||||||
| chr17:78403015 | C | G | 1 | a0001c0002t0002g0209 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.881-553C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403015 | |||||||
| chr17:78403077 | G | T | 1 | a0001c0012t0008g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.881-491G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403077 | |||||||
| chr17:78403323 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(194): Show |
209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.881-245C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403323 | |||||||
| chr17:78403364 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.881-204T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403364 | |||||||
| chr17:78403470 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.881-98C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403470 | |||||||
| chr17:78403471 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(196): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.881-97G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403471 | |||||||
| chr17:78403557 | G | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0341 others(4): Show |
8 | HG02145.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.881-11G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 6/9 | chr17 | 78403557 | |||||||
| chr17:78404093 | C | A | 1 | a0001c0001t0001g0353 | 1 | HG01433.hp2 | splice_region_variant&intron_variant | LOW | c.1402+4C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404093 | |||||||
| chr17:78404140 | T | C | 39 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(36): Show |
40 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1402+51T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404140 | |||||||
| chr17:78404149 | G | A | 62 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0069 others(59): Show |
65 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1402+60G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404149 | |||||||
| chr17:78404155 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(195): Show |
210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1402+66G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404155 | |||||||
| chr17:78404170 | C | G | 75 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(72): Show |
80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1402+81C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404170 | |||||||
| chr17:78404177 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(195): Show |
210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1402+88G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404177 | |||||||
| chr17:78404187 | C | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(195): Show |
210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1402+98C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404187 | |||||||
| chr17:78404240 | A | G | 79 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(76): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1402+151A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404240 | |||||||
| chr17:78404246 | TGGG | T | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+159_1402+161d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404246 | ||||||
| chr17:78404248 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(190): Show |
205 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1402+159G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404248 | |||||||
| chr17:78404256 | C | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(196): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1402+167C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404256 | |||||||
| chr17:78404279 | A | AT | 12 | a0001c0002t0001g0129 a0001c0002t0001g0131 a0001c0002t0001g0132 others(9): Show |
12 | HG00544.hp1 HG01175.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1402+212dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404279 | ||||||
| chr17:78404279 | AT | A | 87 | a0001c0001t0001g0337 a0001c0001t0001g0342 a0001c0001t0001g0356 others(84): Show |
90 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1402+212delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404279 | ||||||
| chr17:78404279 | ATTT | A | 6 | a0001c0001t0001g0106 a0001c0001t0001g0243 a0001c0001t0001g0372 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402+210_1402+212d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404279 | ||||||
| chr17:78404279 | ATTTT | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1402+209_1402+212d others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78404279 | ||||||
| chr17:78404352 | G | A | 1 | a0001c0003t0001g0079 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1402+263G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404352 | |||||||
| chr17:78404368 | A | C | 1 | a0001c0001t0001g0346 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1402+279A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404368 | |||||||
| chr17:78404426 | G | A | 72 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(69): Show |
77 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1402+337G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404426 | |||||||
| chr17:78404485 | G | T | 80 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1402+396G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404485 | |||||||
| chr17:78404628 | G | C | 15 | a0001c0003t0001g0079 a0001c0003t0002g0026 a0001c0003t0002g0081 others(12): Show |
15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1402+539G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404628 | |||||||
| chr17:78404641 | C | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0218 |
2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1402+552C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404641 | |||||||
| chr17:78404709 | G | A | 1 | a0001c0001t0001g0375 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1402+620G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404709 | |||||||
| chr17:78404952 | G | A | 6 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0159 others(3): Show |
6 | HG02723.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402+863G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78404952 | |||||||
| chr17:78405152 | TA | T | 18 | a0001c0001t0001g0335 a0001c0001t0001g0350 a0001c0001t0001g0352 others(15): Show |
18 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1402+1064delA | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405152 | |||||||
| chr17:78405205 | C | T | 1 | a0001c0001t0002g0343 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1402+1116C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405205 | |||||||
| chr17:78405237 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(195): Show |
210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1402+1148C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405237 | |||||||
| chr17:78405247 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(156): Show |
170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1402+1158C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405247 | |||||||
| chr17:78405248 | A | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(275): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1402+1159A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405248 | |||||||
| chr17:78405275 | C | T | 1 | a0001c0002t0001g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1402+1186C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405275 | |||||||
| chr17:78405349 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0006g0224 |
2 | HG00733.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1402+1260C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405349 | |||||||
| chr17:78405406 | T | G | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1402+1317T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405406 | |||||||
| chr17:78405635 | C | G | 1 | a0001c0002t0007g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1402+1546C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405635 | |||||||
| chr17:78405689 | C | T | 1 | a0001c0002t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1402+1600C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405689 | |||||||
| chr17:78405773 | A | C | 2 | a0001c0003t0002g0176 a0001c0003t0008g0018 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1402+1684A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405773 | |||||||
| chr17:78405820 | C | A | 1 | a0001c0001t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1402+1731C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78405820 | |||||||
| chr17:78406024 | A | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
