Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8775 |
| ensemblid | ENSG00000105402.8 |
| hgncid | 7641 |
| symbol | NAPA |
| name | NSF attachment protein alpha |
| refseq_nuc | NM_003827.4 |
| refseq_prot | NP_003818.2 |
| ensembl_nuc | ENST00000263354.8 |
| ensembl_prot | ENSP00000263354.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 47487637 |
| end | 47515063 |
| strand | - |
| ver | v1.2 |
| region | chr19:47487637-47515063 |
| region5000 | chr19:47482637-47520063 |
| regionname0 | NAPA_chr19_47487637_47515063 |
| regionname5000 | NAPA_chr19_47482637_47520063 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 295 | 337 | 83 | 70 | 132 | 14 | 36 | 98 | NAPA_chr19_47482637_47520063 | NAPA | MDNSG others(290): Show |
chr19 | 47482637 | 47520063 |
| a0002 | 0/0 | 295 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | MDNSG others(290): Show |
chr19 | 47482637 | 47520063 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 885 | 329 | 76 | 69 | 132 | 14 | 36 | NAPA_chr19_47482637_47520063 | NAPA | ATGGA others(880): Show |
chr19 | 47482637 | 47520063 | ||
| a0001c0002 | 0/0 | 885 | 5 | 5 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | ATGGA others(880): Show |
chr19 | 47482637 | 47520063 | ||
| a0001c0003 | 0/0 | 885 | 3 | 2 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | ATGGA others(880): Show |
chr19 | 47482637 | 47520063 | ||
| a0002c0004 | 0/0 | 885 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | ATGGA others(880): Show |
chr19 | 47482637 | 47520063 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1662 | 157 | 20 | 36 | 69 | 9 | 22 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0002 | 0/0 | 1662 | 91 | 15 | 22 | 46 | 2 | 6 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0003 | 1/0 | 1662 | 43 | 19 | 1 | 14 | 3 | 5 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0004 | 0/0 | 1662 | 14 | 14 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0005 | 0/0 | 1662 | 7 | 4 | 3 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0006 | 0/0 | 1662 | 6 | 0 | 6 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0007 | 0/0 | 1662 | 2 | 2 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0008 | 0/0 | 1662 | 4 | 1 | 1 | 0 | 0 | 2 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0009 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0010 | 0/0 | 1662 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0011 | 0/0 | 1662 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0012 | 0/0 | 1662 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0001t0013 | 0/0 | 1662 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0002t0003 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0002t0007 | 0/0 | 1662 | 4 | 4 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0001c0003t0002 | 0/0 | 1662 | 3 | 2 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| a0002c0004t0005 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | GCGCG others(1657): Show |
chr19 | 47482637 | 47520063 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 1 | 4 | 0 | 3 | 8 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 2 | 3 | 2 | 2 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0002 | 0/0 | 10 | 0 | 3 | 5 | 0 | 2 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0004 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0007 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0005g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0006g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0007g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0008g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0010g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0012g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0001t0013g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0002t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0002t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0002t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0002t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0003t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0001c0003t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| a0002c0004t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | FIN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0137 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0038 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0124 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0014 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | IBS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0103 | EUR | IBS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0136 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0039 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0040 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | CDX | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CDX | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02602 | hp2 | a0001 | c0001 | t0008 | g0037 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0246 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02717 | hp1 | a0001 | c0002 | t0007 | g0245 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02895 | hp1 | a0002 | c0004 | t0005 | g0042 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0247 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0228 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03098 | hp2 | a0001 | c0002 | t0007 | g0244 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0019 | SAS | BEB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03942 | hp1 | a0001 | c0001 | t0010 | g0051 | SAS | BEB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04204 | hp1 | a0001 | c0001 | t0008 | g0014 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | STU | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | YRI | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | YRI | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | YRI | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18995 | hp1 | a0001 | c0001 | t0011 | g0151 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19009 | hp1 | a0001 | c0001 | t0013 | g0248 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | LWK | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | LWK | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | LWK | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19068 | hp2 | a0001 | c0001 | t0012 | g0111 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | YRI | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | YRI | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0138 | AFR | ASW | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0243 | AFR | ASW | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0092 | EUR | TSI | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | GIH | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0041 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ACB | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0233 | AFR | MSL | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | USA | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | USA | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | USA | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0129 | REF | REF | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0108 | REF | REF | NAPA_chr19_47482637_47520063 | NAPA | chr19 | 47482637 | 47520063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47514859 | A | G | 1 | a0002 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.82T>C | p.Phe28Leu | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/11 | 205/1662 | 82/888 | 28/295 | chr19 | 47514859 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47493039 | G | C | 1 | a0001c0003 | 3 | HG00642.hp1 HG01884.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.483C>G | p.Ala161Ala | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/11 | 606/1662 | 483/888 | 161/295 | chr19 | 47493039 | |||
| chr19:47514863 | G | A | 1 | a0001c0002 | 5 | HG02622.hp1 HG02717.hp1 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.78C>T | p.Ser26Ser | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/11 | 201/1662 | 78/888 | 26/295 | chr19 | 47514863 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47487771 | G | A | 1 | a0001c0001t0011 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*517C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 11/11 | 517 | chr19 | 47487771 | ||||||
| chr19:47487787 | C | T | 1 | a0001c0001t0010 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 11/11 | 501 | chr19 | 47487787 | ||||||
| chr19:47487922 | C | T | 1 | a0001c0001t0009 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*366G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 11/11 | 366 | chr19 | 47487922 | ||||||
| chr19:47487951 | T | C | 1 | a0001c0001t0004 | 14 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*337A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 11/11 | 337 | chr19 | 47487951 | ||||||
| chr19:47487971 | C | T | 2 | a0001c0001t0007 a0001c0002t0007 |
6 | HG02622.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*317G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 11/11 | 317 | chr19 | 47487971 | ||||||
| chr19:47488021 | T | C | 2 | a0001c0001t0005 a0002c0004t0005 |
8 | HG01167.hp1 HG01169.hp2 HG01934.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*267A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 11/11 | 267 | chr19 | 47488021 | ||||||
