Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79187 |
| ensemblid | ENSG00000105255.11 |
| hgncid | 13745 |
| symbol | FSD1 |
| name | fibronectin type III and SPRY domain containing 1 |
| refseq_nuc | NM_024333.3 |
| refseq_prot | NP_077309.1 |
| ensembl_nuc | ENST00000221856.11 |
| ensembl_prot | ENSP00000221856.5 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 4304598 |
| end | 4323836 |
| strand | + |
| ver | v1.2 |
| region | chr19:4304598-4323836 |
| region5000 | chr19:4299598-4328836 |
| regionname0 | FSD1_chr19_4304598_4323836 |
| regionname5000 | FSD1_chr19_4299598_4328836 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 496 | 406 | 98 | 71 | 176 | 15 | 44 | 136 | FSD1_chr19_4299598_4328836 | FSD1 | MEEQR others(491): Show |
chr19 | 4299598 | 4328836 |
| a0002 | 0/0 | 496 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | MEEQR others(491): Show |
chr19 | 4299598 | 4328836 |
| a0003 | 0/0 | 496 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | MEEQR others(491): Show |
chr19 | 4299598 | 4328836 |
| a0004 | 0/0 | 496 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | MEEQR others(491): Show |
chr19 | 4299598 | 4328836 |
| a0005 | 0/0 | 496 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | MEEQR others(491): Show |
chr19 | 4299598 | 4328836 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1488 | 184 | 36 | 28 | 102 | 6 | 10 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0002 | 0/0 | 1488 | 162 | 40 | 28 | 59 | 7 | 28 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0003 | 0/0 | 1488 | 25 | 2 | 7 | 13 | 1 | 2 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0004 | 0/0 | 1488 | 14 | 6 | 6 | 0 | 1 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0005 | 0/0 | 1488 | 9 | 9 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0006 | 0/0 | 1488 | 4 | 1 | 0 | 1 | 0 | 2 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0008 | 0/0 | 1488 | 3 | 0 | 2 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0009 | 0/0 | 1488 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0010 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0011 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0001c0013 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0002c0007 | 0/0 | 1488 | 3 | 0 | 2 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0003c0012 | 0/0 | 1488 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0004c0015 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 | ||
| a0005c0014 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | ATGGA others(1483): Show |
chr19 | 4299598 | 4328836 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1833 | 183 | 36 | 28 | 101 | 6 | 10 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0001t0002 | 0/0 | 1850 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1845): Show |
chr19 | 4299598 | 4328836 |
| a0001c0002t0001 | 0/0 | 1833 | 162 | 40 | 28 | 59 | 7 | 28 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0003t0001 | 0/0 | 1833 | 25 | 2 | 7 | 13 | 1 | 2 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0004t0001 | 0/0 | 1833 | 14 | 6 | 6 | 0 | 1 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0005t0001 | 0/0 | 1833 | 9 | 9 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0006t0001 | 0/0 | 1833 | 4 | 1 | 0 | 1 | 0 | 2 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0008t0001 | 0/0 | 1833 | 3 | 0 | 2 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0009t0001 | 0/0 | 1833 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0010t0001 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0011t0001 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0001c0013t0001 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0002c0007t0001 | 0/0 | 1833 | 3 | 0 | 2 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0003c0012t0001 | 0/0 | 1833 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0004c0015t0001 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| a0005c0014t0001 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | GCAAT others(1828): Show |
chr19 | 4299598 | 4328836 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 1 | 3 | 19 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0003 | 0/0 | 11 | 1 | 2 | 6 | 0 | 2 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0017 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0002 | 0/0 | 21 | 1 | 7 | 13 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0004 | 0/0 | 8 | 0 | 2 | 0 | 1 | 5 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0009 | 0/0 | 6 | 0 | 1 | 1 | 3 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0014 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0016 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0018 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0006 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0007 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0004t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0004t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0004t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0004t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0005t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0005t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0005t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0005t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0005t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0006t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0006t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0008t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0008t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0008t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0009t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0010t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0011t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0001c0013t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0002c0007t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0002c0007t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0003c0012t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0004c0015t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| a0005c0014t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0018 | EUR | GBR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0133 | EUR | GBR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | GBR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0244 | EUR | GBR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0009 | EUR | FIN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | FIN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0009 | EUR | FIN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0094 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | CHS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00733 | hp2 | a0001 | c0008 | t0001 | g0217 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01069 | hp2 | a0002 | c0007 | t0001 | g0043 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01070 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01071 | hp1 | a0002 | c0007 | t0001 | g0043 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01175 | hp1 | a0001 | c0008 | t0001 | g0003 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0032 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0033 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01496 | hp1 | a0001 | c0004 | t0001 | g0033 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01496 | hp2 | a0003 | c0012 | t0001 | g0060 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | IBS | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | CDX | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0145 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | KHV | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0044 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02630 | hp2 | a0001 | c0006 | t0001 | g0006 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0044 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0093 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02976 | hp1 | a0001 | c0011 | t0001 | g0251 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0249 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0116 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03239 | hp2 | a0001 | c0008 | t0001 | g0163 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03486 | hp1 | a0001 | c0010 | t0001 | g0252 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0250 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03491 | hp1 | a0001 | c0006 | t0001 | g0040 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03492 | hp2 | a0001 | c0006 | t0001 | g0040 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0078 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | BEB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | BEB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | BEB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0082 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0122 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | YRI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | YRI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18906 | hp1 | a0001 | c0009 | t0001 | g0036 | AFR | YRI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18942 | hp2 | a0004 | c0015 | t0001 | g0150 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18943 | hp2 | a0005 | c0014 | t0001 | g0151 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18991 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18991 | hp2 | a0001 | c0006 | t0001 | g0069 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0174 | AFR | LWK | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | LWK | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19059 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19062 | hp1 | a0001 | c0013 | t0001 | g0177 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19068 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19078 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | YRI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | YRI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | ASW | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ASW | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0009 | EUR | TSI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20805 | hp1 | a0002 | c0007 | t0001 | g0247 | EUR | TSI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0006 | EUR | TSI | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02109 | hp1 | a0001 | c0009 | t0001 | g0036 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0024 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0248 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | ACB | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | MSL | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | USA | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0089 | AFR | USA | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | USA | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0172 | REF | REF | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0223 | REF | REF | FSD1_chr19_4299598_4328836 | FSD1 | chr19 | 4299598 | 4328836 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4307943 | A | G | 1 | a0004 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.305A>G | p.Asn102Ser | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/13 | 454/1833 | 305/1491 | 102/496 | chr19 | 4307943 | |||
| chr19:4311980 | C | T | 1 | a0003 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.629C>T | p.Pro210Leu | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/13 | 778/1833 | 629/1491 | 210/496 | chr19 | 4311980 | |||
| chr19:4312045 | C | G | 1 | a0002 | 3 | HG01069.hp2 HG01071.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.694C>G | p.Leu232Val | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/13 | 843/1833 | 694/1491 | 232/496 | chr19 | 4312045 | |||
| chr19:4323198 | G | A | 1 | a0005 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.1252G>A | p.Val418Met | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 11/13 | 1401/1833 | 1252/1491 | 418/496 | chr19 | 4323198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4306314 | T | C | 7 | a0001c0002 a0001c0003 a0001c0004 others(4): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
synonymous_variant | LOW | c.228T>C | p.Arg76Arg | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/13 | 377/1833 | 228/1491 | 76/496 | chr19 | 4306314 | |||
| chr19:4307887 | G | A | 1 | a0001c0005 | 9 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(6): Show |
synonymous_variant | LOW | c.249G>A | p.Gln83Gln | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/13 | 398/1833 | 249/1491 | 83/496 | chr19 | 4307887 | |||
| chr19:4311900 | C | A | 1 | a0001c0013 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.549C>A | p.Thr183Thr | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/13 | 698/1833 | 549/1491 | 183/496 | chr19 | 4311900 | |||
| chr19:4311918 | G | A | 2 | a0001c0010 a0001c0011 |
2 | HG02976.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.567G>A | p.Pro189Pro | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/13 | 716/1833 | 567/1491 | 189/496 | chr19 | 4311918 | |||
| chr19:4311945 | C | T | 1 | a0001c0008 | 3 | HG00733.hp2 HG01175.hp1 HG03239.hp2 |
synonymous_variant | LOW | c.594C>T | p.Tyr198Tyr | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/13 | 743/1833 | 594/1491 | 198/496 | chr19 | 4311945 | |||
| chr19:4318368 | G | A | 2 | a0001c0003 a0001c0006 |
29 | HG01099.hp1 HG01256.hp1 HG01257.hp2 others(26): Show |
synonymous_variant | LOW | c.822G>A | p.Ala274Ala | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 9/13 | 971/1833 | 822/1491 | 274/496 | chr19 | 4318368 | |||
| chr19:4318497 | C | T | 1 | a0001c0011 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.951C>T | p.Ser317Ser | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 9/13 | 1100/1833 | 951/1491 | 317/496 | chr19 | 4318497 | |||
| chr19:4322993 | G | A | 2 | a0001c0004 a0001c0009 |
16 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(13): Show |
synonymous_variant | LOW | c.1047G>A | p.Thr349Thr | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 11/13 | 1196/1833 | 1047/1491 | 349/496 | chr19 | 4322993 | |||
| chr19:4323574 | C | T | 1 | a0002c0007 | 3 | HG01069.hp2 HG01071.hp1 NA20805.hp1 |
synonymous_variant | LOW | c.1422C>T | p.Val474Val | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 13/13 | 1571/1833 | 1422/1491 | 474/496 | chr19 | 4323574 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4304628 | G | GGGGCGCG others(10): Show |
1 | a0001c0001t0002 | 1 | NA19005.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114_-98dupGCGGCGG others(10): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/13 | 97 | INFO_REALIGN_3_PRIME | chr19 | 4304628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4304777 | G | A | 120 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(117): Show |
196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.15+16G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/12 | chr19 | 4304777 | |||||||
| chr19:4304850 | C | T | 1 | a0001c0002t0001g0034 | 2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.15+89C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/12 | chr19 | 4304850 | |||||||
| chr19:4304858 | A | G | 126 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0045 others(123): Show |
202 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.15+97A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/12 | chr19 | 4304858 | |||||||
| chr19:4305259 | C | G | 3 | a0001c0002t0001g0139 a0001c0002t0001g0140 a0001c0002t0001g0141 |
3 | HG03209.hp2 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.15+498C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/12 | chr19 | 4305259 | |||||||
| chr19:4305741 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.16-205G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/12 | chr19 | 4305741 | |||||||
| chr19:4305793 | T | C | 29 | a0001c0001t0001g0147 a0001c0002t0001g0019 a0001c0002t0001g0046 others(26): Show |
31 | HG00642.hp2 HG01109.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.16-153T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/12 | chr19 | 4305793 | |||||||
| chr19:4305815 | T | C | 1 | a0001c0002t0001g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.16-131T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/12 | chr19 | 4305815 | |||||||
| chr19:4305821 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.16-125C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/12 | chr19 | 4305821 | |||||||
| chr19:4305904 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.16-42G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 1/12 | chr19 | 4305904 | |||||||
| chr19:4306103 | C | T | 4 | a0001c0002t0001g0019 a0001c0002t0001g0050 a0001c0002t0001g0064 others(1): Show |
6 | HG02145.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+62C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 2/12 | chr19 | 4306103 | |||||||
| chr19:4306489 | C | T | 5 | a0001c0005t0001g0024 a0001c0005t0001g0044 a0001c0005t0001g0248 others(2): Show |