171 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1402+1935A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406024 | |||||||
| chr17:78406035 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(80): Show |
91 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.1402+1946G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406035 | |||||||
| chr17:78406041 | GCGCGGTG others(5): Show |
G | 13 | a0001c0002t0001g0001 a0001c0002t0001g0113 a0001c0002t0001g0155 others(10): Show |
15 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.1402+1956_1402+196 others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78406041 | ||||||
| chr17:78406186 | C | G | 1 | a0001c0001t0001g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1402+2097C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406186 | |||||||
| chr17:78406187 | G | C | 1 | a0001c0001t0001g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1402+2098G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406187 | |||||||
| chr17:78406190 | C | G | 1 | a0001c0002t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1402+2101C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406190 | |||||||
| chr17:78406284 | T | C | 372 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(369): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1402+2195T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406284 | |||||||
| chr17:78406309 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0336 |
3 | HG02145.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1402+2220C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406309 | |||||||
| chr17:78406498 | G | A | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1402+2409G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406498 | |||||||
| chr17:78406546 | G | C | 1 | a0001c0002t0001g0148 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1402+2457G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406546 | |||||||
| chr17:78406591 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1402+2502A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406591 | |||||||
| chr17:78406671 | T | C | 2 | a0001c0001t0003g0339 a0001c0001t0005g0340 |
2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1402+2582T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406671 | |||||||
| chr17:78406947 | T | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(201): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1402+2858T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406947 | |||||||
| chr17:78406984 | C | A | 1 | a0001c0001t0001g0350 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1402+2895C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78406984 | |||||||
| chr17:78407038 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0242 |
2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1402+2949A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407038 | |||||||
| chr17:78407473 | C | G | 3 | a0001c0001t0002g0330 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG02280.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1402+3384C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407473 | |||||||
| chr17:78407509 | C | A | 25 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(22): Show |
25 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1402+3420C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407509 | |||||||
| chr17:78407617 | G | A | 7 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0002g0199 others(4): Show |
7 | HG01069.hp2 HG01243.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1402+3528G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407617 | |||||||
| chr17:78407677 | A | G | 1 | a0001c0003t0002g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1402+3588A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407677 | |||||||
| chr17:78407779 | G | A | 2 | a0001c0002t0001g0166 a0001c0007t0006g0170 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1402+3690G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407779 | |||||||
| chr17:78407822 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1402+3733G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407822 | |||||||
| chr17:78407842 | G | C | 1 | a0001c0002t0001g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1402+3753G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407842 | |||||||
| chr17:78407903 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(156): Show |
170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1402+3814G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78407903 | |||||||
| chr17:78408044 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1402+3955G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408044 | |||||||
| chr17:78408077 | A | G | 1 | a0001c0003t0002g0184 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1402+3988A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408077 | |||||||
| chr17:78408108 | ATCAG | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(156): Show |
170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1402+4023_1402+402 others(8): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78408108 | ||||||
| chr17:78408199 | A | G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0069 others(59): Show |
65 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1402+4110A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408199 | |||||||
| chr17:78408351 | G | A | 11 | a0001c0002t0001g0025 a0001c0002t0001g0027 a0001c0002t0001g0031 others(8): Show |
11 | HG00544.hp2 HG02015.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+4262G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408351 | |||||||
| chr17:78408445 | G | A | 1 | a0001c0001t0001g0353 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1402+4356G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408445 | |||||||
| chr17:78408499 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1402+4410C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408499 | |||||||
| chr17:78408574 | C | T | 41 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(38): Show |
42 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1402+4485C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408574 | |||||||
| chr17:78408660 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1402+4571G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408660 | |||||||
| chr17:78408705 | C | T | 43 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(40): Show |
44 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1402+4616C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408705 | |||||||
| chr17:78408812 | C | T | 72 | a0001c0001t0001g0346 a0001c0002t0001g0001 a0001c0002t0001g0007 others(69): Show |
77 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1402+4723C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408812 | |||||||
| chr17:78408817 | C | T | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1402+4728C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408817 | |||||||
| chr17:78408952 | G | C | 5 | a0001c0002t0001g0115 a0001c0002t0001g0122 a0001c0002t0001g0136 others(2): Show |
5 | NA18946.hp2 NA18950.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+4863G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408952 | |||||||
| chr17:78408993 | G | A | 1 | a0001c0002t0001g0005 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1402+4904G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78408993 | |||||||
| chr17:78409077 | G | A | 1 | a0001c0001t0001g0357 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1402+4988G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409077 | |||||||
| chr17:78409095 | T | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0218 |
2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1402+5006T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409095 | |||||||
| chr17:78409134 | A | G | 1 | a0001c0002t0001g0023 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1402+5045A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409134 | |||||||
| chr17:78409221 | C | T | 43 | a0001c0001t0001g0016 a0001c0001t0001g0333 a0001c0001t0001g0334 others(40): Show |
44 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1402+5132C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409221 | |||||||
| chr17:78409228 | C | T | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1402+5139C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409228 | |||||||
| chr17:78409491 | C | A | 1 | a0001c0001t0001g0353 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1403-5388C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409491 | |||||||
| chr17:78409565 | G | A | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1403-5314G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409565 | |||||||