| chr19:47488180 | G | A | 1 | a0001c0001t0012 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 11/11 | 108 | chr19 | 47488180 | ||||||
| chr19:47488184 | C | G | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(8): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*104G>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 11/11 | 104 | chr19 | 47488184 | ||||||
| chr19:47488194 | A | G | 7 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(4): Show |
106 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*94T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 11/11 | 94 | chr19 | 47488194 | ||||||
| chr19:47514997 | C | T | 1 | a0001c0001t0006 | 6 | HG01069.hp2 HG01123.hp1 HG01978.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-57G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/11 | 57 | chr19 | 47514997 | ||||||
| chr19:47515000 | G | T | 1 | a0001c0001t0008 | 4 | HG01256.hp2 HG02602.hp2 HG04204.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-60C>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/11 | 60 | chr19 | 47515000 | ||||||
| chr19:47515050 | T | C | 1 | a0001c0001t0013 | 1 | NA19009.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/11 | 110 | chr19 | 47515050 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47488617 | T | TA | 95 | a0001c0001t0001g0023 a0001c0001t0001g0121 a0001c0001t0001g0132 others(92): Show |
128 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.787-229dupT | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488617 | |||||||
| chr19:47488666 | T | C | 1 | a0001c0001t0004g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.787-277A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488666 | |||||||
| chr19:47488667 | A | C | 1 | a0001c0001t0002g0071 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.787-278T>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488667 | |||||||
| chr19:47488785 | T | C | 72 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(69): Show |
102 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.787-396A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488785 | |||||||
| chr19:47488872 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.787-483T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488872 | |||||||
| chr19:47488873 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.787-484G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488873 | |||||||
| chr19:47488874 | G | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-485C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488874 | |||||||
| chr19:47488896 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.787-507C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488896 | |||||||
| chr19:47488902 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.787-513C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488902 | |||||||
| chr19:47488916 | C | CA | 67 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0132 others(64): Show |
97 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.787-528dupT | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488916 | |||||||
| chr19:47488958 | G | C | 1 | a0001c0003t0002g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.787-569C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488958 | |||||||
| chr19:47488991 | C | A | 2 | a0001c0001t0004g0227 a0001c0001t0004g0228 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.787-602G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47488991 | |||||||
| chr19:47489004 | T | G | 32 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0026 others(29): Show |
38 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.787-615A>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47489004 | |||||||
| chr19:47489095 | C | T | 13 | a0001c0001t0001g0121 a0001c0001t0001g0229 a0001c0001t0001g0230 others(10): Show |
15 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.786+616G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47489095 | |||||||
| chr19:47489217 | C | T | 1 | a0001c0003t0002g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.786+494G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47489217 | |||||||
| chr19:47489415 | T | C | 1 | a0001c0001t0003g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.786+296A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47489415 | |||||||
| chr19:47489428 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+283G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47489428 | |||||||
| chr19:47489547 | G | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0158 others(1): Show |
4 | HG00642.hp2 NA18943.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+164C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47489547 | |||||||
| chr19:47489571 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0183 others(14): Show |
23 | HG01943.hp1 HG02015.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.786+140C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47489571 | |||||||
| chr19:47489633 | G | C | 1 | a0001c0003t0002g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.786+78C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 10/10 | chr19 | 47489633 | |||||||
| chr19:47489836 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.736-75G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47489836 | |||||||
| chr19:47489920 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.736-159T>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47489920 | |||||||
| chr19:47490014 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.736-253A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490014 | |||||||
| chr19:47490058 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.736-297C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490058 | |||||||
| chr19:47490060 | G | GGT | 4 | a0001c0001t0001g0121 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-301_736-300dup others(2): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490060 | |||||||
| chr19:47490149 | T | G | 1 | a0001c0003t0002g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.736-388A>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490149 | |||||||
| chr19:47490251 | G | T | 1 | a0001c0001t0001g0023 | 2 | HG00733.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.736-490C>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490251 | |||||||
| chr19:47490255 | G | T | 1 | a0001c0001t0008g0036 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.736-494C>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490255 | |||||||
| chr19:47490308 | CGT | C | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
88 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.735+478_735+479del others(2): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490308 | |||||||
| chr19:47490356 | CTGTGTGT others(4): Show |
C | 1 | a0001c0001t0002g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.735+421_735+431del others(11): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490356 | |||||||
| chr19:47490422 | ATGTGTGT others(46): Show |
A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(164): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.735+313_735+365del others(53): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490422 | |||||||
| chr19:47490427 | TGTGGTGT others(49): Show |
T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0094 a0001c0001t0002g0095 |
4 | HG01243.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+305_735+360del others(56): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490427 | |||||||
| chr19:47490449 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.735+339C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490449 | |||||||
| chr19:47490451 | TGTGGTGT others(49): Show |
T | 65 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(62): Show |
93 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.735+281_735+336del others(56): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490451 | |||||||
| chr19:47490454 | GGTGTGTG others(50): Show |
G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+277_735+333del others(57): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490454 | |||||||
| chr19:47490494 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0002g0056 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.735+294T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490494 | |||||||
| chr19:47490502 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0002g0056 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.735+286C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490502 | |||||||
| chr19:47490504 | TGTGGTGT others(44): Show |
T | 1 | a0001c0001t0001g0152 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.735+233_735+283del others(51): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490504 | |||||||
| chr19:47490507 | G | GTGGTGTG others(30): Show |
1 | a0001c0001t0002g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.735+280_735+281ins others(37): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490507 | |||||||
| chr19:47490646 | C | CAAACA | 116 | a0001c0001t0001g0176 a0001c0001t0001g0206 a0001c0001t0001g0212 others(113): Show |
161 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.735+137_735+141dup others(5): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490646 | |||||||