8 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.243+160C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4306489 | |||||||
| chr19:4306507 | G | A | 1 | a0004c0015t0001g0150 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.243+178G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4306507 | |||||||
| chr19:4306580 | A | G | 125 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0008 others(122): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.243+251A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4306580 | |||||||
| chr19:4306640 | G | A | 1 | a0001c0002t0001g0074 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.243+311G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4306640 | |||||||
| chr19:4306736 | G | A | 1 | a0001c0002t0001g0034 | 2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.243+407G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4306736 | |||||||
| chr19:4306738 | G | GC | 47 | a0001c0002t0001g0012 a0001c0002t0001g0019 a0001c0002t0001g0028 others(44): Show |
67 | HG00558.hp2 HG00642.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.243+414dupC | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 4306738 | ||||||
| chr19:4306791 | G | A | 3 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | HG01243.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.243+462G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4306791 | |||||||
| chr19:4307077 | CAG | C | 26 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0009 others(23): Show |
51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.243+751_243+752del others(2): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 4307077 | ||||||
| chr19:4307086 | A | C | 4 | a0001c0002t0001g0046 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+757A>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307086 | |||||||
| chr19:4307123 | T | C | 2 | a0001c0010t0001g0252 a0001c0011t0001g0251 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.244-759T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307123 | |||||||
| chr19:4307128 | C | T | 1 | a0001c0005t0001g0044 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.244-754C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307128 | |||||||
| chr19:4307157 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.244-725C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307157 | |||||||
| chr19:4307367 | T | C | 74 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(71): Show |
126 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.244-515T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307367 | |||||||
| chr19:4307456 | C | G | 1 | a0001c0002t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.244-426C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307456 | |||||||
| chr19:4307461 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.244-421G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307461 | |||||||
| chr19:4307494 | A | G | 1 | a0001c0002t0001g0138 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.244-388A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307494 | |||||||
| chr19:4307681 | A | G | 27 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0009 others(24): Show |
52 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.244-201A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307681 | |||||||
| chr19:4307779 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.244-103G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307779 | |||||||
| chr19:4307797 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.244-85T>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 3/12 | chr19 | 4307797 | |||||||
| chr19:4307992 | C | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01257.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.345+9C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4307992 | |||||||
| chr19:4308030 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.345+47C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308030 | |||||||
| chr19:4308072 | T | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0148 a0001c0001t0001g0149 others(11): Show |
17 | HG01891.hp2 HG02257.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.345+89T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308072 | |||||||
| chr19:4308101 | T | C | 127 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0008 others(124): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.345+118T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308101 | |||||||
| chr19:4308131 | C | T | 22 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0009 others(19): Show |
47 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.345+148C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308131 | |||||||
| chr19:4308132 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0066 |
4 | HG00423.hp1 HG00558.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+149G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308132 | |||||||
| chr19:4308147 | G | A | 1 | a0001c0004t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.345+164G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308147 | |||||||
| chr19:4308203 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.345+220T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308203 | |||||||
| chr19:4308423 | A | G | 25 | a0001c0002t0001g0019 a0001c0002t0001g0046 a0001c0002t0001g0050 others(22): Show |
27 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.345+440A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308423 | |||||||
| chr19:4308488 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.345+505C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308488 | |||||||
| chr19:4308654 | A | G | 1 | a0001c0002t0001g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.345+671A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308654 | |||||||
| chr19:4308661 | T | G | 2 | a0001c0001t0001g0255 a0001c0002t0001g0253 |
2 | HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345+678T>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308661 | |||||||
| chr19:4308681 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0166 |
3 | HG00597.hp2 HG02165.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.345+698G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308681 | |||||||
| chr19:4308726 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.345+743C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308726 | |||||||
| chr19:4308728 | GGCACCTG others(120): Show |
G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG00597.hp1 NA18969.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.345+749_345+875del | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 4308728 | ||||||
| chr19:4308807 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0170 a0001c0002t0001g0104 |
3 | NA18946.hp1 NA18961.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.345+824A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308807 | |||||||
| chr19:4308815 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.345+832G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308815 | |||||||
| chr19:4308837 | A | G | 1 | a0001c0002t0001g0009 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.345+854A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308837 | |||||||
| chr19:4308845 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.345+862G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308845 | |||||||
| chr19:4308853 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.345+870G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308853 | |||||||
| chr19:4308917 | T | C | 2 | a0001c0003t0001g0075 a0001c0003t0001g0076 |
2 | NA18948.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.345+934T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4308917 | |||||||
| chr19:4309046 | G | A | 48 | a0001c0001t0001g0035 a0001c0001t0001g0170 a0001c0001t0001g0171 others(45): Show |
83 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.345+1063G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4309046 | |||||||
| chr19:4309052 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.345+1069G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4309052 | |||||||
| chr19:4309371 | T | A | 1 | a0001c0002t0001g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.346-902T>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4309371 | |||||||
| chr19:4309482 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.346-791G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4309482 | |||||||
| chr19:4309670 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.346-603G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4309670 | |||||||
