Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 375061 |
| ensemblid | ENSG00000182118.8 |
| hgncid | 25057 |
| symbol | FAM89A |
| name | family with sequence similarity 89 member A |
| refseq_nuc | NM_198552.3 |
| refseq_prot | NP_940954.1 |
| ensembl_nuc | ENST00000366654.5 |
| ensembl_prot | ENSP00000355614.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 231018958 |
| end | 231040254 |
| strand | - |
| ver | v1.2 |
| region | chr1:231018958-231040254 |
| region5000 | chr1:231013958-231045254 |
| regionname0 | FAM89A_chr1_231018958_231040254 |
| regionname5000 | FAM89A_chr1_231013958_231045254 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 184 | 449 | 93 | 76 | 214 | 18 | 46 | 174 | FAM89A_chr1_231013958_231045254 | FAM89A | MSGAR others(179): Show |
chr1 | 231013958 | 231045254 |
| a0002 | 0/0 | 184 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | MSGAR others(179): Show |
chr1 | 231013958 | 231045254 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 552 | 449 | 93 | 76 | 214 | 18 | 46 | FAM89A_chr1_231013958_231045254 | FAM89A | ATGAG others(547): Show |
chr1 | 231013958 | 231045254 | ||
| a0002c0002 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | ATGAG others(547): Show |
chr1 | 231013958 | 231045254 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1503 | 434 | 89 | 71 | 209 | 18 | 46 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| a0001c0001t0002 | 0/0 | 1503 | 4 | 3 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| a0001c0001t0003 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| a0001c0001t0004 | 0/0 | 1503 | 2 | 0 | 2 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| a0001c0001t0005 | 0/0 | 1503 | 2 | 0 | 2 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| a0001c0001t0006 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| a0001c0001t0007 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| a0001c0001t0008 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| a0001c0001t0009 | 0/1 | 1504 | 1 | 0 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1499): Show |
chr1 | 231013958 | 231045254 |
| a0001c0001t0010 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| a0002c0002t0001 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | GGTTC others(1498): Show |
chr1 | 231013958 | 231045254 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 0 | 8 | 0 | 3 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0003 | 0/0 | 11 | 0 | 3 | 7 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0004 | 0/0 | 10 | 1 | 0 | 7 | 0 | 2 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0005 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0009g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | FIN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0291 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0315 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0314 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | IBS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0134 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18947 | hp2 | a0001 | c0001 | t0008 | g0250 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18976 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18995 | hp1 | a0001 | c0001 | t0007 | g0210 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19012 | hp1 | a0001 | c0001 | t0010 | g0089 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ASW | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ASW | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | TSI | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | GIH | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | GIH | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | USA | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | USA | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | LWK | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0149 | REF | REF | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0270 | REF | REF | FAM89A_chr1_231013958_231045254 | FAM89A | chr1 | 231013958 | 231045254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231019991 | C | T | 1 | a0002 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.427G>A | p.Asp143Asn | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 470/1503 | 427/555 | 143/184 | chr1 | 231019991 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231019055 | T | C | 1 | a0001c0001t0002 | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*808A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 808 | chr1 | 231019055 | ||||||
| chr1:231019175 | C | CT | 5 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(2): Show |
245 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*687dupA | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 687 | chr1 | 231019175 | ||||||
| chr1:231019175 | C | CTT | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(2): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*686_*687dupAA | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 687 | chr1 | 231019175 | ||||||
| chr1:231019313 | A | G | 1 | a0001c0001t0008 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*550T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 550 | chr1 | 231019313 | ||||||
| chr1:231019392 | C | T | 1 | a0001c0001t0003 | 2 | NA18966.hp2 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*471G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 471 | chr1 | 231019392 | ||||||
| chr1:231019580 | A | G | 1 | a0001c0001t0007 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*283T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 283 | chr1 | 231019580 | ||||||
| chr1:231019615 | A | G | 1 | a0001c0001t0006 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 248 | chr1 | 231019615 | ||||||
| chr1:231019701 | T | A | 1 | a0001c0001t0010 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162A>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 162 | chr1 | 231019701 | ||||||
| chr1:231019753 | G | C | 1 | a0001c0001t0004 | 2 | HG00735.hp1 HG00738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*110C>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 110 | chr1 | 231019753 | ||||||
| chr1:231019808 | G | C | 1 | a0001c0001t0005 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*55C>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 2/2 | 55 | chr1 | 231019808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231020192 | A | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0135 a0001c0001t0001g0143 others(6): Show |
10 | HG01106.hp2 HG02145.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-66T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020192 | |||||||
| chr1:231020203 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0074 others(2): Show |
8 | HG01175.hp1 HG01515.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.292-77C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020203 | |||||||
| chr1:231020207 | T | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0065 others(6): Show |
13 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.292-81A>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020207 | |||||||
| chr1:231020259 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.292-133C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020259 | |||||||
| chr1:231020266 | T | C | 1 | a0001c0001t0006g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.292-140A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020266 | |||||||
| chr1:231020283 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(99): Show |
146 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.292-157T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020283 | |||||||
| chr1:231020295 | T | C | 9 | a0001c0001t0001g0186 a0001c0001t0001g0262 a0001c0001t0001g0267 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-169A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020295 | |||||||
| chr1:231020327 | T | A | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.292-201A>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020327 | |||||||
| chr1:231020483 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-357G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020483 | |||||||
| chr1:231020512 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292-386G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020512 | |||||||
| chr1:231020709 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.292-583A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020709 | |||||||
| chr1:231020767 | A | G | 70 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0017 others(67): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.292-641T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020767 | |||||||
