Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84928 |
| ensemblid | ENSG00000146842.17 |
| hgncid | 21898 |
| symbol | TMEM209 |
| name | transmembrane protein 209 |
| refseq_nuc | NM_032842.4 |
| refseq_prot | NP_116231.2 |
| ensembl_nuc | ENST00000397622.7 |
| ensembl_prot | ENSP00000380747.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 130164713 |
| end | 130205406 |
| strand | - |
| ver | v1.2 |
| region | chr7:130164713-130205406 |
| region5000 | chr7:130159713-130210406 |
| regionname0 | TMEM209_chr7_130164713_130205406 |
| regionname5000 | TMEM209_chr7_130159713_130210406 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 561 | 323 | 90 | 69 | 110 | 12 | 40 | 93 | TMEM209_chr7_130159713_130210406 | TMEM209 | MMQGE others(556): Show |
chr7 | 130159713 | 130210406 |
| a0002 | 0/0 | 561 | 7 | 0 | 3 | 4 | 0 | 0 | 2 | TMEM209_chr7_130159713_130210406 | TMEM209 | MMQGE others(556): Show |
chr7 | 130159713 | 130210406 |
| a0003 | 0/0 | 561 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | MMQGE others(556): Show |
chr7 | 130159713 | 130210406 |
| a0004 | 0/0 | 561 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | MMQGE others(556): Show |
chr7 | 130159713 | 130210406 |
| a0005 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | MMQGE others(556): Show |
chr7 | 130159713 | 130210406 |
| a0006 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | MMQGE others(556): Show |
chr7 | 130159713 | 130210406 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1683 | 218 | 76 | 52 | 54 | 9 | 26 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 | ||
| a0001c0002 | 0/1 | 1683 | 100 | 14 | 15 | 55 | 3 | 12 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 | ||
| a0001c0004 | 0/0 | 1683 | 3 | 0 | 1 | 0 | 0 | 2 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 | ||
| a0001c0007 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 | ||
| a0001c0009 | 0/0 | 1683 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 | ||
| a0002c0003 | 0/0 | 1683 | 7 | 0 | 3 | 4 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 | ||
| a0003c0006 | 0/0 | 1683 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 | ||
| a0004c0005 | 0/0 | 1683 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 | ||
| a0005c0010 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 | ||
| a0006c0008 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | ATGAT others(1678): Show |
chr7 | 130159713 | 130210406 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3455 | 83 | 34 | 27 | 8 | 7 | 6 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3450): Show |
chr7 | 130159713 | 130210406 |
| a0001c0001t0002 | 0/0 | 3456 | 101 | 23 | 18 | 46 | 2 | 12 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3451): Show |
chr7 | 130159713 | 130210406 |
| a0001c0001t0003 | 0/0 | 3454 | 32 | 18 | 6 | 0 | 0 | 8 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3449): Show |
chr7 | 130159713 | 130210406 |
| a0001c0001t0006 | 0/0 | 3456 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3451): Show |
chr7 | 130159713 | 130210406 |
| a0001c0001t0007 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3451): Show |
chr7 | 130159713 | 130210406 |
| a0001c0002t0001 | 0/1 | 3455 | 93 | 10 | 15 | 52 | 3 | 12 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3450): Show |
chr7 | 130159713 | 130210406 |
| a0001c0002t0002 | 0/0 | 3456 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3451): Show |
chr7 | 130159713 | 130210406 |
| a0001c0002t0003 | 0/0 | 3454 | 2 | 1 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3449): Show |
chr7 | 130159713 | 130210406 |
| a0001c0002t0004 | 0/0 | 3456 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3451): Show |
chr7 | 130159713 | 130210406 |
| a0001c0002t0008 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3452): Show |
chr7 | 130159713 | 130210406 |
| a0001c0004t0001 | 0/0 | 3455 | 3 | 0 | 1 | 0 | 0 | 2 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3450): Show |
chr7 | 130159713 | 130210406 |
| a0001c0007t0002 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3451): Show |
chr7 | 130159713 | 130210406 |
| a0001c0009t0002 | 0/0 | 3456 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3451): Show |
chr7 | 130159713 | 130210406 |
| a0002c0003t0003 | 0/0 | 3454 | 7 | 0 | 3 | 4 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3449): Show |
chr7 | 130159713 | 130210406 |
| a0003c0006t0005 | 0/0 | 3455 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3450): Show |
chr7 | 130159713 | 130210406 |
| a0004c0005t0002 | 0/0 | 3456 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3451): Show |
chr7 | 130159713 | 130210406 |
| a0005c0010t0002 | 0/0 | 3456 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3451): Show |
chr7 | 130159713 | 130210406 |
| a0006c0008t0001 | 0/0 | 3455 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | GGCGC others(3450): Show |
chr7 | 130159713 | 130210406 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0002 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0001 | 0/0 | 28 | 1 | 5 | 18 | 0 | 4 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0002t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0007t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0001c0009t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0002c0003t0003g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0002c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0002c0003t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0002c0003t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0003c0006t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0003c0006t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0004c0005t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0004c0005t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0005c0010t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| a0006c0008t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | CHS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00558 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | CHS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | CHS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01070 | hp2 | a0003 | c0006 | t0005 | g0095 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01071 | hp2 | a0003 | c0006 | t0005 | g0096 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0209 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01175 | hp2 | a0001 | c0009 | t0002 | g0221 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01261 | hp2 | a0002 | c0003 | t0003 | g0009 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0008 | EUR | IBS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0184 | EUR | IBS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0087 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01928 | hp2 | a0004 | c0005 | t0002 | g0204 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01934 | hp2 | a0002 | c0003 | t0003 | g0079 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01943 | hp1 | a0001 | c0004 | t0001 | g0118 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02004 | hp1 | a0002 | c0003 | t0003 | g0059 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0173 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02083 | hp2 | a0005 | c0010 | t0002 | g0216 | EAS | KHV | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02293 | hp2 | a0004 | c0005 | t0002 | g0187 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0133 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02895 | hp1 | a0001 | c0002 | t0003 | g0169 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02970 | hp2 | a0001 | c0002 | t0008 | g0088 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0078 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0236 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | STU | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0229 | SAS | PJL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0040 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | STU | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | BEB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0129 | SAS | STU | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | STU | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | YRI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | YRI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18942 | hp1 | a0001 | c0002 | t0003 | g0043 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18957 | hp1 | a0006 | c0008 | t0001 | g0057 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18974 | hp2 | a0002 | c0003 | t0003 | g0055 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18987 | hp1 | a0001 | c0007 | t0002 | g0175 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | LWK | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19058 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | YRI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | YRI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ASW | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ASW | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0054 | EUR | TSI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0034 | EUR | TSI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | TSI | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | GIH | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | GIH | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | USA | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | USA | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | USA | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | USA | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | LWK | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | LWK | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0046 | REF | REF | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0028 | REF | REF | TMEM209_chr7_130159713_130210406 | TMEM209 | chr7 | 130159713 | 130210406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130178510 | A | C | 1 | a0002 | 7 | HG00558.hp2 HG01261.hp2 HG01934.hp2 others(4): Show |
missense_variant | MODERATE | c.1138T>G | p.Leu380Val | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/15 | 1169/3455 | 1138/1686 | 380/561 | chr7 | 130178510 | |||
| chr7:130181712 | T | C | 1 | a0004 | 2 | HG01928.hp2 HG02293.hp2 |
missense_variant | MODERATE | c.1031A>G | p.Asn344Ser | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/15 | 1062/3455 | 1031/1686 | 344/561 | chr7 | 130181712 | |||
| chr7:130184211 | C | T | 1 | a0006 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.996G>A | p.Met332Ile | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/15 | 1027/3455 | 996/1686 | 332/561 | chr7 | 130184211 | |||