| chr19:4309782 | G | A | 3 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | HG01243.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.346-491G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4309782 | |||||||
| chr19:4309908 | C | CA | 8 | a0001c0001t0001g0153 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG02083.hp2 HG02257.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-352dupA | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 4309908 | ||||||
| chr19:4309920 | AAC | A | 9 | a0001c0002t0001g0019 a0001c0002t0001g0050 a0001c0002t0001g0064 others(6): Show |
11 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.346-349_346-348del others(2): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 4309920 | ||||||
| chr19:4309921 | AC | A | 4 | a0001c0002t0001g0046 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.346-351delC | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4309921 | |||||||
| chr19:4310016 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.346-257T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4310016 | |||||||
| chr19:4310061 | C | T | 1 | a0001c0003t0001g0032 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.346-212C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4310061 | |||||||
| chr19:4310071 | A | T | 1 | a0001c0013t0001g0177 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.346-202A>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4310071 | |||||||
| chr19:4310072 | C | A | 1 | a0001c0013t0001g0177 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.346-201C>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4310072 | |||||||
| chr19:4310073 | A | C | 1 | a0001c0013t0001g0177 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.346-200A>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4310073 | |||||||
| chr19:4310220 | G | A | 8 | a0001c0004t0001g0013 a0001c0004t0001g0023 a0001c0004t0001g0033 others(5): Show |
15 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.346-53G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 4/12 | chr19 | 4310220 | |||||||
| chr19:4310330 | C | T | 25 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0239 others(22): Show |
51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.368+35C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 5/12 | chr19 | 4310330 | |||||||
| chr19:4310424 | G | A | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0153 others(2): Show |
5 | HG00735.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.369-51G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 5/12 | chr19 | 4310424 | |||||||
| chr19:4310430 | C | G | 1 | a0001c0002t0001g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.369-45C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 5/12 | chr19 | 4310430 | |||||||
| chr19:4310725 | T | G | 25 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0239 others(22): Show |
51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.490+129T>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4310725 | |||||||
| chr19:4310758 | T | C | 39 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0239 others(36): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.490+162T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4310758 | |||||||
| chr19:4310770 | C | T | 1 | a0001c0002t0001g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.490+174C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4310770 | |||||||
| chr19:4310771 | C | T | 8 | a0001c0004t0001g0013 a0001c0004t0001g0023 a0001c0004t0001g0033 others(5): Show |
15 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.490+175C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4310771 | |||||||
| chr19:4310799 | C | A | 25 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0239 others(22): Show |
51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.490+203C>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4310799 | |||||||
| chr19:4310995 | G | C | 10 | a0001c0002t0001g0004 a0001c0002t0001g0125 a0001c0002t0001g0126 others(7): Show |
21 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.490+399G>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4310995 | |||||||
| chr19:4310995 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.490+399G>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4310995 | |||||||
| chr19:4311049 | CA | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0142 |
4 | HG01074.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+454delA | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4311049 | |||||||
| chr19:4311108 | T | C | 39 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0239 others(36): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.490+512T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4311108 | |||||||
| chr19:4311157 | C | T | 1 | a0001c0002t0001g0077 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.490+561C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4311157 | |||||||
| chr19:4311257 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.491-585A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4311257 | |||||||
| chr19:4311410 | G | A | 1 | a0001c0002t0001g0127 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.491-432G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4311410 | |||||||
| chr19:4311537 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.491-305G>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4311537 | |||||||
| chr19:4311704 | A | G | 1 | a0001c0002t0001g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.491-138A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 6/12 | chr19 | 4311704 | |||||||
| chr19:4312106 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(70): Show |
117 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.700+55C>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312106 | |||||||
| chr19:4312224 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.700+173C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312224 | |||||||
| chr19:4312291 | C | A | 1 | a0001c0002t0001g0064 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.700+240C>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312291 | |||||||
| chr19:4312318 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.700+267A>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312318 | |||||||
| chr19:4312352 | A | G | 20 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0239 others(17): Show |
43 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.700+301A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312352 | |||||||
| chr19:4312447 | C | T | 3 | a0001c0004t0001g0023 a0001c0004t0001g0033 a0001c0004t0001g0244 |
6 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.700+396C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312447 | |||||||
| chr19:4312502 | AAAT | A | 5 | a0001c0002t0001g0052 a0001c0002t0001g0057 a0001c0002t0001g0058 others(2): Show |
5 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+461_700+463del others(3): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4312502 | ||||||
| chr19:4312525 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.700+474C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312525 | |||||||
| chr19:4312535 | A | G | 2 | a0001c0002t0001g0020 a0001c0002t0001g0138 |
4 | HG01358.hp2 HG01361.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+484A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312535 | |||||||
| chr19:4312579 | C | T | 1 | a0001c0003t0001g0051 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.700+528C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312579 | |||||||
| chr19:4312580 | G | A | 20 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0239 others(17): Show |
43 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.700+529G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312580 | |||||||
| chr19:4312601 | A | T | 8 | a0001c0004t0001g0013 a0001c0004t0001g0023 a0001c0004t0001g0033 others(5): Show |
15 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.700+550A>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312601 | |||||||
| chr19:4312685 | G | C | 8 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+634G>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312685 | |||||||
| chr19:4312701 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.700+650A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312701 | |||||||
| chr19:4312748 | T | C | 6 | a0001c0001t0001g0255 a0001c0002t0001g0124 a0001c0002t0001g0139 others(3): Show |
