Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51179 |
| ensemblid | ENSG00000116882.15 |
| hgncid | 4810 |
| symbol | HAO2 |
| name | hydroxyacid oxidase 2 |
| refseq_nuc | NM_016527.4 |
| refseq_prot | NP_057611.1 |
| ensembl_nuc | ENST00000325945.4 |
| ensembl_prot | ENSP00000316339.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 119368785 |
| end | 119394130 |
| strand | + |
| ver | v1.2 |
| region | chr1:119368785-119394130 |
| region5000 | chr1:119363785-119399130 |
| regionname0 | HAO2_chr1_119368785_119394130 |
| regionname5000 | HAO2_chr1_119363785_119399130 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 351 | 403 | 74 | 69 | 192 | 18 | 48 | 144 | HAO2_chr1_119363785_119399130 | HAO2 | MSLVC others(346): Show |
chr1 | 119363785 | 119399130 |
| a0002 | 0/0 | 351 | 20 | 19 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | MSLVC others(346): Show |
chr1 | 119363785 | 119399130 |
| a0003 | 0/0 | 351 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HAO2_chr1_119363785_119399130 | HAO2 | MSLVC others(346): Show |
chr1 | 119363785 | 119399130 |
| a0004 | 0/0 | 194 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | MSLVC others(189): Show |
chr1 | 119363785 | 119399130 |
| a0005 | 0/0 | 210 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | MSLVC others(205): Show |
chr1 | 119363785 | 119399130 |
| a0006 | 0/0 | 351 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | MSLVC others(346): Show |
chr1 | 119363785 | 119399130 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1053 | 272 | 65 | 32 | 132 | 9 | 32 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 | ||
| a0001c0002 | 0/0 | 1053 | 126 | 6 | 37 | 60 | 9 | 14 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 | ||
| a0001c0004 | 0/0 | 1053 | 3 | 3 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 | ||
| a0001c0007 | 0/0 | 1053 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 | ||
| a0001c0011 | 0/0 | 1053 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 | ||
| a0002c0003 | 0/0 | 1053 | 19 | 18 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 | ||
| a0002c0006 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 | ||
| a0003c0005 | 0/0 | 1053 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 | ||
| a0004c0010 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 | ||
| a0005c0009 | 0/0 | 1043 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1038): Show |
chr1 | 119363785 | 119399130 | ||
| a0006c0008 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | ATGTC others(1048): Show |
chr1 | 119363785 | 119399130 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1472 | 266 | 64 | 32 | 131 | 8 | 30 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0001c0001t0002 | 0/0 | 1472 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0001c0001t0004 | 0/1 | 1471 | 4 | 0 | 0 | 0 | 1 | 2 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1466): Show |
chr1 | 119363785 | 119399130 |
| a0001c0001t0007 | 0/0 | 1472 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0001c0002t0001 | 0/0 | 1472 | 120 | 6 | 33 | 58 | 9 | 14 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0001c0002t0003 | 0/0 | 1472 | 5 | 0 | 4 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0001c0002t0008 | 0/0 | 1472 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0001c0004t0006 | 0/0 | 1472 | 3 | 3 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0001c0007t0001 | 0/0 | 1472 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0001c0011t0001 | 0/0 | 1472 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0002c0003t0002 | 0/0 | 1472 | 15 | 15 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0002c0003t0005 | 0/0 | 1472 | 3 | 2 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0002c0003t0009 | 0/0 | 1472 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0002c0006t0002 | 0/0 | 1472 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0003c0005t0001 | 0/0 | 1472 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0004c0010t0001 | 0/0 | 1472 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| a0005c0009t0001 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1457): Show |
chr1 | 119363785 | 119399130 |
| a0006c0008t0001 | 0/0 | 1472 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | AGCCT others(1467): Show |
chr1 | 119363785 | 119399130 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 36 | 0 | 2 | 31 | 0 | 3 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 5 | 5 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0007 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0004g0001 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0002 | 0/0 | 10 | 0 | 6 | 4 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0004 | 0/0 | 8 | 0 | 3 | 4 | 1 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0003g0055 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0002t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0004t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0004t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0004t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0007t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0001c0011t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0003t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0002c0006t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0003c0005t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0004c0010t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0005c0009t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| a0006c0008t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0050 | EUR | GBR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0183 | EUR | GBR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0212 | EUR | FIN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0052 | EUR | FIN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0043 | EUR | FIN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0270 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0214 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01433 | hp1 | a0002 | c0003 | t0005 | g0070 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0049 | EUR | IBS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | IBS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | IBS | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01891 | hp2 | a0002 | c0003 | t0002 | g0069 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0227 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0055 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0185 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0271 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0282 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02145 | hp1 | a0004 | c0010 | t0001 | g0097 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0229 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CDX | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | CDX | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02258 | hp2 | a0002 | c0003 | t0009 | g0286 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0228 | AMR | PEL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02451 | hp2 | a0002 | c0003 | t0002 | g0067 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02647 | hp2 | a0002 | c0003 | t0002 | g0061 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02683 | hp1 | a0001 | c0011 | t0001 | g0001 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02698 | hp2 | a0001 | c0007 | t0001 | g0281 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02809 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02895 | hp1 | a0002 | c0006 | t0002 | g0071 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02896 | hp1 | a0002 | c0003 | t0002 | g0020 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02976 | hp1 | a0001 | c0004 | t0006 | g0284 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0068 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03098 | hp1 | a0002 | c0003 | t0002 | g0074 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03098 | hp2 | a0002 | c0003 | t0005 | g0073 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03195 | hp2 | a0002 | c0003 | t0005 | g0253 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03225 | hp1 | a0002 | c0003 | t0002 | g0022 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03453 | hp2 | a0002 | c0003 | t0002 | g0021 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03486 | hp2 | a0002 | c0003 | t0002 | g0021 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03516 | hp2 | a0002 | c0003 | t0002 | g0022 | AFR | ESN | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0269 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0053 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0184 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | BEB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0188 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18522 | hp2 | a0001 | c0004 | t0006 | g0285 | AFR | YRI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | CHB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | CHB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18941 | hp1 | a0003 | c0005 | t0001 | g0036 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18945 | hp1 | a0001 | c0001 | t0007 | g0244 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18949 | hp2 | a0001 | c0002 | t0008 | g0200 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18991 | hp2 | a0005 | c0009 | t0001 | g0258 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19010 | hp1 | a0006 | c0008 | t0001 | g0264 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | LWK | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19083 | hp1 | a0003 | c0005 | t0001 | g0036 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19240 | hp1 | a0002 | c0003 | t0002 | g0072 | AFR | YRI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA19240 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | YRI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ASW | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ASW | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0255 | EUR | TSI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0053 | EUR | TSI | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | GIH | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0216 | SAS | GIH | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | CLM | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG06807 | hp1 | a0002 | c0003 | t0002 | g0020 | AFR | USA | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | USA | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | USA | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA21309 | hp1 | a0001 | c0004 | t0006 | g0287 | AFR | LWK | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0001 | REF | REF | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0235 | REF | REF | HAO2_chr1_119363785_119399130 | HAO2 | chr1 | 119363785 | 119399130 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119368900 | A | C | 2 | a0001 a0002 |
4 | HG02258.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
splice_region_variant | LOW | c.-11A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/8 | chr1 | 119368900 | |||||||
| chr1:119381101 | T | G | 1 | a0002 | 20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
missense_variant | MODERATE | c.16T>G | p.Leu6Val | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/8 | 142/1472 | 16/1056 | 6/351 | chr1 | 119381101 | |||
| chr1:119381128 | G | A | 1 | a0002 | 20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
missense_variant | MODERATE | c.43G>A | p.Glu15Lys | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/8 | 169/1472 | 43/1056 | 15/351 | chr1 | 119381128 | |||
| chr1:119382926 | G | A | 1 | a0006 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.143G>A | p.Arg48His | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/8 | 269/1472 | 143/1056 | 48/351 | chr1 | 119382926 | |||
| chr1:119384856 | G | A | 1 | a0003 | 2 | NA18941.hp1 NA19083.hp1 |
missense_variant | MODERATE | c.364G>A | p.Glu122Lys | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/8 | 490/1472 | 364/1056 | 122/351 | chr1 | 119384856 | |||
| chr1:119386643 | C | T | 1 | a0004 | 1 | HG02145.hp1 | stop_gained | HIGH | c.583C>T | p.Gln195* | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/8 | 709/1472 | 583/1056 | 195/351 | chr1 | 119386643 | |||
| chr1:119386675 | GAATGATC others(3): Show |