| chr17:78409655 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(196): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1403-5224T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409655 | |||||||
| chr17:78409756 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(196): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1403-5123T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409756 | |||||||
| chr17:78409830 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1403-5049G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409830 | |||||||
| chr17:78409880 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1403-4999G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409880 | |||||||
| chr17:78409947 | C | G | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1403-4932C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78409947 | |||||||
| chr17:78410003 | C | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
203 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1403-4876C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410003 | |||||||
| chr17:78410089 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(193): Show |
208 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1403-4790T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410089 | |||||||
| chr17:78410103 | AAAAAC | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(156): Show |
170 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1403-4754_1403-475 others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410103 | ||||||
| chr17:78410193 | A | G | 3 | a0001c0001t0001g0240 a0001c0001t0001g0249 a0001c0001t0001g0287 |
3 | HG02080.hp1 NA18948.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1403-4686A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410193 | |||||||
| chr17:78410220 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1403-4659G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410220 | |||||||
| chr17:78410290 | A | G | 6 | a0001c0001t0001g0349 a0001c0002t0001g0207 a0001c0003t0002g0179 others(3): Show |
6 | HG02818.hp2 HG02970.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1403-4589A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410290 | |||||||
| chr17:78410316 | C | T | 3 | a0001c0002t0001g0111 a0001c0002t0007g0017 a0001c0002t0007g0112 |
3 | HG01109.hp1 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1403-4563C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410316 | |||||||
| chr17:78410321 | C | CAGG | 72 | a0001c0001t0001g0292 a0001c0001t0001g0296 a0001c0001t0002g0330 others(69): Show |
77 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1403-4554_1403-455 others(7): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410321 | ||||||
| chr17:78410326 | G | A | 10 | a0001c0002t0001g0186 a0001c0002t0001g0192 a0001c0002t0002g0189 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1403-4553G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410326 | |||||||
| chr17:78410462 | CT | C | 23 | a0001c0001t0002g0015 a0001c0002t0001g0001 a0001c0002t0001g0005 others(20): Show |
27 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-4388delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | ||||||
| chr17:78410462 | CTTTTT | C | 9 | a0001c0001t0001g0342 a0001c0002t0001g0025 a0001c0002t0001g0032 others(6): Show |
9 | HG00639.hp2 HG02970.hp2 NA18975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1403-4392_1403-438 others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | ||||||
| chr17:78410462 | CTTTTTT | C | 56 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0106 others(53): Show |
59 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1403-4393_1403-438 others(10): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | ||||||
| chr17:78410462 | CTTTTTTT | C | 130 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0069 others(127): Show |
134 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1403-4394_1403-438 others(11): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | ||||||
| chr17:78410462 | CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0001g0110 a0001c0001t0001g0265 a0001c0001t0001g0354 others(4): Show |
7 | HG01109.hp1 HG01978.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-4395_1403-438 others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | ||||||
| chr17:78410462 | CTTTTTTT others(2): Show |
C | 23 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(20): Show |
23 | HG00099.hp2 HG01074.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1403-4396_1403-438 others(13): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | ||||||
| chr17:78410462 | CTTTTTTT others(3): Show |
C | 14 | a0001c0001t0001g0276 a0001c0001t0001g0344 a0001c0001t0001g0345 others(11): Show |
14 | HG01243.hp1 HG02258.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1403-4397_1403-438 others(14): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | ||||||
| chr17:78410462 | CTTTTTTT others(4): Show |
C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(93): Show |
105 | HG00323.hp1 HG00438.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1403-4398_1403-438 others(15): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | ||||||
| chr17:78410462 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1403-4404_1403-438 others(21): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78410462 | ||||||
| chr17:78410561 | C | G | 6 | a0001c0001t0001g0242 a0001c0001t0002g0015 a0001c0001t0002g0270 others(3): Show |
7 | HG01516.hp2 HG01517.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-4318C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410561 | |||||||
| chr17:78410611 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(190): Show |
209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1403-4268T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410611 | |||||||
| chr17:78410624 | C | G | 6 | a0001c0001t0001g0152 a0001c0001t0001g0345 a0001c0001t0003g0331 others(3): Show |
6 | HG02055.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403-4255C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410624 | |||||||
| chr17:78410630 | T | C | 2 | a0001c0001t0001g0338 a0001c0001t0001g0347 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1403-4249T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410630 | |||||||
| chr17:78410691 | T | C | 36 | a0001c0001t0001g0274 a0001c0001t0001g0280 a0001c0001t0001g0289 others(33): Show |
38 | HG00609.hp1 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1403-4188T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410691 | |||||||
| chr17:78410721 | C | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(39): Show |
50 | HG00408.hp2 HG00558.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1403-4158C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410721 | |||||||
| chr17:78410752 | T | G | 13 | a0001c0001t0001g0281 a0001c0001t0001g0345 a0001c0001t0001g0374 others(10): Show |
13 | HG01123.hp2 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1403-4127T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410752 | |||||||
| chr17:78410876 | T | C | 46 | a0001c0001t0001g0016 a0001c0001t0001g0231 a0001c0001t0001g0281 others(43): Show |
47 | HG00099.hp1 HG00099.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1403-4003T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410876 | |||||||
| chr17:78410915 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1403-3964G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410915 | |||||||
| chr17:78410986 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1403-3893G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78410986 | |||||||
| chr17:78411013 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1403-3866G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411013 | |||||||
| chr17:78411082 | G | T | 373 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(370): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1403-3797G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411082 | |||||||
| chr17:78411088 | G | A | 2 | a0001c0002t0001g0111 a0001c0002t0007g0017 |
2 | HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1403-3791G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411088 | |||||||
| chr17:78411187 | C | T | 1 | a0001c0002t0002g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1403-3692C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411187 | |||||||
| chr17:78411191 | G | A | 1 | a0001c0002t0002g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1403-3688G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411191 | |||||||
| chr17:78411222 | A | G | 373 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(370): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1403-3657A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411222 | |||||||
