Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1384 |
| ensemblid | ENSG00000095321.18 |
| hgncid | 2342 |
| symbol | CRAT |
| name | carnitine O-acetyltransferase |
| refseq_nuc | NM_000755.5 |
| refseq_prot | NP_000746.3 |
| ensembl_nuc | ENST00000318080.7 |
| ensembl_prot | ENSP00000315013.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 129094794 |
| end | 129110793 |
| strand | - |
| ver | v1.2 |
| region | chr9:129094794-129110793 |
| region5000 | chr9:129089794-129115793 |
| regionname0 | CRAT_chr9_129094794_129110793 |
| regionname5000 | CRAT_chr9_129089794_129115793 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 626 | 386 | 98 | 59 | 174 | 16 | 38 | 131 | CRAT_chr9_129089794_129115793 | CRAT | MLAFA others(621): Show |
chr9 | 129089794 | 129115793 |
| a0002 | 0/0 | 626 | 23 | 0 | 9 | 12 | 0 | 2 | 7 | CRAT_chr9_129089794_129115793 | CRAT | MLAFA others(621): Show |
chr9 | 129089794 | 129115793 |
| a0003 | 0/0 | 626 | 4 | 0 | 0 | 1 | 0 | 3 | 1 | CRAT_chr9_129089794_129115793 | CRAT | MLAFA others(621): Show |
chr9 | 129089794 | 129115793 |
| a0004 | 1/0 | 626 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | MLAFA others(621): Show |
chr9 | 129089794 | 129115793 |
| a0005 | 0/0 | 626 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | MLAFA others(621): Show |
chr9 | 129089794 | 129115793 |
| a0006 | 0/0 | 626 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | MLAFA others(621): Show |
chr9 | 129089794 | 129115793 |
| a0007 | 0/0 | 626 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | MLAFA others(621): Show |
chr9 | 129089794 | 129115793 |
| a0008 | 0/0 | 626 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | MLAFA others(621): Show |
chr9 | 129089794 | 129115793 |
| a0009 | 0/0 | 631 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | MLAFA others(626): Show |
chr9 | 129089794 | 129115793 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1878 | 279 | 31 | 52 | 144 | 16 | 35 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0001c0002 | 0/0 | 1878 | 73 | 37 | 6 | 28 | 0 | 2 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0001c0004 | 0/0 | 1878 | 16 | 15 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0001c0005 | 0/0 | 1878 | 14 | 14 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0001c0007 | 0/0 | 1878 | 2 | 0 | 0 | 2 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0001c0010 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0001c0015 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0002c0003 | 0/0 | 1878 | 23 | 0 | 9 | 12 | 0 | 2 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0003c0006 | 0/0 | 1878 | 3 | 0 | 0 | 0 | 0 | 3 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0003c0016 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0004c0008 | 1/0 | 1878 | 2 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0005c0009 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0006c0011 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0007c0014 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0008c0013 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1873): Show |
chr9 | 129089794 | 129115793 | ||
| a0009c0012 | 0/0 | 1893 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | ATGTT others(1888): Show |
chr9 | 129089794 | 129115793 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2768 | 190 | 13 | 38 | 108 | 10 | 21 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0001c0001t0002 | 0/1 | 2762 | 81 | 11 | 14 | 35 | 6 | 14 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0001c0001t0004 | 0/0 | 2768 | 3 | 3 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0001c0001t0005 | 0/0 | 2762 | 2 | 2 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0001c0001t0007 | 0/0 | 2762 | 2 | 1 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0001c0001t0012 | 0/0 | 2768 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0001c0002t0002 | 0/0 | 2762 | 70 | 36 | 6 | 26 | 0 | 2 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0001c0002t0004 | 0/0 | 2768 | 2 | 1 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0001c0002t0010 | 0/0 | 2762 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0001c0004t0003 | 0/0 | 2768 | 16 | 15 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0001c0005t0001 | 0/0 | 2768 | 14 | 14 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0001c0007t0006 | 0/0 | 2762 | 2 | 0 | 0 | 2 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0001c0010t0002 | 0/0 | 2762 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0001c0015t0004 | 0/0 | 2768 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0002c0003t0002 | 0/0 | 2762 | 22 | 0 | 8 | 12 | 0 | 2 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0002c0003t0009 | 0/0 | 2762 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0003c0006t0001 | 0/0 | 2768 | 3 | 0 | 0 | 0 | 0 | 3 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0003c0016t0001 | 0/0 | 2768 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0004c0008t0008 | 1/0 | 2768 | 2 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GTCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0005c0009t0011 | 0/0 | 2768 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0006c0011t0001 | 0/0 | 2768 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0007c0014t0002 | 0/0 | 2762 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2757): Show |
chr9 | 129089794 | 129115793 |
| a0008c0013t0001 | 0/0 | 2768 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2763): Show |
chr9 | 129089794 | 129115793 |
| a0009c0012t0001 | 0/0 | 2783 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | GCCCC others(2778): Show |
chr9 | 129089794 | 129115793 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 57 | 3 | 15 | 27 | 4 | 8 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0002 | 0/0 | 38 | 0 | 0 | 37 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0005 | 0/0 | 18 | 4 | 7 | 3 | 1 | 3 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0012 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0018 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0003 | 0/0 | 35 | 4 | 4 | 20 | 1 | 6 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0008 | 0/0 | 8 | 0 | 5 | 0 | 3 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0016 | 0/0 | 5 | 1 | 2 | 1 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0004 | 0/0 | 24 | 0 | 2 | 20 | 0 | 2 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0007 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0009 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0010 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0002t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0004t0003g0015 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0004t0003g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0004t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0004t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0004t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0004t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0004t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0005t0001g0006 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0007t0006g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0010t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0001c0015t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0002c0003t0002g0011 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0002c0003t0002g0013 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0002c0003t0002g0014 