G | 1 | a0005 | 1 | NA18991.hp2 | frameshift_variant | HIGH | c.616_625delAATGATCT others(2): Show |
p.Asn206fs | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/8 | 742/1472 | 616/1056 | 206/351 | chr1 | 119386675 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119381101 | T | C | 1 | a0001c0002 | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(123): Show |
synonymous_variant | LOW | c.16T>C | p.Leu6Leu | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/8 | 142/1472 | 16/1056 | 6/351 | chr1 | 119381101 | |||
| chr1:119381124 | G | A | 1 | a0001c0004 | 3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.39G>A | p.Ala13Ala | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/8 | 165/1472 | 39/1056 | 13/351 | chr1 | 119381124 | |||
| chr1:119381142 | G | A | 1 | a0001c0007 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.57G>A | p.Lys19Lys | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/8 | 183/1472 | 57/1056 | 19/351 | chr1 | 119381142 | |||
| chr1:119383035 | C | T | 1 | a0001c0011 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.252C>T | p.Val84Val | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/8 | 378/1472 | 252/1056 | 84/351 | chr1 | 119383035 | |||
| chr1:119384861 | C | T | 1 | a0002c0006 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.369C>T | p.Gly123Gly | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/8 | 495/1472 | 369/1056 | 123/351 | chr1 | 119384861 | |||
| chr1:119386627 | T | C | 1 | a0001c0004 | 3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.567T>C | p.Asn189Asn | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/8 | 693/1472 | 567/1056 | 189/351 | chr1 | 119386627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119393908 | T | C | 3 | a0001c0001t0002 a0002c0003t0002 a0002c0006t0002 |
17 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*68T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 8/8 | 68 | chr1 | 119393908 | ||||||
| chr1:119393941 | CG | C | 1 | a0001c0001t0004 | 3 | HG03239.hp2 HG03669.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*103delG | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 8/8 | 103 | INFO_REALIGN_3_PRIME | chr1 | 119393941 | |||||
| chr1:119393969 | T | C | 2 | a0002c0003t0005 a0002c0003t0009 |
4 | HG01433.hp1 HG02258.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*129T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 8/8 | 129 | chr1 | 119393969 | ||||||
| chr1:119394009 | C | T | 1 | a0001c0002t0008 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 8/8 | 169 | chr1 | 119394009 | ||||||
| chr1:119394070 | C | T | 1 | a0001c0002t0003 | 5 | HG01928.hp2 HG01934.hp2 HG02148.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*230C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 8/8 | 230 | chr1 | 119394070 | ||||||
| chr1:119394102 | T | G | 1 | a0001c0001t0007 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 8/8 | 262 | chr1 | 119394102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119368911 | T | A | 1 | a0002c0003t0002g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-9+9T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119368911 | |||||||
| chr1:119368974 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-9+72G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119368974 | |||||||
| chr1:119369050 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-9+148A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369050 | |||||||
| chr1:119369282 | C | T | 4 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(1): Show |
4 | HG02258.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+380C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369282 | |||||||
| chr1:119369453 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0059 others(12): Show |
20 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+551C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369453 | |||||||
| chr1:119369470 | C | T | 3 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 |
3 | HG01099.hp2 HG01106.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-9+568C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369470 | |||||||
| chr1:119369499 | A | G | 4 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(1): Show |
4 | HG02258.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+597A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369499 | |||||||
| chr1:119369535 | G | A | 2 | a0001c0004t0006g0284 a0001c0004t0006g0285 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-9+633G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369535 | |||||||
| chr1:119369644 | A | G | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0004g0269 |
3 | HG02015.hp1 HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-9+742A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369644 | |||||||
| chr1:119369692 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(3): Show |
8 | HG02630.hp1 HG02886.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+790T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369692 | |||||||
| chr1:119369734 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-9+832G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369734 | |||||||
| chr1:119369990 | A | T | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-9+1088A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119369990 | |||||||
| chr1:119370091 | T | A | 13 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(10): Show |
18 | HG01433.hp1 HG01891.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+1189T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370091 | |||||||
| chr1:119370103 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9+1201G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370103 | |||||||
| chr1:119370106 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-9+1204G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370106 | |||||||
| chr1:119370216 | T | G | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
124 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.-9+1314T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370216 | |||||||
| chr1:119370304 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-9+1402T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370304 | |||||||
| chr1:119370421 | T | C | 90 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
121 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-9+1519T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370421 | |||||||
| chr1:119370438 | T | C | 1 | a0001c0002t0001g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-9+1536T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370438 | |||||||
| chr1:119370447 | G | A | 1 | a0002c0003t0009g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-9+1545G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370447 | |||||||
| chr1:119370584 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-9+1682T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370584 | |||||||
| chr1:119370637 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(6): Show |
11 | HG02486.hp1 HG02630.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+1735A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370637 | |||||||
| chr1:119370766 | T | C | 6 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(3): Show |
10 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+1864T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370766 | |||||||
| chr1:119370770 | C | A | 1 | a0001c0001t0001g0273 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-9+1868C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370770 | |||||||
| chr1:119370800 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-9+1898G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119370800 | |||||||
| chr1:119371061 | C | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(36): Show |
90 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.-9+2159C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371061 | |||||||
| chr1:119371099 | G | C | 1 | a0002c0003t0002g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-9+2197G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371099 | |||||||
| chr1:119371160 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(185): Show |
283 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(280): Show |
intron_variant | MODIFIER | c.-9+2258G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371160 | |||||||
| chr1:119371170 | A | G | 1 | a0006c0008t0001g0264 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-9+2268A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371170 | |||||||
| chr1:119371201 | G | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
121 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-9+2299G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371201 | |||||||
| chr1:119371281 | T | C | 4 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(1): Show |
4 | HG02258.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+2379T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371281 | |||||||
| chr1:119371453 | G | A | 1 | a0002c0003t0002g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-9+2551G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371453 | |||||||
| chr1:119371489 | T | C | 2 | a0001c0002t0001g0177 a0001c0002t0001g0178 |
2 | HG01175.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-9+2587T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371489 | |||||||
| chr1:119371514 | C | T | 13 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(10): Show |
18 | HG01433.hp1 HG01891.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+2612C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371514 | |||||||
| chr1:119371525 | C | T | 3 | a0001c0002t0001g0246 a0001c0002t0001g0247 a0001c0002t0001g0248 |
3 | HG01261.hp1 HG01975.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-9+2623C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371525 | |||||||
| chr1:119371693 | T | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(78): Show |
140 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-9+2791T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371693 | |||||||
| chr1:119371695 | A | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(78): Show |
140 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-9+2793A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371695 | |||||||
| chr1:119371781 | A | G | 90 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
121 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-9+2879A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371781 | |||||||
| chr1:119371820 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-9+2918T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371820 | |||||||
| chr1:119371873 | A | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0064 a0001c0001t0001g0065 |
4 | HG02886.hp1 HG03209.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+2971A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371873 | |||||||
| chr1:119371880 | T | G | 1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+2978T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371880 | |||||||
| chr1:119371944 | C | T | 1 | a0002c0003t0002g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-9+3042C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371944 | |||||||
| chr1:119371957 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-9+3055A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119371957 | |||||||
| chr1:119372020 | A | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(24): Show |
73 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.-9+3118A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119372020 | |||||||
| chr1:119372085 | G | T | 4 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(1): Show |
4 | HG02258.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+3183G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119372085 | |||||||
| chr1:119372173 | C | T | 1 | a0001c0002t0001g0245 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9+3271C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119372173 | |||||||
| chr1:119372263 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-9+3361C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119372263 | |||||||
| chr1:119372344 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-9+3442G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119372344 | |||||||