| chr19:47490646 | C | CAAACAAA others(3): Show |
80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(77): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.735+132_735+141dup others(10): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490646 | |||||||
| chr19:47490646 | C | CAAACAAA others(8): Show |
31 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0029 others(28): Show |
40 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.735+127_735+141dup others(15): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490646 | |||||||
| chr19:47490646 | C | CAAACAAA others(13): Show |
1 | a0001c0001t0001g0030 | 2 | HG02015.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.735+122_735+141dup others(20): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490646 | |||||||
| chr19:47490646 | CAAACA | C | 7 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG00639.hp2 HG01261.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+137_735+141del others(5): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490646 | |||||||
| chr19:47490731 | C | T | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.735+57G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 9/10 | chr19 | 47490731 | |||||||
| chr19:47490923 | G | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.667-67C>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47490923 | |||||||
| chr19:47490953 | T | C | 36 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0011 others(33): Show |
54 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.667-97A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47490953 | |||||||
| chr19:47491218 | G | T | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
88 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.667-362C>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491218 | |||||||
| chr19:47491272 | A | G | 4 | a0001c0002t0007g0243 a0001c0002t0007g0244 a0001c0002t0007g0245 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-416T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491272 | |||||||
| chr19:47491464 | T | TA | 6 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
7 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+550dupT | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491464 | |||||||
| chr19:47491494 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.666+521C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491494 | |||||||
| chr19:47491524 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.666+491G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491524 | |||||||
| chr19:47491551 | CCT | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(4): Show |
8 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.666+462_666+463del others(2): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491551 | |||||||
| chr19:47491609 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.666+406G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491609 | |||||||
| chr19:47491905 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.666+110C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491905 | |||||||
| chr19:47491910 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.666+105C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491910 | |||||||
| chr19:47491938 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.666+77C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491938 | |||||||
| chr19:47491997 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0210 |
2 | HG02071.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.666+18C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 8/10 | chr19 | 47491997 | |||||||
| chr19:47492194 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.562-75C>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492194 | |||||||
| chr19:47492224 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.562-105C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492224 | |||||||
| chr19:47492250 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.562-131G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492250 | |||||||
| chr19:47492302 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.562-183C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492302 | |||||||
| chr19:47492463 | T | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.562-344A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492463 | |||||||
| chr19:47492525 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0202 a0001c0001t0001g0220 |
3 | NA18954.hp1 NA18997.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.562-406G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492525 | |||||||
| chr19:47492753 | C | T | 70 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(67): Show |
99 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.561+208G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492753 | |||||||
| chr19:47492838 | C | T | 1 | a0001c0002t0007g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.561+123G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492838 | |||||||
| chr19:47492862 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.561+99C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492862 | |||||||
| chr19:47492905 | A | C | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.561+56T>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 7/10 | chr19 | 47492905 | |||||||
| chr19:47493301 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0066 |
2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.420+115C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 5/10 | chr19 | 47493301 | |||||||
| chr19:47493322 | G | A | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.420+94C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 5/10 | chr19 | 47493322 | |||||||
| chr19:47493385 | C | T | 1 | a0001c0003t0002g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.420+31G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 5/10 | chr19 | 47493385 | |||||||
| chr19:47493389 | C | A | 1 | a0001c0002t0007g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.420+27G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 5/10 | chr19 | 47493389 | |||||||
| chr19:47493541 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.343-48C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47493541 | |||||||
| chr19:47493553 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.343-60A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47493553 | |||||||
| chr19:47493633 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.343-140G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47493633 | |||||||
| chr19:47493641 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-148C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47493641 | |||||||
| chr19:47493695 | G | C | 2 | a0001c0001t0002g0054 a0001c0001t0002g0067 |
2 | NA18948.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.343-202C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47493695 | |||||||
| chr19:47493710 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0180 |
2 | HG00738.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.343-217C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47493710 | |||||||
| chr19:47493862 | A | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
2 | NA18943.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.343-369T>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47493862 | |||||||
| chr19:47493894 | C | G | 1 | a0001c0001t0003g0122 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.343-401G>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47493894 | |||||||
| chr19:47494069 | G | A | 1 | a0001c0002t0007g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.343-576C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494069 | |||||||
| chr19:47494105 | C | T | 2 | a0001c0001t0003g0107 a0001c0001t0003g0116 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.343-612G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494105 | |||||||
| chr19:47494407 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.343-914C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494407 | |||||||
| chr19:47494408 | G | A | 1 | a0001c0003t0002g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.343-915C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494408 | |||||||
| chr19:47494610 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.342+940G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494610 | |||||||
| chr19:47494713 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(201): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.342+837T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494713 | |||||||
| chr19:47494735 | C | CA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(96): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.342+814dupT | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494735 | |||||||
| chr19:47494735 | C | CAA | 13 | a0001c0001t0001g0023 a0001c0001t0001g0121 a0001c0001t0001g0132 others(10): Show |
14 | HG00733.hp1 HG02135.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.342+813_342+814dup others(2): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494735 | |||||||
| chr19:47494735 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0168 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.342+805_342+814del others(10): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494735 | |||||||
