Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29968 |
| ensemblid | ENSG00000135069.14 |
| hgncid | 19129 |
| symbol | PSAT1 |
| name | phosphoserine aminotransferase 1 |
| refseq_nuc | NM_058179.4 |
| refseq_prot | NP_478059.1 |
| ensembl_nuc | ENST00000376588.4 |
| ensembl_prot | ENSP00000365773.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 78297125 |
| end | 78330093 |
| strand | + |
| ver | v1.2 |
| region | chr9:78297125-78330093 |
| region5000 | chr9:78292125-78335093 |
| regionname0 | PSAT1_chr9_78297125_78330093 |
| regionname5000 | PSAT1_chr9_78292125_78335093 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 370 | 412 | 95 | 74 | 181 | 16 | 44 | 137 | PSAT1_chr9_78292125_78335093 | PSAT1 | MDAPR others(365): Show |
chr9 | 78292125 | 78335093 |
| a0002 | 0/0 | 370 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | MDAPR others(365): Show |
chr9 | 78292125 | 78335093 |
| a0003 | 0/0 | 370 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | MDAPR others(365): Show |
chr9 | 78292125 | 78335093 |
| a0004 | 0/0 | 370 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | MDAPR others(365): Show |
chr9 | 78292125 | 78335093 |
| a0005 | 0/0 | 370 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | MDAPR others(365): Show |
chr9 | 78292125 | 78335093 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1110 | 244 | 43 | 39 | 129 | 7 | 25 | PSAT1_chr9_78292125_78335093 | PSAT1 | ATGGA others(1105): Show |
chr9 | 78292125 | 78335093 | ||
| a0001c0002 | 0/1 | 1110 | 164 | 51 | 34 | 51 | 9 | 18 | PSAT1_chr9_78292125_78335093 | PSAT1 | ATGGA others(1105): Show |
chr9 | 78292125 | 78335093 | ||
| a0001c0003 | 0/0 | 1110 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | ATGGA others(1105): Show |
chr9 | 78292125 | 78335093 | ||
| a0001c0005 | 0/0 | 1110 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | ATGGA others(1105): Show |
chr9 | 78292125 | 78335093 | ||
| a0001c0009 | 0/0 | 1110 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | ATGGA others(1105): Show |
chr9 | 78292125 | 78335093 | ||
| a0002c0008 | 0/0 | 1110 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | ATGGA others(1105): Show |
chr9 | 78292125 | 78335093 | ||
| a0003c0006 | 0/0 | 1110 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | ATGGA others(1105): Show |
chr9 | 78292125 | 78335093 | ||
| a0004c0007 | 0/0 | 1110 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | ATGGA others(1105): Show |
chr9 | 78292125 | 78335093 | ||
| a0005c0004 | 0/0 | 1110 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | ATGGA others(1105): Show |
chr9 | 78292125 | 78335093 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2206 | 134 | 21 | 18 | 84 | 4 | 7 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0001t0002 | 1/0 | 2206 | 81 | 4 | 11 | 45 | 3 | 17 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0001t0003 | 0/0 | 2206 | 16 | 7 | 8 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0001t0004 | 0/0 | 2206 | 9 | 8 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0001t0005 | 0/0 | 2206 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0001t0009 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0001t0011 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0002t0001 | 0/1 | 2206 | 123 | 31 | 28 | 39 | 9 | 15 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0002t0002 | 0/0 | 2206 | 23 | 3 | 5 | 12 | 0 | 3 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0002t0003 | 0/0 | 2206 | 9 | 8 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0002t0004 | 0/0 | 2206 | 3 | 3 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0002t0005 | 0/0 | 2206 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0002t0006 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0002t0007 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0002t0008 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0002t0010 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0003t0006 | 0/0 | 2206 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0005t0001 | 0/0 | 2206 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0001c0009t0002 | 0/0 | 2206 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0002c0008t0003 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0003c0006t0001 | 0/0 | 2206 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0004c0007t0001 | 0/0 | 2206 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| a0005c0004t0001 | 0/0 | 2206 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | GCAGA others(2201): Show |
chr9 | 78292125 | 78335093 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0004g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0001t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0001 | 0/0 | 12 | 0 | 4 | 6 | 0 | 2 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0006g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0002t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0003t0006g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0005t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0001c0009t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0002c0008t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0003c0006t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0004c0007t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| a0005c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | GBR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0233 | EUR | GBR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0116 | EUR | GBR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0178 | EUR | GBR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0028 | EUR | FIN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0316 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0330 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01081 | hp2 | a0001 | c0003 | t0006 | g0009 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0279 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0278 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0242 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0346 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0319 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0361 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0066 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0134 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0230 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0304 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0215 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0089 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0287 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0110 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0088 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02145 | hp2 | a0001 | c0002 | t0008 | g0021 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | CDX | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | CDX | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0244 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0352 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0186 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0332 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02698 | hp2 | a0001 | c0005 | t0001 | g0310 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0356 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0090 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0211 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02809 | hp2 | a0001 | c0002 | t0010 | g0044 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0272 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0325 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0274 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0243 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0142 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0345 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0353 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0358 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03130 | hp1 | a0001 | c0003 | t0006 | g0009 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0271 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0276 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0275 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0357 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0190 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0045 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0189 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03579 | hp1 | a0002 | c0008 | t0003 | g0143 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03654 | hp1 | a0003 | c0006 | t0001 | g0324 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0344 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03704 | hp2 | a0004 | c0007 | t0001 | g0177 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0277 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0129 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0333 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0292 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0130 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0335 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18995 | hp1 | a0005 | c0004 | t0001 | g0176 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0355 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19084 | hp1 | a0001 | c0009 | t0002 | g0117 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0139 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0228 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ASW | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ASW | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0256 | EUR | TSI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | TSI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0334 | EUR | TSI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0226 | SAS | GIH | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0311 | SAS | GIH | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0336 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0320 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02486 | hp1 | a0001 | c0002 | t0007 | g0257 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0328 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG03471 | hp2 | a0001 | c0002 | t0006 | g0354 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | USA | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | USA | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | USA | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0299 | AFR | USA | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0207 | REF | REF | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0111 | REF | REF | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:78300603 | T | G | 1 | a0005 | 1 | NA18995.hp1 | missense_variant&splice_region_variant | MODERATE | c.62T>G | p.Val21Gly | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/9 | 148/2206 | 62/1113 | 21/370 | chr9 | 78300603 | |||
| chr9:78304910 | A | G | 1 | a0002 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.367A>G | p.Ile123Val | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/9 | 453/2206 | 367/1113 | 123/370 | chr9 | 78304910 | |||
| chr9:78308568 | C | T | 1 | a0004 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.725C>T | p.Thr242Met | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/9 | 811/2206 | 725/1113 | 242/370 | chr9 | 78308568 | |||
| chr9:78317684 | T | C | 1 | a0003 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.749T>C | p.Val250Ala | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/9 | 835/2206 | 749/1113 | 250/370 | chr9 | 78317684 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:78304840 | T | G | 5 | a0001c0002 a0001c0005 a0002c0008 others(2): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
synonymous_variant | LOW | c.297T>G | p.Ala99Ala | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/9 | 383/2206 | 297/1113 | 99/370 | chr9 | 78304840 | |||
| chr9:78304891 | G | A | 1 | a0001c0005 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.348G>A | p.Lys116Lys | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/9 | 434/2206 | 348/1113 | 116/370 | chr9 | 78304891 | |||
| chr9:78317730 | G | A | 1 | a0001c0003 | 2 | HG01081.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.795G>A | p.Ala265Ala | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/9 | 881/2206 | 795/1113 | 265/370 | chr9 | 78317730 | |||
| chr9:78329032 | C | T | 1 | a0001c0009 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.1059C>T | p.Asp353Asp | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 1145/2206 | 1059/1113 | 353/370 | chr9 | 78329032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:78297173 | G | A | 1 | a0001c0002t0007 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/9 | 38 | chr9 | 78297173 | ||||||
| chr9:78297199 | G | C | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(13): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
5_prime_UTR_variant | MODIFIER | c.-12G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/9 | 12 | chr9 | 78297199 | ||||||
| chr9:78329125 | A | G | 1 | a0001c0001t0011 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 39 | chr9 | 78329125 | ||||||
| chr9:78329337 | C | T | 1 | a0001c0002t0010 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 251 | chr9 | 78329337 | ||||||
| chr9:78329338 | G | C | 4 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0006 others(1): Show |
15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*252G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 252 | chr9 | 78329338 | ||||||
| chr9:78329508 | C | T | 7 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(4): Show |
32 | HG00738.hp2 HG01081.hp1 HG01346.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*422C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 422 | chr9 | 78329508 | ||||||
| chr9:78329678 | A | C | 4 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0006 others(1): Show |
15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*592A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 592 | chr9 | 78329678 | ||||||
| chr9:78329750 | A | G | 1 | a0001c0002t0008 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 664 | chr9 | 78329750 | ||||||
| chr9:78329888 | A | T | 1 | a0001c0001t0009 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 802 | chr9 | 78329888 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:78297385 | A | G | 1 | a0001c0002t0001g0361 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.60+115A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297385 | |||||||
| chr9:78297481 | C | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(242): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.60+211C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297481 | |||||||
| chr9:78297530 | C | T | 2 | a0001c0001t0001g0359 a0001c0001t0001g0360 |
2 | NA18944.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.60+260C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297530 | |||||||
| chr9:78297539 | G | T | 1 | a0001c0002t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.60+269G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297539 | |||||||
| chr9:78297651 | C | G | 3 | a0001c0002t0001g0356 a0001c0002t0001g0357 a0001c0002t0001g0358 |
3 | HG02717.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.60+381C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297651 | |||||||
| chr9:78297680 | C | T | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.60+410C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297680 | |||||||