| chr1:119372388 | A | G | 1 | a0002c0003t0009g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-9+3486A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119372388 | |||||||
| chr1:119372505 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(78): Show |
140 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-9+3603C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119372505 | |||||||
| chr1:119372852 | T | C | 1 | a0001c0002t0001g0270 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-9+3950T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119372852 | |||||||
| chr1:119373046 | C | A | 91 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
123 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.-9+4144C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373046 | |||||||
| chr1:119373053 | C | T | 1 | a0001c0004t0006g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9+4151C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373053 | |||||||
| chr1:119373090 | A | G | 12 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(9): Show |
17 | HG01433.hp1 HG01891.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9+4188A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373090 | |||||||
| chr1:119373229 | G | A | 1 | a0003c0005t0001g0036 | 2 | NA18941.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-9+4327G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373229 | |||||||
| chr1:119373241 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | NA19076.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-9+4339A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373241 | |||||||
| chr1:119373384 | C | T | 1 | a0003c0005t0001g0036 | 2 | NA18941.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-9+4482C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373384 | |||||||
| chr1:119373506 | T | A | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-9+4604T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373506 | |||||||
| chr1:119373536 | G | T | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-9+4634G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373536 | |||||||
| chr1:119373749 | A | C | 1 | a0001c0001t0001g0283 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-9+4847A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373749 | |||||||
| chr1:119373803 | G | A | 43 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(40): Show |
53 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+4901G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119373803 | |||||||
| chr1:119374248 | C | A | 1 | a0001c0004t0006g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9+5346C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119374248 | |||||||
| chr1:119374331 | T | A | 8 | a0002c0003t0002g0010 a0002c0003t0002g0022 a0002c0003t0002g0061 others(5): Show |
11 | HG02647.hp2 HG02809.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+5429T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119374331 | |||||||
| chr1:119374383 | T | G | 1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-9+5481T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119374383 | |||||||
| chr1:119374624 | T | C | 1 | a0001c0002t0001g0179 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-9+5722T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119374624 | |||||||
| chr1:119374630 | G | A | 88 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(85): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-9+5728G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119374630 | |||||||
| chr1:119374757 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-9+5855T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119374757 | |||||||
| chr1:119374813 | A | T | 3 | a0002c0003t0005g0070 a0002c0003t0005g0073 a0002c0003t0009g0286 |
3 | HG01433.hp1 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-9+5911A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119374813 | |||||||
| chr1:119374950 | G | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(76): Show |
138 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.-9+6048G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119374950 | |||||||
| chr1:119375018 | A | T | 1 | a0001c0002t0001g0234 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-8-6060A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375018 | |||||||
| chr1:119375116 | G | A | 88 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(85): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-8-5962G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375116 | |||||||
| chr1:119375154 | A | C | 1 | a0001c0002t0001g0179 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-8-5924A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375154 | |||||||
| chr1:119375328 | T | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-8-5750T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375328 | |||||||
| chr1:119375396 | C | A | 17 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(14): Show |
22 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8-5682C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375396 | |||||||
| chr1:119375480 | C | G | 44 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(41): Show |
54 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8-5598C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375480 | |||||||
| chr1:119375486 | G | A | 17 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(14): Show |
22 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8-5592G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375486 | |||||||
| chr1:119375531 | T | C | 11 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(8): Show |
16 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-5547T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375531 | |||||||
| chr1:119375724 | A | G | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-8-5354A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375724 | |||||||
| chr1:119375780 | A | G | 11 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(8): Show |
16 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-5298A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375780 | |||||||
| chr1:119375864 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-5214C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119375864 | |||||||
| chr1:119376105 | C | T | 14 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(11): Show |
19 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-4973C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376105 | |||||||
| chr1:119376156 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-8-4922G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376156 | |||||||
| chr1:119376204 | C | A | 17 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(14): Show |
22 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8-4874C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376204 | |||||||
| chr1:119376391 | T | C | 3 | a0001c0002t0001g0177 a0001c0002t0001g0178 a0001c0002t0001g0180 |
3 | HG01175.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-8-4687T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376391 | |||||||
| chr1:119376545 | A | C | 1 | a0001c0004t0006g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-8-4533A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376545 | |||||||
| chr1:119376570 | A | G | 1 | a0003c0005t0001g0036 | 2 | NA18941.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-8-4508A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376570 | |||||||
| chr1:119376659 | T | A | 1 | a0002c0003t0002g0020 | 2 | HG02896.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-8-4419T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376659 | |||||||
| chr1:119376691 | A | G | 105 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(102): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-8-4387A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376691 | |||||||
| chr1:119376694 | T | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0062 |
3 | HG02630.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-4384T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376694 | |||||||
| chr1:119376815 | C | T | 14 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(11): Show |
19 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-4263C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376815 | |||||||
| chr1:119376838 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8-4240C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376838 | |||||||
| chr1:119376851 | G | A | 14 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(11): Show |
19 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-4227G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376851 | |||||||
| chr1:119376882 | T | A | 1 | a0001c0001t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8-4196T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376882 | |||||||
| chr1:119376892 | A | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(181): Show |
285 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.-8-4186A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376892 | |||||||
| chr1:119376979 | C | T | 1 | a0001c0002t0001g0282 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-8-4099C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119376979 | |||||||
| chr1:119377136 | A | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3942A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377136 | |||||||
| chr1:119377149 | T | A | 14 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(11): Show |
19 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-3929T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377149 | |||||||
| chr1:119377183 | C | T | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-8-3895C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377183 | |||||||
| chr1:119377380 | C | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0078 a0001c0001t0001g0138 others(6): Show |
10 | HG00609.hp2 HG00621.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-3698C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377380 | |||||||
| chr1:119377397 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-8-3681T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377397 | |||||||
| chr1:119377588 | C | A | 11 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(8): Show |
16 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-3490C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377588 | |||||||
| chr1:119377699 | G | T | 1 | a0001c0002t0001g0233 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-8-3379G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377699 | |||||||
| chr1:119377700 | G | C | 4 | a0002c0003t0005g0070 a0002c0003t0005g0073 a0002c0003t0005g0253 others(1): Show |
4 | HG01433.hp1 HG02258.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-3378G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377700 | |||||||
| chr1:119377814 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-3264C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377814 | |||||||
| chr1:119377912 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-8-3166C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377912 | |||||||
| chr1:119377984 | T | A | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-3094T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119377984 | |||||||
| chr1:119378050 | G | GA | 44 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(41): Show |
54 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8-3021dupA | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 119378050 | ||||||
| chr1:119378138 | C | T | 1 | a0001c0002t0001g0232 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-8-2940C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378138 | |||||||
| chr1:119378139 | G | A | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-8-2939G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378139 | |||||||
| chr1:119378156 | G | A | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-2922G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378156 | |||||||
| chr1:119378353 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-8-2725C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378353 | |||||||
| chr1:119378394 | T | A | 1 | a0001c0002t0001g0181 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8-2684T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378394 | |||||||
