Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 339778 |
| ensemblid | ENSG00000173557.15 |
| hgncid | 27938 |
| symbol | FAM166C |
| name | ciliary microtubule inner protein 2C |
| refseq_nuc | NM_001105519.3 |
| refseq_prot | NP_001098989.1 |
| ensembl_nuc | ENST00000329615.4 |
| ensembl_prot | ENSP00000332875.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 26562587 |
| end | 26579524 |
| strand | + |
| ver | v1.2 |
| region | chr2:26562587-26579524 |
| region5000 | chr2:26557587-26584524 |
| regionname0 | FAM166C_chr2_26562587_26579524 |
| regionname5000 | FAM166C_chr2_26557587_26584524 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 201 | 272 | 82 | 59 | 107 | 7 | 15 | 86 | FAM166C_chr2_26557587_26584524 | FAM166C | MASRS others(196): Show |
chr2 | 26557587 | 26584524 |
| a0002 | 0/0 | 201 | 134 | 10 | 14 | 79 | 5 | 26 | 60 | FAM166C_chr2_26557587_26584524 | FAM166C | MASRS others(196): Show |
chr2 | 26557587 | 26584524 |
| a0003 | 0/0 | 157 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM166C_chr2_26557587_26584524 | FAM166C | MASRS others(152): Show |
chr2 | 26557587 | 26584524 |
| a0004 | 0/0 | 201 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | MASRS others(196): Show |
chr2 | 26557587 | 26584524 |
| a0005 | 0/0 | 201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | MASRS others(196): Show |
chr2 | 26557587 | 26584524 |
| a0006 | 0/0 | 201 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | MASRS others(196): Show |
chr2 | 26557587 | 26584524 |
| a0007 | 0/0 | 201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | MASRS others(196): Show |
chr2 | 26557587 | 26584524 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 603 | 146 | 18 | 42 | 70 | 6 | 10 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0001c0003 | 1/1 | 603 | 118 | 58 | 15 | 37 | 1 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0001c0004 | 0/0 | 603 | 4 | 2 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0001c0005 | 0/0 | 603 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0002c0002 | 0/0 | 603 | 131 | 10 | 13 | 78 | 5 | 25 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0002c0006 | 0/0 | 603 | 2 | 0 | 1 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0002c0013 | 0/0 | 603 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0003c0011 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0003c0012 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0004c0009 | 0/0 | 603 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0005c0007 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0006c0010 | 0/0 | 603 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 | ||
| a0007c0008 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | ATGGC others(598): Show |
chr2 | 26557587 | 26584524 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 718 | 143 | 17 | 41 | 69 | 6 | 10 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0001c0001t0002 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0001c0001t0003 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGAT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0001c0001t0004 | 0/0 | 718 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0001c0003t0001 | 1/1 | 718 | 118 | 58 | 15 | 37 | 1 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0001c0004t0002 | 0/0 | 718 | 4 | 2 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0001c0005t0001 | 0/0 | 718 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0002c0002t0002 | 0/0 | 718 | 131 | 10 | 13 | 78 | 5 | 25 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0002c0006t0001 | 0/0 | 718 | 2 | 0 | 1 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0002c0013t0002 | 0/0 | 718 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0003c0011t0002 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0003c0012t0002 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0004c0009t0001 | 0/0 | 718 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0005c0007t0002 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0006c0010t0001 | 0/0 | 718 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| a0007c0008t0001 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | AGGCT others(713): Show |
chr2 | 26557587 | 26584524 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 43 | 1 | 13 | 25 | 2 | 2 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0005 | 0/0 | 12 | 0 | 1 | 8 | 0 | 3 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0006 | 0/0 | 13 | 0 | 13 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0004 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0007 | 0/0 | 12 | 4 | 3 | 0 | 0 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0034 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0004t0002g0017 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0005t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0005t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0005t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0001c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0002 | 0/0 | 39 | 2 | 5 | 26 | 1 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0003 | 0/0 | 37 | 0 | 3 | 27 | 0 | 7 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0006t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0002c0013t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0003c0011t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0003c0012t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0004c0009t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0005c0007t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0006c0010t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| a0007c0008t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0036 | EUR | GBR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0111 | EUR | FIN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0076 | EUR | FIN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0136 | EUR | FIN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0128 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0123 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0074 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0091 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00738 | hp1 | a0001 | c0004 | t0002 | g0017 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0052 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0036 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0121 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01257 | hp1 | a0002 | c0006 | t0001 | g0087 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0041 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0041 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01346 | hp2 | a0001 | c0004 | t0002 | g0017 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0082 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01433 | hp2 | a0004 | c0009 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0079 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0138 | EUR | IBS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0098 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0099 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02145 | hp1 | a0001 | c0004 | t0002 | g0017 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CDX | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | CDX | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0152 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0069 