| chr17:78411237 | C | T | 1 | a0001c0002t0001g0066 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1403-3642C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411237 | |||||||
| chr17:78411347 | A | G | 1 | a0001c0003t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1403-3532A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411347 | |||||||
| chr17:78411417 | G | T | 1 | a0001c0002t0001g0150 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1403-3462G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411417 | |||||||
| chr17:78411449 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0101 others(2): Show |
5 | NA18959.hp2 NA18960.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-3430G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411449 | |||||||
| chr17:78411545 | C | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0069 others(54): Show |
59 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1403-3334C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411545 | |||||||
| chr17:78411618 | C | A | 5 | a0001c0001t0002g0343 a0001c0002t0002g0075 a0001c0003t0002g0026 others(2): Show |
5 | HG01106.hp1 HG01123.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-3261C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78411618 | |||||||
| chr17:78411707 | T | TG | 3 | a0001c0001t0005g0340 a0001c0002t0005g0077 a0001c0002t0005g0084 |
3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1403-3171dupG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411707 | ||||||
| chr17:78411902 | C | CT | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(150): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1403-2949dupT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | ||||||
| chr17:78411902 | C | CTT | 128 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0091 others(125): Show |
131 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1403-2950_1403-294 others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | ||||||
| chr17:78411902 | C | CTTT | 26 | a0001c0001t0001g0012 a0001c0001t0001g0090 a0001c0001t0001g0093 others(23): Show |
27 | HG00673.hp1 HG02486.hp2 HG02523.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-2951_1403-294 others(7): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | ||||||
| chr17:78411902 | CT | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0281 a0001c0001t0001g0336 others(21): Show |
25 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1403-2949delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | ||||||
| chr17:78411902 | CTT | C | 19 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0304 others(16): Show |
20 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1403-2950_1403-294 others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | ||||||
| chr17:78411902 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0345 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1403-2961_1403-294 others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 78411902 | ||||||
| chr17:78412140 | C | T | 3 | a0001c0001t0003g0331 a0001c0001t0003g0332 a0001c0001t0003g0339 |
3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1403-2739C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412140 | |||||||
| chr17:78412224 | G | A | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1403-2655G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412224 | |||||||
| chr17:78412257 | G | A | 1 | a0001c0001t0001g0374 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1403-2622G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412257 | |||||||
| chr17:78412288 | G | A | 31 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(28): Show |
32 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1403-2591G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412288 | |||||||
| chr17:78412305 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1403-2574G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412305 | |||||||
| chr17:78412451 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1403-2428A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412451 | |||||||
| chr17:78412536 | G | C | 3 | a0001c0001t0005g0340 a0001c0002t0005g0077 a0001c0002t0005g0084 |
3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1403-2343G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412536 | |||||||
| chr17:78412621 | C | T | 1 | a0001c0003t0002g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1403-2258C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412621 | |||||||
| chr17:78412726 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0001g0096 a0001c0001t0001g0101 others(2): Show |
5 | NA18959.hp2 NA18960.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-2153G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412726 | |||||||
| chr17:78412903 | G | A | 5 | a0001c0001t0001g0237 a0001c0001t0001g0245 a0001c0001t0001g0246 others(2): Show |
5 | HG01109.hp2 HG01361.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-1976G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412903 | |||||||
| chr17:78412945 | A | G | 15 | a0001c0001t0002g0343 a0001c0002t0002g0075 a0001c0003t0002g0026 others(12): Show |
15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1403-1934A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78412945 | |||||||
| chr17:78413012 | G | T | 1 | a0001c0001t0001g0249 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1403-1867G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413012 | |||||||
| chr17:78413109 | G | A | 1 | a0001c0002t0001g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1403-1770G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413109 | |||||||
| chr17:78413199 | C | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0217 a0001c0001t0001g0228 others(7): Show |
11 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1403-1680C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413199 | |||||||
| chr17:78413231 | A | G | 4 | a0001c0002t0002g0199 a0001c0002t0002g0202 a0001c0002t0002g0204 others(1): Show |
4 | HG01069.hp2 HG01243.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1403-1648A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413231 | |||||||
| chr17:78413522 | C | T | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1403-1357C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413522 | |||||||
| chr17:78413529 | T | G | 10 | a0001c0001t0009g0366 a0001c0001t0010g0348 a0001c0002t0001g0060 others(7): Show |
10 | HG00408.hp1 HG02523.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.1403-1350T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413529 | |||||||
| chr17:78413601 | C | G | 1 | a0001c0001t0001g0318 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1403-1278C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413601 | |||||||
| chr17:78413703 | C | A | 3 | a0001c0001t0005g0340 a0001c0002t0005g0077 a0001c0002t0005g0084 |
3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1403-1176C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413703 | |||||||
| chr17:78413728 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(26): Show |
36 | HG00408.hp2 HG00558.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1403-1151G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413728 | |||||||
| chr17:78413804 | C | T | 1 | a0001c0001t0001g0374 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1403-1075C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413804 | |||||||
| chr17:78413838 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1403-1041T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78413838 | |||||||
| chr17:78414053 | G | A | 1 | a0001c0003t0016g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1403-826G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414053 | |||||||
| chr17:78414213 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0345 |
4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1403-666C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414213 | |||||||
| chr17:78414217 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1403-662C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414217 | |||||||
| chr17:78414261 | C | G | 2 | a0001c0002t0001g0085 a0001c0002t0001g0120 |
2 | NA18983.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1403-618C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414261 | |||||||
| chr17:78414361 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0307 |
2 | NA19083.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1403-518G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414361 | |||||||
| chr17:78414383 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1403-496G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414383 | |||||||
| chr17:78414432 | C | T | 1 | a0001c0001t0001g0365 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1403-447C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414432 | |||||||