| chr19:47494757 | AAG | A | 12 | a0001c0001t0002g0047 a0001c0001t0002g0049 a0001c0001t0002g0069 others(9): Show |
12 | HG00544.hp2 HG01123.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.342+791_342+792del others(2): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494757 | |||||||
| chr19:47494757 | AAGAG | A | 7 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0058 others(4): Show |
7 | HG01168.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+789_342+792del others(4): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494757 | |||||||
| chr19:47494758 | AGAG | A | 51 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(48): Show |
80 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.342+789_342+791del others(3): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494758 | |||||||
| chr19:47494761 | G | A | 13 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(10): Show |
13 | HG00544.hp2 HG01123.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+789C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494761 | |||||||
| chr19:47494785 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.342+765C>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494785 | |||||||
| chr19:47494804 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.342+746G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494804 | |||||||
| chr19:47494863 | C | T | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.342+687G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494863 | |||||||
| chr19:47494977 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.342+573C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47494977 | |||||||
| chr19:47495041 | C | T | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.342+509G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47495041 | |||||||
| chr19:47495107 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0131 a0001c0001t0001g0139 others(2): Show |
6 | HG00280.hp1 HG00735.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+443T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47495107 | |||||||
| chr19:47495238 | C | T | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.342+312G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47495238 | |||||||
| chr19:47495348 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.342+202G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47495348 | |||||||
| chr19:47495450 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.342+100G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47495450 | |||||||
| chr19:47495451 | G | A | 1 | a0001c0002t0007g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.342+99C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47495451 | |||||||
| chr19:47495512 | G | A | 17 | a0001c0001t0001g0121 a0001c0001t0001g0229 a0001c0001t0001g0230 others(14): Show |
19 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.342+38C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 4/10 | chr19 | 47495512 | |||||||
| chr19:47495628 | A | C | 1 | a0001c0001t0002g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.296-32T>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47495628 | |||||||
| chr19:47495640 | C | T | 3 | a0001c0001t0004g0034 a0001c0001t0004g0234 a0001c0001t0004g0235 |
4 | HG02970.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-44G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47495640 | |||||||
| chr19:47495727 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.296-131C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47495727 | |||||||
| chr19:47495765 | G | A | 1 | a0001c0003t0002g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.296-169C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47495765 | |||||||
| chr19:47495795 | G | A | 1 | a0001c0003t0002g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.296-199C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47495795 | |||||||
| chr19:47495859 | G | A | 61 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(58): Show |
89 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.296-263C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47495859 | |||||||
| chr19:47495875 | A | G | 3 | a0001c0003t0002g0136 a0001c0003t0002g0137 a0001c0003t0002g0138 |
3 | HG00642.hp1 HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.296-279T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47495875 | |||||||
| chr19:47495962 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0173 |
3 | HG01069.hp1 HG01071.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.296-366C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47495962 | |||||||
| chr19:47496058 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.296-462T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47496058 | |||||||
| chr19:47496254 | C | T | 1 | a0001c0001t0008g0037 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.296-658G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47496254 | |||||||
| chr19:47496407 | G | A | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
88 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.296-811C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47496407 | |||||||
| chr19:47496590 | C | CTTCA | 9 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0234 others(6): Show |
11 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.296-998_296-995dup others(4): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47496590 | |||||||
| chr19:47496814 | CCTT | C | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
88 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.296-1221_296-1219d others(5): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47496814 | |||||||
| chr19:47496860 | G | A | 1 | a0001c0001t0004g0035 | 2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.296-1264C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47496860 | |||||||
| chr19:47497073 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.296-1477G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47497073 | |||||||
| chr19:47497452 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0112 |
3 | NA18954.hp2 NA18960.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.296-1856C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47497452 | |||||||
| chr19:47497620 | G | A | 1 | a0001c0001t0004g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.296-2024C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47497620 | |||||||
| chr19:47497860 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-2264C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47497860 | |||||||
| chr19:47497892 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.296-2296G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47497892 | |||||||
| chr19:47497960 | C | T | 1 | a0001c0002t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.296-2364G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47497960 | |||||||
| chr19:47498012 | C | G | 1 | a0001c0003t0002g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.296-2416G>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47498012 | |||||||
| chr19:47498097 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.296-2501C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47498097 | |||||||
| chr19:47498108 | C | T | 3 | a0001c0003t0002g0136 a0001c0003t0002g0137 a0001c0003t0002g0138 |
3 | HG00642.hp1 HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.296-2512G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47498108 | |||||||
| chr19:47498343 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.295+2290C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47498343 | |||||||
| chr19:47498677 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG03041.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+1956G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47498677 | |||||||
| chr19:47498686 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.295+1947A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47498686 | |||||||
| chr19:47498773 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.295+1860T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47498773 | |||||||
| chr19:47498808 | G | A | 1 | a0001c0001t0013g0248 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.295+1825C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47498808 | |||||||
| chr19:47498917 | G | A | 1 | a0001c0001t0004g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295+1716C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47498917 | |||||||
| chr19:47499051 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0094 a0001c0001t0002g0095 |
4 | HG01243.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+1582C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499051 | |||||||
| chr19:47499129 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+1504T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499129 | |||||||
| chr19:47499132 | G | T | 36 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0011 others(33): Show |
54 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.295+1501C>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499132 | |||||||
| chr19:47499137 | G | A | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(63): Show |