| chr1:231020840 | A | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0135 a0001c0001t0001g0192 |
4 | HG02965.hp2 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-714T>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020840 | |||||||
| chr1:231020943 | T | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0135 a0001c0001t0001g0192 others(6): Show |
10 | HG02109.hp2 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-817A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020943 | |||||||
| chr1:231020997 | T | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(89): Show |
130 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.292-871A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231020997 | |||||||
| chr1:231021090 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(79): Show |
116 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.292-964C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021090 | |||||||
| chr1:231021110 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(91): Show |
132 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.292-984A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021110 | |||||||
| chr1:231021151 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.292-1025A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021151 | |||||||
| chr1:231021269 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0192 |
2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.292-1143G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021269 | |||||||
| chr1:231021351 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.292-1225T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021351 | |||||||
| chr1:231021401 | T | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0093 a0001c0001t0001g0306 |
4 | HG02451.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-1275A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021401 | |||||||
| chr1:231021409 | TG | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(74): Show |
110 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.292-1284delC | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021409 | |||||||
| chr1:231021426 | A | G | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.292-1300T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021426 | |||||||
| chr1:231021542 | A | C | 6 | a0001c0001t0001g0135 a0001c0001t0001g0192 a0001c0001t0001g0267 others(3): Show |
6 | HG02109.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-1416T>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021542 | |||||||
| chr1:231021627 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.292-1501C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021627 | |||||||
| chr1:231021754 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0259 a0001c0001t0001g0272 others(2): Show |
6 | HG02615.hp2 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-1628G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021754 | |||||||
| chr1:231021811 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1685A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021811 | |||||||
| chr1:231021819 | T | C | 4 | a0001c0001t0001g0267 a0001c0001t0002g0184 a0001c0001t0002g0264 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-1693A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021819 | |||||||
| chr1:231021833 | A | C | 1 | a0001c0001t0006g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.292-1707T>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021833 | |||||||
| chr1:231021881 | T | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02559.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.292-1755A>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021881 | |||||||
| chr1:231021925 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0144 others(2): Show |
8 | HG02145.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.292-1799G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021925 | |||||||
| chr1:231021971 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.292-1845C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021971 | |||||||
| chr1:231021975 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(131): Show |
180 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.292-1849A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021975 | |||||||
| chr1:231021983 | A | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(62): Show |
96 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.292-1857T>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021983 | |||||||
| chr1:231021984 | G | C | 1 | a0001c0001t0001g0309 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.292-1858C>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231021984 | |||||||
| chr1:231022118 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0144 others(2): Show |
8 | HG02145.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.292-1992C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022118 | |||||||
| chr1:231022250 | T | C | 3 | a0001c0001t0002g0184 a0001c0001t0002g0264 a0001c0001t0002g0268 |
3 | HG02572.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.292-2124A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022250 | |||||||
| chr1:231022303 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-2177G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022303 | |||||||
| chr1:231022366 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.292-2240G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022366 | |||||||
| chr1:231022474 | A | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0020 others(39): Show |
66 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.292-2348T>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022474 | |||||||
| chr1:231022531 | CT | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-2406delA | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022531 | |||||||
| chr1:231022537 | T | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-2411A>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022537 | |||||||
| chr1:231022551 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.292-2425G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022551 | |||||||
| chr1:231022822 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.292-2696C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022822 | |||||||
| chr1:231022898 | A | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(197): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.292-2772T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022898 | |||||||
| chr1:231022931 | C | CCCA | 166 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(163): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.292-2808_292-2806d others(5): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022931 | |||||||
| chr1:231022988 | C | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-2862G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231022988 | |||||||
| chr1:231023027 | G | A | 1 | a0001c0001t0006g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.292-2901C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023027 | |||||||
| chr1:231023082 | C | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-2956G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023082 | |||||||
| chr1:231023099 | G | A | 10 | a0001c0001t0001g0135 a0001c0001t0001g0192 a0001c0001t0001g0196 others(7): Show |
10 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-2973C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023099 | |||||||
| chr1:231023185 | C | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-3059G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023185 | |||||||
| chr1:231023220 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.292-3094C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023220 | |||||||
| chr1:231023337 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(104): Show |
148 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.292-3211C>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023337 | |||||||
| chr1:231023399 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-3273C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023399 | |||||||
| chr1:231023406 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.292-3280G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023406 | |||||||
| chr1:231023416 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.292-3290G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023416 | |||||||
| chr1:231023433 | T | C | 92 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(89): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.292-3307A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023433 | |||||||