6 | HG02145.hp1 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.700+697T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312748 | |||||||
| chr19:4312783 | C | T | 1 | a0001c0002t0001g0114 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.700+732C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312783 | |||||||
| chr19:4312799 | C | T | 8 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+748C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312799 | |||||||
| chr19:4312804 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.700+753C>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312804 | |||||||
| chr19:4312807 | A | AAAAT | 13 | a0001c0001t0001g0072 a0001c0001t0001g0147 a0001c0001t0001g0154 others(10): Show |
15 | HG01109.hp1 HG02145.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.700+787_700+790dup others(4): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4312807 | ||||||
| chr19:4312807 | A | AAAATAAA others(1): Show |
9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0255 others(6): Show |
9 | HG02145.hp1 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.700+783_700+790dup others(8): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4312807 | ||||||
| chr19:4312807 | A | AAAATAAA others(5): Show |
4 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(1): Show |
7 | HG02280.hp1 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.700+779_700+790dup others(12): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4312807 | ||||||
| chr19:4312807 | AAAATAAA others(1): Show |
A | 4 | a0001c0002t0001g0046 a0001c0002t0001g0061 a0001c0002t0001g0062 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+783_700+790del others(8): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4312807 | ||||||
| chr19:4312810 | A | T | 1 | a0001c0013t0001g0177 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.700+759A>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312810 | |||||||
| chr19:4312811 | T | A | 1 | a0001c0013t0001g0177 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.700+760T>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4312811 | |||||||
| chr19:4312835 | TA | T | 5 | a0001c0004t0001g0013 a0001c0004t0001g0089 a0001c0004t0001g0093 others(2): Show |
9 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.700+787delA | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4312835 | ||||||
| chr19:4313053 | A | T | 1 | a0001c0013t0001g0177 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.700+1002A>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313053 | |||||||
| chr19:4313069 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.700+1018C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313069 | |||||||
| chr19:4313182 | TA | T | 8 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0207 others(5): Show |
8 | HG00323.hp1 HG01074.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+1145delA | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4313182 | ||||||
| chr19:4313197 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.700+1146T>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313197 | |||||||
| chr19:4313233 | A | C | 1 | a0001c0002t0001g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.700+1182A>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313233 | |||||||
| chr19:4313265 | C | T | 11 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0153 others(8): Show |
12 | HG00735.hp2 HG01256.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.700+1214C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313265 | |||||||
| chr19:4313348 | CAA | C | 2 | a0002c0007t0001g0043 a0002c0007t0001g0247 |
3 | HG01069.hp2 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.700+1299_700+1300d others(4): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4313348 | ||||||
| chr19:4313378 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.700+1327C>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313378 | |||||||
| chr19:4313385 | C | T | 1 | a0001c0002t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.700+1334C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313385 | |||||||
| chr19:4313412 | A | G | 20 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0156 others(17): Show |
43 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.700+1361A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313412 | |||||||
| chr19:4313432 | C | CTCATGAG others(12): Show |
19 | a0001c0001t0001g0255 a0001c0002t0001g0015 a0001c0002t0001g0048 others(16): Show |
22 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.700+1383_700+1384i others(21): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4313432 | ||||||
| chr19:4313442 | G | A | 2 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.700+1391G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313442 | |||||||
| chr19:4313535 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.700+1484T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313535 | |||||||
| chr19:4313590 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.700+1539C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313590 | |||||||
| chr19:4313598 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.700+1547A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313598 | |||||||
| chr19:4313716 | C | CA | 15 | a0001c0001t0001g0068 a0001c0001t0001g0184 a0001c0001t0001g0185 others(12): Show |
15 | HG00741.hp1 HG01981.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.700+1679dupA | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4313716 | ||||||
| chr19:4313716 | CA | C | 14 | a0001c0001t0001g0168 a0001c0002t0001g0015 a0001c0002t0001g0048 others(11): Show |
17 | HG00597.hp1 HG00642.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.700+1679delA | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4313716 | ||||||
| chr19:4313725 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.700+1674A>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313725 | |||||||
| chr19:4313726 | A | C | 1 | a0003c0012t0001g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.700+1675A>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4313726 | |||||||
| chr19:4314040 | G | GA | 6 | a0001c0001t0001g0215 a0001c0002t0001g0015 a0001c0002t0001g0048 others(3): Show |
9 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.700+1998dupA | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4314040 | ||||||
| chr19:4314067 | G | T | 5 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.700+2016G>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314067 | |||||||
| chr19:4314070 | T | A | 5 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.700+2019T>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314070 | |||||||
| chr19:4314136 | C | T | 1 | a0001c0002t0001g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.700+2085C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314136 | |||||||
| chr19:4314187 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.700+2136G>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314187 | |||||||
| chr19:4314197 | T | C | 1 | a0001c0002t0001g0124 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.700+2146T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314197 | |||||||
| chr19:4314330 | C | T | 1 | a0001c0003t0001g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.700+2279C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314330 | |||||||
| chr19:4314340 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.700+2289T>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314340 | |||||||
| chr19:4314488 | C | CT | 7 | a0001c0001t0001g0168 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG00597.hp1 HG02055.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.700+2453dupT | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4314488 | ||||||
| chr19:4314488 | CT | C | 23 | a0001c0001t0001g0216 a0001c0001t0001g0256 a0001c0002t0001g0015 others(20): Show |
30 | HG00639.hp1 HG00642.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.700+2453delT | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4314488 | ||||||
| chr19:4314504 | T | C | 5 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.700+2453T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314504 | |||||||
| chr19:4314504 | T | TC | 18 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0002t0001g0004 others(15): Show |
41 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.700+2453_700+2454i others(3): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314504 | |||||||
| chr19:4314715 | G | A | 22 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0255 others(19): Show |