95 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.295+1496C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499137 | |||||||
| chr19:47499152 | A | G | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.295+1481T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499152 | |||||||
| chr19:47499450 | C | T | 2 | a0001c0001t0004g0239 a0001c0001t0004g0240 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.295+1183G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499450 | |||||||
| chr19:47499488 | C | T | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.295+1145G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499488 | |||||||
| chr19:47499572 | G | C | 4 | a0001c0001t0003g0021 a0001c0001t0003g0112 a0001c0001t0003g0123 others(1): Show |
5 | NA18954.hp2 NA18960.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1061C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499572 | |||||||
| chr19:47499688 | A | T | 1 | a0001c0003t0002g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.295+945T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499688 | |||||||
| chr19:47499846 | T | C | 1 | a0001c0001t0003g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.295+787A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499846 | |||||||
| chr19:47499995 | C | T | 1 | a0001c0003t0002g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.295+638G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47499995 | |||||||
| chr19:47500023 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.295+610T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500023 | |||||||
| chr19:47500033 | C | T | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 |
3 | HG02615.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.295+600G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500033 | |||||||
| chr19:47500156 | TTCTC | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG03041.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+473_295+476del others(4): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500156 | |||||||
| chr19:47500175 | A | T | 1 | a0001c0001t0003g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.295+458T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500175 | |||||||
| chr19:47500203 | T | C | 4 | a0001c0002t0007g0243 a0001c0002t0007g0244 a0001c0002t0007g0245 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+430A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500203 | |||||||
| chr19:47500258 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.295+375C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500258 | |||||||
| chr19:47500264 | C | T | 1 | a0001c0001t0003g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.295+369G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500264 | |||||||
| chr19:47500321 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+312G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500321 | |||||||
| chr19:47500441 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.295+192G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500441 | |||||||
| chr19:47500442 | G | A | 2 | a0001c0001t0001g0207 a0001c0003t0002g0136 |
2 | HG00733.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.295+191C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 3/10 | chr19 | 47500442 | |||||||
| chr19:47500955 | G | A | 3 | a0001c0003t0002g0136 a0001c0003t0002g0137 a0001c0003t0002g0138 |
3 | HG00642.hp1 HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.179-206C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47500955 | |||||||
| chr19:47501041 | A | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0187 |
3 | NA18957.hp2 NA19068.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.179-292T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47501041 | |||||||
| chr19:47501279 | A | G | 3 | a0001c0001t0004g0034 a0001c0001t0004g0234 a0001c0001t0004g0235 |
4 | HG02970.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-530T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47501279 | |||||||
| chr19:47501447 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.179-698A>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47501447 | |||||||
| chr19:47501628 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(198): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.179-879A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47501628 | |||||||
| chr19:47501738 | TCTC | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0094 a0001c0001t0002g0095 |
4 | HG01243.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-992_179-990del others(3): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47501738 | |||||||
| chr19:47501902 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.179-1153C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47501902 | |||||||
| chr19:47501960 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.179-1211G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47501960 | |||||||
| chr19:47501995 | C | A | 3 | a0001c0002t0007g0243 a0001c0002t0007g0244 a0001c0002t0007g0245 |
3 | HG02717.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.179-1246G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47501995 | |||||||
| chr19:47502024 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.179-1275G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502024 | |||||||
| chr19:47502237 | CA | C | 71 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0026 others(68): Show |
91 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.178+1185delT | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502237 | |||||||
| chr19:47502237 | CAA | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(103): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.178+1184_178+1185d others(4): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502237 | |||||||
| chr19:47502237 | CAAA | C | 27 | a0001c0001t0001g0028 a0001c0001t0001g0140 a0001c0001t0001g0142 others(24): Show |
30 | HG00642.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.178+1183_178+1185d others(5): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502237 | |||||||
| chr19:47502237 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0002g0011 a0001c0001t0002g0045 a0001c0001t0002g0046 others(3): Show |
8 | HG01123.hp2 HG01261.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.178+1177_178+1185d others(11): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502237 | |||||||
| chr19:47502237 | CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0004g0227 a0001c0001t0004g0228 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.178+1168_178+1185d others(20): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502237 | |||||||
| chr19:47502292 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+1131C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502292 | |||||||
| chr19:47502369 | A | G | 8 | a0001c0001t0002g0011 a0001c0001t0002g0045 a0001c0001t0002g0046 others(5): Show |
10 | HG01123.hp2 HG01261.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.178+1054T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502369 | |||||||
| chr19:47502459 | C | T | 3 | a0001c0003t0002g0136 a0001c0003t0002g0137 a0001c0003t0002g0138 |
3 | HG00642.hp1 HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.178+964G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502459 | |||||||
| chr19:47502696 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.178+727G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502696 | |||||||
| chr19:47502739 | C | T | 59 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(56): Show |
87 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.178+684G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502739 | |||||||
| chr19:47502875 | T | C | 2 | a0001c0001t0004g0239 a0001c0001t0004g0240 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.178+548A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502875 | |||||||
| chr19:47502877 | T | A | 5 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(2): Show |
5 | HG00621.hp2 NA19010.hp2 NA19086.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+546A>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502877 | |||||||
| chr19:47502974 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.178+449G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47502974 | |||||||
| chr19:47503159 | A | G | 1 | a0001c0001t0003g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178+264T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47503159 | |||||||
| chr19:47503263 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.178+160C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 2/10 | chr19 | 47503263 | |||||||
| chr19:47503506 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG01928.hp1 | splice_region_variant&intron_variant | LOW | c.99-4C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47503506 | |||||||
| chr19:47503583 | C | T | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.99-81G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47503583 | |||||||
| chr19:47503590 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-88C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47503590 | |||||||
| chr19:47503763 | A | T | 1 | a0001c0001t0001g0183 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.99-261T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47503763 | |||||||