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02698 | hp2 | a0002 | c0013 | t0002 | g0002 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02717 | hp2 | a0001 | c0005 | t0001 | g0054 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0151 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0088 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0107 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0017 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0131 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0072 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03486 | hp2 | a0005 | c0007 | t0002 | g0002 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0071 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0094 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03669 | hp1 | a0006 | c0010 | t0001 | g0104 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0035 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0090 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0093 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0109 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0096 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0053 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0035 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18522 | hp2 | a0007 | c0008 | t0001 | g0048 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0127 | EAS | CHB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | CHB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0141 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18949 | hp1 | a0003 | c0011 | t0002 | g0097 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18965 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18966 | hp2 | a0003 | c0012 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18989 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18997 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0122 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0106 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19055 | hp2 | a0001 | c0003 | t0001 | g0125 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19065 | hp1 | a0002 | c0006 | t0001 | g0092 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19076 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0147 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0025 | SAS | GIH | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | GIH | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0144 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0105 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0055 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0101 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0051 | AFR | USA | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | USA | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0059 | AFR | USA | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0139 | REF | REF | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0034 | REF | REF | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26576006 | G | A | 1 | a0005 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.179G>A | p.Ser60Asn | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 205/718 | 179/606 | 60/201 | chr2 | 26576006 | |||
| chr2:26576025 | A | T | 3 | a0002 a0003 a0005 |
137 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(134): Show |
missense_variant | MODERATE | c.198A>T | p.Gln66His | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 224/718 | 198/606 | 66/201 | chr2 | 26576025 | |||
| chr2:26576093 | G | A | 1 | a0007 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.266G>A | p.Arg89Gln | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 292/718 | 266/606 | 89/201 | chr2 | 26576093 | |||
| chr2:26576165 | A | G | 1 | a0006 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.338A>G | p.Asn113Ser | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 364/718 | 338/606 | 113/201 | chr2 | 26576165 | |||
| chr2:26579306 | C | A | 1 | a0003 | 1 | NA18949.hp1 | stop_gained | HIGH | c.474C>A | p.Cys158* | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 500/718 | 474/606 | 158/201 | chr2 | 26579306 | |||
| chr2:26579320 | G | A | 1 | a0003 | 1 | NA18966.hp2 | stop_gained | HIGH | c.488G>A | p.Trp163* | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 514/718 | 488/606 | 163/201 | chr2 | 26579320 | |||
| chr2:26579343 | G | A | 1 | a0004 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.511G>A | p.Glu171Lys | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 537/718 | 511/606 | 171/201 | chr2 | 26579343 | |||
| chr2:26579362 | A | T | 1 | a0003 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.530A>T | p.Gln177Leu | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 556/718 | 530/606 | 177/201 | chr2 | 26579362 | |||
| chr2:26579524 | A | T | 4 | a0001 a0002 a0003 others(1): Show |
140 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
splice_region_variant | LOW | c.*86A>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | chr2 | 26579524 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26576163 | G | A | 7 | a0001c0004 a0002c0002 a0002c0006 others(4): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
synonymous_variant | LOW | c.336G>A | p.Thr112Thr | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 362/718 | 336/606 | 112/201 | chr2 | 26576163 | |||
| chr2:26577554 | G | A | 3 | a0001c0001 a0002c0006 a0004c0009 |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
synonymous_variant | LOW | c.387G>A | p.Thr129Thr | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/4 | 413/718 | 387/606 | 129/201 | chr2 | 26577554 | |||
| chr2:26577569 | A | G | 1 | a0001c0005 | 4 | HG02451.hp1 HG02559.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.402A>G | p.Arg134Arg | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/4 | 428/718 | 402/606 | 134/201 | chr2 | 26577569 | |||
| chr2:26579354 | G | A | 1 | a0002c0013 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.522G>A | p.Lys174Lys | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 548/718 | 522/606 | 174/201 | chr2 | 26579354 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26562590 | C | A | 1 | a0001c0001t0003 | 1 | NA19080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/4 | 23 | chr2 | 26562590 | ||||||
| chr2:26579480 | G | A | 1 | a0001c0001t0004 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 42 | chr2 | 26579480 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26562694 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0003t0001g0044 |
4 | HG02055.hp2 HG02486.hp2 HG02886.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.74+8C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562694 | |||||||
| chr2:26562695 | G | A | 1 | a0001c0003t0001g0014 | 4 | HG01496.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.74+9G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562695 | |||||||
| chr2:26562738 | C | T | 2 | a0001c0005t0001g0151 a0001c0005t0001g0152 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.74+52C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562738 | |||||||
| chr2:26562766 | C | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0003t0001g0046 |
3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.74+80C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562766 | |||||||