| chr9:78297819 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.60+549C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297819 | |||||||
| chr9:78297870 | G | A | 2 | a0001c0002t0001g0141 a0001c0002t0003g0142 |
2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.60+600G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297870 | |||||||
| chr9:78297907 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0017 others(78): Show |
90 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.60+637G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297907 | |||||||
| chr9:78297913 | C | T | 2 | a0001c0002t0001g0353 a0001c0002t0003g0352 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.60+643C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297913 | |||||||
| chr9:78297914 | C | G | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.60+644C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297914 | |||||||
| chr9:78298118 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.60+848G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298118 | |||||||
| chr9:78298154 | G | C | 88 | a0001c0001t0001g0025 a0001c0001t0001g0146 a0001c0001t0001g0197 others(85): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.60+884G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298154 | |||||||
| chr9:78298170 | C | G | 3 | a0001c0002t0001g0031 a0001c0002t0001g0137 a0001c0002t0001g0138 |
4 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+900C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298170 | |||||||
| chr9:78298405 | C | T | 10 | a0001c0002t0001g0031 a0001c0002t0001g0137 a0001c0002t0001g0138 others(7): Show |
11 | HG02257.hp1 HG02258.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+1135C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298405 | |||||||
| chr9:78298653 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0348 a0001c0001t0001g0349 others(2): Show |
6 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+1383A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298653 | |||||||
| chr9:78298778 | T | G | 1 | a0001c0001t0004g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.60+1508T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298778 | |||||||
| chr9:78299013 | G | A | 30 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0055 others(27): Show |
36 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.61-1589G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299013 | |||||||
| chr9:78299121 | T | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(250): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.61-1481T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299121 | |||||||
| chr9:78299144 | C | CA | 26 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0001t0001g0323 others(23): Show |
28 | HG00642.hp1 HG01106.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.61-1430dupA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299144 | C | CAAAAAAA others(19): Show |
1 | a0001c0002t0001g0031 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.61-1455_61-1430dup others(26): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299144 | C | CAAAAAAA others(23): Show |
1 | a0001c0002t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.61-1430_61-1429ins others(30): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299144 | C | CAAAAAAA others(24): Show |
1 | a0001c0002t0001g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-1430_61-1429ins others(31): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299144 | CA | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
6 | HG02717.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-1430delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299144 | CAA | C | 13 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(10): Show |
14 | HG00544.hp1 HG01978.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-1431_61-1430del others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299144 | CAAA | C | 76 | a0001c0001t0001g0032 a0001c0001t0001g0208 a0001c0001t0001g0212 others(73): Show |
95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.61-1432_61-1430del others(3): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299144 | CAAAAAAA others(2): Show |
C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0154 others(39): Show |
49 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.61-1438_61-1430del others(9): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299144 | CAAAAAAA others(3): Show |
C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0030 others(60): Show |
71 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.61-1439_61-1430del others(10): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299144 | CAAAAAAA others(4): Show |
C | 43 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0055 others(40): Show |
51 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.61-1440_61-1430del others(11): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | ||||||
| chr9:78299158 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61-1444A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299158 | |||||||
| chr9:78299164 | A | G | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.61-1438A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299164 | |||||||
| chr9:78299180 | T | C | 1 | a0001c0002t0001g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.61-1422T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299180 | |||||||
| chr9:78299211 | G | GA | 7 | a0001c0001t0001g0260 a0001c0001t0003g0308 a0001c0002t0001g0279 others(4): Show |
7 | HG01192.hp1 HG01433.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-1380dupA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299211 | ||||||
| chr9:78299211 | G | GAA | 136 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0026 others(133): Show |
166 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.61-1381_61-1380dup others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299211 | ||||||
| chr9:78299211 | G | GAAA | 68 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0030 others(65): Show |
77 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.61-1382_61-1380dup others(3): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299211 | ||||||
| chr9:78299211 | G | GAAAA | 40 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0055 others(37): Show |
47 | HG00408.hp1 HG00544.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.61-1383_61-1380dup others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299211 | ||||||
| chr9:78299269 | CTG | C | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1331_61-1330del others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299269 | ||||||
| chr9:78299271 | G | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(243): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.61-1331G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299271 | |||||||
| chr9:78299273 | T | C | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1329T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299273 | |||||||
| chr9:78299369 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61-1233C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299369 | |||||||
| chr9:78299465 | A | C | 1 | a0001c0002t0001g0319 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.61-1137A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299465 | |||||||
| chr9:78299496 | C | CT | 250 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(247): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.61-1098dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299496 | ||||||
| chr9:78299514 | C | CT | 11 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0347 others(8): Show |
11 | HG01243.hp1 HG01346.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-1070dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299514 | ||||||
| chr9:78299514 | C | CTT | 104 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0026 others(101): Show |
121 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.61-1071_61-1070dup others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299514 | ||||||
| chr9:78299514 | C | CTTT | 133 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0017 others(130): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.61-1072_61-1070dup others(3): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299514 | ||||||
| chr9:78299514 | C | CTTTT | 9 | a0001c0001t0001g0255 a0001c0001t0001g0281 a0001c0002t0001g0137 others(6): Show |
9 | HG00408.hp2 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.61-1073_61-1070dup others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299514 | ||||||
| chr9:78299554 | C | T | 4 | a0001c0001t0001g0306 a0001c0002t0001g0141 a0001c0002t0003g0142 others(1): Show |
4 | HG02976.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1048C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299554 | |||||||
| chr9:78299555 | G | T | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.61-1047G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299555 | |||||||
| chr9:78299571 | C | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(250): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.61-1031C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299571 | |||||||
| chr9:78299581 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.61-1021C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299581 | |||||||
| chr9:78299593 | ACCTCCGC others(25): Show |
A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0348 a0001c0001t0001g0349 others(2): Show |
6 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-997_61-966delCG others(30): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299593 | ||||||
| chr9:78299630 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0004g0194 a0001c0002t0010g0044 |
3 | HG02809.hp2 HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.61-972C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299630 | |||||||
| chr9:78299697 | G | C | 1 | a0001c0001t0004g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.61-905G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299697 | |||||||
| chr9:78299702 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.61-900G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299702 | |||||||
| chr9:78299713 | A | G | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.61-889A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299713 | |||||||
| chr9:78299718 | G | C | 1 | a0001c0002t0001g0141 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.61-884G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299718 | |||||||
| chr9:78300190 | C | T | 16 | a0001c0001t0002g0064 a0001c0001t0004g0148 a0001c0001t0005g0065 others(13): Show |
19 | HG01081.hp2 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-412C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300190 | |||||||
| chr9:78300386 | A | G | 2 | a0001c0002t0001g0353 a0001c0002t0003g0352 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.61-216A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300386 | |||||||
| chr9:78300435 | G | T | 3 | a0001c0002t0001g0031 a0001c0002t0001g0137 a0001c0002t0001g0138 |
4 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-167G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300435 | |||||||
| chr9:78300476 | G | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0030 others(55): Show |
66 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.61-126G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300476 | |||||||
| chr9:78300487 | A | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(247): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.61-115A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300487 | |||||||
| chr9:78300494 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.61-108G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300494 | |||||||
| chr9:78300564 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.61-38A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300564 | |||||||
| chr9:78300580 | A | G | 1 | a0001c0002t0002g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.61-22A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300580 | |||||||
| chr9:78300710 | C | CT | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(181): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.121+70dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 78300710 | ||||||
| chr9:78300710 | C | CTT | 43 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0034 others(40): Show |
49 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.121+69_121+70dupTT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 78300710 | ||||||
| chr9:78300710 | CT | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0001t0002g0091 others(15): Show |
21 | HG00642.hp1 HG01070.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.121+70delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 78300710 | ||||||
| chr9:78300732 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.121+70T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300732 | |||||||
| chr9:78300762 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0002t0003g0271 |
5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+100C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300762 | |||||||
| chr9:78300776 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0348 a0001c0001t0001g0349 others(2): Show |
6 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+114C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300776 | |||||||
| chr9:78300777 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
9 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+115G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300777 | |||||||
| chr9:78300843 | G | C | 2 | a0001c0002t0001g0356 a0001c0002t0001g0357 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.121+181G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300843 | |||||||
| chr9:78300890 | T | A | 1 | a0001c0002t0001g0318 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.121+228T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300890 | |||||||
| chr9:78301090 | G | A | 1 | a0001c0002t0001g0326 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.121+428G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301090 | |||||||
| chr9:78301278 | G | A | 82 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0208 others(79): Show |
102 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.121+616G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301278 | |||||||
| chr9:78301330 | A | G | 90 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0034 others(87): Show |
111 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.122-624A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301330 | |||||||
| chr9:78301367 | TA | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0002t0003g0271 |
5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-585delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 78301367 | ||||||
| chr9:78301442 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122-512G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301442 | |||||||
| chr9:78301460 | T | A | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122-494T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301460 | |||||||
| chr9:78301466 | A | G | 90 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0034 others(87): Show |