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0002c0003t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0002c0003t0009g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0003c0006t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0003c0016t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0004c0008t0008g0039 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0005c0009t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0006c0011t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0007c0014t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0008c0013t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| a0009c0012t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | GBR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01081 | hp1 | a0002 | c0003 | t0002 | g0011 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01099 | hp1 | a0002 | c0003 | t0002 | g0084 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0070 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01167 | hp1 | a0001 | c0004 | t0003 | g0020 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01255 | hp2 | a0002 | c0003 | t0002 | g0081 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01257 | hp2 | a0002 | c0003 | t0002 | g0014 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01884 | hp1 | a0001 | c0004 | t0003 | g0021 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01943 | hp1 | a0002 | c0003 | t0002 | g0011 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01952 | hp1 | a0002 | c0003 | t0002 | g0011 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02055 | hp1 | a0001 | c0005 | t0001 | g0125 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0085 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02074 | hp2 | a0002 | c0003 | t0002 | g0013 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CDX | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02165 | hp2 | a0002 | c0003 | t0002 | g0014 | EAS | CDX | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02273 | hp2 | a0002 | c0003 | t0009 | g0083 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0071 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02293 | hp2 | a0002 | c0003 | t0002 | g0011 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02451 | hp1 | a0001 | c0004 | t0003 | g0021 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02523 | hp1 | a0002 | c0003 | t0002 | g0014 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02523 | hp2 | a0002 | c0003 | t0002 | g0059 | EAS | KHV | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02602 | hp1 | a0003 | c0006 | t0001 | g0019 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02615 | hp1 | a0001 | c0004 | t0003 | g0147 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02622 | hp1 | a0005 | c0009 | t0011 | g0092 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0153 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0127 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0126 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02886 | hp1 | a0001 | c0004 | t0003 | g0146 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0078 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02896 | hp2 | a0001 | c0004 | t0003 | g0015 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02897 | hp2 | a0001 | c0004 | t0003 | g0015 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02970 | hp1 | a0001 | c0004 | t0003 | g0015 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03017 | hp2 | a0006 | c0011 | t0001 | g0105 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03041 | hp2 | a0001 | c0004 | t0003 | g0144 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0094 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0074 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03209 | hp2 | a0001 | c0004 | t0003 | g0020 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03453 | hp2 | a0001 | c0004 | t0003 | g0020 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03490 | hp2 | a0003 | c0006 | t0001 | g0019 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03540 | hp2 | a0001 | c0004 | t0003 | g0015 | AFR | GWD | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03831 | hp2 | a0002 | c0003 | t0002 | g0013 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03927 | hp1 | a0002 | c0003 | t0002 | g0013 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03927 | hp2 | a0003 | c0006 | t0001 | g0019 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03942 | hp1 | a0007 | c0014 | t0002 | g0082 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04115 | hp2 | a0008 | c0013 | t0001 | g0106 | SAS | STU | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04184 | hp1 | a0001 | c0010 | t0002 | g0054 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | BEB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | YRI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | YRI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18612 | hp1 | a0002 | c0003 | t0002 | g0011 | EAS | CHB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | YRI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | YRI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18949 | hp1 | a0001 | c0007 | t0006 | g0029 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18970 | hp2 | a0003 | c0016 | t0001 | g0112 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18980 | hp2 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0014 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18987 | hp2 | a0002 | c0003 | t0002 | g0013 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18988 | hp1 | a0009 | c0012 | t0001 | g0104 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18992 | hp1 | a0001 | c0002 | t0004 | g0149 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18999 | hp1 | a0002 | c0003 | t0002 | g0014 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19005 | hp1 | a0002 | c0003 | t0002 | g0013 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19030 | hp1 | a0001 | c0004 | t0003 | g0145 | AFR | LWK | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | LWK | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | LWK | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | LWK | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19055 | hp1 | a0002 | c0003 | t0002 | g0014 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19056 | hp1 | a0001 | c0007 | t0006 | g0029 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19067 | hp2 | a0002 | c0003 | t0002 | g0013 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19089 | hp2 | a0001 | c0002 | t0010 | g0090 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | YRI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | ASW | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | TSI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | GIH | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG01123 | hp2 | a0002 | c0003 | t0002 | g0011 | AMR | CLM | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02109 | hp2 | a0001 | c0004 | t0003 | g0021 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02486 | hp1 | a0001 | c0015 | t0004 | g0143 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02486 | hp2 | a0004 | c0008 | t0008 | g0039 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | MSL | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG06807 | hp1 | a0001 | c0004 | t0003 | g0015 | AFR | USA | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| HG06807 | hp2 | a0001 | c0004 | t0003 | g0015 | AFR | USA | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | USA | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | USA | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0075 | AFR | LWK | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0066 | REF | REF | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| homoSapiens | grch38p0 | a0004 | c0008 | t0008 | g0039 | REF | REF | CRAT_chr9_129089794_129115793 | CRAT | chr9 | 129089794 | 129115793 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:129095408 | C | G | 2 | a0002 a0007 |