| chr1:231023434 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.292-3308C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023434 | |||||||
| chr1:231023436 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.292-3310G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023436 | |||||||
| chr1:231023477 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0143 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.292-3351A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023477 | |||||||
| chr1:231023484 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.292-3358T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023484 | |||||||
| chr1:231023502 | G | A | 11 | a0001c0001t0001g0053 a0001c0001t0001g0093 a0001c0001t0001g0135 others(8): Show |
12 | HG02109.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.292-3376C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023502 | |||||||
| chr1:231023899 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.292-3773T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023899 | |||||||
| chr1:231023999 | A | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(176): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.292-3873T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231023999 | |||||||
| chr1:231024118 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.292-3992G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024118 | |||||||
| chr1:231024129 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(195): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.292-4003G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024129 | |||||||
| chr1:231024138 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.292-4012T>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024138 | |||||||
| chr1:231024202 | CA | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(132): Show |
179 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.292-4077delT | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024202 | |||||||
| chr1:231024202 | CAA | C | 40 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0037 others(37): Show |
49 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.292-4078_292-4077d others(4): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024202 | |||||||
| chr1:231024231 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-4105C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024231 | |||||||
| chr1:231024249 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.292-4123T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024249 | |||||||
| chr1:231024296 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0192 |
2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.292-4170C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024296 | |||||||
| chr1:231024328 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.292-4202A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024328 | |||||||
| chr1:231024333 | T | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0192 |
2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.292-4207A>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024333 | |||||||
| chr1:231024423 | C | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-4297G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024423 | |||||||
| chr1:231024520 | G | GCA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0033 others(16): Show |
28 | HG00423.hp1 HG00423.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.292-4396_292-4395d others(4): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | G | GCACA | 6 | a0001c0001t0001g0074 a0001c0001t0001g0140 a0001c0001t0001g0192 others(3): Show |
6 | HG02559.hp1 HG03471.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-4398_292-4395d others(6): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0267 others(1): Show |
6 | HG02109.hp2 HG02572.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-4402_292-4395d others(10): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | G | GCACACAC others(3): Show |
37 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0037 others(34): Show |
45 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.292-4404_292-4395d others(12): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | G | GCACACAC others(5): Show |
15 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0053 others(12): Show |
18 | HG00408.hp2 HG00438.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.292-4406_292-4395d others(14): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | G | GCACACAC others(7): Show |
48 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0025 others(45): Show |
65 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.292-4408_292-4395d others(16): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | G | GCACACAC others(9): Show |
23 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0019 others(20): Show |
33 | HG00621.hp2 HG01099.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.292-4410_292-4395d others(18): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | G | GCACACAC others(11): Show |
24 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0034 others(21): Show |
32 | HG01109.hp1 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.292-4412_292-4395d others(20): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | G | GCACACAC others(13): Show |
16 | a0001c0001t0001g0028 a0001c0001t0001g0044 a0001c0001t0001g0046 others(13): Show |
19 | HG00280.hp2 HG01981.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-4414_292-4395d others(22): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | G | GCACACAC others(15): Show |
3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0183 |
3 | NA18982.hp1 NA18998.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.292-4416_292-4395d others(24): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | GCA | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0022 others(24): Show |
41 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.292-4396_292-4395d others(4): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024520 | GCACACA | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0132 others(3): Show |
9 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-4400_292-4395d others(8): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024520 | |||||||
| chr1:231024527 | C | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-4401G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024527 | |||||||
| chr1:231024549 | C | CACACACA others(4): Show |
1 | a0001c0001t0001g0012 | 4 | NA18952.hp1 NA18976.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-4424_292-4423i others(13): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024549 | |||||||
| chr1:231024650 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.292-4524G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024650 | |||||||
| chr1:231024695 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292-4569G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024695 | |||||||
| chr1:231024900 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(195): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.292-4774G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024900 | |||||||
| chr1:231024914 | C | CT | 96 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(93): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.292-4789dupA | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024914 | |||||||
| chr1:231024914 | C | CTT | 12 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0159 others(9): Show |
14 | HG00735.hp2 HG02004.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.292-4790_292-4789d others(4): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024914 | |||||||
| chr1:231024914 | CT | C | 20 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0072 others(17): Show |
22 | HG01069.hp1 HG01106.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.292-4789delA | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024914 | |||||||
| chr1:231024914 | CTT | C | 8 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0267 others(5): Show |
8 | HG00735.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-4790_292-4789d others(4): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024914 | |||||||
| chr1:231024914 | CTTT | C | 15 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0074 others(12): Show |
19 | HG00738.hp2 HG01243.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-4791_292-4789d others(5): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024914 | |||||||
| chr1:231024977 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(195): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.292-4851A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231024977 | |||||||