| chr17:78414559 | G | T | 1 | a0001c0001t0001g0349 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1403-320G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414559 | |||||||
| chr17:78414671 | G | T | 4 | a0001c0002t0001g0140 a0001c0002t0001g0186 a0001c0003t0008g0018 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1403-208G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414671 | |||||||
| chr17:78414710 | G | A | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1403-169G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414710 | |||||||
| chr17:78414790 | G | A | 316 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(313): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1403-89G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414790 | |||||||
| chr17:78414861 | G | A | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1403-18G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 7/9 | chr17 | 78414861 | |||||||
| chr17:78415073 | T | TG | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(284): Show |
305 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(302): Show |
intron_variant | MODIFIER | c.1551+51dupG | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78415073 | ||||||
| chr17:78415088 | A | G | 2 | a0001c0002t0001g0140 a0001c0002t0001g0186 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1551+61A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415088 | |||||||
| chr17:78415229 | C | T | 2 | a0001c0002t0001g0140 a0001c0002t0001g0186 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1551+202C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415229 | |||||||
| chr17:78415232 | G | T | 373 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(370): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1551+205G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415232 | |||||||
| chr17:78415250 | G | T | 1 | a0001c0001t0002g0343 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1551+223G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415250 | |||||||
| chr17:78415344 | A | G | 1 | a0001c0001t0001g0346 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1551+317A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415344 | |||||||
| chr17:78415668 | C | T | 3 | a0001c0001t0003g0331 a0001c0001t0003g0332 a0001c0001t0003g0339 |
3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1551+641C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415668 | |||||||
| chr17:78415936 | G | T | 2 | a0001c0003t0002g0176 a0001c0003t0002g0180 |
2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1551+909G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415936 | |||||||
| chr17:78415949 | G | A | 30 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(27): Show |
30 | HG00099.hp1 HG00099.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1551+922G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78415949 | |||||||
| chr17:78416061 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1551+1034T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416061 | |||||||
| chr17:78416139 | C | T | 1 | a0001c0002t0002g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1551+1112C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416139 | |||||||
| chr17:78416165 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1551+1138G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416165 | |||||||
| chr17:78416190 | G | A | 2 | a0001c0001t0001g0337 a0001c0001t0001g0354 |
2 | HG00673.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1551+1163G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416190 | |||||||
| chr17:78416267 | T | G | 9 | a0001c0001t0001g0281 a0001c0002t0001g0072 a0001c0002t0001g0086 others(6): Show |
9 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1551+1240T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416267 | |||||||
| chr17:78416345 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0345 |
4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1551+1318C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416345 | |||||||
| chr17:78416416 | G | A | 2 | a0001c0003t0008g0018 a0001c0012t0008g0188 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1551+1389G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416416 | |||||||
| chr17:78416536 | CCACTGCC others(10): Show |
C | 4 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0358 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1551+1515_1551+153 others(21): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78416536 | ||||||
| chr17:78416545 | T | C | 24 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(21): Show |
25 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1551+1518T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416545 | |||||||
| chr17:78416593 | C | T | 1 | a0001c0002t0002g0080 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1551+1566C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416593 | |||||||
| chr17:78416594 | G | A | 3 | a0001c0002t0001g0131 a0001c0002t0001g0133 a0001c0002t0001g0208 |
3 | HG03831.hp1 NA18995.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1551+1567G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416594 | |||||||
| chr17:78416755 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1551+1728G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416755 | |||||||
| chr17:78416761 | C | A | 6 | a0001c0002t0001g0086 a0002c0004t0001g0190 a0002c0004t0001g0191 others(3): Show |
6 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1551+1734C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416761 | |||||||
| chr17:78416867 | G | T | 7 | a0001c0001t0009g0366 a0001c0001t0010g0348 a0001c0002t0001g0060 others(4): Show |
7 | HG00408.hp1 HG02523.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1551+1840G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78416867 | |||||||
| chr17:78417106 | C | T | 30 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(27): Show |
30 | HG00099.hp1 HG00099.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1551+2079C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417106 | |||||||
| chr17:78417142 | C | T | 15 | a0001c0001t0001g0090 a0001c0001t0001g0256 a0001c0001t0001g0273 others(12): Show |
15 | HG01993.hp2 HG02738.hp1 NA18951.hp2 others(12): Show |
intron_variant | MODIFIER | c.1551+2115C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417142 | |||||||
| chr17:78417187 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1551+2160G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417187 | |||||||
| chr17:78417236 | A | G | 12 | a0001c0001t0001g0231 a0001c0001t0001g0335 a0001c0001t0001g0350 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1551+2209A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417236 | |||||||
| chr17:78417292 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1552-2254C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417292 | |||||||
| chr17:78417395 | C | T | 25 | a0001c0001t0001g0345 a0001c0001t0002g0015 a0001c0001t0002g0263 others(22): Show |
26 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1552-2151C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417395 | |||||||
| chr17:78417406 | G | A | 4 | a0001c0002t0001g0122 a0001c0002t0002g0114 a0001c0002t0002g0189 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1552-2140G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417406 | |||||||
| chr17:78417576 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0345 |
4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1552-1970C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417576 | |||||||
| chr17:78417753 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1793G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417753 | |||||||
| chr17:78417754 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1792G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417754 | |||||||
| chr17:78417755 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1791T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417755 | |||||||
| chr17:78417756 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1790G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417756 | |||||||
| chr17:78417757 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1789G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417757 | |||||||
| chr17:78417761 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1785G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417761 | |||||||
| chr17:78417765 | T | G | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1781T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417765 | |||||||
| chr17:78417766 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1780G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417766 | |||||||