111 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.122-488A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301466 | |||||||
| chr9:78301474 | C | T | 1 | a0001c0002t0010g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.122-480C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301474 | |||||||
| chr9:78301504 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-450C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301504 | |||||||
| chr9:78301699 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(236): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.122-255G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301699 | |||||||
| chr9:78301885 | G | A | 2 | a0001c0001t0003g0322 a0001c0002t0001g0321 |
2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.122-69G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301885 | |||||||
| chr9:78301937 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.122-17T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301937 | |||||||
| chr9:78302063 | A | G | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191+40A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302063 | |||||||
| chr9:78302154 | C | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0030 others(55): Show |
66 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.191+131C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302154 | |||||||
| chr9:78302180 | C | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(236): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.191+157C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302180 | |||||||
| chr9:78302197 | C | T | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+174C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302197 | |||||||
| chr9:78302442 | A | G | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191+419A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302442 | |||||||
| chr9:78302464 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.191+441C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302464 | |||||||
| chr9:78302494 | C | T | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191+471C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302494 | |||||||
| chr9:78302537 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+514G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302537 | |||||||
| chr9:78302570 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.191+547C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302570 | |||||||
| chr9:78302621 | C | G | 1 | a0001c0002t0002g0088 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.191+598C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302621 | |||||||
| chr9:78302626 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(123): Show |
147 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.191+603C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302626 | |||||||
| chr9:78302733 | C | CA | 41 | a0001c0001t0001g0025 a0001c0001t0001g0096 a0001c0001t0001g0105 others(38): Show |
43 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.191+738dupA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | ||||||
| chr9:78302733 | C | CAA | 6 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0001t0002g0093 others(3): Show |
8 | HG00642.hp1 HG01070.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+737_191+738dup others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | ||||||
| chr9:78302733 | CA | C | 9 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0188 others(6): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.191+738delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | ||||||
| chr9:78302733 | CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0158 others(7): Show |
10 | HG02055.hp1 HG02074.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.191+731_191+738del others(8): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | ||||||
| chr9:78302733 | CAAAAAAA others(2): Show |
C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(195): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.191+730_191+738del others(9): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | ||||||
| chr9:78302733 | CAAAAAAA others(3): Show |
C | 10 | a0001c0001t0002g0069 a0001c0001t0002g0072 a0001c0001t0003g0157 others(7): Show |
10 | HG01168.hp2 HG01975.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.191+729_191+738del others(10): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | ||||||
| chr9:78302788 | G | C | 6 | a0001c0001t0002g0064 a0001c0001t0004g0148 a0001c0001t0005g0065 others(3): Show |
7 | HG01081.hp2 HG01496.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+765G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302788 | |||||||
| chr9:78302810 | G | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+787G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302810 | |||||||
| chr9:78302830 | C | T | 1 | a0001c0002t0003g0242 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.191+807C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302830 | |||||||
| chr9:78302861 | G | A | 15 | a0001c0001t0002g0064 a0001c0001t0004g0148 a0001c0001t0005g0065 others(12): Show |
18 | HG01081.hp2 HG01243.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.191+838G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302861 | |||||||
| chr9:78302877 | C | T | 1 | a0001c0003t0006g0009 | 2 | HG01081.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.191+854C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302877 | |||||||
| chr9:78302997 | G | A | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+974G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302997 | |||||||
| chr9:78303041 | A | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0026 others(52): Show |
68 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.191+1018A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303041 | |||||||
| chr9:78303046 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.191+1023T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303046 | |||||||
| chr9:78303345 | A | C | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+1322A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303345 | |||||||
| chr9:78303417 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(217): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.192-1318A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303417 | |||||||
| chr9:78303504 | C | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(217): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.192-1231C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303504 | |||||||
| chr9:78303548 | T | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(236): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.192-1187T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303548 | |||||||
| chr9:78303684 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.192-1051T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303684 | |||||||
| chr9:78303693 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.192-1042C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303693 | |||||||
| chr9:78303910 | T | G | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192-825T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303910 | |||||||
| chr9:78303921 | C | G | 15 | a0001c0001t0002g0064 a0001c0001t0004g0148 a0001c0001t0005g0065 others(12): Show |
18 | HG01081.hp2 HG01243.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.192-814C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303921 | |||||||
| chr9:78303980 | T | C | 8 | a0001c0001t0001g0032 a0001c0001t0004g0005 a0001c0001t0004g0276 others(5): Show |
11 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.192-755T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303980 | |||||||
| chr9:78304037 | T | C | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192-698T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304037 | |||||||
| chr9:78304079 | T | G | 279 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(276): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.192-656T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304079 | |||||||
| chr9:78304268 | C | T | 1 | a0001c0002t0001g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.192-467C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304268 | |||||||
| chr9:78304348 | G | A | 1 | a0001c0001t0004g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.192-387G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304348 | |||||||
| chr9:78304353 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.192-382G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304353 | |||||||
| chr9:78304547 | C | G | 1 | a0001c0002t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.192-188C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304547 | |||||||
| chr9:78304612 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0034 others(6): Show |
11 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.192-123G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304612 | |||||||
| chr9:78304687 | T | C | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-48T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304687 | |||||||
| chr9:78305039 | G | GT | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.397+100dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | 78305039 | ||||||
| chr9:78305137 | C | T | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.397+197C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305137 | |||||||
| chr9:78305217 | C | T | 2 | a0001c0002t0001g0254 a0001c0002t0005g0139 |
2 | NA18961.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.397+277C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305217 | |||||||
| chr9:78305269 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.397+329C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305269 | |||||||
| chr9:78305272 | G | A | 1 | a0001c0002t0002g0051 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.397+332G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305272 | |||||||
| chr9:78305370 | C | T | 10 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0140 others(7): Show |
12 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.397+430C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305370 | |||||||
| chr9:78305413 | C | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0034 others(6): Show |
11 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.397+473C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305413 | |||||||
| chr9:78305526 | C | G | 2 | a0001c0001t0002g0107 a0001c0001t0002g0125 |
2 | HG01109.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.397+586C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305526 | |||||||
| chr9:78305573 | G | C | 9 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0187 others(6): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+633G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305573 | |||||||
| chr9:78305841 | C | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.398-473C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305841 | |||||||
| chr9:78305869 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.398-445T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305869 | |||||||
| chr9:78305991 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.398-323G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305991 | |||||||
| chr9:78306102 | G | C | 1 | a0001c0002t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.398-212G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78306102 | |||||||
| chr9:78306105 | G | A | 35 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0031 others(32): Show |
39 | HG00323.hp2 HG01074.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.398-209G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78306105 | |||||||
| chr9:78306172 | T | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(253): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.398-142T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78306172 | |||||||
| chr9:78306229 | C | T | 27 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0031 others(24): Show |
31 | HG00323.hp2 HG01074.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.398-85C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78306229 | |||||||
| chr9:78306530 | G | T | 255 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(252): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.570+44G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306530 | |||||||
| chr9:78306565 | AAGAACCA others(18): Show |
A | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.570+86_570+110delA others(24): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 78306565 | ||||||
| chr9:78306683 | C | T | 86 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0016 others(83): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.570+197C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306683 | |||||||
| chr9:78306816 | C | T | 86 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0016 others(83): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.570+330C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306816 | |||||||
| chr9:78306888 | C | T | 2 | a0001c0002t0001g0239 a0001c0002t0001g0240 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.570+402C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306888 | |||||||
| chr9:78306921 | G | C | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+435G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306921 | |||||||
| chr9:78307041 | A | G | 1 | a0001c0002t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.570+555A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307041 | |||||||
| chr9:78307208 | G | A | 1 | a0001c0002t0001g0220 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.570+722G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307208 | |||||||
| chr9:78307251 | A | G | 1 | a0001c0001t0003g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+765A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307251 | |||||||
| chr9:78307373 | G | C | 35 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0031 others(32): Show |
39 | HG00323.hp2 HG01074.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.570+887G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307373 | |||||||
| chr9:78307381 | A | T | 1 | a0001c0002t0001g0033 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.570+895A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307381 | |||||||
| chr9:78307401 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.570+915G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307401 | |||||||
| chr9:78307478 | A | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.571-936A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307478 | |||||||
| chr9:78307517 | C | T | 2 | a0001c0002t0001g0237 a0001c0002t0001g0238 |
2 | HG00733.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.571-897C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307517 | |||||||
| chr9:78307542 | G | A | 35 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0031 others(32): Show |
39 | HG00323.hp2 HG01074.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.571-872G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307542 | |||||||
| chr9:78307621 | C | A | 1 | a0002c0008t0003g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.571-793C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307621 | |||||||
| chr9:78307745 | T | TAAAAAAT others(322): Show |