| chr1:231025031 | T | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-4905A>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025031 | |||||||
| chr1:231025063 | C | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(178): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.292-4937G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025063 | |||||||
| chr1:231025067 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.292-4941G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025067 | |||||||
| chr1:231025068 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-4942C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025068 | |||||||
| chr1:231025072 | G | A | 3 | a0001c0001t0001g0254 a0001c0001t0005g0314 a0001c0001t0005g0315 |
3 | HG01167.hp2 HG01169.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.292-4946C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025072 | |||||||
| chr1:231025133 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.292-5007T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025133 | |||||||
| chr1:231025168 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-5042G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025168 | |||||||
| chr1:231025202 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-5076C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025202 | |||||||
| chr1:231025292 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.292-5166C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025292 | |||||||
| chr1:231025341 | C | CA | 3 | a0001c0001t0001g0053 a0001c0001t0001g0093 a0001c0001t0001g0306 |
4 | HG02451.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-5216_292-5215i others(3): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025341 | |||||||
| chr1:231025342 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(90): Show |
129 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.292-5216C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025342 | |||||||
| chr1:231025455 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0263 |
3 | HG02109.hp1 HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.292-5329G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025455 | |||||||
| chr1:231025917 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.292-5791A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231025917 | |||||||
| chr1:231026027 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0020 others(39): Show |
66 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.292-5901G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026027 | |||||||
| chr1:231026071 | T | TA | 63 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0037 others(60): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.292-5946dupT | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026071 | |||||||
| chr1:231026071 | T | TAA | 59 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(56): Show |
89 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.292-5947_292-5946d others(4): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026071 | |||||||
| chr1:231026071 | T | TAAA | 6 | a0001c0001t0001g0047 a0001c0001t0001g0086 a0001c0001t0001g0115 others(3): Show |
7 | HG01433.hp2 HG01981.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-5948_292-5946d others(5): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026071 | |||||||
| chr1:231026071 | TA | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(15): Show |
24 | HG00735.hp1 HG00738.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.292-5946delT | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026071 | |||||||
| chr1:231026130 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.292-6004G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026130 | |||||||
| chr1:231026210 | A | G | 53 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0034 others(50): Show |
65 | HG00280.hp2 HG01109.hp1 HG01496.hp1 others(62): Show |
intron_variant | MODIFIER | c.292-6084T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026210 | |||||||
| chr1:231026326 | C | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(193): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.292-6200G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026326 | |||||||
| chr1:231026334 | T | C | 1 | a0001c0001t0006g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.292-6208A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026334 | |||||||
| chr1:231026549 | C | G | 1 | a0001c0001t0001g0290 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.292-6423G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026549 | |||||||
| chr1:231026578 | G | C | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-6452C>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026578 | |||||||
| chr1:231026623 | C | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-6497G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026623 | |||||||
| chr1:231026686 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.292-6560C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026686 | |||||||
| chr1:231026691 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-6565G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026691 | |||||||
| chr1:231026783 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(101): Show |
144 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.292-6657C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026783 | |||||||
| chr1:231026840 | A | T | 88 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0019 others(85): Show |
107 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.292-6714T>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026840 | |||||||
| chr1:231026863 | A | G | 88 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0019 others(85): Show |
107 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.292-6737T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026863 | |||||||
| chr1:231026865 | T | C | 74 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0034 others(71): Show |
88 | HG00280.hp2 HG01109.hp1 HG01243.hp1 others(85): Show |
intron_variant | MODIFIER | c.292-6739A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026865 | |||||||
| chr1:231026871 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.292-6745C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026871 | |||||||
| chr1:231026897 | C | T | 88 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0019 others(85): Show |
107 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.292-6771G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026897 | |||||||
| chr1:231026910 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-6784A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026910 | |||||||
| chr1:231026916 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0132 others(5): Show |
11 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-6790C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026916 | |||||||
| chr1:231026955 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(101): Show |
144 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.292-6829G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231026955 | |||||||
| chr1:231027041 | T | C | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-6915A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027041 | |||||||
| chr1:231027104 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.292-6978C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027104 | |||||||
| chr1:231027179 | T | A | 1 | a0001c0001t0001g0285 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.292-7053A>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027179 | |||||||
| chr1:231027191 | A | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-7065T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027191 | |||||||
| chr1:231027211 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.292-7085G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027211 | |||||||
| chr1:231027223 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-7097C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027223 | |||||||
| chr1:231027314 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02559.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.292-7188G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027314 | |||||||
| chr1:231027475 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0236 a0001c0001t0001g0259 others(3): Show |
7 | HG02615.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-7349G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027475 | |||||||