| chr1:119378409 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-2669A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378409 | |||||||
| chr1:119378424 | C | T | 1 | a0001c0004t0006g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-8-2654C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378424 | |||||||
| chr1:119378593 | G | A | 44 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(41): Show |
54 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8-2485G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378593 | |||||||
| chr1:119378789 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-8-2289G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378789 | |||||||
| chr1:119378858 | C | A | 1 | a0001c0002t0001g0282 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-8-2220C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378858 | |||||||
| chr1:119378909 | A | T | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-8-2169A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119378909 | |||||||
| chr1:119379107 | A | G | 1 | a0001c0007t0001g0281 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-8-1971A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379107 | |||||||
| chr1:119379119 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-8-1959C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379119 | |||||||
| chr1:119379156 | GACACATG others(15): Show |
G | 1 | a0001c0001t0004g0261 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-8-1921_-8-1900del others(22): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379156 | |||||||
| chr1:119379223 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8-1855A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379223 | |||||||
| chr1:119379312 | T | C | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG00140.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-8-1766T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379312 | |||||||
| chr1:119379514 | G | GA | 18 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(15): Show |
23 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-1564_-8-1563ins others(1): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379514 | |||||||
| chr1:119379623 | A | G | 2 | a0001c0004t0006g0284 a0001c0004t0006g0285 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-8-1455A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379623 | |||||||
| chr1:119379704 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8-1374C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379704 | |||||||
| chr1:119379734 | C | T | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-1344C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379734 | |||||||
| chr1:119379792 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8-1286G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379792 | |||||||
| chr1:119379822 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0280 |
2 | HG02723.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-8-1256A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379822 | |||||||
| chr1:119379981 | C | G | 1 | a0001c0002t0001g0272 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-8-1097C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119379981 | |||||||
| chr1:119380027 | C | A | 44 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(41): Show |
54 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8-1051C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380027 | |||||||
| chr1:119380190 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0242 a0001c0001t0001g0243 |
4 | HG01257.hp2 HG01258.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-888C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380190 | |||||||
| chr1:119380191 | G | A | 1 | a0003c0005t0001g0036 | 2 | NA18941.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-8-887G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380191 | |||||||
| chr1:119380246 | C | T | 1 | a0001c0002t0001g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-8-832C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380246 | |||||||
| chr1:119380304 | G | A | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-774G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380304 | |||||||
| chr1:119380408 | G | A | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-8-670G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380408 | |||||||
| chr1:119380476 | T | C | 3 | a0001c0002t0001g0246 a0001c0002t0001g0247 a0001c0002t0001g0248 |
3 | HG01261.hp1 HG01975.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-8-602T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380476 | |||||||
| chr1:119380618 | C | T | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-460C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380618 | |||||||
| chr1:119380624 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(3): Show |
8 | HG02630.hp1 HG02886.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-454C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380624 | |||||||
| chr1:119380640 | G | A | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-438G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380640 | |||||||
| chr1:119380645 | G | A | 1 | a0001c0004t0006g0284 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-8-433G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380645 | |||||||
| chr1:119380694 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8-384T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380694 | |||||||
| chr1:119380786 | G | C | 1 | a0001c0004t0006g0284 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-8-292G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380786 | |||||||
| chr1:119380809 | T | C | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-269T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380809 | |||||||
| chr1:119380809 | TGGA | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
6 | HG02074.hp1 HG02129.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-264_-8-262delGA others(1): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 119380809 | ||||||
| chr1:119380810 | G | A | 2 | a0002c0003t0005g0073 a0002c0003t0009g0286 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-8-268G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380810 | |||||||
| chr1:119380908 | A | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(182): Show |
286 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.-8-170A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380908 | |||||||
| chr1:119380952 | G | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-8-126G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119380952 | |||||||
| chr1:119381025 | G | T | 1 | a0001c0001t0001g0260 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-8-53G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 1/7 | chr1 | 119381025 | |||||||
| chr1:119381332 | T | C | 4 | a0002c0003t0005g0070 a0002c0003t0005g0073 a0002c0003t0005g0253 others(1): Show |
4 | HG01433.hp1 HG02258.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+116T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119381332 | |||||||
| chr1:119381359 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0079 others(2): Show |
11 | NA18951.hp2 NA18961.hp2 NA18975.hp2 others(8): Show |
intron_variant | MODIFIER | c.131+143G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119381359 | |||||||
| chr1:119381413 | T | A | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.131+197T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119381413 | |||||||
| chr1:119381421 | T | C | 11 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(8): Show |
16 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.131+205T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119381421 | |||||||
| chr1:119381437 | G | C | 11 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(8): Show |
16 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.131+221G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119381437 | |||||||
| chr1:119381623 | G | A | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.131+407G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119381623 | |||||||
| chr1:119381669 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.131+453G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119381669 | |||||||
| chr1:119381681 | A | C | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.131+465A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119381681 | |||||||
| chr1:119382028 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.131+812G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382028 | |||||||
| chr1:119382138 | T | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(6): Show |
11 | HG02486.hp1 HG02630.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.132-777T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382138 | |||||||
| chr1:119382140 | T | C | 1 | a0002c0003t0002g0069 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.132-775T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382140 | |||||||
| chr1:119382303 | C | T | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.132-612C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382303 | |||||||
| chr1:119382404 | A | G | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.132-511A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382404 | |||||||
| chr1:119382413 | A | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(21): Show |
70 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.132-502A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382413 | |||||||
| chr1:119382552 | T | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | NA18965.hp1 NA19057.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-363T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382552 | |||||||
| chr1:119382644 | A | G | 1 | a0001c0004t0006g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132-271A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382644 | |||||||
| chr1:119382722 | G | A | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.132-193G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382722 | |||||||
| chr1:119382780 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(85): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.132-135C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382780 | |||||||
| chr1:119382841 | G | A | 88 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(85): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.132-74G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382841 | |||||||
| chr1:119382845 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.132-70C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 2/7 | chr1 | 119382845 | |||||||
| chr1:119383313 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(181): Show |
285 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.283+247T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119383313 | |||||||
| chr1:119383659 | C | T | 1 | a0001c0001t0001g0003 | 10 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+593C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119383659 | |||||||
| chr1:119383662 | C | CAAT | 2 | a0001c0001t0001g0060 a0001c0001t0001g0279 |
3 | HG00438.hp1 HG00597.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.283+617_283+619dup others(3): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 119383662 | ||||||
| chr1:119383730 | C | T | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+664C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119383730 | |||||||
| chr1:119383731 | G | A | 1 | a0003c0005t0001g0036 | 2 | NA18941.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.283+665G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119383731 | |||||||
| chr1:119383935 | C | T | 1 | a0001c0002t0001g0231 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.284-841C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119383935 | |||||||
| chr1:119383994 | C | T | 1 | a0003c0005t0001g0036 | 2 | NA18941.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.284-782C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119383994 | |||||||
| chr1:119384139 | T | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(5): Show |
10 | HG02630.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-637T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119384139 | |||||||