1 | a0001c0002t0001g0355 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571-654_571-653ins others(329): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 78307745 | ||||||
| chr9:78307745 | T | TAAAAAAT others(323): Show |
1 | a0001c0002t0006g0354 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571-654_571-653ins others(330): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 78307745 | ||||||
| chr9:78307781 | C | A | 1 | a0001c0001t0004g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-633C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307781 | |||||||
| chr9:78307894 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(143): Show |
166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.571-520A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307894 | |||||||
| chr9:78307912 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.571-502C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307912 | |||||||
| chr9:78307964 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.571-450G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307964 | |||||||
| chr9:78307980 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0034 others(7): Show |
12 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.571-434A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307980 | |||||||
| chr9:78308053 | AT | A | 4 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0001g0342 others(1): Show |
4 | NA18942.hp1 NA19010.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-360delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308053 | |||||||
| chr9:78308131 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(103): Show |
120 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.571-283G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308131 | |||||||
| chr9:78308207 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.571-207C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308207 | |||||||
| chr9:78308210 | G | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0001t0003g0322 |
5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-204G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308210 | |||||||
| chr9:78308249 | G | A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
125 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.571-165G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308249 | |||||||
| chr9:78308334 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
125 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.571-80C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308334 | |||||||
| chr9:78308644 | G | A | 1 | a0001c0002t0002g0003 | 4 | NA18943.hp2 NA18952.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.740+61G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308644 | |||||||
| chr9:78308682 | G | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0260 a0001c0001t0001g0262 others(4): Show |
8 | HG00438.hp2 NA18952.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.740+99G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308682 | |||||||
| chr9:78308693 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(142): Show |
165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.740+110C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308693 | |||||||
| chr9:78308694 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(143): Show |
166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.740+111A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308694 | |||||||
| chr9:78308712 | T | C | 2 | a0001c0001t0005g0065 a0001c0001t0005g0066 |
2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.740+129T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308712 | |||||||
| chr9:78308713 | T | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0001t0003g0322 others(36): Show |
45 | HG00323.hp2 HG00642.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.740+130T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308713 | |||||||
| chr9:78308759 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.740+176T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308759 | |||||||
| chr9:78308791 | A | G | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.740+208A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308791 | |||||||
| chr9:78308816 | G | A | 3 | a0001c0001t0001g0286 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | NA18950.hp1 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.740+233G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308816 | |||||||
| chr9:78308903 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(256): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.740+320C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308903 | |||||||
| chr9:78308918 | G | GCACT | 8 | a0001c0002t0001g0141 a0001c0002t0001g0353 a0001c0002t0001g0356 others(5): Show |
8 | HG02572.hp2 HG02717.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.740+337_740+340dup others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78308918 | ||||||
| chr9:78308967 | T | C | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.740+384T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308967 | |||||||
| chr9:78309092 | A | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(142): Show |
165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.740+509A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309092 | |||||||
| chr9:78309174 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0034 others(8): Show |
13 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.740+591C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309174 | |||||||
| chr9:78309193 | C | G | 1 | a0001c0002t0001g0253 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.740+610C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309193 | |||||||
| chr9:78309203 | C | G | 2 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
2 | NA18970.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.740+620C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309203 | |||||||
| chr9:78309232 | C | G | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+649C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309232 | |||||||
| chr9:78309246 | A | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0001t0003g0322 |
5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.740+663A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309246 | |||||||
| chr9:78309305 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.740+722G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309305 | |||||||
| chr9:78309335 | A | G | 1 | a0001c0002t0002g0060 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.740+752A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309335 | |||||||
| chr9:78309386 | C | T | 4 | a0001c0001t0002g0085 a0001c0001t0002g0092 a0001c0001t0002g0106 others(1): Show |
4 | NA18978.hp1 NA18983.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.740+803C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309386 | |||||||
| chr9:78309395 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(103): Show |
120 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.740+812G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309395 | |||||||
| chr9:78309423 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(142): Show |
165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.740+840C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309423 | |||||||
| chr9:78309451 | C | T | 1 | a0001c0002t0001g0182 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.740+868C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309451 | |||||||
| chr9:78309485 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.740+902C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309485 | |||||||
| chr9:78309507 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.740+924T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309507 | |||||||
| chr9:78309517 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.740+934T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309517 | |||||||
| chr9:78309620 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.740+1037T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309620 | |||||||
| chr9:78309726 | C | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.740+1143C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309726 | |||||||
| chr9:78309737 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(105): Show |
122 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.740+1154G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309737 | |||||||
| chr9:78309765 | G | A | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+1182G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309765 | |||||||
| chr9:78309933 | C | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(141): Show |
162 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.740+1350C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309933 | |||||||
| chr9:78310109 | G | C | 3 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | NA18941.hp2 NA18980.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.740+1526G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310109 | |||||||
| chr9:78310159 | G | A | 2 | a0001c0002t0003g0243 a0001c0002t0003g0244 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.740+1576G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310159 | |||||||
| chr9:78310162 | A | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(141): Show |
162 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.740+1579A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310162 | |||||||
| chr9:78310197 | T | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+1614T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310197 | |||||||
| chr9:78310303 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+1720T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310303 | |||||||
| chr9:78310382 | G | T | 1 | a0002c0008t0003g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.740+1799G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310382 | |||||||
| chr9:78310484 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.740+1901C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310484 | |||||||
| chr9:78310616 | A | ATTT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(98): Show |
115 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.740+2045_740+2047d others(5): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78310616 | ||||||
| chr9:78310616 | A | ATTTT | 41 | a0001c0001t0001g0049 a0001c0001t0001g0184 a0001c0001t0001g0297 others(38): Show |
45 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.740+2044_740+2047d others(6): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78310616 | ||||||
| chr9:78310641 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+2058T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310641 | |||||||
| chr9:78310643 | C | T | 2 | a0001c0002t0001g0147 a0001c0002t0001g0335 |
2 | NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.740+2060C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310643 | |||||||
| chr9:78310703 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+2120C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310703 | |||||||
| chr9:78310734 | A | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+2151A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310734 | |||||||
| chr9:78310787 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(106): Show |
123 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.740+2204T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310787 | |||||||
| chr9:78310844 | G | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0026 others(49): Show |
62 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.740+2261G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310844 | |||||||
| chr9:78310883 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+2300C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310883 | |||||||
| chr9:78310920 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.740+2337G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310920 | |||||||
| chr9:78310942 | G | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+2359G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310942 | |||||||
| chr9:78310961 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+2378C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310961 | |||||||
| chr9:78310966 | C | T | 10 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0140 others(7): Show |
12 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.740+2383C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310966 | |||||||
| chr9:78311219 | A | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+2636A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311219 | |||||||
| chr9:78311257 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+2674T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311257 | |||||||
| chr9:78311284 | C | T | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.740+2701C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311284 | |||||||
| chr9:78311470 | T | C | 1 | a0002c0008t0003g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.740+2887T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311470 | |||||||
| chr9:78311535 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.740+2952T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311535 | |||||||
| chr9:78311571 | C | T | 1 | a0001c0002t0001g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.740+2988C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311571 | |||||||
| chr9:78311604 | C | T | 1 | a0001c0002t0001g0180 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.740+3021C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311604 | |||||||
| chr9:78311618 | G | A | 1 | a0001c0002t0001g0256 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.740+3035G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311618 | |||||||
| chr9:78311635 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+3052C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311635 | |||||||
| chr9:78311651 | G | A | 2 | a0001c0002t0001g0249 a0001c0002t0001g0273 |
2 | HG00735.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.740+3068G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311651 | |||||||
| chr9:78311780 | C | T | 79 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0016 others(76): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.740+3197C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311780 | |||||||
| chr9:78311828 | T | TCAAAAC | 76 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0026 others(73): Show |
88 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.740+3245_740+3246i others(8): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311828 | |||||||
| chr9:78311828 | T | TCAAAACA others(5): Show |
15 | a0001c0002t0001g0007 a0001c0002t0001g0033 a0001c0002t0001g0141 others(12): Show |
17 | HG01070.hp2 HG01192.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.740+3245_740+3246i others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311828 | |||||||
| chr9:78311829 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0026 others(88): Show |
105 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.740+3246G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311829 | |||||||
| chr9:78311829 | G | C | 54 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0096 others(51): Show |
58 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.740+3246G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311829 | |||||||