| chr1:231027476 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.292-7350C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027476 | |||||||
| chr1:231027550 | C | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
4 | HG00099.hp2 HG00735.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-7424G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027550 | |||||||
| chr1:231027654 | TA | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
19 | HG00735.hp1 HG00738.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-7529delT | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027654 | |||||||
| chr1:231027746 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0132 others(5): Show |
11 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-7620A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027746 | |||||||
| chr1:231027886 | G | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(123): Show |
174 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.292-7760C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231027886 | |||||||
| chr1:231028194 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0262 |
2 | NA19043.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.292-8068G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028194 | |||||||
| chr1:231028256 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(101): Show |
144 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.292-8130G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028256 | |||||||
| chr1:231028259 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02559.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.292-8133G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028259 | |||||||
| chr1:231028316 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.292-8190G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028316 | |||||||
| chr1:231028436 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0236 a0001c0001t0001g0259 others(3): Show |
7 | HG02615.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-8310G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028436 | |||||||
| chr1:231028515 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.292-8389C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028515 | |||||||
| chr1:231028559 | C | T | 1 | a0001c0001t0001g0051 | 2 | NA18978.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.292-8433G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028559 | |||||||
| chr1:231028687 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-8561G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028687 | |||||||
| chr1:231028757 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0236 a0001c0001t0001g0259 others(3): Show |
7 | HG02615.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-8631G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028757 | |||||||
| chr1:231028768 | T | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(198): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.292-8642A>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028768 | |||||||
| chr1:231028783 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.292-8657G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028783 | |||||||
| chr1:231028907 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0093 a0001c0001t0001g0306 |
4 | HG02451.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-8781G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028907 | |||||||
| chr1:231028918 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0273 |
3 | HG02622.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.292-8792C>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028918 | |||||||
| chr1:231028968 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292-8842T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028968 | |||||||
| chr1:231028981 | C | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0142 |
2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.292-8855G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028981 | |||||||
| chr1:231028982 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.292-8856C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231028982 | |||||||
| chr1:231029153 | A | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0132 others(4): Show |
10 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-9027T>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231029153 | |||||||
| chr1:231029226 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0272 |
2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.292-9100C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231029226 | |||||||
| chr1:231029309 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0020 others(43): Show |
70 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.292-9183G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231029309 | |||||||
| chr1:231029491 | C | CA | 67 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0034 others(64): Show |
79 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.292-9366dupT | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231029491 | |||||||
| chr1:231029732 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0262 |
2 | NA19043.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.292-9606C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231029732 | |||||||
| chr1:231029764 | C | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0262 |
2 | NA19043.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.292-9638G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231029764 | |||||||
| chr1:231029945 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-9819T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231029945 | |||||||
| chr1:231029957 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.292-9831C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231029957 | |||||||
| chr1:231029990 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0274 a0001c0001t0001g0318 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-9864C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231029990 | |||||||
| chr1:231030033 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.291+9888A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231030033 | |||||||
| chr1:231030131 | T | C | 21 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0033 others(18): Show |
29 | HG00735.hp1 HG00738.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.291+9790A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231030131 | |||||||
| chr1:231030245 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0020 others(42): Show |
69 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.291+9676G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231030245 | |||||||
| chr1:231030264 | C | G | 5 | a0001c0001t0001g0112 a0001c0001t0001g0276 a0001c0001t0001g0279 others(2): Show |
5 | NA18963.hp1 NA18980.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+9657G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231030264 | |||||||
| chr1:231030375 | T | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0317 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.291+9546A>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231030375 | |||||||
| chr1:231030379 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.291+9542A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231030379 | |||||||
| chr1:231030430 | T | C | 2 | a0001c0001t0001g0311 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.291+9491A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231030430 | |||||||
| chr1:231030538 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0122 others(4): Show |
14 | HG01496.hp1 HG01943.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.291+9383A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231030538 | |||||||
| chr1:231031020 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.291+8901C>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231031020 | |||||||
| chr1:231031109 | C | CAAT | 20 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0079 others(17): Show |
22 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.291+8809_291+8811d others(5): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231031109 | |||||||
| chr1:231031109 | C | CAATAAT | 5 | a0001c0001t0001g0053 a0001c0001t0001g0093 a0001c0001t0001g0145 others(2): Show |
6 | HG02451.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+8806_291+8811d others(8): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231031109 | |||||||
| chr1:231031109 | CAAT | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(102): Show |
145 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.291+8809_291+8811d others(5): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231031109 | |||||||