| chr2:26562842 | G | T | 1 | a0001c0003t0001g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.74+156G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562842 | |||||||
| chr2:26562901 | G | A | 1 | a0007c0008t0001g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.74+215G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562901 | |||||||
| chr2:26562968 | G | A | 5 | a0001c0001t0001g0049 a0001c0003t0001g0021 a0001c0003t0001g0050 others(2): Show |
7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+282G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562968 | |||||||
| chr2:26562969 | G | A | 5 | a0001c0001t0001g0049 a0001c0003t0001g0021 a0001c0003t0001g0050 others(2): Show |
7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+283G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562969 | |||||||
| chr2:26562998 | G | T | 1 | a0001c0003t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.74+312G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562998 | |||||||
| chr2:26563113 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.74+427A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563113 | |||||||
| chr2:26563160 | C | T | 1 | a0001c0003t0001g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.74+474C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563160 | |||||||
| chr2:26563206 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.74+520G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563206 | |||||||
| chr2:26563239 | T | C | 1 | a0002c0002t0002g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.74+553T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563239 | |||||||
| chr2:26563392 | T | C | 1 | a0001c0005t0001g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.74+706T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563392 | |||||||
| chr2:26563420 | T | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0031 others(20): Show |
38 | HG00609.hp2 HG01106.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.74+734T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563420 | |||||||
| chr2:26563458 | G | A | 1 | a0001c0003t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.74+772G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563458 | |||||||
| chr2:26563460 | A | G | 2 | a0001c0003t0001g0009 a0001c0003t0001g0028 |
10 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.74+774A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563460 | |||||||
| chr2:26563462 | C | G | 1 | a0002c0002t0002g0144 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.74+776C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563462 | |||||||
| chr2:26563511 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0070 |
3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.74+825T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563511 | |||||||
| chr2:26563967 | C | T | 2 | a0001c0003t0001g0009 a0001c0003t0001g0028 |
10 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.74+1281C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563967 | |||||||
| chr2:26563981 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0031 others(19): Show |
37 | HG00609.hp2 HG01106.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.74+1295G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563981 | |||||||
| chr2:26564259 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.74+1573A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564259 | |||||||
| chr2:26564284 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.74+1598A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564284 | |||||||
| chr2:26564325 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.74+1639A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564325 | |||||||
| chr2:26564419 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0003t0001g0046 |
3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.74+1733C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564419 | |||||||
| chr2:26564518 | C | G | 1 | a0001c0003t0001g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.74+1832C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564518 | |||||||
| chr2:26564623 | A | G | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.74+1937A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564623 | |||||||
| chr2:26564669 | C | T | 1 | a0002c0002t0002g0140 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.74+1983C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564669 | |||||||
| chr2:26564815 | G | A | 2 | a0001c0003t0001g0072 a0001c0003t0001g0073 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.74+2129G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564815 | |||||||
| chr2:26565015 | T | TTTC | 1 | a0001c0001t0001g0020 | 4 | NA18953.hp2 NA18954.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+2346_74+2348dup others(3): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565015 | ||||||
| chr2:26565029 | T | TCTTCTC | 4 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0002g0056 others(1): Show |
10 | HG00639.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.74+2367_74+2372dup others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565029 | ||||||
| chr2:26565029 | TCTTCTC | T | 4 | a0002c0002t0002g0136 a0002c0002t0002g0137 a0002c0002t0002g0138 others(1): Show |
4 | HG00323.hp2 HG01515.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+2367_74+2372del others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565029 | ||||||
| chr2:26565053 | CCTTCTT | C | 2 | a0001c0003t0001g0029 a0001c0003t0001g0055 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.74+2372_74+2377del others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565053 | ||||||
| chr2:26565059 | T | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0031 others(18): Show |
35 | HG00609.hp2 HG01106.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.74+2373T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565059 | |||||||
| chr2:26565059 | T | TCTTCCC | 3 | a0002c0002t0002g0003 a0002c0002t0002g0076 a0002c0002t0002g0086 |
5 | HG00323.hp1 HG01981.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+2400_74+2405dup others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565059 | ||||||
| chr2:26565059 | TCTTCCC | T | 3 | a0001c0003t0001g0009 a0001c0003t0001g0018 a0001c0003t0001g0150 |
12 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.74+2400_74+2405del others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565059 | ||||||
| chr2:26565223 | T | C | 46 | a0001c0001t0001g0037 a0001c0003t0001g0036 a0001c0003t0001g0079 others(43): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.74+2537T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565223 | |||||||
| chr2:26565239 | C | T | 6 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0003t0001g0044 others(3): Show |
7 | HG01074.hp1 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.74+2553C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565239 | |||||||
| chr2:26565337 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.74+2651C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565337 | |||||||
| chr2:26565377 | C | T | 1 | a0002c0002t0002g0038 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.74+2691C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565377 | |||||||
| chr2:26565382 | C | T | 1 | a0007c0008t0001g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.74+2696C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565382 | |||||||