25 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.701-2467G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314715 | |||||||
| chr19:4314721 | A | T | 22 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0255 others(19): Show |
25 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.701-2461A>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314721 | |||||||
| chr19:4314745 | C | T | 1 | a0002c0007t0001g0043 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.701-2437C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314745 | |||||||
| chr19:4314806 | C | T | 1 | a0001c0004t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.701-2376C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314806 | |||||||
| chr19:4314918 | G | A | 2 | a0001c0002t0001g0124 a0001c0005t0001g0174 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.701-2264G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4314918 | |||||||
| chr19:4315120 | CCTTTTTT others(7): Show |
C | 5 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-2054_701-2041d others(16): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4315120 | ||||||
| chr19:4315156 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(75): Show |
124 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.701-2026C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315156 | |||||||
| chr19:4315265 | A | G | 1 | a0001c0011t0001g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.701-1917A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315265 | |||||||
| chr19:4315301 | A | AT | 72 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0037 others(69): Show |
95 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.701-1856dupT | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4315301 | ||||||
| chr19:4315301 | A | ATT | 10 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0048 others(7): Show |
13 | HG00099.hp2 HG00140.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.701-1857_701-1856d others(4): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4315301 | ||||||
| chr19:4315301 | AT | A | 30 | a0001c0001t0001g0038 a0001c0001t0001g0071 a0001c0001t0001g0171 others(27): Show |
47 | HG00738.hp2 HG01099.hp1 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.701-1856delT | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4315301 | ||||||
| chr19:4315347 | T | C | 1 | a0001c0003t0001g0079 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.701-1835T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315347 | |||||||
| chr19:4315369 | T | C | 1 | a0001c0004t0001g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.701-1813T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315369 | |||||||
| chr19:4315371 | C | G | 1 | a0001c0004t0001g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.701-1811C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315371 | |||||||
| chr19:4315372 | T | C | 1 | a0002c0007t0001g0043 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.701-1810T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315372 | |||||||
| chr19:4315372 | T | G | 1 | a0001c0004t0001g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.701-1810T>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315372 | |||||||
| chr19:4315395 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.701-1787G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315395 | |||||||
| chr19:4315409 | C | T | 37 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0045 others(34): Show |
48 | HG00423.hp2 HG00558.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.701-1773C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315409 | |||||||
| chr19:4315509 | C | T | 38 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0045 others(35): Show |
49 | HG00423.hp2 HG00558.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.701-1673C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315509 | |||||||
| chr19:4315597 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.701-1585C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315597 | |||||||
| chr19:4315607 | C | CT | 44 | a0001c0001t0001g0070 a0001c0001t0001g0167 a0001c0001t0001g0187 others(41): Show |
48 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.701-1554dupT | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4315607 | ||||||
| chr19:4315607 | CT | C | 8 | a0001c0002t0001g0091 a0001c0002t0001g0098 a0001c0002t0001g0099 others(5): Show |
8 | HG01167.hp1 HG03209.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-1554delT | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4315607 | ||||||
| chr19:4315699 | C | T | 1 | a0001c0002t0001g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.701-1483C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315699 | |||||||
| chr19:4315742 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.701-1440G>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315742 | |||||||
| chr19:4315913 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701-1269G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315913 | |||||||
| chr19:4315918 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.701-1264C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315918 | |||||||
| chr19:4315922 | C | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0047 |
3 | HG02040.hp2 NA18971.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.701-1260C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4315922 | |||||||
| chr19:4316254 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.701-928C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4316254 | |||||||
| chr19:4316314 | C | T | 1 | a0001c0005t0001g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.701-868C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4316314 | |||||||
| chr19:4316370 | A | AC | 9 | a0001c0001t0001g0160 a0001c0001t0001g0185 a0001c0001t0001g0194 others(6): Show |
9 | HG00741.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-806dupC | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 4316370 | ||||||
| chr19:4316444 | C | T | 5 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-738C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4316444 | |||||||
| chr19:4316907 | C | T | 8 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-275C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4316907 | |||||||
| chr19:4316983 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0142 others(4): Show |
13 | HG01074.hp2 HG01109.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.701-199C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4316983 | |||||||
| chr19:4317006 | G | A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0202 a0001c0001t0001g0210 others(2): Show |
5 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-176G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4317006 | |||||||
| chr19:4317036 | AGCCAGTG others(24): Show |
A | 1 | a0001c0002t0001g0100 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.701-145_701-115del others(31): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 7/12 | chr19 | 4317036 | |||||||
| chr19:4317657 | G | C | 1 | a0001c0002t0001g0102 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.799+377G>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 8/12 | chr19 | 4317657 | |||||||
| chr19:4317794 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.799+514G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 8/12 | chr19 | 4317794 | |||||||
| chr19:4317845 | C | A | 5 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.800-501C>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 8/12 | chr19 | 4317845 | |||||||
| chr19:4317846 | G | A | 7 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0055 others(4): Show |
7 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.800-500G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 8/12 | chr19 | 4317846 | |||||||
| chr19:4318004 | G | A | 2 | a0001c0002t0001g0109 a0001c0010t0001g0252 |
2 | HG00621.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.800-342G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 8/12 | chr19 | 4318004 | |||||||
| chr19:4318137 | C | T | 1 | a0001c0002t0001g0107 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.800-209C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 8/12 | chr19 | 4318137 | |||||||
| chr19:4318181 | G | A | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0139 others(2): Show |
5 | HG02615.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-165G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 8/12 | chr19 | 4318181 | |||||||