| chr19:47503840 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(100): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.99-338C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47503840 | |||||||
| chr19:47504092 | A | T | 16 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(13): Show |
18 | HG01891.hp2 HG01978.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.99-590T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504092 | |||||||
| chr19:47504106 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.99-604C>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504106 | |||||||
| chr19:47504211 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99-709G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504211 | |||||||
| chr19:47504261 | G | C | 1 | a0001c0001t0001g0163 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.99-759C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504261 | |||||||
| chr19:47504397 | C | CA | 11 | a0001c0001t0001g0121 a0001c0001t0001g0140 a0001c0001t0001g0142 others(8): Show |
12 | HG02080.hp1 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.99-896dupT | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504397 | |||||||
| chr19:47504397 | CA | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(161): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.99-896delT | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504397 | |||||||
| chr19:47504397 | CAA | C | 18 | a0001c0001t0001g0130 a0001c0001t0001g0145 a0001c0001t0001g0148 others(15): Show |
18 | HG01074.hp2 HG01256.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.99-897_99-896delTT | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504397 | |||||||
| chr19:47504421 | GAGAA | G | 4 | a0001c0001t0003g0021 a0001c0001t0003g0112 a0001c0001t0003g0123 others(1): Show |
5 | NA18954.hp2 NA18960.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-923_99-920delTT others(2): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504421 | |||||||
| chr19:47504579 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-1077G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504579 | |||||||
| chr19:47504673 | A | G | 1 | a0001c0001t0004g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99-1171T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504673 | |||||||
| chr19:47504675 | A | G | 1 | a0001c0001t0004g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99-1173T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504675 | |||||||
| chr19:47504679 | GTA | G | 3 | a0001c0003t0002g0136 a0001c0003t0002g0137 a0001c0003t0002g0138 |
3 | HG00642.hp1 HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.99-1179_99-1178del others(2): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504679 | |||||||
| chr19:47504692 | T | A | 1 | a0001c0001t0001g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.99-1190A>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504692 | |||||||
| chr19:47504733 | A | G | 1 | a0001c0002t0007g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.99-1231T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504733 | |||||||
| chr19:47504736 | G | GAC | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 |
3 | HG02615.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.99-1236_99-1235dup others(2): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504736 | |||||||
| chr19:47504813 | C | A | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | HG01261.hp2 HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99-1311G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504813 | |||||||
| chr19:47504911 | T | C | 76 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(73): Show |
106 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.99-1409A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504911 | |||||||
| chr19:47504998 | A | G | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | NA18974.hp2 NA18984.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-1496T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47504998 | |||||||
| chr19:47505003 | C | A | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | NA18974.hp2 NA18984.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-1501G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505003 | |||||||
| chr19:47505104 | G | A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0057 a0001c0001t0002g0058 others(1): Show |
7 | HG02451.hp2 HG02486.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-1602C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505104 | |||||||
| chr19:47505128 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.99-1626C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505128 | |||||||
| chr19:47505146 | T | C | 95 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(92): Show |
127 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.99-1644A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505146 | |||||||
| chr19:47505167 | T | A | 9 | a0001c0001t0002g0004 a0001c0001t0002g0053 a0001c0001t0002g0060 others(6): Show |
15 | HG00544.hp2 HG01168.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.99-1665A>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505167 | |||||||
| chr19:47505417 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.99-1915G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505417 | |||||||
| chr19:47505419 | C | G | 1 | a0001c0001t0002g0078 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.99-1917G>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505419 | |||||||
| chr19:47505489 | C | G | 1 | a0001c0002t0007g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.99-1987G>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505489 | |||||||
| chr19:47505542 | G | A | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.99-2040C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505542 | |||||||
| chr19:47505659 | C | T | 15 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(12): Show |
17 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.99-2157G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505659 | |||||||
| chr19:47505742 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.99-2240G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505742 | |||||||
| chr19:47505944 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.99-2442T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505944 | |||||||
| chr19:47505994 | C | CT | 23 | a0001c0001t0001g0139 a0001c0001t0001g0149 a0001c0001t0001g0152 others(20): Show |
25 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.99-2493dupA | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505994 | |||||||
| chr19:47505994 | CT | C | 14 | a0001c0001t0001g0121 a0001c0001t0001g0135 a0001c0001t0001g0164 others(11): Show |
15 | HG01070.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.99-2493delA | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47505994 | |||||||
| chr19:47506200 | G | A | 1 | a0001c0001t0004g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99-2698C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506200 | |||||||
| chr19:47506217 | C | T | 1 | a0001c0003t0002g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99-2715G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506217 | |||||||
| chr19:47506312 | T | C | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | NA18974.hp2 NA18984.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-2810A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506312 | |||||||
| chr19:47506425 | G | A | 13 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
15 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.99-2923C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506425 | |||||||
| chr19:47506618 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.99-3116T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506618 | |||||||
| chr19:47506795 | T | G | 1 | a0001c0001t0002g0077 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.99-3293A>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506795 | |||||||
| chr19:47506799 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.99-3297A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506799 | |||||||
| chr19:47506803 | C | A | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
88 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.99-3301G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506803 | |||||||
| chr19:47506815 | G | A | 2 | a0001c0002t0007g0243 a0001c0002t0007g0245 |
2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.99-3313C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506815 | |||||||
| chr19:47506983 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99-3481G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47506983 | |||||||
| chr19:47507004 | C | T | 1 | a0001c0002t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.99-3502G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47507004 | |||||||
| chr19:47507030 | G | C | 1 | a0001c0001t0002g0063 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.99-3528C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47507030 | |||||||
| chr19:47507227 | A | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG03041.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-3725T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47507227 | |||||||
| chr19:47507287 | A | ACCAACCT others(9): Show |