| chr9:78311829 | G | GAAAACA | 5 | a0001c0001t0001g0030 a0001c0001t0001g0348 a0001c0001t0001g0349 others(2): Show |
6 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+3274_740+3279d others(8): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78311829 | ||||||
| chr9:78311908 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.740+3325C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311908 | |||||||
| chr9:78311982 | C | T | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3399C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311982 | |||||||
| chr9:78311989 | C | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+3406C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311989 | |||||||
| chr9:78312004 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.740+3421A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312004 | |||||||
| chr9:78312047 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(143): Show |
164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+3464C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312047 | |||||||
| chr9:78312050 | C | CT | 7 | a0001c0001t0001g0340 a0001c0001t0002g0109 a0001c0001t0002g0121 others(4): Show |
7 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.740+3480dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78312050 | ||||||
| chr9:78312062 | TTC | T | 9 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0187 others(6): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.740+3480_740+3481d others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312062 | |||||||
| chr9:78312063 | TC | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(156): Show |
178 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.740+3484delC | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78312063 | ||||||
| chr9:78312064 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0270 others(89): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.740+3481C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312064 | |||||||
| chr9:78312144 | C | T | 2 | a0001c0002t0001g0237 a0001c0002t0001g0238 |
2 | HG00733.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.740+3561C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312144 | |||||||
| chr9:78312319 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0002t0001g0033 |
5 | HG00642.hp1 HG01070.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.740+3736G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312319 | |||||||
| chr9:78312323 | G | C | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3740G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312323 | |||||||
| chr9:78312375 | A | T | 1 | a0001c0001t0001g0105 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.740+3792A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312375 | |||||||
| chr9:78312474 | T | G | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3891T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312474 | |||||||
| chr9:78312475 | C | T | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3892C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312475 | |||||||
| chr9:78312476 | A | T | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3893A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312476 | |||||||
| chr9:78312493 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(106): Show |
123 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.740+3910C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312493 | |||||||
| chr9:78312575 | A | C | 36 | a0001c0001t0002g0080 a0001c0002t0001g0007 a0001c0002t0001g0028 others(33): Show |
40 | HG00323.hp2 HG01074.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.740+3992A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312575 | |||||||
| chr9:78312586 | C | T | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.740+4003C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312586 | |||||||
| chr9:78312588 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(143): Show |
164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+4005C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312588 | |||||||
| chr9:78312656 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.740+4073A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312656 | |||||||
| chr9:78312899 | A | G | 37 | a0001c0001t0002g0080 a0001c0002t0001g0007 a0001c0002t0001g0028 others(34): Show |
41 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.740+4316A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312899 | |||||||
| chr9:78313030 | C | T | 37 | a0001c0001t0002g0080 a0001c0002t0001g0007 a0001c0002t0001g0028 others(34): Show |
41 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.740+4447C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313030 | |||||||
| chr9:78313103 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+4520C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313103 | |||||||
| chr9:78313297 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.741-4379G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313297 | |||||||
| chr9:78313448 | C | T | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-4228C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313448 | |||||||
| chr9:78313483 | T | TGG | 37 | a0001c0001t0002g0080 a0001c0002t0001g0007 a0001c0002t0001g0028 others(34): Show |
41 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.741-4193_741-4192i others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313483 | |||||||
| chr9:78313584 | C | T | 1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.741-4092C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313584 | |||||||
| chr9:78313727 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.741-3949C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313727 | |||||||
| chr9:78313728 | G | A | 1 | a0001c0002t0001g0221 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.741-3948G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313728 | |||||||
| chr9:78313802 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0270 a0001c0001t0003g0322 |
5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.741-3874G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313802 | |||||||
| chr9:78313863 | T | C | 1 | a0001c0001t0001g0349 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.741-3813T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313863 | |||||||
| chr9:78313922 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.741-3754C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313922 | |||||||
| chr9:78313940 | C | T | 85 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0016 others(82): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.741-3736C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313940 | |||||||
| chr9:78314027 | G | A | 1 | a0001c0001t0003g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.741-3649G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314027 | |||||||
| chr9:78314178 | G | C | 1 | a0001c0001t0002g0062 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.741-3498G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314178 | |||||||
| chr9:78314239 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.741-3437C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314239 | |||||||
| chr9:78314301 | A | ATCCTGTG others(73): Show |
35 | a0001c0001t0002g0080 a0001c0002t0001g0007 a0001c0002t0001g0028 others(32): Show |
39 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.741-3358_741-3357i others(82): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314301 | ||||||
| chr9:78314301 | A | ATCCTGTG others(73): Show |
2 | a0001c0002t0001g0147 a0001c0002t0001g0335 |
2 | NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.741-3358_741-3357i others(82): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314301 | ||||||
| chr9:78314319 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.741-3357T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314319 | |||||||
| chr9:78314379 | T | C | 257 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(254): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.741-3297T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314379 | |||||||
| chr9:78314381 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(104): Show |
121 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.741-3295A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314381 | |||||||
| chr9:78314399 | C | CCACAGGG others(73): Show |
102 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(99): Show |
110 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.741-3213_741-3212i others(82): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314399 | ||||||
| chr9:78314399 | C | T | 38 | a0001c0001t0002g0042 a0001c0001t0002g0080 a0001c0002t0001g0007 others(35): Show |
42 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.741-3277C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314399 | |||||||
| chr9:78314431 | G | T | 84 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0016 others(81): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.741-3245G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314431 | |||||||
| chr9:78314445 | G | A | 1 | a0001c0002t0001g0336 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.741-3231G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314445 | |||||||
| chr9:78314464 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0297 a0001c0001t0001g0307 others(3): Show |
12 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.741-3212T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314464 | |||||||
| chr9:78314479 | T | TCACAGGG others(73): Show |
1 | a0001c0002t0001g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.741-3132_741-3131i others(82): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314479 | ||||||
| chr9:78314489 | T | TAGACATC others(70): Show |
1 | a0001c0001t0001g0307 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.741-3133_741-3132i others(79): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314489 | ||||||
| chr9:78314604 | T | G | 141 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(138): Show |
153 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.741-3072T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314604 | |||||||
| chr9:78314756 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0297 |
8 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.741-2920C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314756 | |||||||
| chr9:78314822 | C | G | 140 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(137): Show |
152 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.741-2854C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314822 | |||||||
| chr9:78314878 | C | T | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.741-2798C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314878 | |||||||
| chr9:78314968 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.741-2708T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314968 | |||||||
| chr9:78314973 | C | T | 2 | a0001c0001t0002g0067 a0001c0001t0002g0084 |
2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.741-2703C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314973 | |||||||
| chr9:78315010 | CA | C | 22 | a0001c0001t0002g0080 a0001c0002t0001g0028 a0001c0002t0001g0031 others(19): Show |
24 | HG00323.hp2 HG01074.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.741-2665delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315010 | |||||||
| chr9:78315069 | G | A | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.741-2607G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315069 | |||||||
| chr9:78315145 | T | G | 2 | a0001c0001t0001g0312 a0001c0001t0002g0311 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.741-2531T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315145 | |||||||
| chr9:78315157 | A | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0270 |
4 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.741-2519A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315157 | |||||||
| chr9:78315278 | T | C | 1 | a0001c0002t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.741-2398T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315278 | |||||||
| chr9:78315327 | C | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(139): Show |
154 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.741-2349C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315327 | |||||||
| chr9:78315343 | T | C | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-2333T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315343 | |||||||
| chr9:78315462 | C | G | 1 | a0001c0001t0002g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.741-2214C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315462 | |||||||
| chr9:78315523 | C | T | 22 | a0001c0001t0002g0080 a0001c0002t0001g0028 a0001c0002t0001g0031 others(19): Show |
24 | HG00323.hp2 HG01074.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.741-2153C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315523 | |||||||
| chr9:78315525 | G | A | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-2151G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315525 | |||||||
| chr9:78315686 | C | A | 83 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0016 others(80): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.741-1990C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315686 | |||||||
| chr9:78315806 | G | A | 1 | a0001c0002t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.741-1870G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315806 | |||||||
| chr9:78315835 | C | T | 9 | a0001c0002t0001g0008 a0001c0002t0001g0016 a0001c0002t0001g0164 others(6): Show |
12 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.741-1841C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315835 | |||||||
| chr9:78315925 | AT | A | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-1746delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78315925 | ||||||
| chr9:78315948 | G | C | 1 | a0001c0002t0001g0279 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.741-1728G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315948 | |||||||
| chr9:78316027 | C | T | 3 | a0001c0002t0001g0247 a0001c0002t0001g0252 a0001c0002t0001g0258 |
3 | HG00423.hp1 NA18941.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.741-1649C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316027 | |||||||
| chr9:78316034 | C | A | 1 | a0001c0002t0001g0033 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.741-1642C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316034 | |||||||
| chr9:78316055 | G | A | 1 | a0001c0002t0001g0222 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.741-1621G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316055 | |||||||
| chr9:78316074 | G | A | 1 | a0001c0002t0003g0352 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.741-1602G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316074 | |||||||
| chr9:78316134 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
5 | HG02055.hp1 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.741-1542G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316134 | |||||||
| chr9:78316300 | A | G | 2 | a0001c0002t0001g0355 a0001c0002t0006g0354 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.741-1376A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316300 | |||||||
| chr9:78316330 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0034 others(6): Show |