24 | HG01081.hp1 HG01099.hp1 HG01123.hp2 others(21): Show |
missense_variant | MODERATE | c.1870G>C | p.Ala624Pro | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 14/14 | 2154/2768 | 1870/1881 | 624/626 | chr9 | 129095408 | |||
| chr9:129095434 | C | A | 1 | a0008 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1844G>T | p.Arg615Leu | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 14/14 | 2128/2768 | 1844/1881 | 615/626 | chr9 | 129095434 | |||
| chr9:129097250 | C | CCGGTCGG others(8): Show |
1 | a0009 | 1 | NA18988.hp1 | disruptive_inframe_insertion&splice_region_variant | MODERATE | c.1512_1526dupAGGCTA others(9): Show |
p.Arg509_Ala510insGl others(13): Show |
CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 12/14 | 1810/2768 | 1526/1881 | 509/626 | chr9 | 129097250 | |||
| chr9:129098295 | T | G | 1 | a0007 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.1282A>C | p.Ser428Arg | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 10/14 | 1566/2768 | 1282/1881 | 428/626 | chr9 | 129098295 | |||
| chr9:129098622 | G | T | 8 | a0001 a0002 a0003 others(5): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
missense_variant | MODERATE | c.1114C>A | p.Leu372Met | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 9/14 | 1398/2768 | 1114/1881 | 372/626 | chr9 | 129098622 | |||
| chr9:129099915 | C | T | 1 | a0006 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1036G>A | p.Ala346Thr | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/14 | 1320/2768 | 1036/1881 | 346/626 | chr9 | 129099915 | |||
| chr9:129100624 | T | C | 1 | a0003 | 4 | HG02602.hp1 HG03490.hp2 HG03927.hp2 others(1): Show |
missense_variant | MODERATE | c.871A>G | p.Thr291Ala | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/14 | 1155/2768 | 871/1881 | 291/626 | chr9 | 129100624 | |||
| chr9:129108040 | A | G | 1 | a0005 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.65T>C | p.Met22Thr | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/14 | 349/2768 | 65/1881 | 22/626 | chr9 | 129108040 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:129095481 | G | A | 1 | a0001c0007 | 2 | NA18949.hp1 NA19056.hp1 |
synonymous_variant | LOW | c.1797C>T | p.Asn599Asn | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 14/14 | 2081/2768 | 1797/1881 | 599/626 | chr9 | 129095481 | |||
| chr9:129098025 | G | A | 1 | a0001c0007 | 2 | NA18949.hp1 NA19056.hp1 |
synonymous_variant | LOW | c.1452C>T | p.Asp484Asp | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/14 | 1736/2768 | 1452/1881 | 484/626 | chr9 | 129098025 | |||
| chr9:129098142 | G | A | 1 | a0001c0004 | 16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
synonymous_variant | LOW | c.1335C>T | p.Tyr445Tyr | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/14 | 1619/2768 | 1335/1881 | 445/626 | chr9 | 129098142 | |||
| chr9:129098638 | C | T | 1 | a0003c0006 | 3 | HG02602.hp1 HG03490.hp2 HG03927.hp2 |
synonymous_variant | LOW | c.1098G>A | p.Glu366Glu | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 9/14 | 1382/2768 | 1098/1881 | 366/626 | chr9 | 129098638 | |||
| chr9:129100526 | G | A | 1 | a0001c0005 | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
synonymous_variant | LOW | c.969C>T | p.Phe323Phe | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/14 | 1253/2768 | 969/1881 | 323/626 | chr9 | 129100526 | |||
| chr9:129100541 | G | A | 1 | a0001c0015 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.954C>T | p.Ser318Ser | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/14 | 1238/2768 | 954/1881 | 318/626 | chr9 | 129100541 | |||
| chr9:129100598 | C | T | 1 | a0001c0010 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.897G>A | p.Val299Val | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/14 | 1181/2768 | 897/1881 | 299/626 | chr9 | 129100598 | |||
| chr9:129104244 | C | G | 2 | a0001c0002 a0001c0007 |
75 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(72): Show |
synonymous_variant | LOW | c.354G>C | p.Ser118Ser | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 3/14 | 638/2768 | 354/1881 | 118/626 | chr9 | 129104244 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:129094828 | C | G | 3 | a0001c0001t0005 a0001c0004t0003 a0001c0007t0006 |
20 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*569G>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 14/14 | 569 | chr9 | 129094828 | ||||||
| chr9:129094955 | C | T | 1 | a0001c0004t0003 | 16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*442G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 14/14 | 442 | chr9 | 129094955 | ||||||
| chr9:129095133 | C | T | 1 | a0001c0001t0005 | 2 | HG02055.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*264G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 14/14 | 264 | chr9 | 129095133 | ||||||
| chr9:129095167 | C | T | 1 | a0002c0003t0009 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*230G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 14/14 | 230 | chr9 | 129095167 | ||||||
| chr9:129095175 | C | T | 1 | a0005c0009t0011 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 14/14 | 222 | chr9 | 129095175 | ||||||
| chr9:129095351 | C | T | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(8): Show |
183 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*46G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 14/14 | 46 | chr9 | 129095351 | ||||||
| chr9:129110533 | G | C | 1 | a0001c0002t0010 | 1 | NA19089.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/14 | 24 | chr9 | 129110533 | ||||||
| chr9:129110568 | GCGCCGC | G | 10 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(7): Show |
182 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
5_prime_UTR_variant | MODIFIER | c.-65_-60delGCGGCG | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/14 | 60 | chr9 | 129110568 | ||||||
| chr9:129110675 | C | A | 1 | a0001c0001t0012 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-166G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/14 | 166 | chr9 | 129110675 | ||||||
| chr9:129110696 | A | C | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(20): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-187T>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/14 | chr9 | 129110696 | |||||||
| chr9:129110792 | A | G | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(20): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
5_prime_UTR_variant | MODIFIER | c.-283T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/14 | 283 | chr9 | 129110792 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:129095655 | C | T | 4 | a0001c0001t0004g0038 a0001c0001t0004g0150 a0001c0001t0012g0153 others(1): Show |
5 | HG02486.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1666-43G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 13/13 | chr9 | 129095655 | |||||||
| chr9:129095767 | C | T | 1 | a0001c0002t0002g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1666-155G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 13/13 | chr9 | 129095767 | |||||||
| chr9:129095910 | A | G | 1 | a0001c0002t0002g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1665+88T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 13/13 | chr9 | 129095910 | |||||||