1 | a0001c0001t0001g0131 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.99-3801_99-3786dup others(16): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47507287 | |||||||
| chr19:47507454 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.99-3952G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47507454 | |||||||
| chr19:47507473 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.99-3971C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47507473 | |||||||
| chr19:47507821 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0130 a0001c0001t0001g0166 others(2): Show |
6 | HG02523.hp1 NA18939.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-4319C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47507821 | |||||||
| chr19:47508049 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.99-4547C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508049 | |||||||
| chr19:47508106 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.99-4604C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508106 | |||||||
| chr19:47508111 | C | T | 3 | a0001c0001t0003g0020 a0001c0001t0003g0110 a0001c0001t0003g0126 |
4 | HG02572.hp2 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-4609G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508111 | |||||||
| chr19:47508291 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(101): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.99-4789C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508291 | |||||||
| chr19:47508310 | T | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG03041.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-4808A>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508310 | |||||||
| chr19:47508427 | G | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG03041.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-4925C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508427 | |||||||
| chr19:47508639 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.99-5137A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508639 | |||||||
| chr19:47508643 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99-5141G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508643 | |||||||
| chr19:47508669 | C | CT | 6 | a0001c0001t0004g0034 a0001c0001t0004g0234 a0001c0001t0004g0235 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-5168dupA | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508669 | |||||||
| chr19:47508875 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99-5373G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47508875 | |||||||
| chr19:47509163 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.99-5661A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509163 | |||||||
| chr19:47509177 | C | T | 1 | a0001c0001t0004g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98+5666G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509177 | |||||||
| chr19:47509212 | C | T | 90 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(87): Show |
121 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.98+5631G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509212 | |||||||
| chr19:47509230 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.98+5613G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509230 | |||||||
| chr19:47509289 | A | AAAAATAA others(3): Show |
4 | a0001c0001t0003g0104 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG02155.hp1 HG02622.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+5544_98+5553dup others(10): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509289 | |||||||
| chr19:47509289 | AAAAAT | A | 72 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0027 others(69): Show |
97 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.98+5549_98+5553del others(5): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509289 | |||||||
| chr19:47509289 | AAAAATAA others(3): Show |
A | 42 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0131 others(39): Show |
55 | HG00280.hp1 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.98+5544_98+5553del others(10): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509289 | |||||||
| chr19:47509289 | AAAAATAA others(8): Show |
A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(58): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.98+5539_98+5553del others(15): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509289 | |||||||
| chr19:47509289 | AAAAATAA others(13): Show |
A | 23 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(20): Show |
31 | HG01123.hp2 HG01261.hp1 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.98+5534_98+5553del others(20): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509289 | |||||||
| chr19:47509289 | AAAAATAA others(23): Show |
A | 1 | a0001c0001t0001g0219 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.98+5524_98+5553del others(30): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509289 | |||||||
| chr19:47509313 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.98+5530T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509313 | |||||||
| chr19:47509329 | TAAAATAA others(18): Show |
T | 1 | a0001c0001t0002g0049 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.98+5489_98+5513del others(25): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509329 | |||||||
| chr19:47509334 | TAAAATAA others(13): Show |
T | 1 | a0001c0001t0001g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.98+5489_98+5508del others(20): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509334 | |||||||
| chr19:47509339 | TA | T | 5 | a0001c0001t0002g0050 a0001c0001t0002g0052 a0001c0001t0002g0092 others(2): Show |
5 | HG01496.hp2 HG03540.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+5503delT | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509339 | |||||||
| chr19:47509344 | TAAAATAA others(3): Show |
T | 1 | a0001c0001t0003g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.98+5489_98+5498del others(10): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509344 | |||||||
| chr19:47509345 | AAAAT | A | 5 | a0001c0001t0002g0050 a0001c0001t0002g0052 a0001c0001t0002g0092 others(2): Show |
5 | HG01496.hp2 HG03540.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+5494_98+5497del others(4): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509345 | |||||||
| chr19:47509348 | A | T | 2 | a0001c0001t0001g0229 a0001c0001t0004g0232 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.98+5495T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509348 | |||||||
| chr19:47509349 | T | A | 2 | a0001c0001t0001g0229 a0001c0001t0004g0232 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.98+5494A>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509349 | |||||||
| chr19:47509349 | T | TAAAATAA others(8): Show |
1 | a0001c0001t0004g0034 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.98+5493_98+5494ins others(15): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509349 | |||||||
| chr19:47509349 | T | TAAAATAA others(3): Show |
6 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0234 others(3): Show |
7 | HG02280.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+5493_98+5494ins others(10): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509349 | |||||||
| chr19:47509353 | T | A | 1 | a0001c0002t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98+5490A>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509353 | |||||||
| chr19:47509354 | A | T | 2 | a0001c0001t0001g0130 a0001c0002t0007g0243 |
2 | NA18985.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.98+5489T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509354 | |||||||
| chr19:47509452 | T | A | 2 | a0001c0001t0004g0237 a0001c0001t0004g0238 |
2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.98+5391A>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509452 | |||||||
| chr19:47509508 | A | G | 1 | a0001c0001t0002g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.98+5335T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509508 | |||||||
| chr19:47509521 | G | A | 70 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(67): Show |
99 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.98+5322C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509521 | |||||||
| chr19:47509553 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.98+5290C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509553 | |||||||
| chr19:47509664 | A | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.98+5179T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509664 | |||||||
| chr19:47509741 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(53): Show |
83 | HG00280.hp2 HG00408.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.98+5102A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509741 | |||||||
| chr19:47509752 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.98+5091C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509752 | |||||||
| chr19:47509792 | A | T | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.98+5051T>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509792 | |||||||
| chr19:47509814 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.98+5029G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509814 | |||||||
| chr19:47509860 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.98+4983G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509860 | |||||||