| chr2:26565468 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.74+2782G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565468 | |||||||
| chr2:26565503 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0003t0001g0074 |
9 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+2817C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565503 | |||||||
| chr2:26565664 | CT | C | 3 | a0001c0005t0001g0101 a0001c0005t0001g0151 a0001c0005t0001g0152 |
3 | HG02451.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.74+2979delT | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565664 | |||||||
| chr2:26565665 | T | C | 1 | a0001c0005t0001g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.74+2979T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565665 | |||||||
| chr2:26565808 | G | A | 1 | a0001c0003t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.74+3122G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565808 | |||||||
| chr2:26565822 | C | T | 1 | a0001c0001t0001g0032 | 2 | NA18943.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.74+3136C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565822 | |||||||
| chr2:26565862 | G | A | 1 | a0002c0002t0002g0075 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.74+3176G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565862 | |||||||
| chr2:26565865 | G | A | 1 | a0002c0002t0002g0076 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.74+3179G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565865 | |||||||
| chr2:26566118 | C | A | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.74+3432C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566118 | |||||||
| chr2:26566346 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0002g0056 |
2 | HG01891.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.74+3660G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566346 | |||||||
| chr2:26566381 | G | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
16 | HG01081.hp1 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.74+3695G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566381 | |||||||
| chr2:26566384 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.74+3698G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566384 | |||||||
| chr2:26566436 | G | A | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0145 others(4): Show |
8 | HG01109.hp2 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+3750G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566436 | |||||||
| chr2:26566463 | C | G | 1 | a0002c0002t0002g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.74+3777C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566463 | |||||||
| chr2:26566500 | C | T | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.74+3814C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566500 | |||||||
| chr2:26566583 | G | A | 1 | a0006c0010t0001g0104 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.74+3897G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566583 | |||||||
| chr2:26566954 | C | A | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0145 others(4): Show |
8 | HG01109.hp2 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+4268C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566954 | |||||||
| chr2:26566991 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.74+4305C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566991 | |||||||
| chr2:26566992 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.74+4306C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566992 | |||||||
| chr2:26567118 | G | A | 1 | a0002c0002t0002g0077 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.74+4432G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567118 | |||||||
| chr2:26567129 | C | G | 16 | a0001c0001t0001g0011 a0001c0003t0001g0004 a0001c0003t0001g0019 others(13): Show |
45 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.74+4443C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567129 | |||||||
| chr2:26567170 | G | A | 1 | a0006c0010t0001g0104 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.74+4484G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567170 | |||||||
| chr2:26567390 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.74+4704A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567390 | |||||||
| chr2:26567505 | G | A | 3 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 |
3 | HG01074.hp1 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.74+4819G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567505 | |||||||
| chr2:26567592 | G | A | 1 | a0002c0002t0002g0078 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.74+4906G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567592 | |||||||
| chr2:26567624 | C | G | 1 | a0001c0003t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.74+4938C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567624 | |||||||
| chr2:26567653 | C | T | 7 | a0001c0001t0001g0120 a0001c0003t0001g0007 a0001c0003t0001g0041 others(4): Show |
19 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.74+4967C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567653 | |||||||
| chr2:26567853 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(117): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.74+5167T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567853 | |||||||
| chr2:26567947 | A | G | 1 | a0001c0003t0001g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.74+5261A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567947 | |||||||
| chr2:26567966 | T | C | 1 | a0001c0005t0001g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.74+5280T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567966 | |||||||
| chr2:26568040 | G | A | 1 | a0001c0003t0001g0125 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.74+5354G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568040 | |||||||
| chr2:26568096 | G | T | 1 | a0002c0002t0002g0138 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.74+5410G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568096 | |||||||
| chr2:26568186 | C | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
4 | NA18956.hp1 NA18984.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+5500C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568186 | |||||||
| chr2:26568235 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.74+5549C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568235 | |||||||
| chr2:26568468 | C | A | 1 | a0001c0003t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.74+5782C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568468 | |||||||
| chr2:26568572 | G | A | 3 | a0001c0003t0001g0042 a0001c0003t0001g0126 a0001c0003t0001g0149 |
4 | NA18965.hp1 NA18989.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+5886G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568572 | |||||||
| chr2:26568586 | A | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(101): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.74+5900A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568586 | |||||||
| chr2:26568791 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.74+6105C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568791 | |||||||
| chr2:26568793 | G | C | 1 | a0001c0003t0001g0071 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.74+6107G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568793 | |||||||