11 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.741-1346C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316330 | |||||||
| chr9:78316380 | C | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.741-1296C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316380 | |||||||
| chr9:78316387 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.741-1289G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316387 | |||||||
| chr9:78316406 | G | A | 2 | a0001c0002t0001g0223 a0001c0002t0001g0224 |
2 | NA18971.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.741-1270G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316406 | |||||||
| chr9:78316442 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0270 |
4 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.741-1234C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316442 | |||||||
| chr9:78316486 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.741-1190C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316486 | |||||||
| chr9:78316608 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.741-1068C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316608 | |||||||
| chr9:78316695 | C | T | 4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-981C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316695 | |||||||
| chr9:78316789 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0270 |
4 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.741-887C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316789 | |||||||
| chr9:78316843 | TA | T | 3 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG01168.hp2 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.741-831delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78316843 | ||||||
| chr9:78316848 | A | C | 321 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(318): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.741-828A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316848 | |||||||
| chr9:78316852 | G | C | 2 | a0001c0002t0001g0321 a0001c0002t0001g0358 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.741-824G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316852 | |||||||
| chr9:78316871 | C | T | 4 | a0001c0001t0002g0076 a0001c0001t0002g0097 a0001c0001t0002g0103 others(1): Show |
4 | NA18961.hp1 NA19010.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-805C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316871 | |||||||
| chr9:78316941 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0348 others(1): Show |
5 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.741-735G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316941 | |||||||
| chr9:78317001 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.741-675C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317001 | |||||||
| chr9:78317088 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.741-588T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317088 | |||||||
| chr9:78317173 | T | A | 4 | a0001c0001t0002g0098 a0001c0001t0002g0136 a0001c0002t0001g0033 others(1): Show |
4 | HG01070.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.741-503T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317173 | |||||||
| chr9:78317249 | TTTTC | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0112 others(90): Show |
103 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.741-419_741-416del others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78317249 | ||||||
| chr9:78317257 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.741-419C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317257 | |||||||
| chr9:78317279 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0105 others(93): Show |
106 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.741-397A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317279 | |||||||
| chr9:78317283 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0105 others(90): Show |
103 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.741-393C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317283 | |||||||
| chr9:78317440 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.741-236C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317440 | |||||||
| chr9:78317530 | C | T | 1 | a0001c0002t0001g0236 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.741-146C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317530 | |||||||
| chr9:78317599 | C | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0105 others(91): Show |
104 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.741-77C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317599 | |||||||
| chr9:78317658 | T | A | 243 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(240): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.741-18T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317658 | |||||||
| chr9:78317873 | T | G | 248 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(245): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.869+69T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78317873 | |||||||
| chr9:78317971 | C | T | 247 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(244): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.869+167C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78317971 | |||||||
| chr9:78318082 | T | C | 247 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(244): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.869+278T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318082 | |||||||
| chr9:78318104 | C | T | 247 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(244): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.869+300C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318104 | |||||||
| chr9:78318218 | G | A | 1 | a0001c0002t0001g0277 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.869+414G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318218 | |||||||
| chr9:78318508 | A | G | 106 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0055 others(103): Show |
127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.869+704A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318508 | |||||||
| chr9:78318642 | T | C | 109 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0055 others(106): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.869+838T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318642 | |||||||
| chr9:78318704 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.869+900C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318704 | |||||||
| chr9:78318706 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.869+902A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318706 | |||||||
| chr9:78318719 | T | C | 1 | a0002c0008t0003g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.869+915T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318719 | |||||||
| chr9:78318757 | A | G | 1 | a0001c0001t0001g0360 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.869+953A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318757 | |||||||
| chr9:78318828 | G | A | 26 | a0001c0001t0001g0193 a0001c0001t0001g0294 a0001c0001t0001g0304 others(23): Show |
28 | HG01192.hp1 HG01346.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.869+1024G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318828 | |||||||
| chr9:78318890 | C | T | 1 | a0001c0002t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.869+1086C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318890 | |||||||
| chr9:78318997 | T | C | 1 | a0001c0002t0001g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.869+1193T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318997 | |||||||
| chr9:78319019 | C | T | 1 | a0001c0002t0005g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.869+1215C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319019 | |||||||
| chr9:78319052 | C | T | 16 | a0001c0001t0002g0046 a0001c0001t0002g0064 a0001c0001t0003g0149 others(13): Show |
16 | HG01496.hp2 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.869+1248C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319052 | |||||||
| chr9:78319095 | C | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0270 others(25): Show |
31 | HG00642.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.869+1291C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319095 | |||||||
| chr9:78319249 | G | A | 2 | a0001c0001t0001g0350 a0001c0001t0011g0215 |
2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.869+1445G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319249 | |||||||
| chr9:78319331 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.869+1527T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319331 | |||||||
| chr9:78319386 | G | A | 1 | a0002c0008t0003g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.869+1582G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319386 | |||||||
| chr9:78319390 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0285 a0001c0001t0001g0302 others(2): Show |
5 | NA18939.hp2 NA18966.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.869+1586G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319390 | |||||||
| chr9:78319449 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.869+1645A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319449 | |||||||
| chr9:78319538 | TGTGTGAG others(7): Show |
T | 1 | a0001c0002t0002g0060 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.869+1736_869+1749d others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78319538 | ||||||
| chr9:78319884 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.869+2080C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319884 | |||||||
| chr9:78319902 | C | T | 6 | a0001c0001t0002g0119 a0001c0002t0001g0022 a0001c0002t0001g0210 others(3): Show |
7 | NA18946.hp2 NA18954.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.869+2098C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319902 | |||||||
| chr9:78319903 | G | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(60): Show |
68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.869+2099G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319903 | |||||||
| chr9:78319987 | CTCAT | C | 102 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0055 others(99): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.869+2196_869+2199d others(6): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78319987 | ||||||
| chr9:78320215 | G | A | 1 | a0001c0002t0001g0274 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.869+2411G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320215 | |||||||
| chr9:78320296 | C | T | 102 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0055 others(99): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.869+2492C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320296 | |||||||
| chr9:78320322 | T | TTCCA | 102 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0055 others(99): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.869+2529_869+2532d others(6): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320322 | ||||||
| chr9:78320322 | T | TTCCATCC others(1): Show |
128 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(125): Show |
144 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.869+2525_869+2532d others(10): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320322 | ||||||
| chr9:78320322 | T | TTCCATCC others(5): Show |
1 | a0002c0008t0003g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.869+2521_869+2532d others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320322 | ||||||
| chr9:78320333 | C | CATCCATC others(5): Show |
11 | a0001c0001t0001g0193 a0001c0001t0002g0064 a0001c0001t0004g0148 others(8): Show |
13 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.869+2532_869+2533i others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320333 | ||||||
| chr9:78320337 | T | C | 11 | a0001c0001t0001g0193 a0001c0001t0002g0064 a0001c0001t0004g0148 others(8): Show |
13 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.869+2533T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320337 | |||||||
| chr9:78320362 | G | T | 3 | a0001c0001t0003g0322 a0001c0001t0004g0194 a0001c0002t0006g0354 |
3 | HG03471.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.869+2558G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320362 | |||||||
| chr9:78320427 | C | A | 2 | a0001c0002t0001g0356 a0001c0002t0001g0357 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.869+2623C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320427 | |||||||
| chr9:78320479 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.869+2675C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320479 | |||||||
| chr9:78320642 | T | TCCACCCA others(1): Show |
6 | a0001c0002t0001g0031 a0001c0002t0001g0137 a0001c0002t0001g0138 others(3): Show |
7 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.869+2846_869+2853d others(10): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320642 | ||||||
| chr9:78320672 | TGTCCATC others(9): Show |
T | 105 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0055 others(102): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.869+2882_869+2897d others(18): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320672 | ||||||
| chr9:78320675 | CCATCCAT others(8): Show |
C | 1 | a0001c0002t0002g0060 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.869+2873_869+2887d others(17): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320675 | ||||||
| chr9:78320699 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.869+2895C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320699 | |||||||
| chr9:78320758 | G | T | 1 | a0001c0002t0002g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.869+2954G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320758 | |||||||
| chr9:78320883 | C | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(116): Show |
132 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.869+3079C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320883 | |||||||
| chr9:78320929 | C | T | 17 | a0001c0001t0001g0294 a0001c0001t0001g0304 a0001c0002t0001g0147 others(14): Show |
17 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.869+3125C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320929 | |||||||
| chr9:78321010 | TC | T | 244 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(241): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.869+3214delC | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78321010 | ||||||
| chr9:78321016 | C | G | 1 | a0001c0001t0002g0052 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.869+3212C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321016 | |||||||
| chr9:78321241 | C | T | 2 | a0001c0002t0001g0179 a0001c0002t0002g0129 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.869+3437C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321241 | |||||||
| chr9:78321402 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.869+3598T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321402 | |||||||
| chr9:78321422 | A | G | 2 | a0001c0001t0001g0155 a0001c0002t0001g0321 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.869+3618A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321422 | |||||||
| chr9:78321483 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0348 a0001c0001t0001g0349 others(1): Show |
5 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.869+3679A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321483 | |||||||
| chr9:78321708 | T | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(82): Show |