| chr1:119384148 | T | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.284-628T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119384148 | |||||||
| chr1:119384174 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0259 |
2 | NA18956.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.284-602A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119384174 | |||||||
| chr1:119384186 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(85): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.284-590C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119384186 | |||||||
| chr1:119384335 | G | A | 1 | a0001c0001t0004g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.284-441G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119384335 | |||||||
| chr1:119384398 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(183): Show |
287 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.284-378C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119384398 | |||||||
| chr1:119384575 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.284-201C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119384575 | |||||||
| chr1:119384615 | CA | C | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-158delA | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 119384615 | ||||||
| chr1:119384693 | A | C | 1 | a0001c0002t0001g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.284-83A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 3/7 | chr1 | 119384693 | |||||||
| chr1:119385057 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(181): Show |
285 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(282): Show |
splice_region_variant&intron_variant | LOW | c.561+4A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385057 | |||||||
| chr1:119385147 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG00738.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.561+94A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385147 | |||||||
| chr1:119385208 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.561+155T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385208 | |||||||
| chr1:119385340 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(6): Show |
11 | HG02486.hp1 HG02630.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.561+287G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385340 | |||||||
| chr1:119385346 | T | G | 115 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(112): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.561+293T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385346 | |||||||
| chr1:119385359 | A | G | 2 | a0002c0003t0002g0061 a0002c0003t0002g0072 |
2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.561+306A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385359 | |||||||
| chr1:119385370 | A | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.561+317A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385370 | |||||||
| chr1:119385462 | A | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA18941.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.561+409A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385462 | |||||||
| chr1:119385491 | C | A | 1 | a0001c0002t0001g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.561+438C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385491 | |||||||
| chr1:119385564 | G | A | 18 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(15): Show |
23 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.561+511G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385564 | |||||||
| chr1:119385570 | T | G | 48 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0012 others(45): Show |
71 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.561+517T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385570 | |||||||
| chr1:119385697 | G | T | 1 | a0001c0001t0001g0034 | 2 | NA18942.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.561+644G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385697 | |||||||
| chr1:119385760 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(181): Show |
285 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.561+707A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385760 | |||||||
| chr1:119385869 | G | A | 18 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(15): Show |
23 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.562-753G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385869 | |||||||
| chr1:119385955 | C | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.562-667C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119385955 | |||||||
| chr1:119386207 | GTTGT | G | 6 | a0001c0001t0001g0040 a0001c0001t0001g0154 a0001c0001t0001g0169 others(3): Show |
7 | HG02145.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-396_562-393del others(4): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 119386207 | ||||||
| chr1:119386316 | C | T | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.562-306C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119386316 | |||||||
| chr1:119386317 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.562-305G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119386317 | |||||||
| chr1:119386334 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(6): Show |
11 | HG02486.hp1 HG02630.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.562-288C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119386334 | |||||||
| chr1:119386412 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(21): Show |
70 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.562-210C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 4/7 | chr1 | 119386412 | |||||||
| chr1:119386980 | CTG | C | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.771+151_771+152del others(2): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119386980 | ||||||
| chr1:119387041 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG00558.hp2 HG02015.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.771+210C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387041 | |||||||
| chr1:119387056 | T | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.771+225T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387056 | |||||||
| chr1:119387090 | A | T | 27 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(24): Show |
34 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(31): Show |
intron_variant | MODIFIER | c.771+259A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387090 | |||||||
| chr1:119387172 | A | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0078 a0001c0001t0001g0138 others(7): Show |
11 | HG00609.hp2 HG00621.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.771+341A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387172 | |||||||
| chr1:119387204 | C | T | 3 | a0001c0002t0001g0246 a0001c0002t0001g0247 a0001c0002t0001g0248 |
3 | HG01261.hp1 HG01975.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.771+373C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387204 | |||||||
| chr1:119387205 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.771+374G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387205 | |||||||
| chr1:119387313 | T | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0078 a0001c0001t0001g0138 others(7): Show |
11 | HG00609.hp2 HG00621.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.771+482T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387313 | |||||||
| chr1:119387522 | A | T | 1 | a0001c0004t0006g0284 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.771+691A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387522 | |||||||
| chr1:119387661 | C | T | 1 | a0005c0009t0001g0258 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.771+830C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387661 | |||||||
| chr1:119387715 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0079 others(2): Show |
11 | NA18951.hp2 NA18961.hp2 NA18975.hp2 others(8): Show |
intron_variant | MODIFIER | c.771+884C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387715 | |||||||
| chr1:119387745 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(21): Show |
70 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.771+914A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387745 | |||||||
| chr1:119387933 | G | C | 2 | a0001c0004t0006g0284 a0001c0004t0006g0285 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.771+1102G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387933 | |||||||
| chr1:119387999 | C | T | 4 | a0002c0003t0005g0070 a0002c0003t0005g0073 a0002c0003t0005g0253 others(1): Show |
4 | HG01433.hp1 HG02258.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+1168C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119387999 | |||||||
| chr1:119388036 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.771+1205G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388036 | |||||||
| chr1:119388079 | T | C | 18 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(15): Show |
23 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.771+1248T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388079 | |||||||
| chr1:119388105 | G | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.771+1274G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388105 | |||||||
| chr1:119388152 | G | T | 1 | a0001c0002t0001g0210 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.771+1321G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388152 | |||||||
| chr1:119388199 | A | G | 4 | a0001c0002t0003g0055 a0001c0002t0003g0227 a0001c0002t0003g0228 others(1): Show |
5 | HG01928.hp2 HG01934.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+1368A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388199 | |||||||
| chr1:119388203 | G | C | 1 | a0001c0002t0001g0186 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.771+1372G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388203 | |||||||
| chr1:119388216 | C | G | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.771+1385C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388216 | |||||||
| chr1:119388217 | C | G | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.771+1386C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388217 | |||||||
| chr1:119388267 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.771+1436C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388267 | |||||||
| chr1:119388340 | T | C | 1 | a0001c0002t0001g0187 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.771+1509T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388340 | |||||||
| chr1:119388386 | T | G | 18 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 others(15): Show |
23 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.771+1555T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388386 | |||||||
| chr1:119388442 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.771+1611C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388442 | |||||||
| chr1:119388457 | T | G | 1 | a0001c0002t0001g0188 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.771+1626T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388457 | |||||||
| chr1:119388594 | C | T | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.771+1763C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388594 | |||||||
| chr1:119388923 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(21): Show |
70 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.771+2092C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119388923 | |||||||
| chr1:119389091 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.771+2260C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389091 | |||||||
| chr1:119389096 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(21): Show |
70 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.771+2265G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389096 | |||||||
| chr1:119389137 | C | CATATATA others(79): Show |
1 | a0001c0001t0001g0138 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.771+2319_771+2320i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
1 | a0001c0001t0001g0139 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.771+2319_771+2320i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(99): Show |
1 | a0001c0001t0001g0063 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.771+2323_771+2324i others(108): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(65): Show |