| chr17:78417768 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1778A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417768 | |||||||
| chr17:78417769 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1552-1777G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417769 | |||||||
| chr17:78417848 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1552-1698A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417848 | |||||||
| chr17:78417889 | C | CAAAG | 3 | a0001c0002t0001g0060 a0001c0002t0001g0063 a0001c0002t0001g0068 |
3 | NA18959.hp1 NA18985.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1552-1655_1552-165 others(8): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78417889 | ||||||
| chr17:78417928 | AT | A | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(284): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1552-1597delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78417928 | ||||||
| chr17:78417928 | ATT | A | 55 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0095 others(52): Show |
58 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1552-1598_1552-159 others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78417928 | ||||||
| chr17:78417991 | A | G | 29 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(26): Show |
30 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1552-1555A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417991 | |||||||
| chr17:78417999 | G | T | 1 | a0001c0002t0002g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1552-1547G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78417999 | |||||||
| chr17:78418087 | G | A | 15 | a0001c0001t0002g0343 a0001c0002t0002g0075 a0001c0003t0002g0026 others(12): Show |
15 | HG01106.hp1 HG01123.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1552-1459G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418087 | |||||||
| chr17:78418090 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0341 others(1): Show |
5 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1552-1456C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418090 | |||||||
| chr17:78418131 | C | T | 2 | a0001c0002t0001g0140 a0001c0002t0001g0186 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1552-1415C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418131 | |||||||
| chr17:78418149 | C | T | 3 | a0001c0001t0003g0331 a0001c0001t0003g0332 a0001c0001t0003g0339 |
3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1552-1397C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418149 | |||||||
| chr17:78418219 | C | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(222): Show |
240 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.1552-1327C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418219 | |||||||
| chr17:78418274 | CAT | C | 9 | a0001c0001t0001g0281 a0001c0002t0001g0072 a0001c0002t0001g0086 others(6): Show |
9 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1552-1271_1552-127 others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418274 | |||||||
| chr17:78418304 | G | A | 315 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(312): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1552-1242G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418304 | |||||||
| chr17:78418313 | C | G | 3 | a0001c0001t0003g0331 a0001c0001t0003g0332 a0001c0001t0003g0339 |
3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1552-1233C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418313 | |||||||
| chr17:78418332 | A | G | 1 | a0001c0002t0003g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1552-1214A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418332 | |||||||
| chr17:78418361 | C | T | 373 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(370): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1552-1185C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418361 | |||||||
| chr17:78418433 | A | C | 1 | a0001c0001t0002g0330 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1552-1113A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418433 | |||||||
| chr17:78418605 | G | A | 1 | a0001c0002t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1552-941G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418605 | |||||||
| chr17:78418761 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1552-785C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418761 | |||||||
| chr17:78418806 | C | T | 1 | a0001c0010t0001g0227 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1552-740C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78418806 | |||||||
| chr17:78418861 | CTG | C | 9 | a0001c0001t0009g0366 a0001c0001t0010g0348 a0001c0002t0001g0060 others(6): Show |
9 | HG00408.hp1 HG02523.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1552-681_1552-680d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 78418861 | ||||||
| chr17:78419072 | G | C | 45 | a0001c0001t0001g0283 a0001c0001t0002g0015 a0001c0001t0002g0263 others(42): Show |
46 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1552-474G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419072 | |||||||
| chr17:78419074 | A | G | 45 | a0001c0001t0001g0283 a0001c0001t0002g0015 a0001c0001t0002g0263 others(42): Show |
46 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1552-472A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419074 | |||||||
| chr17:78419129 | T | C | 1 | a0001c0002t0001g0037 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1552-417T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419129 | |||||||
| chr17:78419134 | A | G | 45 | a0001c0001t0001g0283 a0001c0001t0002g0015 a0001c0001t0002g0263 others(42): Show |
46 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1552-412A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419134 | |||||||
| chr17:78419249 | G | A | 2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1552-297G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419249 | |||||||
| chr17:78419439 | G | C | 4 | a0001c0002t0001g0140 a0001c0002t0001g0186 a0001c0003t0008g0018 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1552-107G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419439 | |||||||
| chr17:78419510 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1552-36G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 8/9 | chr17 | 78419510 | |||||||
| chr17:78419890 | C | T | 1 | a0001c0002t0001g0115 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.*10+215C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78419890 | |||||||
| chr17:78419923 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*10+248C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78419923 | |||||||
| chr17:78419964 | A | G | 44 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(41): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*10+289A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78419964 | |||||||
| chr17:78420117 | C | T | 1 | a0001c0002t0001g0040 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.*10+442C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420117 | |||||||
| chr17:78420179 | G | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0345 |
4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*10+504G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420179 | |||||||
| chr17:78420220 | G | A | 2 | a0001c0003t0008g0018 a0001c0012t0008g0188 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*10+545G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420220 | |||||||
| chr17:78420236 | G | A | 1 | a0001c0001t0001g0350 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*10+561G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420236 | |||||||
| chr17:78420251 | G | A | 3 | a0001c0001t0003g0331 a0001c0001t0003g0332 a0001c0001t0003g0339 |
3 | HG02280.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.*10+576G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420251 | |||||||
| chr17:78420329 | C | T | 1 | a0001c0002t0001g0035 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.*10+654C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420329 | |||||||
| chr17:78420331 | T | TGGACTGT others(5): Show |
2 | a0001c0001t0009g0366 a0001c0001t0010g0348 |
2 | NA18939.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.*10+657_*10+668dup others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78420331 | ||||||
| chr17:78420356 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0253 |
2 | NA18959.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.*10+681C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420356 | |||||||
| chr17:78420460 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0217 a0001c0001t0001g0228 others(7): Show |
11 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.*10+785C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420460 | |||||||