| chr9:129095935 | C | T | 1 | a0006c0011t0001g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1665+63G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 13/13 | chr9 | 129095935 | |||||||
| chr9:129095974 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1665+24C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 13/13 | chr9 | 129095974 | |||||||
| chr9:129096382 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1528-247G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 12/13 | chr9 | 129096382 | |||||||
| chr9:129096414 | G | T | 1 | a0001c0007t0006g0029 | 2 | NA18949.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1528-279C>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 12/13 | chr9 | 129096414 | |||||||
| chr9:129096479 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1528-344G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 12/13 | chr9 | 129096479 | |||||||
| chr9:129096811 | A | G | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1527+439T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 12/13 | chr9 | 129096811 | |||||||
| chr9:129097067 | CA | C | 19 | a0001c0001t0001g0091 a0001c0001t0002g0063 a0001c0002t0002g0007 others(16): Show |
42 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1527+182delT | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 12/13 | chr9 | 129097067 | |||||||
| chr9:129097067 | CAA | C | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1527+181_1527+182d others(4): Show |
CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 12/13 | chr9 | 129097067 | |||||||
| chr9:129097114 | A | G | 5 | a0001c0001t0002g0043 a0001c0001t0002g0049 a0001c0001t0002g0061 others(2): Show |
5 | NA18941.hp2 NA18982.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1527+136T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 12/13 | chr9 | 129097114 | |||||||
| chr9:129097178 | C | T | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1527+72G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 12/13 | chr9 | 129097178 | |||||||
| chr9:129097634 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1465-322C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/13 | chr9 | 129097634 | |||||||
| chr9:129097706 | C | T | 1 | a0001c0001t0007g0085 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1464+307G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/13 | chr9 | 129097706 | |||||||
| chr9:129097707 | T | TA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(70): Show |
217 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1464+305dupT | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/13 | chr9 | 129097707 | |||||||
| chr9:129097707 | TA | T | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1464+305delT | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/13 | chr9 | 129097707 | |||||||
| chr9:129097875 | G | A | 1 | a0001c0001t0001g0012 | 7 | HG01069.hp2 HG01496.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1464+138C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/13 | chr9 | 129097875 | |||||||
| chr9:129097899 | C | T | 17 | a0001c0002t0002g0007 a0001c0002t0002g0009 a0001c0002t0002g0010 others(14): Show |
40 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1464+114G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/13 | chr9 | 129097899 | |||||||
| chr9:129097965 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1464+48C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/13 | chr9 | 129097965 | |||||||
| chr9:129097988 | C | T | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
17 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1464+25G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 11/13 | chr9 | 129097988 | |||||||
| chr9:129098188 | G | C | 1 | a0001c0001t0002g0063 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1329-40C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 10/13 | chr9 | 129098188 | |||||||
| chr9:129098189 | C | A | 1 | a0001c0001t0002g0063 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1329-41G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 10/13 | chr9 | 129098189 | |||||||
| chr9:129098190 | A | C | 1 | a0001c0001t0002g0063 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1329-42T>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 10/13 | chr9 | 129098190 | |||||||
| chr9:129098197 | C | T | 1 | a0001c0001t0001g0035 | 2 | NA18968.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1329-49G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 10/13 | chr9 | 129098197 | |||||||
| chr9:129098244 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18989.hp1 | splice_region_variant&intron_variant | LOW | c.1328+5G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 10/13 | chr9 | 129098244 | |||||||
| chr9:129098375 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18983.hp1 | splice_region_variant&intron_variant | LOW | c.1206-4C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 9/13 | chr9 | 129098375 | |||||||
| chr9:129098429 | C | T | 1 | a0001c0007t0006g0029 | 2 | NA18949.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1206-58G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 9/13 | chr9 | 129098429 | |||||||
| chr9:129098668 | C | A | 1 | a0001c0001t0001g0103 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1086-18G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098668 | |||||||
| chr9:129098704 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1086-54G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098704 | |||||||
| chr9:129098815 | TC | T | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1086-166delG | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098815 | |||||||
| chr9:129098816 | CTT | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(139): Show |
392 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(389): Show |
intron_variant | MODIFIER | c.1086-168_1086-167d others(4): Show |
CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098816 | |||||||
| chr9:129098825 | T | G | 1 | a0001c0001t0002g0056 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1086-175A>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098825 | |||||||
| chr9:129098839 | A | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(71): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1086-189T>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098839 | |||||||
| chr9:129098876 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.1086-226A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098876 | |||||||
| chr9:129098916 | C | T | 2 | a0001c0001t0005g0044 a0001c0001t0005g0045 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1086-266G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098916 | |||||||
| chr9:129098962 | C | T | 1 | a0001c0007t0006g0029 | 2 | NA18949.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1086-312G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098962 | |||||||
| chr9:129098996 | A | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(71): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1086-346T>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129098996 | |||||||
| chr9:129099044 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18942.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1086-394C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099044 | |||||||
| chr9:129099104 | A | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(71): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1086-454T>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099104 | |||||||