| chr2:26568842 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0003t0001g0009 others(5): Show |
25 | HG00639.hp2 HG01496.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.74+6156A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568842 | |||||||
| chr2:26568861 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.74+6175A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568861 | |||||||
| chr2:26569016 | CA | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
78 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.74+6345delA | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26569016 | ||||||
| chr2:26569016 | CAA | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.74+6344_74+6345del others(2): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26569016 | ||||||
| chr2:26569020 | A | C | 1 | a0002c0002t0002g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.74+6334A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569020 | |||||||
| chr2:26569167 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(115): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.74+6481G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569167 | |||||||
| chr2:26569187 | T | C | 1 | a0002c0002t0002g0082 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.74+6501T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569187 | |||||||
| chr2:26569205 | G | A | 4 | a0001c0003t0001g0021 a0001c0003t0001g0050 a0001c0003t0001g0051 others(1): Show |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.74+6519G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569205 | |||||||
| chr2:26569220 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.74+6534C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569220 | |||||||
| chr2:26569228 | A | C | 4 | a0001c0003t0001g0106 a0001c0005t0001g0101 a0001c0005t0001g0151 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+6542A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569228 | |||||||
| chr2:26569266 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(105): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.74+6580C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569266 | |||||||
| chr2:26569493 | G | A | 1 | a0002c0002t0002g0083 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.75-6409G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569493 | |||||||
| chr2:26569554 | A | C | 1 | a0003c0011t0002g0097 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.75-6348A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569554 | |||||||
| chr2:26569647 | G | T | 1 | a0002c0002t0002g0096 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.75-6255G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569647 | |||||||
| chr2:26569903 | T | C | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-5999T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569903 | |||||||
| chr2:26569946 | G | A | 1 | a0001c0003t0001g0021 | 3 | HG00733.hp2 HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.75-5956G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569946 | |||||||
| chr2:26570035 | A | G | 1 | a0007c0008t0001g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75-5867A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570035 | |||||||
| chr2:26570043 | C | T | 13 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0120 others(10): Show |
39 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.75-5859C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570043 | |||||||
| chr2:26570247 | A | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(85): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.75-5655A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570247 | |||||||
| chr2:26570278 | G | A | 1 | a0001c0003t0001g0027 | 3 | NA18940.hp2 NA19076.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75-5624G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570278 | |||||||
| chr2:26570302 | C | A | 1 | a0001c0003t0001g0043 | 2 | NA18981.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.75-5600C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570302 | |||||||
| chr2:26570344 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.75-5558C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570344 | |||||||
| chr2:26570363 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.75-5539C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570363 | |||||||
| chr2:26570429 | T | C | 1 | a0002c0002t0002g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75-5473T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570429 | |||||||
| chr2:26570491 | C | T | 1 | a0001c0001t0001g0040 | 2 | NA18949.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.75-5411C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570491 | |||||||
| chr2:26570496 | G | A | 1 | a0001c0003t0001g0127 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.75-5406G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570496 | |||||||
| chr2:26570740 | T | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.75-5162T>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570740 | |||||||
| chr2:26570776 | T | C | 7 | a0001c0001t0001g0120 a0001c0003t0001g0007 a0001c0003t0001g0041 others(4): Show |
19 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.75-5126T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570776 | |||||||
| chr2:26570779 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.75-5123A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570779 | |||||||
| chr2:26570787 | C | A | 1 | a0001c0003t0001g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.75-5115C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570787 | |||||||
| chr2:26570797 | G | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0030 others(18): Show |
41 | HG00438.hp2 HG00609.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.75-5105G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570797 | |||||||
| chr2:26570940 | GTGGAGGG others(3): Show |
G | 1 | a0001c0003t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75-4946_75-4937del others(10): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26570940 | ||||||
| chr2:26571008 | G | A | 1 | a0001c0003t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.75-4894G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571008 | |||||||
| chr2:26571023 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0003t0001g0074 |
9 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-4879T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571023 | |||||||
| chr2:26571050 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.75-4852G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571050 | |||||||
| chr2:26571121 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.75-4781G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571121 | |||||||
| chr2:26571141 | TAG | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.75-4756_75-4755del others(2): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26571141 | ||||||
| chr2:26571258 | G | A | 1 | a0002c0002t0002g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.75-4644G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571258 | |||||||
| chr2:26571653 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75-4249T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571653 | |||||||