1 | a0001c0002t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.771+2333_771+2334i others(74): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(57): Show |
1 | a0001c0001t0001g0076 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.771+2335_771+2336i others(66): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.771+2335_771+2336i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(47): Show |
1 | a0001c0001t0001g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.771+2340_771+2341i others(56): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0002t0001g0047 | 2 | NA18988.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
1 | a0001c0002t0001g0048 | 2 | HG02080.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
1 | a0001c0002t0001g0190 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0002t0001g0191 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
2 | a0001c0002t0001g0186 a0001c0002t0001g0192 |
2 | HG00673.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(55): Show |
1 | a0001c0001t0001g0160 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(64): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(57): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0161 |
3 | HG02895.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(66): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(59): Show |
1 | a0001c0001t0001g0162 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(68): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(95): Show |
1 | a0001c0001t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(104): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(65): Show |
1 | a0001c0001t0001g0133 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(74): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(67): Show |
1 | a0001c0001t0001g0236 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(76): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(69): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0057 |
4 | HG01257.hp2 HG01258.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(69): Show |
1 | a0001c0001t0001g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(57): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0163 |
3 | HG02109.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(66): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(59): Show |
1 | a0001c0001t0001g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(68): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(63): Show |
1 | a0001c0001t0001g0165 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(72): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(53): Show |
2 | a0001c0001t0001g0166 a0001c0001t0001g0274 |
2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(62): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(55): Show |
1 | a0001c0001t0001g0280 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(64): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(65): Show |
1 | a0001c0001t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(74): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(69): Show |
3 | a0001c0001t0001g0025 a0001c0001t0001g0084 a0001c0001t0001g0237 |
4 | HG01106.hp2 HG01884.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
1 | a0001c0001t0001g0093 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(77): Show |
1 | a0001c0002t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(86): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
2 | a0001c0002t0001g0180 a0001c0002t0001g0193 |
2 | HG02486.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(83): Show |
1 | a0001c0002t0001g0194 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(92): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(63): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0159 |
2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(72): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(55): Show |
1 | a0001c0001t0001g0059 | 2 | HG01169.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(64): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(57): Show |
1 | a0001c0001t0001g0273 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(66): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(65): Show |
1 | a0001c0001t0001g0041 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(74): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(67): Show |
1 | a0001c0001t0001g0174 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(76): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(127): Show |
1 | a0001c0001t0001g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(136): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0001t0001g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(81): Show |
1 | a0001c0001t0001g0095 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(90): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(67): Show |
1 | a0001c0001t0001g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(76): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(69): Show |
1 | a0001c0001t0001g0238 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
5 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
6 | HG00099.hp1 HG00280.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
3 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0004c0010t0001g0097 |
4 | HG01192.hp2 HG02145.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
1 | a0001c0002t0001g0195 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(81): Show |
6 | a0001c0002t0001g0042 a0001c0002t0001g0153 a0001c0002t0001g0179 others(3): Show |
7 | HG01257.hp1 HG01978.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(90): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(83): Show |
1 | a0001c0002t0001g0043 | 2 | HG00323.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(92): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(85): Show |
3 | a0001c0002t0001g0049 a0001c0002t0001g0198 a0001c0002t0001g0270 |
4 | HG01106.hp1 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(94): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(87): Show |
1 | a0001c0002t0001g0199 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(96): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(69): Show |
3 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0136 |
3 | HG01981.hp2 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
3 | a0001c0001t0001g0080 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG02622.hp2 HG02717.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
1 | a0001c0001t0001g0102 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(59): Show |
1 | a0001c0001t0001g0027 | 2 | HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(68): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
1 | a0001c0001t0001g0103 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(57): Show |
2 | a0001c0001t0001g0279 a0001c0001t0007g0244 |
2 | HG02155.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(66): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(97): Show |
1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(106): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
8 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0034 others(5): Show |
13 | HG00609.hp2 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
2 | a0001c0001t0001g0087 a0001c0001t0001g0267 |
2 | HG02015.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(77): Show |
1 | a0001c0001t0001g0127 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(86): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
1 | a0001c0001t0001g0028 | 2 | HG00544.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(81): Show |
1 | a0001c0001t0001g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(90): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(85): Show |
1 | a0001c0001t0001g0104 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(94): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0001t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
1 | a0001c0001t0001g0105 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(74): Show |
1 | a0001c0001t0001g0106 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(83): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(85): Show |
1 | a0001c0002t0001g0231 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(94): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(87): Show |
1 | a0001c0002t0008g0200 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(96): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
1 | a0001c0002t0001g0044 | 2 | HG02273.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(81): Show |
4 | a0001c0002t0001g0050 a0001c0002t0001g0184 a0001c0002t0001g0201 others(1): Show |
5 | HG00099.hp2 HG00280.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(90): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(83): Show |
10 | a0001c0002t0001g0004 a0001c0002t0001g0009 a0001c0002t0001g0051 others(7): Show |
21 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(92): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(85): Show |
6 | a0001c0002t0001g0012 a0001c0002t0001g0045 a0001c0002t0001g0052 others(3): Show |
10 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(94): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(87): Show |
1 | a0001c0002t0001g0214 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(96): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(89): Show |
1 | a0001c0002t0001g0215 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(98): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(87): Show |
1 | a0001c0002t0001g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(96): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(83): Show |
1 | a0001c0002t0001g0217 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(92): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(67): Show |
1 | a0001c0001t0001g0107 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(76): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0001t0001g0008 | 4 | HG00735.hp1 NA18945.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0147 |
7 | HG02109.hp1 HG02257.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
1 | a0001c0001t0001g0108 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(81): Show |
1 | a0001c0001t0002g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(90): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(63): Show |
1 | a0001c0001t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(72): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(59): Show |
1 | a0001c0001t0001g0060 | 2 | HG00438.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(68): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0001t0001g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(65): Show |
2 | a0001c0001t0001g0149 a0001c0001t0001g0239 |
2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(74): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
1 | a0001c0001t0001g0240 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
4 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0109 others(1): Show |
7 | HG00140.hp1 HG00639.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(81): Show |
1 | a0001c0002t0001g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(90): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(83): Show |
4 | a0001c0002t0001g0177 a0001c0002t0001g0202 a0001c0002t0001g0219 others(1): Show |
4 | HG01175.hp1 HG01175.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(92): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(85): Show |
6 | a0001c0002t0001g0002 a0001c0002t0001g0182 a0001c0002t0001g0187 others(3): Show |
15 | HG00597.hp2 HG00642.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(94): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(87): Show |
4 | a0001c0002t0001g0053 a0001c0002t0001g0151 a0001c0002t0001g0178 others(1): Show |
5 | HG01074.hp1 HG02970.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(96): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(69): Show |
1 | a0001c0001t0001g0112 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0001t0001g0030 | 2 | HG02523.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
5 | a0001c0001t0001g0007 a0001c0001t0001g0113 a0001c0001t0001g0128 others(2): Show |
9 | HG00423.hp2 HG02080.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0129 |
3 | NA18941.hp2 NA18971.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0114 |
2 | HG00609.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(83): Show |