| chr9:129099118 | G | A | 2 | a0001c0001t0005g0044 a0001c0001t0005g0045 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1086-468C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099118 | |||||||
| chr9:129099134 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1086-484C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099134 | |||||||
| chr9:129099141 | A | G | 1 | a0001c0007t0006g0029 | 2 | NA18949.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1086-491T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099141 | |||||||
| chr9:129099142 | C | CT | 10 | a0001c0001t0001g0036 a0001c0001t0002g0049 a0001c0001t0002g0079 others(7): Show |
27 | HG01081.hp1 HG01123.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1086-493dupA | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099142 | |||||||
| chr9:129099142 | CT | C | 13 | a0001c0001t0001g0108 a0001c0001t0001g0123 a0001c0001t0001g0137 others(10): Show |
37 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1086-493delA | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099142 | |||||||
| chr9:129099147 | T | A | 1 | a0001c0001t0002g0056 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1086-497A>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099147 | |||||||
| chr9:129099182 | A | C | 1 | a0001c0001t0002g0063 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1086-532T>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099182 | |||||||
| chr9:129099182 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
414 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(411): Show |
intron_variant | MODIFIER | c.1086-532T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099182 | |||||||
| chr9:129099236 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.1086-586C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099236 | |||||||
| chr9:129099237 | G | T | 1 | a0001c0001t0002g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1086-587C>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099237 | |||||||
| chr9:129099399 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.1085+467A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099399 | |||||||
| chr9:129099412 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1085+454G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099412 | |||||||
| chr9:129099426 | AT | A | 15 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(12): Show |
25 | HG01167.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1085+439delA | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099426 | |||||||
| chr9:129099426 | ATT | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(128): Show |
385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.1085+438_1085+439d others(4): Show |
CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099426 | |||||||
| chr9:129099503 | C | T | 5 | a0001c0002t0002g0009 a0001c0002t0002g0025 a0001c0002t0002g0070 others(2): Show |
12 | HG01099.hp2 HG01943.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1085+363G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099503 | |||||||
| chr9:129099509 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(71): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1085+357G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099509 | |||||||
| chr9:129099590 | G | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.1085+276C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099590 | |||||||
| chr9:129099593 | AT | A | 55 | a0001c0001t0001g0109 a0001c0001t0001g0148 a0001c0001t0002g0003 others(52): Show |
150 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1085+272delA | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099593 | |||||||
| chr9:129099593 | ATT | A | 14 | a0001c0001t0005g0045 a0001c0002t0002g0007 a0001c0002t0002g0010 others(11): Show |
31 | HG00639.hp1 HG01109.hp1 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.1085+271_1085+272d others(4): Show |
CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099593 | |||||||
| chr9:129099595 | T | A | 8 | a0001c0002t0002g0004 a0001c0002t0002g0040 a0001c0002t0002g0046 others(5): Show |
31 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1085+271A>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099595 | |||||||
| chr9:129099596 | T | A | 1 | a0001c0002t0002g0028 | 2 | NA18957.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1085+270A>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099596 | |||||||
| chr9:129099752 | AAC | A | 17 | a0001c0002t0002g0007 a0001c0002t0002g0009 a0001c0002t0002g0010 others(14): Show |
40 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1085+112_1085+113d others(4): Show |
CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099752 | |||||||
| chr9:129099794 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.1085+72C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099794 | |||||||
| chr9:129099804 | C | T | 1 | a0001c0001t0002g0024 | 2 | HG01978.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1085+62G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099804 | |||||||
| chr9:129099809 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1085+57C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099809 | |||||||
| chr9:129099823 | A | G | 1 | a0001c0001t0002g0023 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1085+43T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 8/13 | chr9 | 129099823 | |||||||
| chr9:129099989 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.985-23G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/13 | chr9 | 129099989 | |||||||
| chr9:129100157 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.985-191C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/13 | chr9 | 129100157 | |||||||
| chr9:129100159 | G | A | 4 | a0001c0002t0002g0027 a0001c0002t0002g0072 a0001c0002t0002g0073 others(1): Show |
5 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-193C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/13 | chr9 | 129100159 | |||||||
| chr9:129100426 | AGG | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(122): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.984+83_984+84delCC | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/13 | chr9 | 129100426 | |||||||
| chr9:129100437 | C | G | 10 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0004t0003g0015 others(7): Show |
20 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.984+74G>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/13 | chr9 | 129100437 | |||||||
| chr9:129100438 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0100 |
6 | HG00140.hp2 NA18941.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.984+73C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/13 | chr9 | 129100438 | |||||||
| chr9:129100451 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(61): Show |
207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.984+60G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/13 | chr9 | 129100451 | |||||||
| chr9:129100499 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.984+12C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/13 | chr9 | 129100499 | |||||||
| chr9:129100502 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(60): Show |
192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.984+9C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 7/13 | chr9 | 129100502 | |||||||
| chr9:129100708 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.806-19C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129100708 | |||||||
| chr9:129100715 | C | T | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.806-26G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129100715 | |||||||