| chr19:47509900 | C | A | 1 | a0001c0001t0002g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.98+4943G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47509900 | |||||||
| chr19:47510025 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.98+4818C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510025 | |||||||
| chr19:47510099 | T | C | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.98+4744A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510099 | |||||||
| chr19:47510106 | T | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03017.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.98+4737A>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510106 | |||||||
| chr19:47510202 | G | C | 1 | a0001c0001t0002g0092 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.98+4641C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510202 | |||||||
| chr19:47510217 | G | A | 83 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(80): Show |
113 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.98+4626C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510217 | |||||||
| chr19:47510322 | G | C | 1 | a0001c0001t0005g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.98+4521C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510322 | |||||||
| chr19:47510436 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.98+4407A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510436 | |||||||
| chr19:47510476 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0226 |
2 | HG00738.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.98+4367G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510476 | |||||||
| chr19:47510621 | T | C | 1 | a0001c0001t0004g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98+4222A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510621 | |||||||
| chr19:47510747 | C | A | 1 | a0001c0001t0006g0041 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.98+4096G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510747 | |||||||
| chr19:47510747 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | NA18975.hp1 NA19012.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.98+4096G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510747 | |||||||
| chr19:47510839 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.98+4004A>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47510839 | |||||||
| chr19:47511041 | T | A | 1 | a0001c0001t0004g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.98+3802A>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47511041 | |||||||
| chr19:47511134 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.98+3709T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47511134 | |||||||
| chr19:47511150 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.98+3693G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47511150 | |||||||
| chr19:47511290 | C | T | 6 | a0001c0001t0003g0018 a0001c0001t0003g0099 a0001c0001t0003g0100 others(3): Show |
7 | HG02145.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+3553G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47511290 | |||||||
| chr19:47511816 | G | A | 1 | a0001c0001t0009g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.98+3027C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47511816 | |||||||
| chr19:47511823 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.98+3020G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47511823 | |||||||
| chr19:47511887 | C | T | 1 | a0001c0001t0004g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.98+2956G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47511887 | |||||||
| chr19:47512029 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98+2814G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47512029 | |||||||
| chr19:47512288 | C | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG03041.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+2555G>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47512288 | |||||||
| chr19:47512315 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.98+2528T>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47512315 | |||||||
| chr19:47512695 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.98+2148T>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47512695 | |||||||
| chr19:47512812 | C | T | 2 | a0001c0001t0004g0227 a0001c0001t0004g0228 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.98+2031G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47512812 | |||||||
| chr19:47512922 | C | A | 1 | a0001c0001t0001g0226 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.98+1921G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47512922 | |||||||
| chr19:47513007 | G | A | 9 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0234 others(6): Show |
11 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.98+1836C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513007 | |||||||
| chr19:47513098 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(104): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.98+1745C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513098 | |||||||
| chr19:47513135 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.98+1708G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513135 | |||||||
| chr19:47513451 | T | C | 1 | a0001c0001t0004g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.98+1392A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513451 | |||||||
| chr19:47513483 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.98+1360A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513483 | |||||||
| chr19:47513562 | G | A | 15 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(12): Show |
17 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.98+1281C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513562 | |||||||
| chr19:47513751 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.98+1092A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513751 | |||||||
| chr19:47513752 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.98+1091G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513752 | |||||||
| chr19:47513842 | CTTTCTT | C | 9 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0234 others(6): Show |
11 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.98+995_98+1000delA others(5): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513842 | |||||||
| chr19:47513846 | C | CT | 24 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(21): Show |
26 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.98+996dupA | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513846 | |||||||
| chr19:47513846 | CT | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0148 a0001c0001t0001g0222 others(14): Show |
17 | HG00735.hp2 HG01069.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+996delA | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513846 | |||||||
| chr19:47513847 | T | TTTC | 5 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00733.hp1 HG01070.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.98+995_98+996insGA others(1): Show |
NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513847 | |||||||
| chr19:47513935 | T | C | 2 | a0001c0001t0004g0239 a0001c0001t0004g0240 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.98+908A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513935 | |||||||
| chr19:47513941 | C | CT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.98+901_98+902insA | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47513941 | |||||||
| chr19:47514077 | C | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(198): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.98+766G>C | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47514077 | |||||||
| chr19:47514159 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.98+684A>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47514159 | |||||||
| chr19:47514190 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.98+653G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47514190 | |||||||
| chr19:47514320 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.98+523G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47514320 | |||||||
| chr19:47514603 | G | C | 7 | a0001c0001t0002g0017 a0001c0001t0002g0094 a0001c0001t0002g0095 others(4): Show |
8 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.98+240C>G | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47514603 | |||||||
| chr19:47514700 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(68): Show |
100 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+143G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47514700 | |||||||
| chr19:47514728 | G | A | 9 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0234 others(6): Show |
11 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.98+115C>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47514728 | |||||||
| chr19:47514765 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.98+78G>A | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47514765 | |||||||
| chr19:47514820 | C | A | 2 | a0001c0001t0002g0241 a0001c0001t0002g0242 |
2 | NA18951.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.98+23G>T | NAPA | ENSG00000105402.8 | transcript | ENST00000263354.8 | protein_coding | 1/10 | chr19 | 47514820 |