| chr7:130192636 | T | C | 1 | a0005 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.761A>G | p.His254Arg | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/15 | 792/3455 | 761/1686 | 254/561 | chr7 | 130192636 | |||
| chr7:130202586 | T | C | 1 | a0003 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.277A>G | p.Thr93Ala | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 4/15 | 308/3455 | 277/1686 | 93/561 | chr7 | 130202586 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130173898 | T | C | 3 | a0001c0002 a0003c0006 a0006c0008 |
102 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(99): Show |
synonymous_variant | LOW | c.1386A>G | p.Leu462Leu | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 12/15 | 1417/3455 | 1386/1686 | 462/561 | chr7 | 130173898 | |||
| chr7:130175515 | A | G | 1 | a0001c0009 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1341T>C | p.Ser447Ser | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 11/15 | 1372/3455 | 1341/1686 | 447/561 | chr7 | 130175515 | |||
| chr7:130181711 | A | G | 1 | a0001c0004 | 3 | HG01943.hp1 HG02602.hp1 HG04228.hp1 |
synonymous_variant | LOW | c.1032T>C | p.Asn344Asn | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/15 | 1063/3455 | 1032/1686 | 344/561 | chr7 | 130181711 | |||
| chr7:130192653 | A | G | 1 | a0001c0007 | 1 | NA18987.hp1 | synonymous_variant | LOW | c.744T>C | p.Ser248Ser | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/15 | 775/3455 | 744/1686 | 248/561 | chr7 | 130192653 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130164721 | T | TA | 2 | a0001c0002t0004 a0001c0002t0008 |
3 | HG01891.hp1 HG02970.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1729dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 15/15 | 1729 | chr7 | 130164721 | ||||||
| chr7:130165395 | G | A | 1 | a0003c0006t0005 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1056C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 15/15 | 1056 | chr7 | 130165395 | ||||||
| chr7:130165699 | T | TA | 9 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(6): Show |
111 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*751dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 15/15 | 751 | chr7 | 130165699 | ||||||
| chr7:130165699 | TA | T | 3 | a0001c0001t0003 a0001c0002t0003 a0002c0003t0003 |
41 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*751delT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 15/15 | 751 | chr7 | 130165699 | ||||||
| chr7:130166034 | C | T | 1 | a0001c0001t0007 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 15/15 | 417 | chr7 | 130166034 | ||||||
| chr7:130166424 | A | G | 1 | a0001c0001t0006 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 15/15 | 27 | chr7 | 130166424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130166513 | G | A | 1 | a0001c0001t0003g0111 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.1632-8C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130166513 | |||||||
| chr7:130166523 | A | T | 26 | a0001c0001t0001g0156 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
31 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1632-18T>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130166523 | |||||||
| chr7:130166576 | A | C | 25 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(22): Show |
32 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1632-71T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130166576 | |||||||
| chr7:130166601 | C | T | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
333 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(330): Show |
intron_variant | MODIFIER | c.1632-96G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130166601 | |||||||
| chr7:130166607 | T | C | 5 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0135 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1632-102A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130166607 | |||||||
| chr7:130166660 | C | T | 1 | a0001c0002t0001g0069 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1632-155G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130166660 | |||||||
| chr7:130167009 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(16): Show |
25 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1632-504C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130167009 | |||||||
| chr7:130167245 | T | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(16): Show |
25 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1632-740A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130167245 | |||||||
| chr7:130167466 | C | T | 5 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0135 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1632-961G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130167466 | |||||||
| chr7:130167541 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1632-1036A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130167541 | |||||||
| chr7:130167778 | A | C | 1 | a0001c0002t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1632-1273T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130167778 | |||||||
| chr7:130167975 | C | G | 1 | a0001c0002t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1632-1470G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130167975 | |||||||
| chr7:130168401 | C | T | 3 | a0001c0001t0002g0200 a0001c0001t0006g0209 a0001c0009t0002g0221 |
3 | HG01106.hp1 HG01175.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1632-1896G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130168401 | |||||||
| chr7:130168471 | C | T | 1 | a0001c0001t0001g0005 | 6 | HG00642.hp2 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1631+1929G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130168471 | |||||||
| chr7:130168714 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1631+1686G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130168714 | |||||||
| chr7:130168719 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(16): Show |
25 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1631+1681G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130168719 | |||||||
| chr7:130168756 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1631+1644T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130168756 | |||||||
| chr7:130168875 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1631+1525T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130168875 | |||||||
| chr7:130168900 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0002g0184 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1631+1500T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130168900 | |||||||
| chr7:130169011 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1631+1389G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169011 | |||||||
| chr7:130169061 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1631+1339T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169061 | |||||||
| chr7:130169065 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(16): Show |
25 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1631+1335G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169065 | |||||||
| chr7:130169078 | A | T | 5 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0135 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1631+1322T>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169078 | |||||||
| chr7:130169095 | C | T | 2 | a0001c0001t0002g0157 a0001c0001t0002g0186 |
2 | NA18950.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1631+1305G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169095 | |||||||
| chr7:130169182 | G | A | 1 | a0001c0002t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1631+1218C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169182 | |||||||
| chr7:130169194 | C | CA | 83 | a0001c0001t0001g0114 a0001c0001t0001g0156 a0001c0001t0001g0179 others(80): Show |
108 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1631+1205dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169194 | |||||||
| chr7:130169379 | T | A | 1 | a0001c0001t0002g0191 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1631+1021A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169379 | |||||||
| chr7:130169385 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1631+1015G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169385 | |||||||
| chr7:130169633 | A | G | 2 | a0001c0002t0001g0018 a0001c0002t0001g0065 |
3 | NA18945.hp2 NA19011.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1631+767T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169633 | |||||||
| chr7:130169662 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1631+738C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169662 | |||||||
| chr7:130169734 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(10): Show |
28 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1631+666G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130169734 | |||||||
| chr7:130170102 | T | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0211 |
2 | NA18980.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1631+298A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130170102 | |||||||
| chr7:130170237 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1631+163A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 14/14 | chr7 | 130170237 | |||||||
| chr7:130170657 | A | G | 1 | a0001c0002t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1558-184T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130170657 | |||||||
| chr7:130170733 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1558-260A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130170733 | |||||||
| chr7:130170794 | G | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0100 others(7): Show |
13 | HG01099.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1558-321C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130170794 | |||||||
| chr7:130170830 | A | AT | 12 | a0001c0001t0001g0207 a0001c0001t0002g0162 a0001c0001t0002g0174 others(9): Show |
12 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1558-358dupA | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130170830 | |||||||
| chr7:130170868 | G | A | 1 | a0001c0002t0001g0083 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1558-395C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130170868 | |||||||
| chr7:130170974 | G | A | 2 | a0001c0001t0003g0020 a0001c0001t0003g0141 |
3 | HG02615.hp1 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1558-501C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130170974 | |||||||