| chr9:129100800 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(80): Show |
242 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.806-111A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129100800 | |||||||
| chr9:129100828 | G | A | 3 | a0001c0001t0004g0038 a0001c0001t0004g0150 a0001c0015t0004g0143 |
4 | HG02486.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.806-139C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129100828 | |||||||
| chr9:129100914 | C | T | 1 | a0001c0001t0002g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.806-225G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129100914 | |||||||
| chr9:129100958 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(65): Show |
211 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.806-269C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129100958 | |||||||
| chr9:129101094 | CG | C | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.806-406delC | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129101094 | |||||||
| chr9:129101294 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.805+589T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129101294 | |||||||
| chr9:129101483 | G | A | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.805+400C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129101483 | |||||||
| chr9:129101490 | T | C | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.805+393A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129101490 | |||||||
| chr9:129101581 | T | C | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.805+302A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129101581 | |||||||
| chr9:129101647 | G | C | 25 | a0001c0002t0002g0007 a0001c0002t0002g0009 a0001c0002t0002g0010 others(22): Show |
58 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.805+236C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129101647 | |||||||
| chr9:129101699 | GC | G | 2 | a0001c0002t0002g0010 a0001c0002t0002g0048 |
8 | HG00639.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.805+183delG | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129101699 | |||||||
| chr9:129101795 | T | C | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.805+88A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 6/13 | chr9 | 129101795 | |||||||
| chr9:129102129 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.631-72G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 5/13 | chr9 | 129102129 | |||||||
| chr9:129102232 | G | A | 11 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0002t0002g0004 others(8): Show |
35 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.630+168C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 5/13 | chr9 | 129102232 | |||||||
| chr9:129102243 | G | C | 1 | a0001c0005t0001g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.630+157C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 5/13 | chr9 | 129102243 | |||||||
| chr9:129102296 | G | T | 3 | a0001c0001t0004g0038 a0001c0001t0004g0150 a0001c0015t0004g0143 |
4 | HG02486.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+104C>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 5/13 | chr9 | 129102296 | |||||||
| chr9:129102592 | A | G | 8 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(5): Show |
18 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.465-27T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 4/13 | chr9 | 129102592 | |||||||
| chr9:129102671 | C | T | 33 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0016 others(30): Show |
82 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.465-106G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 4/13 | chr9 | 129102671 | |||||||
| chr9:129102676 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.465-111G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 4/13 | chr9 | 129102676 | |||||||
| chr9:129102748 | C | T | 34 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0016 others(31): Show |
83 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.465-183G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 4/13 | chr9 | 129102748 | |||||||
| chr9:129102760 | G | A | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.465-195C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 4/13 | chr9 | 129102760 | |||||||
| chr9:129102821 | G | A | 17 | a0001c0002t0002g0007 a0001c0002t0002g0009 a0001c0002t0002g0010 others(14): Show |
40 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.464+192C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 4/13 | chr9 | 129102821 | |||||||
| chr9:129102938 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.464+75G>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 4/13 | chr9 | 129102938 | |||||||
| chr9:129102939 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.464+74A>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 4/13 | chr9 | 129102939 | |||||||
| chr9:129102981 | G | A | 1 | a0001c0002t0002g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.464+32C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 4/13 | chr9 | 129102981 | |||||||
| chr9:129103098 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.411-32C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 3/13 | chr9 | 129103098 | |||||||
| chr9:129103214 | C | T | 34 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0016 others(31): Show |
83 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.411-148G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 3/13 | chr9 | 129103214 | |||||||
| chr9:129103311 | T | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG01074.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.411-245A>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 3/13 | chr9 | 129103311 | |||||||
| chr9:129103719 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0031 others(22): Show |
70 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.410+469C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 3/13 | chr9 | 129103719 | |||||||
| chr9:129104020 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.410+168C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 3/13 | chr9 | 129104020 | |||||||
| chr9:129104064 | C | G | 1 | a0001c0007t0006g0029 | 2 | NA18949.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.410+124G>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 3/13 | chr9 | 129104064 | |||||||
| chr9:129104109 | C | T | 38 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0016 others(35): Show |
103 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.410+79G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 3/13 | chr9 | 129104109 | |||||||
| chr9:129104142 | T | C | 4 | a0001c0001t0004g0038 a0001c0001t0004g0150 a0001c0001t0012g0153 others(1): Show |
5 | HG02486.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+46A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 3/13 | chr9 | 129104142 | |||||||
| chr9:129104330 | C | T | 12 | a0001c0002t0002g0007 a0001c0002t0002g0010 a0001c0002t0002g0026 others(9): Show |
28 | HG00639.hp1 HG01109.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.292-24G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104330 | |||||||
| chr9:129104378 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.292-72C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104378 | |||||||
| chr9:129104525 | C | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.292-219G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104525 | |||||||
| chr9:129104531 | T | C | 4 | a0001c0004t0003g0020 a0001c0004t0003g0144 a0001c0004t0003g0145 others(1): Show |