| chr17:78420476 | T | C | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.*10+801T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420476 | |||||||
| chr17:78420512 | A | C | 2 | a0001c0002t0001g0140 a0001c0002t0001g0186 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.*10+837A>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420512 | |||||||
| chr17:78420516 | CTGGGCCT others(9): Show |
C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0345 |
4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*10+842_*10+857del others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420516 | |||||||
| chr17:78420526 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.*10+851G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420526 | |||||||
| chr17:78420677 | A | G | 1 | a0001c0002t0003g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*10+1002A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420677 | |||||||
| chr17:78420722 | C | A | 1 | a0001c0001t0001g0317 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.*10+1047C>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420722 | |||||||
| chr17:78420744 | G | A | 44 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(41): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*10+1069G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420744 | |||||||
| chr17:78420847 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*10+1172G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420847 | |||||||
| chr17:78420859 | A | G | 11 | a0001c0001t0002g0343 a0001c0003t0002g0176 a0001c0003t0002g0177 others(8): Show |
11 | HG02055.hp1 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.*10+1184A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78420859 | |||||||
| chr17:78420970 | A | AATGGTGT others(8): Show |
1 | a0001c0001t0004g0351 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*10+1296_*10+1310d others(17): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78420970 | ||||||
| chr17:78421098 | T | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0336 |
3 | HG02145.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*10+1423T>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421098 | |||||||
| chr17:78421270 | CAG | C | 27 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(24): Show |
28 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.*10+1601_*10+1602d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421270 | ||||||
| chr17:78421273 | A | G | 1 | a0001c0002t0002g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*10+1598A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421273 | |||||||
| chr17:78421275 | A | G | 2 | a0001c0001t0002g0270 a0001c0011t0002g0315 |
2 | HG01256.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*10+1600A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421275 | |||||||
| chr17:78421286 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.*10+1611G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421286 | |||||||
| chr17:78421403 | T | TGTCA | 358 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(355): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.*10+1729_*10+1732d others(6): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421403 | ||||||
| chr17:78421435 | A | G | 370 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(367): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.*10+1760A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421435 | |||||||
| chr17:78421436 | G | T | 1 | a0001c0001t0001g0354 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*10+1761G>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421436 | |||||||
| chr17:78421518 | C | T | 2 | a0001c0002t0001g0074 a0001c0002t0001g0083 |
2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.*10+1843C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421518 | |||||||
| chr17:78421567 | C | T | 1 | a0001c0002t0001g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.*10+1892C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421567 | |||||||
| chr17:78421611 | A | G | 1 | a0001c0002t0001g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*10+1936A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421611 | |||||||
| chr17:78421674 | C | T | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.*10+1999C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421674 | |||||||
| chr17:78421690 | C | CATTCCTC others(3): Show |
1 | a0002c0004t0001g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*10+2020_*10+2029d others(12): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421690 | ||||||
| chr17:78421782 | A | ACTG | 3 | a0001c0002t0001g0008 a0001c0002t0001g0043 a0001c0002t0001g0128 |
4 | HG00609.hp2 HG00639.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.*10+2110_*10+2112d others(5): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421782 | ||||||
| chr17:78421802 | T | C | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(308): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.*10+2127T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421802 | |||||||
| chr17:78421898 | A | AGCGGGCG | 4 | a0001c0001t0001g0223 a0001c0001t0001g0286 a0001c0002t0007g0017 others(1): Show |
4 | HG00733.hp1 HG01109.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.*11-2151_*11-2145d others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421898 | ||||||
| chr17:78421898 | AGCGGGCG | A | 46 | a0001c0001t0001g0016 a0001c0001t0001g0219 a0001c0001t0001g0242 others(43): Show |
49 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.*11-2151_*11-2145d others(9): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78421898 | ||||||
| chr17:78421905 | G | A | 1 | a0001c0002t0001g0065 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.*11-2156G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421905 | |||||||
| chr17:78421912 | G | C | 1 | a0001c0001t0001g0287 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.*11-2149G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421912 | |||||||
| chr17:78421915 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0341 others(10): Show |
14 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.*11-2146G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421915 | |||||||
| chr17:78421918 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.*11-2143C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421918 | |||||||
| chr17:78421919 | G | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0341 others(9): Show |
13 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.*11-2142G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421919 | |||||||
| chr17:78421932 | C | T | 2 | a0001c0001t0003g0331 a0001c0001t0003g0332 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.*11-2129C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421932 | |||||||
| chr17:78421957 | C | T | 5 | a0001c0001t0001g0341 a0001c0001t0001g0371 a0001c0001t0001g0372 others(2): Show |
5 | HG03516.hp1 NA18939.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.*11-2104C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421957 | |||||||
| chr17:78421969 | CCT | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(276): Show |
297 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.*11-2091_*11-2090d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421969 | |||||||
| chr17:78421993 | C | T | 3 | a0001c0001t0005g0340 a0001c0002t0005g0077 a0001c0002t0005g0084 |
3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.*11-2068C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78421993 | |||||||
| chr17:78422228 | A | T | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*11-1833A>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422228 | |||||||
| chr17:78422333 | C | T | 2 | a0001c0001t0001g0362 a0001c0001t0001g0363 |
2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.*11-1728C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422333 | |||||||
| chr17:78422349 | C | T | 4 | a0001c0001t0001g0371 a0001c0001t0001g0372 a0001c0001t0001g0373 others(1): Show |
4 | NA18939.hp2 NA18984.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.*11-1712C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422349 | |||||||
| chr17:78422382 | T | G | 9 | a0001c0001t0001g0281 a0001c0002t0001g0072 a0001c0002t0001g0086 others(6): Show |
9 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.*11-1679T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422382 | |||||||
| chr17:78422421 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0311 |
2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.*11-1640G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422421 | |||||||
| chr17:78422469 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.*11-1592C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422469 | |||||||