| chr7:130170979 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1558-506G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130170979 | |||||||
| chr7:130171042 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1558-569C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171042 | |||||||
| chr7:130171053 | G | C | 1 | a0001c0001t0003g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1558-580C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171053 | |||||||
| chr7:130171136 | A | G | 5 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0135 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-663T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171136 | |||||||
| chr7:130171164 | T | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
333 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(330): Show |
intron_variant | MODIFIER | c.1558-691A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171164 | |||||||
| chr7:130171296 | A | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(10): Show |
28 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1558-823T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171296 | |||||||
| chr7:130171436 | A | G | 88 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(85): Show |
113 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1558-963T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171436 | |||||||
| chr7:130171464 | AAGAT | A | 25 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(22): Show |
32 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1558-995_1558-992d others(6): Show |
TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171464 | |||||||
| chr7:130171534 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(16): Show |
25 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1558-1061C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171534 | |||||||
| chr7:130171560 | A | C | 2 | a0001c0001t0001g0112 a0001c0001t0003g0111 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1558-1087T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171560 | |||||||
| chr7:130171654 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0003g0111 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1558-1181A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171654 | |||||||
| chr7:130171703 | T | C | 1 | a0001c0001t0002g0190 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1558-1230A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171703 | |||||||
| chr7:130171734 | T | A | 1 | a0001c0002t0001g0049 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1558-1261A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171734 | |||||||
| chr7:130171750 | A | C | 1 | a0001c0002t0001g0049 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1558-1277T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171750 | |||||||
| chr7:130171845 | C | A | 25 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(22): Show |
32 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1558-1372G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171845 | |||||||
| chr7:130171847 | G | A | 25 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(22): Show |
32 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1558-1374C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171847 | |||||||
| chr7:130171961 | A | G | 5 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0135 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-1488T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130171961 | |||||||
| chr7:130172380 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1557+1252G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172380 | |||||||
| chr7:130172424 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1557+1208C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172424 | |||||||
| chr7:130172432 | T | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0140 a0001c0001t0003g0141 |
4 | HG02572.hp1 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1557+1200A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172432 | |||||||
| chr7:130172468 | C | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(10): Show |
28 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1557+1164G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172468 | |||||||
| chr7:130172497 | C | T | 68 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0013 others(65): Show |
102 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.1557+1135G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172497 | |||||||
| chr7:130172538 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1557+1094C>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172538 | |||||||
| chr7:130172719 | C | T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0163 |
2 | HG01943.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1557+913G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172719 | |||||||
| chr7:130172860 | G | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0120 others(13): Show |
22 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1557+772C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172860 | |||||||
| chr7:130172872 | G | T | 1 | a0001c0002t0001g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1557+760C>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172872 | |||||||
| chr7:130172891 | T | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
333 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(330): Show |
intron_variant | MODIFIER | c.1557+741A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172891 | |||||||
| chr7:130172908 | A | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0100 others(7): Show |
13 | HG01099.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1557+724T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172908 | |||||||
| chr7:130172924 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0002g0184 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1557+708C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172924 | |||||||
| chr7:130172998 | C | CA | 104 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0029 others(101): Show |
135 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.1557+633dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172998 | |||||||
| chr7:130172998 | CA | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(47): Show |
75 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1557+633delT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130172998 | |||||||
| chr7:130173062 | T | C | 1 | a0001c0001t0001g0019 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1557+570A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130173062 | |||||||
| chr7:130173293 | G | A | 6 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0171 others(3): Show |
6 | HG00639.hp1 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+339C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130173293 | |||||||
| chr7:130173516 | A | G | 5 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0104 others(2): Show |
5 | HG01943.hp2 HG02280.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557+116T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 13/14 | chr7 | 130173516 | |||||||
| chr7:130174005 | T | C | 4 | a0001c0001t0002g0012 a0001c0001t0002g0026 a0001c0001t0002g0215 others(1): Show |
8 | HG00544.hp1 HG02040.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345-66A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 11/14 | chr7 | 130174005 | |||||||
| chr7:130174811 | A | G | 1 | a0001c0001t0003g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1344+701T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 11/14 | chr7 | 130174811 | |||||||
| chr7:130175217 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1344+295A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 11/14 | chr7 | 130175217 | |||||||
| chr7:130175372 | G | A | 88 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(85): Show |
113 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1344+140C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 11/14 | chr7 | 130175372 | |||||||
| chr7:130176115 | C | CT | 46 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(43): Show |
59 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.1247-507dupA | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176115 | |||||||
| chr7:130176115 | C | CTT | 86 | a0001c0001t0001g0125 a0001c0001t0001g0156 a0001c0001t0001g0177 others(83): Show |
111 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1247-508_1247-507d others(4): Show |
TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176115 | |||||||
| chr7:130176269 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0220 |
4 | HG01934.hp1 NA18945.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1247-660G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176269 | |||||||
| chr7:130176274 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(155): Show |
203 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.1247-665T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176274 | |||||||
| chr7:130176280 | T | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(10): Show |
28 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1247-671A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176280 | |||||||
| chr7:130176358 | T | A | 1 | a0001c0001t0002g0181 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1247-749A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176358 | |||||||
| chr7:130176372 | G | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(155): Show |
203 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.1247-763C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176372 | |||||||
| chr7:130176441 | T | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(10): Show |
28 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1247-832A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176441 | |||||||
| chr7:130176683 | T | C | 2 | a0001c0001t0001g0206 a0001c0001t0002g0205 |
2 | NA18939.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1247-1074A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176683 | |||||||
| chr7:130176759 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1247-1150T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176759 | |||||||
| chr7:130176954 | C | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(14): Show |
23 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1247-1345G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130176954 | |||||||
| chr7:130177013 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1246+1389C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130177013 | |||||||