1 | a0001c0001t0001g0115 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(92): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(61): Show |
1 | a0001c0007t0001g0281 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(70): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(65): Show |
1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(74): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(67): Show |
1 | a0001c0001t0001g0037 | 2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(76): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0001t0001g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
1 | a0001c0001t0001g0040 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(67): Show |
1 | a0001c0001t0001g0275 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(76): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(67): Show |
1 | a0001c0001t0001g0241 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(76): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
1 | a0001c0002t0001g0282 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(83): Show |
1 | a0001c0002t0001g0205 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(92): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(85): Show |
2 | a0001c0002t0001g0013 a0001c0002t0001g0206 |
4 | HG02004.hp1 HG03942.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(94): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(87): Show |
3 | a0001c0002t0001g0046 a0001c0002t0001g0188 a0001c0002t0001g0220 |
4 | HG01993.hp2 HG04204.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(96): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
1 | a0001c0001t0001g0006 | 6 | NA18951.hp2 NA18961.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0135 |
3 | NA18964.hp2 NA18979.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(77): Show |
1 | a0001c0001t0001g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(86): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(65): Show |
1 | a0001c0001t0001g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(74): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(67): Show |
1 | a0001c0001t0001g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(76): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(63): Show |
1 | a0001c0001t0001g0016 | 3 | NA18939.hp2 NA18966.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(72): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(65): Show |
1 | a0001c0001t0001g0283 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(74): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(69): Show |
1 | a0001c0001t0001g0017 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0001t0001g0155 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
1 | a0001c0001t0001g0169 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(81): Show |
1 | a0001c0001t0001g0276 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(90): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(97): Show |
1 | a0001c0001t0001g0265 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(106): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(79): Show |
1 | a0001c0001t0001g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(88): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(87): Show |
1 | a0001c0002t0001g0207 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(96): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(89): Show |
1 | a0001c0002t0001g0208 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(98): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
1 | a0001c0001t0001g0079 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(77): Show |
1 | a0001c0001t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(86): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(69): Show |
1 | a0001c0001t0001g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
1 | a0001c0001t0001g0156 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(77): Show |
1 | a0001c0001t0001g0157 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(86): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(91): Show |
2 | a0001c0002t0001g0209 a0001c0002t0001g0248 |
2 | HG01975.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(100): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(75): Show |
1 | a0001c0002t0001g0120 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(77): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0089 |
3 | HG03579.hp1 NA18975.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(86): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(73): Show |
1 | a0001c0001t0001g0158 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(82): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(81): Show |
1 | a0001c0001t0001g0131 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(90): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(85): Show |
1 | a0001c0001t0001g0121 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(94): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(89): Show |
1 | a0001c0001t0001g0122 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(98): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(91): Show |
1 | a0001c0001t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(100): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(71): Show |
1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(59): Show |
1 | a0001c0001t0001g0277 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(68): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(57): Show |
1 | a0001c0001t0001g0278 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(66): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(65): Show |
1 | a0001c0001t0001g0176 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(74): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(69): Show |
1 | a0001c0001t0001g0171 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(49): Show |
1 | a0001c0002t0003g0227 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(58): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(95): Show |
1 | a0001c0001t0001g0019 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(104): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(47): Show |
1 | a0001c0002t0003g0228 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(56): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(45): Show |
2 | a0001c0002t0001g0222 a0001c0002t0003g0055 |
3 | HG01934.hp2 NA18954.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(54): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(41): Show |
1 | a0001c0002t0001g0223 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(50): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(43): Show |
2 | a0001c0002t0001g0054 a0001c0002t0003g0229 |
3 | HG02027.hp1 HG02148.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(52): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(45): Show |
3 | a0001c0002t0001g0224 a0001c0002t0001g0225 a0001c0002t0001g0233 |
3 | HG00673.hp2 HG02165.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(54): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(47): Show |
1 | a0001c0002t0001g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(56): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389137 | C | CATATATA others(43): Show |
1 | a0002c0003t0009g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.771+2336_771+2337i others(52): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389137 | ||||||
| chr1:119389138 | A | ATATATAT others(43): Show |
1 | a0002c0003t0005g0073 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(52): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389138 | ||||||
| chr1:119389138 | A | ATATATAT others(37): Show |
1 | a0002c0003t0005g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.771+2330_771+2331i others(46): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389138 | ||||||
| chr1:119389140 | A | ATATATAT others(69): Show |
1 | a0001c0001t0001g0018 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.771+2327_771+2328i others(78): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389140 | ||||||
| chr1:119389140 | A | ATATATAT others(81): Show |
1 | a0001c0001t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(90): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389140 | ||||||
| chr1:119389140 | A | ATATATAT others(83): Show |
1 | a0001c0001t0001g0023 | 2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.771+2337_771+2338i others(92): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389140 | ||||||
| chr1:119389140 | A | ATATATAT others(53): Show |
1 | a0001c0001t0001g0098 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(62): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389140 | ||||||
| chr1:119389140 | A | ATATATAT others(57): Show |
1 | a0001c0001t0001g0111 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(66): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389140 | ||||||
| chr1:119389142 | A | ATATATAT others(71): Show |
1 | a0001c0002t0001g0221 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(80): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389142 | ||||||
| chr1:119389142 | A | ATATATAT others(49): Show |
1 | a0002c0003t0005g0070 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(58): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389142 | ||||||
| chr1:119389146 | A | ATATATAT others(51): Show |
1 | a0001c0001t0001g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(60): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389146 | ||||||
| chr1:119389146 | A | ATATATAT others(51): Show |
1 | a0001c0001t0001g0125 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(60): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389146 | ||||||
| chr1:119389146 | A | ATATATAT others(55): Show |
1 | a0001c0001t0001g0243 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(64): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389146 | ||||||
| chr1:119389146 | A | ATATATAT others(29): Show |
1 | a0002c0003t0002g0068 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.771+2330_771+2331i others(38): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389146 | ||||||
| chr1:119389146 | A | ATATATAT others(27): Show |
4 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(1): Show |
8 | HG01891.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.771+2328_771+2329i others(36): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389146 | ||||||
| chr1:119389146 | A | ATATATAT others(25): Show |
1 | a0002c0003t0002g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.771+2328_771+2329i others(34): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389146 | ||||||
| chr1:119389146 | A | ATATATAT others(25): Show |
5 | a0002c0003t0002g0022 a0002c0003t0002g0061 a0002c0003t0002g0072 others(2): Show |
6 | HG02647.hp2 HG02895.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.771+2326_771+2327i others(34): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389146 | ||||||
| chr1:119389148 | A | ATGTGTAT others(45): Show |
2 | a0001c0004t0006g0284 a0001c0004t0006g0285 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.771+2318_771+2319i others(54): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389148 | ||||||
| chr1:119389148 | A | ATGTGTAT others(43): Show |
1 | a0001c0004t0006g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.771+2318_771+2319i others(52): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389148 | ||||||
| chr1:119389150 | A | ATG | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(22): Show |
72 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.771+2320_771+2321i others(4): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389150 | ||||||
| chr1:119389152 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(22): Show |
72 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.771+2321A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389152 | |||||||
| chr1:119389154 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(22): Show |
72 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.771+2323A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389154 | |||||||
| chr1:119389156 | A | ATATATAT others(41): Show |
1 | a0001c0001t0001g0110 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(50): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389156 | ||||||