| chr17:78422487 | A | ATGGGTGT others(43): Show |
24 | a0001c0001t0002g0263 a0001c0001t0002g0270 a0001c0001t0002g0367 others(21): Show |
24 | HG00558.hp2 HG00733.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.*11-1573_*11-1524d others(52): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78422487 | ||||||
| chr17:78422605 | C | T | 4 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0358 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.*11-1456C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422605 | |||||||
| chr17:78422617 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0247 a0001c0001t0001g0285 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.*11-1444C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422617 | |||||||
| chr17:78422659 | G | A | 44 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(41): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-1402G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422659 | |||||||
| chr17:78422726 | C | CTGGGCTC others(7): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0336 |
3 | HG02145.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*11-1334_*11-1321d others(16): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78422726 | ||||||
| chr17:78422747 | G | A | 2 | a0001c0003t0008g0018 a0001c0012t0008g0188 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*11-1314G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422747 | |||||||
| chr17:78422763 | CGT | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0336 a0001c0001t0001g0345 |
4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*11-1296_*11-1295d others(4): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78422763 | ||||||
| chr17:78422779 | G | A | 9 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.*11-1282G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422779 | |||||||
| chr17:78422790 | CTTTGAAG others(10): Show |
C | 2 | a0001c0002t0007g0017 a0001c0002t0007g0112 |
2 | HG01109.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.*11-1270_*11-1254d others(19): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422790 | |||||||
| chr17:78422856 | G | A | 1 | a0001c0001t0009g0366 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.*11-1205G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422856 | |||||||
| chr17:78422857 | A | G | 1 | a0001c0001t0009g0366 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.*11-1204A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422857 | |||||||
| chr17:78422883 | G | A | 3 | a0001c0002t0002g0114 a0001c0002t0002g0189 a0001c0002t0002g0196 |
3 | HG01891.hp2 HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.*11-1178G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422883 | |||||||
| chr17:78422929 | C | T | 5 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0206 others(2): Show |
5 | HG00558.hp2 HG02129.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.*11-1132C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422929 | |||||||
| chr17:78422972 | T | C | 1 | a0001c0002t0002g0067 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.*11-1089T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422972 | |||||||
| chr17:78422995 | T | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(279): Show |
300 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.*11-1066T>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78422995 | |||||||
| chr17:78423011 | G | A | 2 | a0001c0002t0007g0017 a0001c0002t0007g0112 |
2 | HG01109.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.*11-1050G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423011 | |||||||
| chr17:78423055 | G | A | 1 | a0001c0013t0011g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*11-1006G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423055 | |||||||
| chr17:78423089 | ACT | A | 44 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(41): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-968_*11-967del others(2): Show |
PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78423089 | ||||||
| chr17:78423104 | C | T | 44 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(41): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-957C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423104 | |||||||
| chr17:78423105 | G | GA | 275 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(272): Show |
292 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.*11-942dupA | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr17 | 78423105 | ||||||
| chr17:78423106 | A | G | 24 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(21): Show |
25 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.*11-955A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423106 | |||||||
| chr17:78423119 | AT | A | 44 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(41): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-941delT | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423119 | |||||||
| chr17:78423129 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*11-932T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423129 | |||||||
| chr17:78423136 | G | C | 3 | a0001c0001t0005g0340 a0001c0002t0005g0077 a0001c0002t0005g0084 |
3 | HG01243.hp1 HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.*11-925G>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423136 | |||||||
| chr17:78423146 | G | A | 4 | a0001c0002t0001g0140 a0001c0003t0008g0018 a0001c0012t0008g0188 others(1): Show |
4 | HG01884.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.*11-915G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423146 | |||||||
| chr17:78423170 | G | A | 6 | a0001c0002t0001g0086 a0001c0002t0001g0192 a0002c0004t0001g0190 others(3): Show |
6 | HG01261.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.*11-891G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423170 | |||||||
| chr17:78423204 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0299 |
2 | NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.*11-857T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423204 | |||||||
| chr17:78423260 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*11-801C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423260 | |||||||
| chr17:78423275 | C | G | 209 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(206): Show |
219 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.*11-786C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423275 | |||||||
| chr17:78423345 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0103 |
2 | NA18967.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.*11-716G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423345 | |||||||
| chr17:78423364 | C | T | 1 | a0001c0002t0001g0198 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*11-697C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423364 | |||||||
| chr17:78423398 | A | G | 44 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(41): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-663A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423398 | |||||||
| chr17:78423518 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0280 |
2 | NA19054.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.*11-543A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423518 | |||||||
| chr17:78423548 | A | G | 2 | a0001c0002t0001g0027 a0001c0002t0001g0054 |
2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.*11-513A>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423548 | |||||||
| chr17:78423556 | T | C | 44 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(41): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-505T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423556 | |||||||
| chr17:78423570 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.*11-491C>T | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423570 | |||||||
| chr17:78423704 | C | G | 1 | a0001c0001t0001g0346 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*11-357C>G | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423704 | |||||||
| chr17:78423801 | G | A | 44 | a0001c0001t0002g0015 a0001c0001t0002g0263 a0001c0001t0002g0270 others(41): Show |
45 | HG00140.hp1 HG00558.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*11-260G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423801 | |||||||
| chr17:78423993 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.*11-68G>A | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78423993 | |||||||
| chr17:78424004 | T | C | 18 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0001g0326 others(15): Show |
18 | HG00609.hp1 HG00673.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.*11-57T>C | PGS1 | ENSG00000087157.19 | transcript | ENST00000262764.11 | protein_coding | 9/9 | chr17 | 78424004 |