| chr7:130177025 | T | G | 1 | a0001c0001t0002g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1246+1377A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130177025 | |||||||
| chr7:130177028 | CA | C | 170 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0099 others(167): Show |
235 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.1246+1373delT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130177028 | |||||||
| chr7:130177028 | CAA | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
60 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1246+1372_1246+137 others(6): Show |
TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130177028 | |||||||
| chr7:130177091 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(14): Show |
23 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1246+1311C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130177091 | |||||||
| chr7:130177348 | CA | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(11): Show |
29 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1246+1053delT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130177348 | |||||||
| chr7:130177352 | A | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0121 others(12): Show |
21 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1246+1050T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130177352 | |||||||
| chr7:130177629 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1246+773A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130177629 | |||||||
| chr7:130177664 | G | A | 66 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0013 others(63): Show |
100 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1246+738C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130177664 | |||||||
| chr7:130178075 | A | G | 25 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(22): Show |
32 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1246+327T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 10/14 | chr7 | 130178075 | |||||||
| chr7:130178548 | G | C | 1 | a0001c0002t0001g0066 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1121-21C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130178548 | |||||||
| chr7:130178657 | C | T | 7 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0153 others(4): Show |
9 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1121-130G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130178657 | |||||||
| chr7:130178985 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1121-458T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130178985 | |||||||
| chr7:130179002 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1121-475C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130179002 | |||||||
| chr7:130179304 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1121-777A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130179304 | |||||||
| chr7:130179581 | G | C | 1 | a0001c0001t0002g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1121-1054C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130179581 | |||||||
| chr7:130179856 | T | C | 1 | a0001c0002t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1121-1329A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130179856 | |||||||
| chr7:130179897 | C | T | 25 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(22): Show |
32 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1121-1370G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130179897 | |||||||
| chr7:130179919 | T | C | 1 | a0001c0001t0002g0025 | 2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1121-1392A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130179919 | |||||||
| chr7:130180246 | C | G | 25 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(22): Show |
32 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1120+1377G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130180246 | |||||||
| chr7:130180414 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120+1209G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130180414 | |||||||
| chr7:130180483 | C | T | 1 | a0001c0002t0001g0091 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1120+1140G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130180483 | |||||||
| chr7:130180528 | T | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
333 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(330): Show |
intron_variant | MODIFIER | c.1120+1095A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130180528 | |||||||
| chr7:130180535 | AT | A | 3 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0136 |
3 | HG02257.hp1 HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1120+1087delA | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130180535 | |||||||
| chr7:130180556 | C | T | 68 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0013 others(65): Show |
102 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.1120+1067G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130180556 | |||||||
| chr7:130180599 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0021 others(2): Show |
14 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1120+1024G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130180599 | |||||||
| chr7:130180648 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1120+975G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130180648 | |||||||
| chr7:130180673 | A | C | 1 | a0001c0002t0001g0061 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1120+950T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130180673 | |||||||
| chr7:130181069 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1120+554A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130181069 | |||||||
| chr7:130181287 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0002g0184 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1120+336C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130181287 | |||||||
| chr7:130181330 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1120+293G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130181330 | |||||||
| chr7:130181334 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1120+289A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130181334 | |||||||
| chr7:130181410 | C | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(10): Show |
28 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1120+213G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130181410 | |||||||
| chr7:130181440 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1120+183A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 9/14 | chr7 | 130181440 | |||||||
| chr7:130181777 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1024-58A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130181777 | |||||||
| chr7:130181799 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1024-80G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130181799 | |||||||
| chr7:130181893 | G | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
6 | HG02055.hp2 HG02451.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-174C>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130181893 | |||||||
| chr7:130181909 | T | C | 1 | a0001c0002t0001g0035 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1024-190A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130181909 | |||||||
| chr7:130182002 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1024-283C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130182002 | |||||||
| chr7:130182441 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0002g0205 |
2 | NA18939.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1024-722C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130182441 | |||||||
| chr7:130182489 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1024-770G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130182489 | |||||||
| chr7:130182517 | G | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0231 |
2 | HG01884.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1024-798C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130182517 | |||||||
| chr7:130182600 | T | C | 5 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0135 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-881A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130182600 | |||||||
| chr7:130182634 | G | A | 4 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0136 others(1): Show |
4 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-915C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130182634 | |||||||
| chr7:130182664 | T | C | 1 | a0001c0001t0002g0024 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1024-945A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130182664 | |||||||
| chr7:130182957 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(155): Show |
203 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.1023+1227T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130182957 | |||||||
| chr7:130182990 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(15): Show |
24 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1023+1194G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130182990 | |||||||
| chr7:130183163 | A | G | 7 | a0001c0001t0003g0020 a0001c0001t0003g0137 a0001c0001t0003g0138 others(4): Show |
8 | HG02572.hp1 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+1021T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130183163 | |||||||
| chr7:130183192 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1023+992G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130183192 | |||||||
| chr7:130183317 | T | A | 5 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0135 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+867A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130183317 | |||||||
| chr7:130183349 | A | G | 1 | a0001c0002t0001g0076 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1023+835T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130183349 | |||||||
| chr7:130183507 | C | G | 3 | a0001c0002t0001g0008 a0001c0002t0001g0044 a0001c0002t0001g0045 |
6 | HG00642.hp1 HG01069.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1023+677G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130183507 | |||||||
| chr7:130183755 | A | T | 1 | a0001c0001t0002g0166 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1023+429T>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 8/14 | chr7 | 130183755 | |||||||
| chr7:130184345 | A | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0100 others(7): Show |