| chr19:4318188 | C | T | 1 | a0002c0007t0001g0043 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.800-158C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 8/12 | chr19 | 4318188 | |||||||
| chr19:4318261 | C | G | 3 | a0001c0002t0001g0046 a0001c0002t0001g0061 a0001c0002t0001g0063 |
3 | HG02559.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.800-85C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 8/12 | chr19 | 4318261 | |||||||
| chr19:4318528 | T | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0218 a0001c0001t0001g0220 |
4 | HG02040.hp1 HG02074.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+23T>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 9/12 | chr19 | 4318528 | |||||||
| chr19:4318614 | G | GT | 3 | a0001c0001t0001g0039 a0001c0001t0001g0194 a0001c0001t0001g0201 |
4 | NA18971.hp1 NA19000.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+110dupT | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 4318614 | ||||||
| chr19:4318658 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(181): Show |
285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.959+153A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 9/12 | chr19 | 4318658 | |||||||
| chr19:4318857 | C | G | 1 | a0001c0003t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.960-15C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 9/12 | chr19 | 4318857 | |||||||
| chr19:4319011 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1039+60G>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319011 | |||||||
| chr19:4319289 | A | G | 1 | a0001c0002t0001g0034 | 2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1039+338A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319289 | |||||||
| chr19:4319312 | T | A | 8 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039+361T>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319312 | |||||||
| chr19:4319418 | G | A | 1 | a0001c0002t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1039+467G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319418 | |||||||
| chr19:4319486 | A | G | 1 | a0001c0010t0001g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1039+535A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319486 | |||||||
| chr19:4319547 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1039+596T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319547 | |||||||
| chr19:4319630 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1039+679G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319630 | |||||||
| chr19:4319654 | C | T | 19 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0015 others(16): Show |
22 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039+703C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319654 | |||||||
| chr19:4319702 | T | C | 3 | a0001c0002t0001g0085 a0001c0002t0001g0243 a0001c0003t0001g0007 |
8 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039+751T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319702 | |||||||
| chr19:4319778 | G | A | 13 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(10): Show |
16 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1039+827G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319778 | |||||||
| chr19:4319890 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0196 |
2 | HG00738.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1039+939T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4319890 | |||||||
| chr19:4320025 | A | G | 14 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(11): Show |
17 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1039+1074A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320025 | |||||||
| chr19:4320189 | G | C | 8 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039+1238G>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320189 | |||||||
| chr19:4320193 | C | G | 2 | a0001c0001t0001g0255 a0001c0002t0001g0253 |
2 | HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1039+1242C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320193 | |||||||
| chr19:4320204 | G | A | 8 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039+1253G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320204 | |||||||
| chr19:4320221 | A | G | 17 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0255 others(14): Show |
24 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1039+1270A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320221 | |||||||
| chr19:4320226 | A | G | 1 | a0001c0011t0001g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1039+1275A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320226 | |||||||
| chr19:4320471 | C | G | 14 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0139 others(11): Show |
21 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1039+1520C>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320471 | |||||||
| chr19:4320572 | A | G | 14 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(11): Show |
17 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1039+1621A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320572 | |||||||
| chr19:4320786 | AGTATCTG others(5): Show |
A | 1 | a0001c0003t0001g0075 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1039+1837_1039+184 others(16): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4320786 | ||||||
| chr19:4320827 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1039+1876G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320827 | |||||||
| chr19:4320846 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1039+1895G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320846 | |||||||
| chr19:4320954 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1039+2003C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320954 | |||||||
| chr19:4320984 | A | G | 1 | a0001c0011t0001g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1040-2002A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4320984 | |||||||
| chr19:4321058 | G | A | 8 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040-1928G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321058 | |||||||
| chr19:4321096 | C | T | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1040-1890C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321096 | |||||||
| chr19:4321161 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1040-1825G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321161 | |||||||
| chr19:4321175 | C | CTGAGGAG others(22): Show |
1 | a0001c0002t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1040-1811_1040-181 others(33): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321175 | |||||||
| chr19:4321180 | G | A | 5 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1040-1806G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321180 | |||||||
| chr19:4321184 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1040-1802C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321184 | |||||||
| chr19:4321199 | A | G | 1 | a0001c0002t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1040-1787A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321199 | |||||||
| chr19:4321204 | A | G | 1 | a0001c0002t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1040-1782A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321204 | |||||||
| chr19:4321206 | C | A | 1 | a0001c0002t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1040-1780C>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321206 | |||||||
| chr19:4321225 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1040-1761G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321225 | |||||||
| chr19:4321225 | G | GAATAGCT others(83): Show |
1 | a0001c0003t0001g0075 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1040-1675_1040-167 others(94): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4321225 | ||||||
| chr19:4321225 | G | GAATAGCT others(84): Show |
237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1040-1675_1040-167 others(95): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4321225 | ||||||
| chr19:4321225 | G | GAATAGCT others(571): Show |
1 | a0001c0001t0001g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1040-1697_1040-169 others(582): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4321225 | ||||||
| chr19:4321302 | G | GGAGTATC others(81): Show |
1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1040-1675_1040-167 others(92): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4321302 | ||||||
| chr19:4321310 | T | TG | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0096 others(4): Show |
7 | HG00621.hp1 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1040-1675dupG | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4321310 | ||||||