| chr1:231031221 | C | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0034 others(53): Show |
68 | HG00280.hp2 HG01109.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.291+8700G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231031221 | |||||||
| chr1:231031558 | T | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0093 a0001c0001t0001g0306 |
4 | HG02451.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+8363A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231031558 | |||||||
| chr1:231031778 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02155.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.291+8143T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231031778 | |||||||
| chr1:231031811 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0200 |
2 | NA19004.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.291+8110A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231031811 | |||||||
| chr1:231031948 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(74): Show |
111 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.291+7973C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231031948 | |||||||
| chr1:231032044 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(125): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.291+7877G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032044 | |||||||
| chr1:231032055 | A | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0273 a0001c0001t0001g0274 others(3): Show |
7 | HG02615.hp2 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.291+7866T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032055 | |||||||
| chr1:231032121 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02559.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.291+7800T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032121 | |||||||
| chr1:231032152 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(119): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.291+7769A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032152 | |||||||
| chr1:231032153 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.291+7768A>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032153 | |||||||
| chr1:231032250 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0318 |
3 | HG02572.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.291+7671C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032250 | |||||||
| chr1:231032335 | C | CA | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.291+7585dupT | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032335 | |||||||
| chr1:231032364 | C | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(41): Show |
69 | HG00140.hp2 HG00639.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.291+7557G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032364 | |||||||
| chr1:231032366 | A | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
149 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.291+7555T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032366 | |||||||
| chr1:231032376 | G | GC | 5 | a0001c0001t0001g0016 a0001c0001t0001g0165 a0001c0001t0001g0256 others(2): Show |
7 | HG00642.hp2 HG03516.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.291+7544dupG | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032376 | |||||||
| chr1:231032382 | G | A | 22 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0161 others(19): Show |
24 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.291+7539C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032382 | |||||||
| chr1:231032398 | C | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0303 |
4 | HG01175.hp1 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+7523G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032398 | |||||||
| chr1:231032491 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0017 others(27): Show |
48 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.291+7430T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032491 | |||||||
| chr1:231032492 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0302 |
3 | NA18977.hp2 NA19065.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.291+7429A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032492 | |||||||
| chr1:231032584 | T | G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG01106.hp1 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+7337A>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032584 | |||||||
| chr1:231032615 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.291+7306G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032615 | |||||||
| chr1:231032625 | TTTTG | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(143): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.291+7292_291+7295d others(6): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032625 | |||||||
| chr1:231032731 | A | G | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(149): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.291+7190T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032731 | |||||||
| chr1:231032735 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0303 a0001c0001t0001g0304 others(1): Show |
6 | HG01175.hp1 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+7186C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032735 | |||||||
| chr1:231032791 | C | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0017 others(31): Show |
51 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.291+7130G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032791 | |||||||
| chr1:231032798 | G | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0183 a0001c0001t0001g0194 others(3): Show |
7 | HG02258.hp2 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.291+7123C>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032798 | |||||||
| chr1:231032903 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.291+7018G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231032903 | |||||||
| chr1:231033001 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0187 a0001c0001t0001g0188 others(3): Show |
7 | HG01109.hp1 HG01243.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.291+6920G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033001 | |||||||
| chr1:231033188 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.291+6733C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033188 | |||||||
| chr1:231033200 | C | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG00323.hp2 HG00642.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.291+6721G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033200 | |||||||
| chr1:231033248 | C | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(150): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.291+6673G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033248 | |||||||
| chr1:231033401 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0001g0196 others(1): Show |
5 | HG02258.hp1 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+6520G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033401 | |||||||
| chr1:231033407 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0001g0196 others(1): Show |
5 | HG02258.hp1 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+6514A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033407 | |||||||
| chr1:231033486 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.291+6435G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033486 | |||||||
| chr1:231033568 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0273 a0001c0001t0001g0274 |
4 | HG02622.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+6353C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033568 | |||||||
| chr1:231033639 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0204 a0001c0001t0001g0229 others(1): Show |
6 | HG02040.hp1 NA18948.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+6282A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033639 | |||||||
| chr1:231033833 | AAGAACTC others(20): Show |
A | 1 | a0001c0001t0001g0307 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.291+6061_291+6087d others(29): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033833 | |||||||
| chr1:231033919 | C | T | 2 | a0001c0001t0001g0041 a0002c0002t0001g0185 |
3 | HG02965.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.291+6002G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033919 | |||||||
| chr1:231033946 | C | A | 1 | a0001c0001t0001g0306 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.291+5975G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033946 | |||||||