90 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.869+3904T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321708 | |||||||
| chr9:78321743 | C | T | 1 | a0001c0002t0002g0061 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.869+3939C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321743 | |||||||
| chr9:78321837 | A | G | 1 | a0001c0001t0001g0297 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.869+4033A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321837 | |||||||
| chr9:78321913 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.869+4109A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321913 | |||||||
| chr9:78321913 | AATAT | A | 6 | a0001c0001t0004g0005 a0001c0001t0004g0276 a0001c0002t0001g0356 others(3): Show |
10 | HG01081.hp2 HG01123.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.869+4113_869+4116d others(6): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78321913 | ||||||
| chr9:78321914 | A | G | 93 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(90): Show |
100 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.869+4110A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321914 | |||||||
| chr9:78322114 | T | C | 2 | a0001c0002t0001g0140 a0001c0002t0003g0228 |
2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.869+4310T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322114 | |||||||
| chr9:78322151 | T | A | 2 | a0001c0001t0001g0350 a0001c0001t0011g0215 |
2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.869+4347T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322151 | |||||||
| chr9:78322358 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0270 |
5 | HG00642.hp1 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+4554G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322358 | |||||||
| chr9:78322359 | T | C | 1 | a0001c0001t0009g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.869+4555T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322359 | |||||||
| chr9:78322365 | T | C | 4 | a0001c0001t0002g0109 a0001c0001t0002g0128 a0001c0002t0001g0258 others(1): Show |
4 | NA18959.hp2 NA19005.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.869+4561T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322365 | |||||||
| chr9:78322537 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.869+4733C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322537 | |||||||
| chr9:78322994 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.870-5057T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322994 | |||||||
| chr9:78323061 | G | T | 1 | a0001c0002t0001g0319 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.870-4990G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323061 | |||||||
| chr9:78323085 | G | A | 123 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0036 others(120): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.870-4966G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323085 | |||||||
| chr9:78323121 | G | A | 6 | a0001c0001t0004g0005 a0001c0001t0004g0276 a0001c0002t0001g0356 others(3): Show |
10 | HG01081.hp2 HG01123.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-4930G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323121 | |||||||
| chr9:78323241 | G | C | 1 | a0001c0002t0002g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.870-4810G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323241 | |||||||
| chr9:78323358 | C | A | 1 | a0001c0002t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.870-4693C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323358 | |||||||
| chr9:78323401 | G | A | 9 | a0001c0001t0001g0193 a0001c0001t0001g0341 a0001c0002t0001g0007 others(6): Show |
11 | HG01192.hp1 HG02258.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-4650G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323401 | |||||||
| chr9:78323427 | A | T | 1 | a0001c0002t0002g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.870-4624A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323427 | |||||||
| chr9:78323450 | C | T | 3 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG01168.hp2 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.870-4601C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323450 | |||||||
| chr9:78323494 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(60): Show |
68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.870-4557C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323494 | |||||||
| chr9:78323539 | C | T | 9 | a0001c0001t0001g0193 a0001c0001t0001g0341 a0001c0002t0001g0007 others(6): Show |
11 | HG01192.hp1 HG02258.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-4512C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323539 | |||||||
| chr9:78323627 | T | G | 1 | a0001c0002t0001g0279 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.870-4424T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323627 | |||||||
| chr9:78323691 | A | C | 1 | a0001c0002t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.870-4360A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323691 | |||||||
| chr9:78323703 | G | A | 1 | a0001c0002t0003g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.870-4348G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323703 | |||||||
| chr9:78323809 | A | G | 1 | a0001c0002t0001g0279 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.870-4242A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323809 | |||||||
| chr9:78323986 | G | A | 2 | a0001c0001t0001g0350 a0001c0001t0011g0215 |
2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.870-4065G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323986 | |||||||
| chr9:78323999 | C | A | 6 | a0001c0001t0004g0005 a0001c0001t0004g0276 a0001c0002t0001g0356 others(3): Show |
10 | HG01081.hp2 HG01123.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-4052C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323999 | |||||||
| chr9:78324050 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.870-4001A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324050 | |||||||
| chr9:78324083 | G | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0036 others(114): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.870-3968G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324083 | |||||||
| chr9:78324101 | G | A | 21 | a0001c0001t0001g0294 a0001c0001t0001g0304 a0001c0001t0003g0322 others(18): Show |
21 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.870-3950G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324101 | |||||||
| chr9:78324109 | G | A | 3 | a0001c0002t0001g0353 a0001c0002t0003g0142 a0001c0002t0003g0352 |
3 | HG02572.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870-3942G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324109 | |||||||
| chr9:78324215 | G | A | 17 | a0001c0001t0001g0294 a0001c0001t0001g0304 a0001c0002t0001g0147 others(14): Show |
17 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.870-3836G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324215 | |||||||
| chr9:78324257 | T | C | 253 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(250): Show |
292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.870-3794T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324257 | |||||||
| chr9:78324301 | A | G | 17 | a0001c0001t0001g0294 a0001c0001t0001g0304 a0001c0002t0001g0147 others(14): Show |
17 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.870-3750A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324301 | |||||||
| chr9:78324347 | C | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0270 |
5 | HG00642.hp1 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-3704C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324347 | |||||||
| chr9:78324416 | T | A | 16 | a0001c0001t0002g0064 a0001c0001t0003g0149 a0001c0001t0003g0200 others(13): Show |
16 | HG01496.hp2 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.870-3635T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324416 | |||||||
| chr9:78324428 | C | G | 1 | a0001c0001t0003g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870-3623C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324428 | |||||||
| chr9:78324492 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.870-3559C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324492 | |||||||
| chr9:78324917 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.870-3134G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324917 | |||||||
| chr9:78324963 | T | G | 127 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0030 others(124): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.870-3088T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324963 | |||||||
| chr9:78324995 | A | G | 1 | a0001c0002t0001g0318 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.870-3056A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324995 | |||||||
| chr9:78325097 | T | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(72): Show |
80 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.870-2954T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325097 | |||||||
| chr9:78325186 | G | A | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.870-2865G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325186 | |||||||
| chr9:78325285 | G | A | 1 | a0001c0001t0002g0013 | 2 | NA18945.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.870-2766G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325285 | |||||||
| chr9:78325305 | C | T | 18 | a0001c0001t0001g0294 a0001c0001t0001g0304 a0001c0002t0001g0147 others(15): Show |
18 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.870-2746C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325305 | |||||||
| chr9:78325306 | C | T | 1 | a0001c0002t0001g0355 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.870-2745C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325306 | |||||||
| chr9:78325377 | T | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0036 others(10): Show |
16 | HG00642.hp1 HG01255.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.870-2674T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325377 | |||||||
| chr9:78325382 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.870-2669C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325382 | |||||||
| chr9:78325516 | C | G | 3 | a0001c0002t0001g0356 a0001c0002t0001g0357 a0002c0008t0003g0143 |
3 | HG02717.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.870-2535C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325516 | |||||||
| chr9:78325638 | T | C | 33 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0294 others(30): Show |
33 | HG01081.hp1 HG01109.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.870-2413T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325638 | |||||||
| chr9:78325660 | G | A | 19 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0294 others(16): Show |
19 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.870-2391G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325660 | |||||||
| chr9:78325696 | A | T | 1 | a0001c0001t0001g0349 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.870-2355A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325696 | |||||||
| chr9:78325734 | C | T | 21 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0294 others(18): Show |
21 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.870-2317C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325734 | |||||||
| chr9:78325933 | G | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(208): Show |
234 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(231): Show |
intron_variant | MODIFIER | c.870-2118G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325933 | |||||||
| chr9:78325992 | C | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(93): Show |
106 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.870-2059C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325992 | |||||||
| chr9:78326025 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.870-2026G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326025 | |||||||
| chr9:78326064 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0112 |
2 | NA19004.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.870-1987A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326064 | |||||||
| chr9:78326129 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-1922G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326129 | |||||||
| chr9:78326186 | A | G | 11 | a0001c0001t0004g0005 a0001c0001t0004g0148 a0001c0001t0004g0194 others(8): Show |
15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.870-1865A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326186 | |||||||
| chr9:78326249 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.870-1802C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326249 | |||||||
| chr9:78326250 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.870-1801G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326250 | |||||||
| chr9:78326492 | T | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0030 others(11): Show |
18 | HG00642.hp1 HG01255.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.870-1559T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326492 | |||||||
| chr9:78326669 | C | T | 11 | a0001c0001t0004g0005 a0001c0001t0004g0148 a0001c0001t0004g0194 others(8): Show |
15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.870-1382C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326669 | |||||||
| chr9:78326724 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-1327C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326724 | |||||||
| chr9:78326794 | C | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
223 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.870-1257C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326794 | |||||||
| chr9:78326808 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.870-1243C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326808 | |||||||
| chr9:78326845 | A | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0032 others(82): Show |
94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.870-1206A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326845 | |||||||
| chr9:78326934 | A | AATATATA others(7): Show |
2 | a0001c0002t0003g0142 a0001c0002t0003g0352 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.870-1108_870-1095d others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326934 | ||||||
| chr9:78326934 | AAT | A | 11 | a0001c0001t0004g0005 a0001c0001t0004g0148 a0001c0001t0004g0194 others(8): Show |
15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.870-1096_870-1095d others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326934 | ||||||
| chr9:78326953 | A | AT | 14 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
16 | HG01168.hp2 HG01169.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.870-1097dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326953 | ||||||
| chr9:78326955 | A | AT | 9 | a0001c0001t0001g0341 a0001c0001t0002g0102 a0001c0002t0001g0016 others(6): Show |
10 | HG00733.hp2 HG01106.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-1078dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATAT | 45 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0146 others(42): Show |
53 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(5): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(54): Show |
1 | a0001c0002t0003g0243 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(63): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(35): Show |