6 | HG01167.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-225A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104531 | |||||||
| chr9:129104608 | CT | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
415 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(412): Show |
intron_variant | MODIFIER | c.292-303delA | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104608 | |||||||
| chr9:129104665 | C | T | 1 | a0001c0002t0002g0026 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.292-359G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104665 | |||||||
| chr9:129104753 | A | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(125): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.292-447T>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104753 | |||||||
| chr9:129104754 | G | A | 2 | a0001c0001t0005g0044 a0001c0001t0005g0045 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.292-448C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104754 | |||||||
| chr9:129104815 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.292-509T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104815 | |||||||
| chr9:129104829 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.292-523A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104829 | |||||||
| chr9:129104851 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(63): Show |
211 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.292-545C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104851 | |||||||
| chr9:129104884 | A | G | 7 | a0001c0001t0001g0117 a0001c0002t0002g0009 a0001c0002t0002g0025 others(4): Show |
19 | HG01109.hp2 HG01255.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.292-578T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104884 | |||||||
| chr9:129104895 | T | C | 2 | a0002c0003t0002g0014 a0002c0003t0002g0081 |
7 | HG01255.hp2 HG01257.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-589A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104895 | |||||||
| chr9:129104903 | C | CT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(67): Show |
212 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.292-598dupA | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104903 | |||||||
| chr9:129104969 | C | T | 9 | a0001c0002t0002g0004 a0001c0002t0002g0028 a0001c0002t0002g0040 others(6): Show |
33 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.292-663G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104969 | |||||||
| chr9:129104981 | A | T | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.292-675T>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129104981 | |||||||
| chr9:129105001 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
102 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.292-695G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105001 | |||||||
| chr9:129105031 | G | C | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.292-725C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105031 | |||||||
| chr9:129105082 | G | T | 1 | a0001c0002t0002g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.292-776C>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105082 | |||||||
| chr9:129105086 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(70): Show |
217 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.292-780A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105086 | |||||||
| chr9:129105106 | C | T | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.292-800G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105106 | |||||||
| chr9:129105107 | G | C | 1 | a0001c0001t0002g0069 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.292-801C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105107 | |||||||
| chr9:129105195 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.292-889C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105195 | |||||||
| chr9:129105203 | C | A | 1 | a0001c0002t0002g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.292-897G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105203 | |||||||
| chr9:129105303 | G | A | 2 | a0001c0001t0005g0044 a0001c0001t0005g0045 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.292-997C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105303 | |||||||
| chr9:129105436 | T | G | 9 | a0001c0002t0002g0004 a0001c0002t0002g0028 a0001c0002t0002g0040 others(6): Show |
33 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.292-1130A>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105436 | |||||||
| chr9:129105438 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.292-1132T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105438 | |||||||
| chr9:129105498 | T | G | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.292-1192A>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105498 | |||||||
| chr9:129105530 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0095 |
3 | HG01069.hp1 HG01071.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.292-1224G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105530 | |||||||
| chr9:129105596 | C | A | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.292-1290G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105596 | |||||||
| chr9:129105613 | C | G | 5 | a0001c0002t0002g0009 a0001c0002t0002g0025 a0001c0002t0002g0070 others(2): Show |
12 | HG01099.hp2 HG01943.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.292-1307G>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105613 | |||||||
| chr9:129105664 | A | G | 1 | a0001c0002t0002g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.292-1358T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105664 | |||||||
| chr9:129105917 | C | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0016 others(40): Show |
109 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.292-1611G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105917 | |||||||
| chr9:129105969 | C | T | 5 | a0001c0002t0002g0009 a0001c0002t0002g0025 a0001c0002t0002g0070 others(2): Show |
12 | HG01099.hp2 HG01943.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.292-1663G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105969 | |||||||
| chr9:129105970 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG01934.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.292-1664G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129105970 | |||||||
| chr9:129106095 | C | T | 8 | a0001c0002t0002g0004 a0001c0002t0002g0028 a0001c0002t0002g0040 others(5): Show |
32 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.291+1719G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129106095 | |||||||
| chr9:129106195 | T | C | 1 | a0007c0014t0002g0082 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.291+1619A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129106195 | |||||||
| chr9:129106212 | G | A | 1 | a0001c0002t0002g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.291+1602C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129106212 | |||||||
| chr9:129106506 | C | T | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.291+1308G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129106506 | |||||||
| chr9:129106712 | A | G | 35 | a0001c0001t0001g0148 a0001c0001t0002g0003 a0001c0001t0002g0008 others(32): Show |
84 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.291+1102T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129106712 | |||||||
| chr9:129106719 | G | A | 9 | a0001c0002t0002g0004 a0001c0002t0002g0028 a0001c0002t0002g0040 others(6): Show |