| chr19:4321310 | T | TGGGGGAA others(24): Show |
15 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(12): Show |
18 | HG00408.hp1 HG00642.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1040-1675_1040-167 others(35): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4321310 | ||||||
| chr19:4321312 | T | G | 28 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0015 others(25): Show |
35 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1040-1674T>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321312 | |||||||
| chr19:4321318 | T | C | 15 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(12): Show |
18 | HG00408.hp1 HG00642.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1040-1668T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321318 | |||||||
| chr19:4321340 | GGAGGGGA others(23): Show |
G | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0096 others(4): Show |
7 | HG00621.hp1 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1040-1644_1040-161 others(34): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4321340 | ||||||
| chr19:4321372 | G | GGGAAATA others(53): Show |
1 | a0001c0001t0001g0222 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1040-1554_1040-149 others(64): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4321372 | ||||||
| chr19:4321372 | G | T | 1 | a0001c0002t0001g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1040-1614G>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321372 | |||||||
| chr19:4321378 | T | C | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0096 others(4): Show |
7 | HG00621.hp1 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1040-1608T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321378 | |||||||
| chr19:4321400 | G | GGAGGGGA others(52): Show |
14 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(11): Show |
17 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1040-1555_1040-155 others(63): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4321400 | ||||||
| chr19:4321432 | T | G | 1 | a0001c0002t0001g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1040-1554T>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321432 | |||||||
| chr19:4321455 | T | C | 1 | a0001c0002t0001g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1040-1531T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321455 | |||||||
| chr19:4321457 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1040-1529T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321457 | |||||||
| chr19:4321466 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0038 others(7): Show |
22 | HG01074.hp2 HG01109.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.1040-1520G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321466 | |||||||
| chr19:4321492 | G | T | 1 | a0001c0002t0001g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1040-1494G>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321492 | |||||||
| chr19:4321660 | C | T | 8 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040-1326C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321660 | |||||||
| chr19:4321739 | A | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0139 others(2): Show |
5 | HG02615.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1040-1247A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321739 | |||||||
| chr19:4321857 | A | G | 1 | a0001c0002t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1040-1129A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321857 | |||||||
| chr19:4321867 | A | G | 1 | a0001c0002t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1040-1119A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321867 | |||||||
| chr19:4321928 | G | A | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0139 others(2): Show |
5 | HG02615.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1040-1058G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4321928 | |||||||
| chr19:4322151 | A | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0139 others(2): Show |
5 | HG02615.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1040-835A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322151 | |||||||
| chr19:4322307 | T | G | 1 | a0001c0002t0001g0103 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1040-679T>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322307 | |||||||
| chr19:4322363 | C | T | 6 | a0001c0004t0001g0013 a0001c0004t0001g0082 a0001c0004t0001g0089 others(3): Show |
10 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1040-623C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322363 | |||||||
| chr19:4322382 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1040-604A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322382 | |||||||
| chr19:4322454 | C | T | 3 | a0001c0001t0001g0026 a0001c0002t0001g0095 a0001c0002t0001g0110 |
4 | HG00597.hp2 NA18960.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-532C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322454 | |||||||
| chr19:4322485 | G | A | 1 | a0001c0005t0001g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1040-501G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322485 | |||||||
| chr19:4322602 | T | C | 19 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0015 others(16): Show |
22 | HG00642.hp2 HG01175.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1040-384T>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322602 | |||||||
| chr19:4322683 | G | GGGGAATA others(24): Show |
257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(254): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1040-291_1040-261d others(33): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4322683 | ||||||
| chr19:4322683 | G | GGGGAATA others(55): Show |
1 | a0001c0003t0001g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1040-292_1040-291i others(64): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4322683 | ||||||
| chr19:4322683 | G | GGGGAATA others(24): Show |
2 | a0001c0001t0001g0170 a0001c0002t0001g0104 |
2 | NA18961.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1040-292_1040-291i others(33): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4322683 | ||||||
| chr19:4322695 | C | CGGCCCAA others(55): Show |
1 | a0001c0002t0001g0100 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1040-261_1040-260i others(64): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4322695 | ||||||
| chr19:4322696 | G | GGCCCAAG others(23): Show |
1 | a0001c0003t0001g0075 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1040-261_1040-260i others(32): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4322696 | ||||||
| chr19:4322703 | G | GGAGTATC others(23): Show |
1 | a0001c0001t0001g0227 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1040-261_1040-260i others(32): Show |
FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 4322703 | ||||||
| chr19:4322768 | C | T | 1 | a0001c0011t0001g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1040-218C>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322768 | |||||||
| chr19:4322807 | A | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0002t0001g0139 others(2): Show |
5 | HG02615.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1040-179A>G | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322807 | |||||||
| chr19:4322908 | G | T | 2 | a0001c0003t0001g0032 a0001c0003t0001g0081 |
3 | HG01257.hp2 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1040-78G>T | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 10/12 | chr19 | 4322908 | |||||||
| chr19:4323260 | G | A | 6 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0182 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+23G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 11/12 | chr19 | 4323260 | |||||||
| chr19:4323287 | C | A | 1 | a0001c0002t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1291+50C>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 11/12 | chr19 | 4323287 | |||||||
| chr19:4323316 | G | C | 1 | a0001c0011t0001g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1292-32G>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 11/12 | chr19 | 4323316 | |||||||
| chr19:4323317 | G | A | 1 | a0001c0011t0001g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1292-31G>A | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 11/12 | chr19 | 4323317 | |||||||
| chr19:4323459 | G | C | 1 | a0001c0001t0001g0220 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1380+23G>C | FSD1 | ENSG00000105255.11 | transcript | ENST00000221856.11 | protein_coding | 12/12 | chr19 | 4323459 |