| chr1:231033971 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.291+5950A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033971 | |||||||
| chr1:231033999 | T | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0018 others(54): Show |
78 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.291+5922A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231033999 | |||||||
| chr1:231034019 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0306 |
3 | HG02451.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.291+5902C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034019 | |||||||
| chr1:231034255 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291+5666G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034255 | |||||||
| chr1:231034267 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.291+5654A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034267 | |||||||
| chr1:231034467 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.291+5454G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034467 | |||||||
| chr1:231034563 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.291+5358T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034563 | |||||||
| chr1:231034628 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG02258.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.291+5293G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034628 | |||||||
| chr1:231034643 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.291+5278T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034643 | |||||||
| chr1:231034650 | T | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.291+5271A>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034650 | |||||||
| chr1:231034726 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.291+5195G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034726 | |||||||
| chr1:231034729 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.291+5192C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034729 | |||||||
| chr1:231034771 | T | TA | 5 | a0001c0001t0001g0104 a0001c0001t0001g0135 a0001c0001t0001g0186 others(2): Show |
5 | HG01243.hp2 HG02083.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+5149_291+5150i others(3): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034771 | |||||||
| chr1:231034771 | TC | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(123): Show |
198 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.291+5149delG | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034771 | |||||||
| chr1:231034771 | TCA | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0138 a0001c0001t0001g0204 |
3 | HG01167.hp1 HG02976.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.291+5148_291+5149d others(4): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034771 | |||||||
| chr1:231034772 | C | A | 26 | a0001c0001t0001g0058 a0001c0001t0001g0096 a0001c0001t0001g0097 others(23): Show |
26 | HG00140.hp2 HG00408.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.291+5149G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034772 | |||||||
| chr1:231034772 | CA | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(130): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.291+5148delT | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034772 | |||||||
| chr1:231034772 | CAA | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(21): Show |
27 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.291+5147_291+5148d others(4): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034772 | |||||||
| chr1:231034773 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.291+5148T>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034773 | |||||||
| chr1:231034864 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.291+5057T>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231034864 | |||||||
| chr1:231035173 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0318 |
3 | HG02572.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.291+4748A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231035173 | |||||||
| chr1:231035269 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.291+4652A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231035269 | |||||||
| chr1:231035393 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(157): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.291+4528C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231035393 | |||||||
| chr1:231035426 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.291+4495G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231035426 | |||||||
| chr1:231035443 | A | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
70 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.291+4478T>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231035443 | |||||||
| chr1:231035572 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.291+4349G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231035572 | |||||||
| chr1:231035758 | C | T | 1 | a0001c0001t0006g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.291+4163G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231035758 | |||||||
| chr1:231035921 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.291+4000G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231035921 | |||||||
| chr1:231035947 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0055 |
3 | HG02258.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.291+3974C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231035947 | |||||||
| chr1:231036061 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.291+3860C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036061 | |||||||
| chr1:231036327 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.291+3594G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036327 | |||||||
| chr1:231036392 | C | T | 1 | a0001c0001t0006g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.291+3529G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036392 | |||||||
| chr1:231036503 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(159): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.291+3418C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036503 | |||||||
| chr1:231036520 | G | C | 1 | a0001c0001t0001g0033 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.291+3401C>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036520 | |||||||
| chr1:231036535 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.291+3386G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036535 | |||||||
| chr1:231036693 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.291+3228C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036693 | |||||||
| chr1:231036699 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0001g0196 others(1): Show |
5 | HG02258.hp1 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+3222G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036699 | |||||||
| chr1:231036767 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.291+3154G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036767 | |||||||
| chr1:231036910 | GTGAT | G | 6 | a0001c0001t0001g0041 a0001c0001t0001g0183 a0001c0001t0001g0194 others(3): Show |
7 | HG02258.hp2 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.291+3007_291+3010d others(6): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036910 | |||||||
| chr1:231036940 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(159): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.291+2981A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231036940 | |||||||
| chr1:231037018 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.291+2903C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037018 | |||||||
| chr1:231037064 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(159): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.291+2857T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037064 | |||||||
| chr1:231037135 | T | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(149): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.291+2786A>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037135 | |||||||
| chr1:231037171 | A | T | 1 | a0001c0001t0001g0307 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.291+2750T>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037171 | |||||||
| chr1:231037173 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.291+2748C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037173 | |||||||
| chr1:231037193 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.291+2728G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037193 | |||||||
| chr1:231037199 | C | A | 1 | a0001c0001t0001g0307 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.291+2722G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037199 | |||||||