13 | HG01099.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.952-90T>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130184345 | |||||||
| chr7:130184494 | CT | C | 224 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(221): Show |
303 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(300): Show |
intron_variant | MODIFIER | c.952-240delA | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130184494 | |||||||
| chr7:130184525 | C | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
333 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(330): Show |
intron_variant | MODIFIER | c.952-270G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130184525 | |||||||
| chr7:130184605 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0100 others(7): Show |
13 | HG01099.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.952-350C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130184605 | |||||||
| chr7:130184641 | C | T | 73 | a0001c0001t0001g0033 a0001c0001t0002g0194 a0001c0001t0003g0060 others(70): Show |
110 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.952-386G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130184641 | |||||||
| chr7:130184734 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.951+458G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130184734 | |||||||
| chr7:130184936 | T | C | 6 | a0001c0002t0001g0022 a0001c0002t0001g0056 a0001c0002t0001g0067 others(3): Show |
7 | HG00741.hp1 HG01256.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+256A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130184936 | |||||||
| chr7:130185004 | A | G | 2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | NA18993.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.951+188T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130185004 | |||||||
| chr7:130185022 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.951+170A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130185022 | |||||||
| chr7:130185190 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG01123.hp2 | splice_donor_variant&intron_variant | HIGH | c.951+2T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 7/14 | chr7 | 130185190 | |||||||
| chr7:130185375 | T | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(17): Show |
26 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
splice_region_variant&intron_variant | LOW | c.776-8A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130185375 | |||||||
| chr7:130185672 | A | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(9): Show |
27 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.776-305T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130185672 | |||||||
| chr7:130185871 | AC | A | 4 | a0001c0002t0001g0089 a0001c0002t0004g0078 a0001c0002t0004g0087 others(1): Show |
4 | HG01891.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.776-505delG | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130185871 | |||||||
| chr7:130186375 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.776-1008C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130186375 | |||||||
| chr7:130186430 | A | C | 90 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(87): Show |
115 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.776-1063T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130186430 | |||||||
| chr7:130186589 | C | T | 3 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0136 |
3 | HG02257.hp1 HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.776-1222G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130186589 | |||||||
| chr7:130186610 | G | A | 1 | a0001c0001t0003g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.776-1243C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130186610 | |||||||
| chr7:130186760 | T | C | 1 | a0001c0002t0001g0068 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.776-1393A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130186760 | |||||||
| chr7:130186803 | A | C | 1 | a0001c0001t0002g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.776-1436T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130186803 | |||||||
| chr7:130186950 | A | G | 1 | a0006c0008t0001g0057 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.776-1583T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130186950 | |||||||
| chr7:130187063 | T | G | 4 | a0001c0002t0001g0089 a0001c0002t0004g0078 a0001c0002t0004g0087 others(1): Show |
4 | HG01891.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.776-1696A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187063 | |||||||
| chr7:130187389 | T | G | 2 | a0001c0001t0002g0171 a0001c0001t0002g0218 |
2 | HG00639.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.776-2022A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187389 | |||||||
| chr7:130187415 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(9): Show |
27 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.776-2048A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187415 | |||||||
| chr7:130187525 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.776-2158A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187525 | |||||||
| chr7:130187638 | T | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0105 others(9): Show |
16 | HG01496.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.776-2271A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187638 | |||||||
| chr7:130187651 | T | TA | 7 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0100 others(4): Show |
10 | HG01099.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.776-2285dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187651 | |||||||
| chr7:130187651 | TA | T | 6 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0001t0002g0145 others(3): Show |
6 | HG01069.hp1 HG01433.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-2285delT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187651 | |||||||
| chr7:130187852 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.776-2485C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187852 | |||||||
| chr7:130187915 | C | T | 72 | a0001c0001t0001g0033 a0001c0001t0003g0060 a0001c0002t0001g0001 others(69): Show |
109 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.776-2548G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187915 | |||||||
| chr7:130187939 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(15): Show |
24 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.776-2572G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187939 | |||||||
| chr7:130187953 | T | A | 3 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0136 |
3 | HG02257.hp1 HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.776-2586A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130187953 | |||||||
| chr7:130188193 | C | T | 2 | a0001c0002t0001g0090 a0001c0002t0001g0091 |
2 | NA18971.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.776-2826G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188193 | |||||||
| chr7:130188323 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.776-2956C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188323 | |||||||
| chr7:130188363 | A | G | 1 | a0001c0002t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.776-2996T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188363 | |||||||
| chr7:130188371 | C | T | 1 | a0001c0001t0003g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.776-3004G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188371 | |||||||
| chr7:130188391 | T | G | 1 | a0001c0002t0001g0069 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.776-3024A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188391 | |||||||
| chr7:130188406 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0003g0111 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.776-3039G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188406 | |||||||
| chr7:130188412 | T | C | 2 | a0001c0002t0001g0053 a0001c0002t0001g0054 |
2 | HG01167.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.776-3045A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188412 | |||||||
| chr7:130188424 | G | A | 1 | a0001c0002t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.776-3057C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188424 | |||||||
| chr7:130188428 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.776-3061G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188428 | |||||||
| chr7:130188453 | A | G | 1 | a0001c0001t0003g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.776-3086T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188453 | |||||||
| chr7:130188458 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0112 a0001c0001t0001g0116 others(3): Show |
8 | HG02258.hp1 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.776-3091A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188458 | |||||||
| chr7:130188465 | A | G | 68 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0002g0153 others(65): Show |
106 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.776-3098T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188465 | |||||||
| chr7:130188470 | C | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.776-3103G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188470 | |||||||
| chr7:130188499 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.776-3132T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188499 | |||||||
| chr7:130188570 | G | T | 61 | a0001c0001t0001g0033 a0001c0001t0003g0060 a0001c0002t0001g0001 others(58): Show |
98 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.776-3203C>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188570 | |||||||
| chr7:130188574 | T | C | 61 | a0001c0001t0001g0033 a0001c0001t0003g0060 a0001c0002t0001g0001 others(58): Show |
98 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.776-3207A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188574 | |||||||
| chr7:130188595 | C | CA | 29 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0103 others(26): Show |
31 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.776-3229dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188595 | |||||||
| chr7:130188595 | CA | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(13): Show |
31 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.776-3229delT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188595 | |||||||
| chr7:130188595 | CAAAAAAA | C | 6 | a0001c0001t0001g0128 a0001c0001t0002g0176 a0001c0002t0001g0049 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.776-3235_776-3229d others(9): Show |
TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188595 | |||||||