| chr2:26571658 | C | T | 1 | a0002c0002t0002g0095 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.75-4244C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571658 | |||||||
| chr2:26571659 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.75-4243G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571659 | |||||||
| chr2:26571739 | C | T | 26 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0120 others(23): Show |
69 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.75-4163C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571739 | |||||||
| chr2:26571882 | A | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0003t0001g0074 |
9 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-4020A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571882 | |||||||
| chr2:26571927 | GAACTT | G | 56 | a0001c0003t0001g0014 a0001c0003t0001g0018 a0001c0003t0001g0024 others(53): Show |
153 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.75-3970_75-3966del others(5): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26571927 | ||||||
| chr2:26571976 | AT | A | 56 | a0001c0003t0001g0014 a0001c0003t0001g0018 a0001c0003t0001g0024 others(53): Show |
153 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.75-3923delT | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26571976 | ||||||
| chr2:26572122 | T | G | 2 | a0001c0003t0001g0019 a0002c0002t0002g0083 |
5 | HG02015.hp1 HG02074.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-3780T>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572122 | |||||||
| chr2:26572125 | G | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0003t0001g0046 |
3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.75-3777G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572125 | |||||||
| chr2:26572223 | G | A | 1 | a0002c0002t0002g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.75-3679G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572223 | |||||||
| chr2:26572278 | T | C | 1 | a0001c0003t0001g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.75-3624T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572278 | |||||||
| chr2:26572347 | TG | T | 5 | a0001c0003t0001g0018 a0001c0003t0001g0024 a0001c0003t0001g0072 others(2): Show |
10 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.75-3553delG | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26572347 | ||||||
| chr2:26572349 | GT | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(114): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.75-3538delT | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26572349 | ||||||
| chr2:26572349 | GTT | G | 5 | a0001c0001t0001g0070 a0001c0003t0001g0021 a0001c0003t0001g0106 others(2): Show |
7 | HG00733.hp2 HG01167.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.75-3539_75-3538del others(2): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26572349 | ||||||
| chr2:26572367 | C | T | 56 | a0001c0003t0001g0009 a0001c0003t0001g0014 a0001c0003t0001g0018 others(53): Show |
161 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.75-3535C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572367 | |||||||
| chr2:26572655 | G | T | 1 | a0002c0002t0002g0023 | 3 | HG01884.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.75-3247G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572655 | |||||||
| chr2:26572780 | G | A | 1 | a0001c0003t0001g0014 | 4 | HG01496.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-3122G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572780 | |||||||
| chr2:26573093 | T | C | 10 | a0001c0001t0001g0120 a0001c0003t0001g0007 a0001c0003t0001g0009 others(7): Show |
30 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.75-2809T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573093 | |||||||
| chr2:26573189 | G | C | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-2713G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573189 | |||||||
| chr2:26573211 | C | T | 1 | a0001c0001t0001g0022 | 3 | HG01884.hp1 HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.75-2691C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573211 | |||||||
| chr2:26573223 | C | T | 1 | a0001c0003t0001g0019 | 4 | HG02015.hp1 HG02074.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-2679C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573223 | |||||||
| chr2:26573294 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.75-2608G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573294 | |||||||
| chr2:26573398 | G | GGGGAAGA others(38): Show |
3 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0003t0001g0015 |
12 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-2500_75-2456dup others(45): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26573398 | ||||||
| chr2:26573400 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0070 |
3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.75-2502G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573400 | |||||||
| chr2:26573442 | A | G | 21 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0009 others(18): Show |
65 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.75-2460A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573442 | |||||||
| chr2:26573592 | A | C | 1 | a0001c0001t0002g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.75-2310A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573592 | |||||||
| chr2:26573609 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
39 | HG00438.hp2 HG00609.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.75-2293G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573609 | |||||||
| chr2:26573659 | G | A | 1 | a0001c0003t0001g0121 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.75-2243G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573659 | |||||||
| chr2:26573660 | C | T | 2 | a0002c0002t0002g0038 a0002c0002t0002g0124 |
3 | HG02280.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.75-2242C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573660 | |||||||
| chr2:26573666 | A | G | 2 | a0002c0002t0002g0093 a0002c0002t0002g0094 |
2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.75-2236A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573666 | |||||||
| chr2:26573706 | A | G | 1 | a0001c0003t0001g0041 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.75-2196A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573706 | |||||||
| chr2:26573710 | G | C | 14 | a0001c0003t0001g0004 a0001c0003t0001g0019 a0001c0003t0001g0027 others(11): Show |
41 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.75-2192G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573710 | |||||||
| chr2:26573917 | C | T | 2 | a0002c0002t0002g0025 a0002c0002t0002g0107 |
4 | HG03017.hp2 HG03239.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-1985C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573917 | |||||||
| chr2:26573988 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.75-1914C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573988 | |||||||
| chr2:26574051 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.75-1851G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574051 | |||||||
| chr2:26574119 | C | T | 2 | a0002c0002t0002g0016 a0002c0006t0001g0092 |
5 | HG02056.hp2 NA18945.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-1783C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574119 | |||||||