| chr1:119389156 | A | G | 3 | a0001c0004t0006g0284 a0001c0004t0006g0285 a0001c0004t0006g0287 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.771+2325A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389156 | |||||||
| chr1:119389167 | T | TATATATA others(75): Show |
1 | a0001c0001t0001g0088 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.771+2337_771+2338i others(84): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389167 | ||||||
| chr1:119389167 | T | TATATATA others(21): Show |
1 | a0001c0001t0001g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.771+2337_771+2338i others(30): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389167 | ||||||
| chr1:119389169 | C | T | 55 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(52): Show |
68 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.771+2338C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389169 | |||||||
| chr1:119389266 | G | T | 1 | a0001c0002t0001g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.771+2435G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389266 | |||||||
| chr1:119389305 | A | G | 1 | a0001c0002t0001g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.771+2474A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389305 | |||||||
| chr1:119389340 | T | C | 1 | a0001c0002t0001g0045 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.771+2509T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389340 | |||||||
| chr1:119389384 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(181): Show |
285 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.771+2553A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389384 | |||||||
| chr1:119389507 | G | C | 88 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(85): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.772-2603G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389507 | |||||||
| chr1:119389606 | G | A | 11 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(8): Show |
16 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.772-2504G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389606 | |||||||
| chr1:119389632 | AT | A | 17 | a0001c0001t0001g0075 a0001c0001t0001g0100 a0001c0001t0001g0273 others(14): Show |
20 | HG00280.hp2 HG00597.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.772-2463delT | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389632 | ||||||
| chr1:119389632 | ATT | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(67): Show |
127 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.772-2464_772-2463d others(4): Show |
HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119389632 | ||||||
| chr1:119389688 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.772-2422A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389688 | |||||||
| chr1:119389766 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(40): Show |
95 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(92): Show |
intron_variant | MODIFIER | c.772-2344C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119389766 | |||||||
| chr1:119390162 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.772-1948C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390162 | |||||||
| chr1:119390213 | C | T | 3 | a0001c0002t0001g0051 a0001c0002t0001g0214 a0001c0002t0001g0219 |
4 | HG01099.hp1 HG01109.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-1897C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390213 | |||||||
| chr1:119390222 | G | C | 1 | a0002c0003t0005g0070 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.772-1888G>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390222 | |||||||
| chr1:119390227 | T | G | 1 | a0001c0001t0001g0101 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.772-1883T>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390227 | |||||||
| chr1:119390230 | T | C | 1 | a0001c0002t0001g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.772-1880T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390230 | |||||||
| chr1:119390248 | T | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(22): Show |
72 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.772-1862T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390248 | |||||||
| chr1:119390260 | A | AT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(37): Show |
92 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.772-1841dupT | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119390260 | ||||||
| chr1:119390260 | AT | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0062 others(3): Show |
8 | HG02630.hp1 HG02886.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.772-1841delT | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 119390260 | ||||||
| chr1:119390385 | G | A | 3 | a0002c0003t0002g0022 a0002c0003t0002g0061 a0002c0003t0002g0072 |
4 | HG02647.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-1725G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390385 | |||||||
| chr1:119390629 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0035 others(21): Show |
70 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.772-1481T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390629 | |||||||
| chr1:119390769 | G | A | 1 | a0001c0002t0001g0206 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.772-1341G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390769 | |||||||
| chr1:119390794 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.772-1316T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390794 | |||||||
| chr1:119390901 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.772-1209G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390901 | |||||||
| chr1:119390921 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.772-1189A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119390921 | |||||||
| chr1:119391043 | G | T | 15 | a0002c0003t0002g0010 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.772-1067G>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391043 | |||||||
| chr1:119391091 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.772-1019C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391091 | |||||||
| chr1:119391096 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(85): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.772-1014C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391096 | |||||||
| chr1:119391200 | G | A | 1 | a0003c0005t0001g0036 | 2 | NA18941.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.772-910G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391200 | |||||||
| chr1:119391314 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.772-796G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391314 | |||||||
| chr1:119391463 | T | C | 1 | a0001c0001t0001g0034 | 2 | NA18942.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.772-647T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391463 | |||||||
| chr1:119391526 | T | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | NA18965.hp1 NA19057.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-584T>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391526 | |||||||
| chr1:119391590 | A | C | 1 | a0001c0002t0001g0196 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.772-520A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391590 | |||||||
| chr1:119391671 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(183): Show |
287 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.772-439T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391671 | |||||||
| chr1:119391682 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.772-428T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391682 | |||||||
| chr1:119391820 | A | C | 48 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(45): Show |
58 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.772-290A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391820 | |||||||
| chr1:119391955 | G | A | 6 | a0001c0002t0001g0186 a0001c0002t0001g0190 a0001c0002t0001g0191 others(3): Show |
6 | HG00673.hp1 NA18747.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-155G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119391955 | |||||||
| chr1:119392068 | C | A | 1 | a0001c0002t0001g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.772-42C>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 5/7 | chr1 | 119392068 | |||||||
| chr1:119392362 | C | G | 3 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 |
3 | HG01099.hp2 HG01106.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.930+94C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 6/7 | chr1 | 119392362 | |||||||
| chr1:119392438 | T | C | 63 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
80 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.930+170T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 6/7 | chr1 | 119392438 | |||||||
| chr1:119392513 | A | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.931-105A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 6/7 | chr1 | 119392513 | |||||||
| chr1:119392698 | A | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0154 a0001c0001t0001g0169 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+11A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119392698 | |||||||
| chr1:119392771 | C | G | 1 | a0001c0001t0001g0257 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1000+84C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119392771 | |||||||
| chr1:119392777 | C | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02015.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1000+90C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119392777 | |||||||
| chr1:119392884 | A | T | 152 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(149): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1000+197A>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119392884 | |||||||
| chr1:119392920 | T | C | 45 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(42): Show |
55 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1000+233T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119392920 | |||||||
| chr1:119393139 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG00558.hp2 HG02015.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1000+452C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393139 | |||||||
| chr1:119393201 | A | G | 45 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(42): Show |
55 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1000+514A>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393201 | |||||||
| chr1:119393223 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1000+536T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393223 | |||||||
| chr1:119393293 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1001-492C>G | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393293 | |||||||
| chr1:119393424 | C | T | 22 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(19): Show |
28 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1001-361C>T | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393424 | |||||||
| chr1:119393538 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1001-247A>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393538 | |||||||
| chr1:119393640 | G | A | 107 | a0001c0001t0001g0075 a0001c0001t0002g0077 a0001c0002t0001g0002 others(104): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1001-145G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393640 | |||||||
| chr1:119393664 | T | C | 1 | a0001c0002t0001g0213 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1001-121T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393664 | |||||||
| chr1:119393675 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1001-110T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393675 | |||||||
| chr1:119393687 | T | C | 3 | a0001c0001t0001g0109 a0001c0001t0001g0145 a0004c0010t0001g0097 |
3 | HG02145.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1001-98T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393687 | |||||||
| chr1:119393695 | G | A | 2 | a0001c0002t0001g0177 a0001c0002t0001g0178 |
2 | HG01175.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1001-90G>A | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393695 | |||||||
| chr1:119393725 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0288 |
2 | HG02698.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1001-60T>C | HAO2 | ENSG00000116882.15 | transcript | ENST00000325945.4 | protein_coding | 7/7 | chr1 | 119393725 |