33 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.291+1095C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129106719 | |||||||
| chr9:129106816 | T | C | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.291+998A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129106816 | |||||||
| chr9:129107153 | C | T | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.291+661G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129107153 | |||||||
| chr9:129107159 | C | G | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.291+655G>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129107159 | |||||||
| chr9:129107215 | G | A | 2 | a0001c0004t0003g0144 a0001c0004t0003g0147 |
2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.291+599C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129107215 | |||||||
| chr9:129107278 | C | T | 1 | a0001c0004t0003g0144 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.291+536G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129107278 | |||||||
| chr9:129107279 | G | A | 4 | a0001c0001t0007g0085 a0002c0003t0002g0011 a0002c0003t0002g0084 others(1): Show |
10 | HG01081.hp1 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.291+535C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129107279 | |||||||
| chr9:129107455 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.291+359C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129107455 | |||||||
| chr9:129107643 | G | A | 1 | a0001c0002t0002g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.291+171C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129107643 | |||||||
| chr9:129107668 | A | G | 1 | a0001c0002t0002g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.291+146T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129107668 | |||||||
| chr9:129107756 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.291+58G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 2/13 | chr9 | 129107756 | |||||||
| chr9:129108154 | C | T | 1 | a0001c0002t0002g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.28-77G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129108154 | |||||||
| chr9:129108184 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0091 |
3 | NA18948.hp2 NA18977.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.28-107G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129108184 | |||||||
| chr9:129108389 | C | T | 1 | a0001c0002t0002g0046 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.28-312G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129108389 | |||||||
| chr9:129108394 | C | A | 3 | a0001c0001t0004g0038 a0001c0001t0004g0150 a0001c0015t0004g0143 |
4 | HG02486.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-317G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129108394 | |||||||
| chr9:129108449 | T | C | 9 | a0001c0001t0007g0085 a0001c0007t0006g0029 a0002c0003t0002g0011 others(6): Show |
26 | HG01081.hp1 HG01099.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.28-372A>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129108449 | |||||||
| chr9:129108620 | A | C | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.28-543T>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129108620 | |||||||
| chr9:129108712 | C | T | 1 | a0001c0001t0002g0022 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-635G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129108712 | |||||||
| chr9:129108865 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.28-788T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129108865 | |||||||
| chr9:129108970 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.28-893T>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129108970 | |||||||
| chr9:129109077 | G | T | 7 | a0001c0004t0003g0015 a0001c0004t0003g0020 a0001c0004t0003g0021 others(4): Show |
16 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.28-1000C>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129109077 | |||||||
| chr9:129109156 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
417 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.28-1079T>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129109156 | |||||||
| chr9:129109406 | C | T | 2 | a0001c0001t0005g0044 a0001c0001t0005g0045 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.27+1077G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129109406 | |||||||
| chr9:129109408 | A | G | 1 | a0001c0001t0002g0043 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.27+1075T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129109408 | |||||||
| chr9:129109457 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.27+1026G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129109457 | |||||||
| chr9:129109648 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(71): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.27+835T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129109648 | |||||||
| chr9:129109901 | G | C | 1 | a0001c0001t0004g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.27+582C>G | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129109901 | |||||||
| chr9:129109963 | G | A | 1 | a0001c0001t0002g0086 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.27+520C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129109963 | |||||||
| chr9:129110124 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.27+359G>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110124 | |||||||
| chr9:129110272 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.27+211A>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110272 | |||||||
| chr9:129110306 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.27+177A>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110306 | |||||||
| chr9:129110340 | C | A | 1 | a0001c0001t0002g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.27+143G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110340 | |||||||
| chr9:129110428 | G | A | 3 | a0001c0001t0002g0030 a0001c0001t0002g0088 a0001c0001t0002g0089 |
4 | HG02723.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+55C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110428 | |||||||
| chr9:129110453 | G | A | 1 | a0001c0002t0002g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27+30C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110453 | |||||||
| chr9:129110455 | C | A | 1 | a0001c0002t0002g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27+28G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110455 | |||||||
| chr9:129110458 | C | A | 1 | a0001c0002t0002g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27+25G>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110458 | |||||||
| chr9:129110459 | A | G | 1 | a0001c0002t0002g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27+24T>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110459 | |||||||
| chr9:129110460 | G | A | 1 | a0001c0002t0002g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27+23C>T | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110460 | |||||||
| chr9:129110461 | G | T | 1 | a0001c0002t0002g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27+22C>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110461 | |||||||
| chr9:129110463 | C | G | 1 | a0001c0002t0002g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27+20G>C | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110463 | |||||||
| chr9:129110466 | G | T | 1 | a0001c0002t0002g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27+17C>A | CRAT | ENSG00000095321.18 | transcript | ENST00000318080.7 | protein_coding | 1/13 | chr9 | 129110466 |