| chr1:231037200 | T | TATTTGTG others(14): Show |
1 | a0001c0001t0001g0307 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.291+2720_291+2721i others(23): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037200 | |||||||
| chr1:231037227 | T | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | NA18953.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.291+2694A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037227 | |||||||
| chr1:231037264 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.291+2657T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037264 | |||||||
| chr1:231037287 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(155): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.291+2634G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037287 | |||||||
| chr1:231037311 | C | G | 11 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0183 others(8): Show |
13 | HG01109.hp1 HG01243.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.291+2610G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037311 | |||||||
| chr1:231037328 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.291+2593A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037328 | |||||||
| chr1:231037353 | T | A | 1 | a0001c0001t0001g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.291+2568A>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037353 | |||||||
| chr1:231037421 | T | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG02258.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.291+2500A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037421 | |||||||
| chr1:231037469 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.291+2452T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037469 | |||||||
| chr1:231037544 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG02258.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.291+2377G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037544 | |||||||
| chr1:231037633 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(155): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.291+2288G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037633 | |||||||
| chr1:231037681 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
174 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.291+2240G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037681 | |||||||
| chr1:231037789 | G | A | 2 | a0001c0001t0001g0311 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.291+2132C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037789 | |||||||
| chr1:231037850 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(155): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.291+2071A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037850 | |||||||
| chr1:231037925 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(121): Show |
180 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.291+1996G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037925 | |||||||
| chr1:231037926 | C | A | 1 | a0001c0001t0001g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.291+1995G>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037926 | |||||||
| chr1:231037938 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.291+1983C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231037938 | |||||||
| chr1:231038158 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(161): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.291+1763T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231038158 | |||||||
| chr1:231038266 | GCGTAATT others(3): Show |
G | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.291+1645_291+1654d others(12): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231038266 | |||||||
| chr1:231038496 | G | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0183 a0001c0001t0001g0194 others(3): Show |
7 | HG02258.hp2 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.291+1425C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231038496 | |||||||
| chr1:231038685 | C | T | 43 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(40): Show |
51 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.291+1236G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231038685 | |||||||
| chr1:231038722 | T | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0313 |
3 | HG00609.hp2 NA18991.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.291+1199A>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231038722 | |||||||
| chr1:231038781 | G | GA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0017 others(30): Show |
50 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.291+1139dupT | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231038781 | |||||||
| chr1:231038878 | A | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0183 a0001c0001t0002g0184 others(1): Show |
5 | HG02572.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+1043T>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231038878 | |||||||
| chr1:231038925 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0017 others(30): Show |
50 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.291+996G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231038925 | |||||||
| chr1:231039075 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0117 others(6): Show |
14 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.291+846C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039075 | |||||||
| chr1:231039124 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.291+797C>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039124 | |||||||
| chr1:231039252 | A | G | 33 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0035 others(30): Show |
42 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.291+669T>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039252 | |||||||
| chr1:231039400 | C | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0017 others(34): Show |
54 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.291+521G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039400 | |||||||
| chr1:231039452 | T | C | 2 | a0001c0001t0005g0314 a0001c0001t0005g0315 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.291+469A>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039452 | |||||||
| chr1:231039533 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.291+388C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039533 | |||||||
| chr1:231039548 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.291+373G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039548 | |||||||
| chr1:231039549 | CT | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0318 |
3 | HG02572.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.291+371delA | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039549 | |||||||
| chr1:231039590 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.291+331C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039590 | |||||||
| chr1:231039740 | G | C | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.291+181C>G | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039740 | |||||||
| chr1:231039803 | G | A | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | NA18978.hp2 NA18982.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+118C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039803 | |||||||
| chr1:231039810 | CCGAAAGG others(73): Show |
C | 1 | a0001c0001t0001g0320 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.291+31_291+110delC others(79): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039810 | |||||||
| chr1:231039830 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0030 others(23): Show |
40 | HG00741.hp2 HG01070.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.291+91C>T | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039830 | |||||||
| chr1:231039830 | G | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0222 |
3 | NA18990.hp2 NA18994.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.291+91C>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039830 | |||||||
| chr1:231039869 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0161 |
3 | HG01496.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.291+52G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039869 | |||||||
| chr1:231039886 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.291+35G>A | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039886 | |||||||
| chr1:231039898 | C | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(87): Show |
136 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.291+23G>C | FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | 231039898 |