| chr7:130188595 | CAAAAAAA others(1): Show |
C | 70 | a0001c0001t0001g0033 a0001c0001t0001g0143 a0001c0001t0003g0060 others(67): Show |
107 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.776-3236_776-3229d others(10): Show |
TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188595 | |||||||
| chr7:130188620 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0116 |
4 | HG02258.hp1 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.776-3253T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188620 | |||||||
| chr7:130188651 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.776-3284A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188651 | |||||||
| chr7:130188771 | A | G | 22 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
29 | HG01099.hp1 HG01496.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.776-3404T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188771 | |||||||
| chr7:130188788 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.776-3421G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188788 | |||||||
| chr7:130188820 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.776-3453G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188820 | |||||||
| chr7:130188882 | A | G | 1 | a0001c0002t0001g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.776-3515T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188882 | |||||||
| chr7:130188965 | T | C | 1 | a0001c0001t0002g0213 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.776-3598A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188965 | |||||||
| chr7:130188995 | C | G | 90 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(87): Show |
115 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.775+3627G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130188995 | |||||||
| chr7:130189177 | A | G | 2 | a0001c0002t0001g0053 a0001c0002t0001g0054 |
2 | HG01167.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.775+3445T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130189177 | |||||||
| chr7:130189219 | C | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(15): Show |
24 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.775+3403G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130189219 | |||||||
| chr7:130189443 | T | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(17): Show |
26 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.775+3179A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130189443 | |||||||
| chr7:130189576 | C | T | 73 | a0001c0001t0001g0033 a0001c0001t0002g0189 a0001c0001t0003g0060 others(70): Show |
110 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.775+3046G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130189576 | |||||||
| chr7:130189732 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.775+2890G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130189732 | |||||||
| chr7:130190000 | G | A | 3 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0136 |
3 | HG02257.hp1 HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.775+2622C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130190000 | |||||||
| chr7:130190035 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(9): Show |
27 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.775+2587A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130190035 | |||||||
| chr7:130190199 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(17): Show |
26 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.775+2423G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130190199 | |||||||
| chr7:130190232 | A | G | 1 | a0001c0002t0001g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.775+2390T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130190232 | |||||||
| chr7:130190517 | T | G | 1 | a0001c0001t0002g0025 | 2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.775+2105A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130190517 | |||||||
| chr7:130190574 | T | TA | 21 | a0001c0001t0001g0014 a0001c0001t0001g0108 a0001c0001t0001g0109 others(18): Show |
27 | HG00639.hp2 HG00735.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.775+2047dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130190574 | |||||||
| chr7:130191081 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.775+1541A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130191081 | |||||||
| chr7:130191243 | A | G | 90 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(87): Show |
115 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.775+1379T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130191243 | |||||||
| chr7:130191510 | A | G | 1 | a0001c0002t0001g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.775+1112T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130191510 | |||||||
| chr7:130191569 | A | C | 3 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0136 |
3 | HG02257.hp1 HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.775+1053T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130191569 | |||||||
| chr7:130191887 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0147 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.775+735A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130191887 | |||||||
| chr7:130191910 | T | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(39): Show |
55 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.775+712A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130191910 | |||||||
| chr7:130191942 | A | G | 1 | a0001c0001t0003g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.775+680T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130191942 | |||||||
| chr7:130192389 | C | G | 4 | a0001c0001t0003g0110 a0001c0001t0003g0134 a0001c0001t0003g0135 others(1): Show |
4 | HG02257.hp1 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+233G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130192389 | |||||||
| chr7:130192480 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.775+142A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130192480 | |||||||
| chr7:130192537 | G | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(17): Show |
26 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.775+85C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130192537 | |||||||
| chr7:130192544 | T | C | 1 | a0001c0002t0001g0070 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.775+78A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130192544 | |||||||
| chr7:130192546 | T | G | 3 | a0001c0001t0003g0020 a0001c0001t0003g0140 a0001c0001t0003g0141 |
4 | HG02572.hp1 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+76A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130192546 | |||||||
| chr7:130192570 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.775+52T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 6/14 | chr7 | 130192570 | |||||||
| chr7:130193020 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.574-197T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193020 | |||||||
| chr7:130193322 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.574-499C>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193322 | |||||||
| chr7:130193435 | G | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(42): Show |
58 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.574-612C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193435 | |||||||
| chr7:130193475 | G | T | 1 | a0001c0001t0002g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.574-652C>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193475 | |||||||
| chr7:130193667 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.574-844A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193667 | |||||||
| chr7:130193745 | A | T | 1 | a0001c0002t0001g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.574-922T>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193745 | |||||||
| chr7:130193972 | G | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(9): Show |
27 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.574-1149C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193972 | |||||||
| chr7:130193975 | A | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(15): Show |
24 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.574-1152T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193975 | |||||||
| chr7:130193981 | G | A | 1 | a0001c0002t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.574-1158C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193981 | |||||||
| chr7:130193994 | C | T | 1 | a0001c0001t0003g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.574-1171G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130193994 | |||||||
| chr7:130194147 | C | G | 13 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0027 others(10): Show |
16 | HG00639.hp2 HG00735.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.574-1324G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194147 | |||||||
| chr7:130194198 | C | CA | 7 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(4): Show |
7 | HG00639.hp2 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-1376dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194198 | |||||||
| chr7:130194217 | T | C | 11 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0232 others(8): Show |
13 | HG00639.hp2 HG00735.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.574-1394A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194217 | |||||||
| chr7:130194338 | C | CA | 21 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0002g0239 others(18): Show |
24 | HG00639.hp2 HG00735.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.574-1516dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194338 | |||||||
| chr7:130194384 | G | A | 1 | a0001c0002t0001g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.574-1561C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194384 | |||||||
| chr7:130194437 | C | A | 1 | a0001c0002t0001g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.574-1614G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194437 | |||||||
| chr7:130194444 | C | G | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.574-1621G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194444 | |||||||
| chr7:130194633 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(9): Show |
27 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.574-1810G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194633 | |||||||
| chr7:130194776 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0003g0111 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.574-1953C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194776 | |||||||