1 | a0001c0002t0003g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(44): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(36): Show |
1 | a0001c0001t0003g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(45): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(37): Show |
1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(46): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(44): Show |
1 | a0001c0002t0003g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(53): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(49): Show |
2 | a0001c0001t0003g0292 a0001c0002t0003g0244 |
2 | HG02451.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(58): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(53): Show |
1 | a0001c0001t0003g0308 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(62): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(35): Show |
1 | a0001c0001t0003g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(44): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(38): Show |
1 | a0001c0001t0003g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(47): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(42): Show |
1 | a0001c0001t0003g0149 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(51): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(48): Show |
1 | a0001c0001t0005g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(57): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(50): Show |
1 | a0001c0001t0005g0066 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(59): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(26): Show |
1 | a0001c0001t0003g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(35): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(32): Show |
1 | a0001c0001t0003g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(41): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0287 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(25): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(27): Show |
1 | a0001c0002t0003g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(36): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(36): Show |
1 | a0001c0002t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(45): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(41): Show |
1 | a0001c0001t0009g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(50): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(32): Show |
1 | a0001c0002t0001g0356 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(41): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(33): Show |
1 | a0001c0002t0001g0357 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(42): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(40): Show |
1 | a0001c0001t0003g0330 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(49): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(43): Show |
1 | a0001c0001t0003g0248 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(52): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(54): Show |
1 | a0001c0001t0003g0288 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(63): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(25): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(44): Show |
1 | a0001c0001t0003g0152 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(53): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(57): Show |
1 | a0001c0001t0003g0153 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(66): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(25): Show |
1 | a0002c0008t0003g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(34): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(38): Show |
1 | a0001c0001t0003g0157 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(47): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0010 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(21): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(7): Show |
1 | a0001c0002t0010g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0167 a0001c0001t0001g0338 a0001c0002t0002g0087 |
3 | HG02523.hp1 NA18960.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(19): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0294 a0001c0001t0001g0304 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0159 a0001c0002t0001g0137 others(1): Show |
7 | HG02257.hp1 HG02258.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(17): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
5 | HG00438.hp2 NA18747.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(19): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATTT others(5): Show |
1 | a0001c0002t0001g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATTT others(6): Show |
1 | a0001c0002t0005g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(15): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATTT others(7): Show |
1 | a0001c0002t0001g0147 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATTT others(8): Show |
3 | a0001c0001t0001g0175 a0001c0001t0001g0185 a0005c0004t0001g0176 |
3 | NA18995.hp1 NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(17): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATTT others(9): Show |
2 | a0001c0001t0001g0295 a0001c0009t0002g0117 |
2 | NA18960.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(18): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATTT others(10): Show |
10 | a0001c0001t0001g0096 a0001c0001t0001g0160 a0001c0001t0001g0172 others(7): Show |
10 | HG00423.hp1 HG02074.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(19): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATATTT others(11): Show |
4 | a0001c0001t0001g0281 a0001c0001t0001g0309 a0001c0001t0001g0317 others(1): Show |
4 | HG02071.hp1 NA18989.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(20): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATTTTT others(3): Show |
4 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0348 others(1): Show |
7 | HG00642.hp1 HG01255.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(12): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATTTTT others(4): Show |
3 | a0001c0002t0001g0018 a0001c0002t0001g0345 a0003c0006t0001g0324 |
4 | HG02559.hp1 HG02723.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(13): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATTTTT others(5): Show |
10 | a0001c0001t0001g0112 a0001c0001t0001g0300 a0001c0002t0001g0213 others(7): Show |
10 | HG01346.hp1 HG01952.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATTTTT others(6): Show |
4 | a0001c0001t0001g0105 a0001c0002t0001g0150 a0001c0002t0001g0182 others(1): Show |
4 | NA18953.hp1 NA18956.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(15): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATTTTT others(7): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0173 a0001c0001t0001g0283 others(2): Show |
6 | HG00621.hp2 HG00673.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATTTTT others(8): Show |
11 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0174 others(8): Show |
11 | HG00558.hp2 HG00673.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(17): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATATTTTT others(9): Show |
1 | a0001c0001t0001g0166 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(18): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATT | 6 | a0001c0001t0001g0029 a0001c0001t0001g0184 a0001c0001t0001g0297 others(3): Show |
6 | HG02965.hp2 HG03209.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1079_870-1078d others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.870-1087_870-1078d others(12): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0349 a0001c0002t0001g0353 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870-1088_870-1078d others(13): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0195 a0001c0002t0001g0355 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.870-1090_870-1078d others(15): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0031 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.870-1091_870-1078d others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326955 | A | T | 43 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(40): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.870-1096A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326955 | |||||||
| chr9:78326955 | AT | A | 6 | a0001c0001t0002g0068 a0001c0001t0002g0134 a0001c0002t0001g0232 others(3): Show |
6 | HG01070.hp1 HG01515.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1078delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | ||||||
| chr9:78326956 | T | TA | 7 | a0001c0001t0002g0076 a0001c0002t0001g0226 a0001c0002t0001g0231 others(4): Show |
7 | HG01099.hp2 HG01257.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(3): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326956 | |||||||
| chr9:78326956 | T | TATA | 15 | a0001c0001t0001g0169 a0001c0001t0001g0217 a0001c0001t0001g0218 others(12): Show |
15 | HG00423.hp2 HG02135.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(5): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326956 | |||||||
| chr9:78326957 | T | A | 21 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0001g0260 others(18): Show |
22 | HG00621.hp1 HG01070.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.870-1094T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326957 | |||||||
| chr9:78326958 | T | A | 6 | a0001c0001t0001g0217 a0001c0001t0001g0264 a0001c0001t0002g0123 others(3): Show |
6 | HG00423.hp2 HG03710.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.870-1093T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326958 | |||||||
| chr9:78326959 | T | A | 1 | a0001c0001t0001g0307 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.870-1092T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326959 | |||||||
| chr9:78327013 | T | C | 1 | a0001c0001t0003g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870-1038T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327013 | |||||||
| chr9:78327042 | A | G | 327 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(324): Show |
375 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.870-1009A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327042 | |||||||
| chr9:78327130 | AT | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0032 others(82): Show |
94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.870-910delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78327130 | ||||||
| chr9:78327149 | G | A | 1 | a0001c0001t0003g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870-902G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327149 | |||||||
| chr9:78327196 | C | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): Show |
220 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(217): Show |
intron_variant | MODIFIER | c.870-855C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327196 | |||||||
| chr9:78327213 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.870-838G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327213 | |||||||
| chr9:78327225 | T | G | 1 | a0001c0002t0001g0346 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.870-826T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327225 | |||||||
| chr9:78327284 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-767C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327284 | |||||||
| chr9:78327348 | A | T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(211): Show |
239 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.870-703A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327348 | |||||||
| chr9:78327409 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.870-642A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327409 | |||||||
| chr9:78327489 | T | C | 3 | a0001c0001t0001g0010 a0001c0002t0001g0137 a0001c0002t0001g0138 |
4 | HG02257.hp1 HG02258.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-562T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327489 | |||||||
| chr9:78327759 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.870-292C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327759 | |||||||
| chr9:78327912 | G | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
224 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.870-139G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327912 | |||||||
| chr9:78327913 | G | A | 21 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0294 others(18): Show |
21 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.870-138G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327913 | |||||||
| chr9:78328005 | C | G | 1 | a0001c0001t0001g0285 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.870-46C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78328005 | |||||||
| chr9:78328355 | A | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0032 others(82): Show |
94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1007+167A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328355 | |||||||
| chr9:78328356 | C | A | 1 | a0001c0002t0001g0277 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1007+168C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328356 | |||||||
| chr9:78328513 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1007+325A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328513 | |||||||
| chr9:78328520 | TTATTATT others(5): Show |
T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0036 others(5): Show |
11 | HG00642.hp1 HG01255.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1007+334_1007+345d others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 78328520 | ||||||
| chr9:78328584 | C | T | 25 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0294 others(22): Show |
27 | HG01243.hp2 HG01346.hp1 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.1007+396C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328584 | |||||||
| chr9:78328605 | GGAATGTC others(7): Show |
G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1008-373_1008-360d others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 78328605 | ||||||
| chr9:78328623 | AAT | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1008-356_1008-355d others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 78328623 | ||||||
| chr9:78328626 | A | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1008-355A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328626 | |||||||
| chr9:78328685 | G | A | 30 | a0001c0001t0003g0149 a0001c0001t0003g0151 a0001c0001t0003g0152 others(27): Show |
30 | HG00738.hp2 HG01081.hp1 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.1008-296G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328685 | |||||||
| chr9:78328704 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): Show |
222 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.1008-277C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328704 | |||||||
| chr9:78328821 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(43): Show |
52 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1008-160C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328821 | |||||||
| chr9:78328946 | T | G | 1 | a0001c0001t0002g0080 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1008-35T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328946 | |||||||
| chr9:78328970 | G | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0298 |
3 | HG02083.hp2 HG02602.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1008-11G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328970 |