| chr2:26574208 | A | T | 1 | a0002c0002t0002g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.75-1694A>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574208 | |||||||
| chr2:26574232 | G | A | 1 | a0002c0002t0002g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.75-1670G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574232 | |||||||
| chr2:26574246 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75-1656G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574246 | |||||||
| chr2:26574423 | G | A | 50 | a0001c0004t0002g0017 a0002c0002t0002g0002 a0002c0002t0002g0003 others(47): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.75-1479G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574423 | |||||||
| chr2:26574599 | C | T | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-1303C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574599 | |||||||
| chr2:26574660 | G | A | 1 | a0001c0003t0001g0014 | 4 | HG01496.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-1242G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574660 | |||||||
| chr2:26574662 | A | G | 1 | a0001c0003t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.75-1240A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574662 | |||||||
| chr2:26574754 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.75-1148G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574754 | |||||||
| chr2:26574768 | C | T | 6 | a0001c0003t0001g0007 a0001c0003t0001g0009 a0001c0003t0001g0028 others(3): Show |
26 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.75-1134C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574768 | |||||||
| chr2:26574775 | G | A | 2 | a0001c0004t0002g0017 a0002c0002t0002g0093 |
5 | HG00738.hp1 HG01346.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.75-1127G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574775 | |||||||
| chr2:26574820 | C | T | 1 | a0001c0003t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75-1082C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574820 | |||||||
| chr2:26574850 | G | A | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-1052G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574850 | |||||||
| chr2:26574938 | T | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.75-964T>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574938 | |||||||
| chr2:26574939 | G | C | 1 | a0001c0001t0001g0008 | 9 | NA18950.hp2 NA18977.hp1 NA18994.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-963G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574939 | |||||||
| chr2:26574939 | G | T | 2 | a0001c0001t0001g0064 a0001c0003t0001g0123 |
2 | HG00639.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.75-963G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574939 | |||||||
| chr2:26574953 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.75-949G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574953 | |||||||
| chr2:26575033 | T | G | 1 | a0001c0003t0001g0126 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.75-869T>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575033 | |||||||
| chr2:26575114 | C | T | 50 | a0001c0004t0002g0017 a0002c0002t0002g0002 a0002c0002t0002g0003 others(47): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.75-788C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575114 | |||||||
| chr2:26575188 | T | A | 12 | a0002c0002t0002g0003 a0002c0002t0002g0075 a0002c0002t0002g0076 others(9): Show |
48 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.75-714T>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575188 | |||||||
| chr2:26575227 | G | A | 2 | a0001c0003t0001g0021 a0001c0003t0001g0072 |
4 | HG00733.hp2 HG01167.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-675G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575227 | |||||||
| chr2:26575262 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
42 | HG00438.hp2 HG00609.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.75-640G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575262 | |||||||
| chr2:26575277 | C | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.75-625C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575277 | |||||||
| chr2:26575306 | C | T | 1 | a0001c0003t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75-596C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575306 | |||||||
| chr2:26575381 | G | C | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-521G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575381 | |||||||
| chr2:26575470 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.75-432G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575470 | |||||||
| chr2:26575470 | G | T | 1 | a0001c0003t0001g0126 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.75-432G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575470 | |||||||
| chr2:26575475 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.75-427G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575475 | |||||||
| chr2:26575610 | A | T | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-292A>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575610 | |||||||
| chr2:26575692 | T | A | 1 | a0001c0003t0001g0009 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.75-210T>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575692 | |||||||
| chr2:26575723 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.75-179G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575723 | |||||||
| chr2:26576223 | C | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
42 | HG00438.hp2 HG00609.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.348+48C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576223 | |||||||
| chr2:26576256 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.348+81C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576256 | |||||||
| chr2:26576355 | G | A | 2 | a0002c0002t0002g0136 a0002c0002t0002g0138 |
2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.348+180G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576355 | |||||||
| chr2:26576523 | A | G | 6 | a0001c0003t0001g0013 a0001c0003t0001g0046 a0001c0003t0001g0059 others(3): Show |
10 | HG00639.hp2 HG01106.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+348A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576523 | |||||||
| chr2:26576588 | C | T | 1 | a0001c0001t0001g0022 | 3 | HG01884.hp1 HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.348+413C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576588 | |||||||
| chr2:26576600 | C | T | 3 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 |
3 | HG01074.hp1 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.348+425C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576600 | |||||||
| chr2:26576623 | G | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0067 a0001c0001t0002g0056 |
3 | HG01243.hp2 HG01891.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.348+448G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576623 | |||||||
| chr2:26576671 | G | A | 1 | a0001c0003t0001g0021 | 3 | HG00733.hp2 HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.348+496G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576671 | |||||||
| chr2:26576742 | G | A | 1 | a0001c0003t0001g0128 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.348+567G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576742 | |||||||