| chr7:130194859 | G | A | 2 | a0001c0002t0001g0073 a0001c0002t0001g0085 |
2 | NA18982.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.574-2036C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194859 | |||||||
| chr7:130194934 | C | A | 2 | a0001c0001t0001g0156 a0001c0001t0002g0184 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.574-2111G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194934 | |||||||
| chr7:130194988 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0100 others(7): Show |
13 | HG01099.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.574-2165A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130194988 | |||||||
| chr7:130195562 | A | G | 3 | a0001c0001t0003g0020 a0001c0001t0003g0140 a0001c0001t0003g0141 |
4 | HG02572.hp1 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-2739T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130195562 | |||||||
| chr7:130195631 | GA | G | 100 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0015 others(97): Show |
148 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.574-2809delT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130195631 | |||||||
| chr7:130195631 | GAA | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0106 others(4): Show |
9 | HG01496.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-2810_574-2809d others(4): Show |
TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130195631 | |||||||
| chr7:130195695 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.574-2872A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130195695 | |||||||
| chr7:130195782 | G | A | 4 | a0001c0001t0003g0137 a0001c0001t0003g0138 a0001c0001t0003g0139 others(1): Show |
4 | HG02965.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-2959C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130195782 | |||||||
| chr7:130195784 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.574-2961T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130195784 | |||||||
| chr7:130195950 | T | C | 1 | a0001c0002t0001g0074 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.574-3127A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130195950 | |||||||
| chr7:130196326 | CT | C | 74 | a0001c0001t0001g0033 a0001c0001t0002g0159 a0001c0001t0002g0239 others(71): Show |
114 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.574-3504delA | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130196326 | |||||||
| chr7:130196339 | T | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(17): Show |
26 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.574-3516A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130196339 | |||||||
| chr7:130196400 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0132 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.574-3577A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130196400 | |||||||
| chr7:130196702 | A | G | 2 | a0001c0001t0002g0239 a0001c0001t0003g0232 |
2 | HG01192.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.574-3879T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130196702 | |||||||
| chr7:130196870 | C | T | 72 | a0001c0001t0001g0033 a0001c0001t0003g0060 a0001c0002t0001g0001 others(69): Show |
109 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.574-4047G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130196870 | |||||||
| chr7:130197060 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0120 others(14): Show |
23 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-4237G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130197060 | |||||||
| chr7:130197200 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.574-4377A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130197200 | |||||||
| chr7:130197351 | C | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(152): Show |
197 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.573+4499G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130197351 | |||||||
| chr7:130197647 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.573+4203G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130197647 | |||||||
| chr7:130197677 | C | T | 1 | a0001c0002t0001g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.573+4173G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130197677 | |||||||
| chr7:130197703 | G | C | 1 | a0001c0002t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.573+4147C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130197703 | |||||||
| chr7:130197743 | T | G | 1 | a0001c0001t0002g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.573+4107A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130197743 | |||||||
| chr7:130197758 | T | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0026 a0001c0001t0002g0215 others(1): Show |
8 | HG00544.hp1 HG02040.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+4092A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130197758 | |||||||
| chr7:130198038 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.573+3812G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130198038 | |||||||
| chr7:130198336 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(9): Show |
27 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.573+3514G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130198336 | |||||||
| chr7:130198373 | G | A | 1 | a0001c0002t0001g0092 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.573+3477C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130198373 | |||||||
| chr7:130198440 | G | A | 20 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(17): Show |
24 | HG00639.hp2 HG00735.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.573+3410C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130198440 | |||||||
| chr7:130198521 | G | A | 13 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0027 others(10): Show |
16 | HG00639.hp2 HG00735.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.573+3329C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130198521 | |||||||
| chr7:130198560 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573+3290C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130198560 | |||||||
| chr7:130198585 | T | C | 1 | a0001c0002t0001g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.573+3265A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130198585 | |||||||
| chr7:130198806 | G | A | 47 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(44): Show |
60 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.573+3044C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130198806 | |||||||
| chr7:130199258 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.573+2592C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199258 | |||||||
| chr7:130199287 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.573+2563C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199287 | |||||||
| chr7:130199320 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0003g0111 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.573+2530G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199320 | |||||||
| chr7:130199342 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0003g0111 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.573+2508G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199342 | |||||||
| chr7:130199462 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.573+2388G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199462 | |||||||
| chr7:130199512 | GC | G | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0186 |
3 | NA18950.hp2 NA18985.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.573+2337delG | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199512 | |||||||
| chr7:130199519 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0002t0001g0045 |
3 | HG00642.hp1 HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.573+2331G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199519 | |||||||
| chr7:130199520 | G | A | 3 | a0001c0002t0001g0036 a0001c0002t0001g0037 a0001c0002t0003g0043 |
3 | HG02886.hp2 NA18942.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.573+2330C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199520 | |||||||
| chr7:130199606 | C | T | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
333 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(330): Show |
intron_variant | MODIFIER | c.573+2244G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199606 | |||||||
| chr7:130199811 | G | C | 1 | a0001c0002t0001g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.573+2039C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199811 | |||||||
| chr7:130199864 | T | C | 3 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0136 |
3 | HG02257.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.573+1986A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199864 | |||||||
| chr7:130199906 | C | T | 5 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(2): Show |
5 | HG03831.hp1 NA18942.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+1944G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199906 | |||||||
| chr7:130199912 | A | G | 4 | a0001c0001t0003g0137 a0001c0001t0003g0138 a0001c0001t0003g0139 others(1): Show |
4 | HG02965.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+1938T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130199912 | |||||||
| chr7:130200045 | GA | G | 3 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0136 |
3 | HG02257.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.573+1804delT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200045 | |||||||
| chr7:130200046 | A | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(61): Show |
81 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.573+1804T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200046 | |||||||
| chr7:130200151 | C | A | 48 | a0001c0001t0001g0199 a0001c0001t0001g0206 a0001c0001t0001g0207 others(45): Show |
64 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.573+1699G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200151 | |||||||
| chr7:130200153 | A | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
225 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(222): Show |
intron_variant | MODIFIER | c.573+1697T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200153 | |||||||
| chr7:130200155 | A | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(55): Show |
70 | HG00738.hp1 HG01069.hp2 HG01081.hp2 others(67): Show |
intron_variant | MODIFIER | c.573+1695T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200155 | |||||||
| chr7:130200157 | A | C | 22 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0099 others(19): Show |
27 | HG01099.hp1 HG01496.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.573+1693T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200157 | |||||||
| chr7:130200263 | A | T | 20 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(17): Show |
24 | HG00639.hp2 HG00735.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.573+1587T>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200263 | |||||||
| chr7:130200361 | T | A | 87 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(84): Show |
112 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.573+1489A>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200361 | |||||||
| chr7:130200433 | G | A | 4 | a0001c0001t0001g0130 a0001c0004t0001g0118 a0001c0004t0001g0129 others(1): Show |
4 | HG01346.hp1 HG01943.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+1417C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200433 | |||||||
| chr7:130200445 | C | A | 65 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(62): Show |
88 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.573+1405G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200445 | |||||||
| chr7:130200556 | A | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.573+1294T>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200556 | |||||||
| chr7:130200732 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.573+1118G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200732 | |||||||
| chr7:130200754 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.573+1096T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200754 | |||||||
| chr7:130200908 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.573+942G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130200908 | |||||||
| chr7:130201054 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.573+796T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201054 | |||||||
| chr7:130201083 | T | C | 73 | a0001c0001t0001g0033 a0001c0001t0002g0047 a0001c0001t0003g0060 others(70): Show |
110 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.573+767A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201083 | |||||||
| chr7:130201088 | C | CA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
16 | HG01099.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.573+761dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201088 | |||||||
| chr7:130201088 | CA | C | 24 | a0001c0001t0001g0105 a0001c0001t0001g0131 a0001c0001t0001g0132 others(21): Show |
25 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.573+761delT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201088 | |||||||
| chr7:130201088 | CAA | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
165 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.573+760_573+761del others(2): Show |
TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201088 | |||||||
| chr7:130201088 | CAAA | C | 72 | a0001c0001t0001g0033 a0001c0001t0001g0156 a0001c0001t0002g0047 others(69): Show |
110 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.573+759_573+761del others(3): Show |
TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201088 | |||||||
| chr7:130201112 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.573+738T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201112 | |||||||
| chr7:130201217 | G | T | 1 | a0001c0001t0002g0152 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.573+633C>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201217 | |||||||
| chr7:130201249 | C | A | 3 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0136 |
3 | HG02257.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.573+601G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201249 | |||||||
| chr7:130201250 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0242 |
3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.573+600C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201250 | |||||||
| chr7:130201393 | A | G | 1 | a0001c0001t0003g0027 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.573+457T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201393 | |||||||
| chr7:130201459 | C | T | 1 | a0001c0002t0001g0038 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.573+391G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201459 | |||||||
| chr7:130201649 | T | C | 3 | a0001c0001t0003g0020 a0001c0001t0003g0140 a0001c0001t0003g0141 |
4 | HG02572.hp1 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+201A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201649 | |||||||
| chr7:130201689 | T | C | 1 | a0001c0002t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.573+161A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 5/14 | chr7 | 130201689 | |||||||
| chr7:130202099 | G | GA | 20 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0119 others(17): Show |
26 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.332-9dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 4/14 | chr7 | 130202099 | |||||||
| chr7:130202178 | T | C | 1 | a0001c0001t0003g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.332-87A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 4/14 | chr7 | 130202178 | |||||||
| chr7:130202301 | AAGTT | A | 3 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0136 |
3 | HG02257.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.332-214_332-211del others(4): Show |
TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 4/14 | chr7 | 130202301 | |||||||
| chr7:130202367 | A | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.331+165T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 4/14 | chr7 | 130202367 | |||||||
| chr7:130202389 | T | C | 20 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0020 others(17): Show |
24 | HG00639.hp2 HG00735.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.331+143A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 4/14 | chr7 | 130202389 | |||||||
| chr7:130202430 | G | T | 2 | a0001c0002t0001g0036 a0001c0002t0001g0037 |
2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.331+102C>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 4/14 | chr7 | 130202430 | |||||||
| chr7:130202480 | A | G | 1 | a0001c0001t0003g0027 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.331+52T>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 4/14 | chr7 | 130202480 | |||||||
| chr7:130202694 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.200-31C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 3/14 | chr7 | 130202694 | |||||||
| chr7:130202783 | T | C | 1 | a0001c0002t0002g0097 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.200-120A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 3/14 | chr7 | 130202783 | |||||||
| chr7:130202911 | A | C | 4 | a0001c0001t0001g0033 a0001c0002t0001g0032 a0001c0002t0001g0034 others(1): Show |
4 | HG01978.hp2 HG03927.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-248T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 3/14 | chr7 | 130202911 | |||||||
| chr7:130202913 | A | AC | 9 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
12 | HG01099.hp1 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.200-251dupG | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 3/14 | chr7 | 130202913 | |||||||
| chr7:130203010 | A | C | 87 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(84): Show |
112 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.200-347T>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 3/14 | chr7 | 130203010 | |||||||
| chr7:130203031 | G | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(9): Show |
27 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.200-368C>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 3/14 | chr7 | 130203031 | |||||||
| chr7:130203072 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.200-409C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 3/14 | chr7 | 130203072 | |||||||
| chr7:130203562 | C | G | 73 | a0001c0001t0001g0033 a0001c0001t0002g0047 a0001c0001t0003g0060 others(70): Show |
110 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.199+226G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 3/14 | chr7 | 130203562 | |||||||
| chr7:130203849 | G | GA | 87 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(84): Show |
112 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(109): Show |
splice_region_variant&intron_variant | LOW | c.141-4dupT | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 2/14 | chr7 | 130203849 | |||||||
| chr7:130203875 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.141-29A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 2/14 | chr7 | 130203875 | |||||||
| chr7:130203954 | T | G | 1 | a0001c0002t0001g0022 | 2 | NA18949.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.140+20A>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 2/14 | chr7 | 130203954 | |||||||
| chr7:130204389 | T | C | 87 | a0001c0001t0001g0156 a0001c0001t0001g0177 a0001c0001t0001g0179 others(84): Show |
112 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.4-279A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 1/14 | chr7 | 130204389 | |||||||
| chr7:130204763 | C | G | 1 | a0001c0001t0002g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3+610G>C | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 1/14 | chr7 | 130204763 | |||||||
| chr7:130204770 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3+603G>A | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 1/14 | chr7 | 130204770 | |||||||
| chr7:130204875 | C | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
333 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(330): Show |
intron_variant | MODIFIER | c.3+498G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 1/14 | chr7 | 130204875 | |||||||
| chr7:130204926 | T | C | 1 | a0001c0002t0001g0229 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3+447A>G | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 1/14 | chr7 | 130204926 | |||||||
| chr7:130205014 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3+359C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 1/14 | chr7 | 130205014 | |||||||
| chr7:130205252 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3+121C>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 1/14 | chr7 | 130205252 | |||||||
| chr7:130205362 | C | A | 13 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0027 others(10): Show |
16 | HG00639.hp2 HG00735.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.3+11G>T | TMEM209 | ENSG00000146842.17 | transcript | ENST00000397622.7 | protein_coding | 1/14 | chr7 | 130205362 |