| chr2:26576851 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.349-665T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576851 | |||||||
| chr2:26576865 | C | A | 2 | a0002c0002t0002g0088 a0002c0002t0002g0098 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.349-651C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576865 | |||||||
| chr2:26576870 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.349-646A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576870 | |||||||
| chr2:26576955 | C | G | 1 | a0002c0002t0002g0035 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.349-561C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576955 | |||||||
| chr2:26576955 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.349-561C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576955 | |||||||
| chr2:26577002 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.349-514G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577002 | |||||||
| chr2:26577042 | G | A | 1 | a0001c0003t0001g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349-474G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577042 | |||||||
| chr2:26577213 | C | T | 1 | a0001c0001t0001g0031 | 2 | NA18984.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.349-303C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577213 | |||||||
| chr2:26577219 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.349-297C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577219 | |||||||
| chr2:26577312 | A | C | 1 | a0002c0002t0002g0058 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.349-204A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577312 | |||||||
| chr2:26577325 | G | A | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.349-191G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577325 | |||||||
| chr2:26577327 | C | T | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.349-189C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577327 | |||||||
| chr2:26577365 | G | A | 1 | a0007c0008t0001g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.349-151G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577365 | |||||||
| chr2:26577384 | C | T | 1 | a0002c0002t0002g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.349-132C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577384 | |||||||
| chr2:26577395 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.349-121C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577395 | |||||||
| chr2:26577838 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0070 |
3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.461+210A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26577838 | |||||||
| chr2:26577915 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0047 |
2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.461+287A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26577915 | |||||||
| chr2:26577975 | T | A | 5 | a0001c0003t0001g0018 a0001c0003t0001g0024 a0001c0003t0001g0072 others(2): Show |
10 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.461+347T>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26577975 | |||||||
| chr2:26578040 | C | CT | 4 | a0001c0003t0001g0014 a0001c0003t0001g0050 a0001c0003t0001g0051 others(1): Show |
7 | HG01074.hp1 HG01496.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+413dupT | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 26578040 | ||||||
| chr2:26578046 | C | T | 1 | a0001c0003t0001g0060 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.461+418C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578046 | |||||||
| chr2:26578051 | C | T | 1 | a0001c0003t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.461+423C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578051 | |||||||
| chr2:26578123 | C | G | 1 | a0001c0005t0001g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.461+495C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578123 | |||||||
| chr2:26578273 | G | A | 1 | a0001c0003t0001g0009 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.461+645G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578273 | |||||||
| chr2:26578275 | G | T | 1 | a0002c0002t0002g0086 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.461+647G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578275 | |||||||
| chr2:26578295 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(10): Show |
38 | HG00438.hp2 HG00609.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.461+667G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578295 | |||||||
| chr2:26578443 | G | C | 50 | a0001c0003t0001g0036 a0001c0003t0001g0079 a0001c0004t0002g0017 others(47): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.461+815G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578443 | |||||||
| chr2:26578523 | G | A | 4 | a0001c0003t0001g0046 a0001c0003t0001g0059 a0001c0003t0001g0060 others(1): Show |
4 | HG01106.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.462-771G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578523 | |||||||
| chr2:26578523 | G | C | 1 | a0001c0003t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.462-771G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578523 | |||||||
| chr2:26578524 | C | A | 1 | a0001c0003t0001g0065 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.462-770C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578524 | |||||||
| chr2:26578532 | A | G | 1 | a0002c0002t0002g0089 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.462-762A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578532 | |||||||
| chr2:26578546 | G | T | 1 | a0001c0003t0001g0013 | 5 | HG02257.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.462-748G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578546 | |||||||
| chr2:26578661 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.462-633T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578661 | |||||||
| chr2:26578718 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.462-576G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578718 | |||||||
| chr2:26578878 | C | G | 1 | a0001c0003t0001g0014 | 4 | HG01496.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.462-416C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578878 | |||||||
| chr2:26578927 | C | T | 6 | a0001c0003t0001g0007 a0001c0003t0001g0009 a0001c0003t0001g0028 others(3): Show |
26 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.462-367C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578927 | |||||||
| chr2:26578944 | C | G | 1 | a0001c0003t0001g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.462-350C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578944 | |||||||
| chr2:26578973 | T | C | 3 | a0001c0005t0001g0101 a0001c0005t0001g0151 a0001c0005t0001g0152 |
3 | HG02451.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.462-321T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578973 | |||||||
| chr2:26579067 | C | T | 1 | a0006c0010t0001g0104 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.462-227C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26579067 | |||||||
| chr2:26579153 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.462-141G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26579153 | |||||||
| chr2:26579276 | TC | T | 1 | a0001c0003t0001g0024 | 3 | HG02109.hp2 HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.462-15delC | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 26579276 |