Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 283635 |
| ensemblid | ENSG00000151327.14 |
| hgncid | 19829 |
| symbol | FAM177A1 |
| name | family with sequence similarity 177 member A1 |
| refseq_nuc | NM_173607.5 |
| refseq_prot | NP_775878.2 |
| ensembl_nuc | ENST00000280987.9 |
| ensembl_prot | ENSP00000280987.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 35046272 |
| end | 35083378 |
| strand | + |
| ver | v1.2 |
| region | chr14:35046272-35083378 |
| region5000 | chr14:35041272-35088378 |
| regionname0 | FAM177A1_chr14_35046272_35083378 |
| regionname5000 | FAM177A1_chr14_35041272_35088378 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 236 | 368 | 96 | 76 | 143 | 13 | 38 | 110 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | MEVGL others(231): Show |
chr14 | 35041272 | 35088378 |
| a0002 | 0/0 | 236 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | MEVGL others(231): Show |
chr14 | 35041272 | 35088378 |
| a0003 | 0/0 | 236 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | MEVGL others(231): Show |
chr14 | 35041272 | 35088378 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 708 | 324 | 72 | 69 | 138 | 12 | 31 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | ATGGA others(703): Show |
chr14 | 35041272 | 35088378 | ||
| a0001c0002 | 0/0 | 708 | 43 | 24 | 6 | 5 | 1 | 7 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | ATGGA others(703): Show |
chr14 | 35041272 | 35088378 | ||
| a0001c0005 | 0/0 | 708 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | ATGGA others(703): Show |
chr14 | 35041272 | 35088378 | ||
| a0002c0003 | 0/0 | 708 | 1 | 0 | 0 | 0 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | ATGGA others(703): Show |
chr14 | 35041272 | 35088378 | ||
| a0003c0004 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | ATGGA others(703): Show |
chr14 | 35041272 | 35088378 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3046 | 111 | 13 | 19 | 64 | 6 | 8 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3041): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0002 | 0/0 | 3051 | 69 | 7 | 13 | 39 | 2 | 8 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0003 | 1/0 | 3053 | 67 | 25 | 10 | 25 | 2 | 4 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3048): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0004 | 0/0 | 3051 | 34 | 2 | 18 | 5 | 2 | 7 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0006 | 0/0 | 3051 | 12 | 7 | 3 | 0 | 0 | 2 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0007 | 0/0 | 3050 | 9 | 0 | 4 | 4 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3045): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0008 | 0/0 | 3051 | 9 | 9 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0010 | 0/0 | 3051 | 6 | 5 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACA others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0011 | 0/0 | 3051 | 2 | 2 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0012 | 0/0 | 3051 | 2 | 1 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0014 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3045): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0015 | 0/0 | 3051 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0001t0018 | 0/0 | 3053 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3048): Show |
chr14 | 35041272 | 35088378 |
| a0001c0002t0005 | 0/0 | 3049 | 32 | 20 | 1 | 5 | 0 | 6 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3044): Show |
chr14 | 35041272 | 35088378 |
| a0001c0002t0009 | 0/0 | 3047 | 7 | 1 | 4 | 0 | 1 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3042): Show |
chr14 | 35041272 | 35088378 |
| a0001c0002t0013 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0002t0016 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| a0001c0002t0017 | 0/0 | 3044 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3039): Show |
chr14 | 35041272 | 35088378 |
| a0001c0002t0019 | 0/0 | 3047 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3042): Show |
chr14 | 35041272 | 35088378 |
| a0001c0005t0005 | 0/0 | 3049 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3044): Show |
chr14 | 35041272 | 35088378 |
| a0002c0003t0003 | 0/0 | 3053 | 1 | 0 | 0 | 0 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3048): Show |
chr14 | 35041272 | 35088378 |
| a0003c0004t0002 | 0/0 | 3051 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | AGACT others(3046): Show |
chr14 | 35041272 | 35088378 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 3 | 8 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 3 | 0 | 1 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0007 | 0/0 | 5 | 1 | 1 | 0 | 2 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0011 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0001 | 0/0 | 18 | 0 | 5 | 11 | 1 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0004 | 0/0 | 7 | 3 | 0 | 3 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0005 | 1/0 | 6 | 0 | 0 | 4 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0007g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0007g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0010g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0010g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0010g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0011g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0012g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0015g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0001t0018g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0009g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0009g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0009g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0009g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0009g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0017g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0002t0019g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0001c0005t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0002c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| a0003c0004t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0009 | g0017 | EUR | GBR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0210 | EUR | GBR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0226 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00639 | hp1 | a0001 | c0002 | t0009 | g0034 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0202 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0024 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG00741 | hp2 | a0001 | c0002 | t0009 | g0031 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0183 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01099 | hp1 | a0001 | c0002 | t0017 | g0081 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01106 | hp1 | a0001 | c0005 | t0005 | g0101 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0242 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0212 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0115 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0117 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0230 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0220 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0118 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0233 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0208 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0232 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01257 | hp1 | a0001 | c0002 | t0009 | g0032 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0203 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01346 | hp1 | a0001 | c0002 | t0005 | g0100 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0211 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0105 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01433 | hp2 | a0001 | c0002 | t0009 | g0036 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01496 | hp2 | a0001 | c0001 | t0012 | g0180 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0285 | EUR | IBS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01516 | hp2 | a0002 | c0003 | t0003 | g0059 | EUR | IBS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0028 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0073 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0224 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0209 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0200 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02015 | hp2 | a0001 | c0001 | t0015 | g0275 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02055 | hp2 | a0001 | c0002 | t0005 | g0027 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0074 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02165 | hp1 | a0003 | c0004 | t0002 | g0274 | EAS | CDX | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | CDX | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0198 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0246 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0236 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0240 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02615 | hp1 | a0001 | c0002 | t0009 | g0033 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0184 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0072 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0186 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02647 | hp1 | a0001 | c0002 | t0005 | g0069 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0241 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02683 | hp1 | a0001 | c0002 | t0005 | g0019 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0191 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02735 | hp1 | a0001 | c0002 | t0005 | g0019 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0197 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02818 | hp1 | a0001 | c0002 | t0019 | g0035 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0190 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0016 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0070 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0192 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02896 | hp2 | a0001 | c0002 | t0005 | g0039 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0193 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0235 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0041 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02970 | hp1 | a0001 | c0002 | t0005 | g0009 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0231 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0237 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0187 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0018 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03225 | hp2 | a0001 | c0002 | t0005 | g0009 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03453 | hp1 | a0001 | c0002 | t0005 | g0016 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03453 | hp2 | a0001 | c0002 | t0013 | g0109 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0199 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03491 | hp1 | a0001 | c0002 | t0005 | g0102 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0204 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0089 | AFR | ESN | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0071 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0239 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0189 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03710 | hp1 | a0001 | c0002 | t0009 | g0017 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0201 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03927 | hp1 | a0001 | c0001 | t0018 | g0005 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0219 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04115 | hp1 | a0001 | c0002 | t0005 | g0080 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0229 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | BEB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG04228 | hp2 | a0001 | c0002 | t0005 | g0085 | SAS | STU | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | YRI | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0194 | AFR | YRI | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18612 | hp2 | a0001 | c0001 | t0007 | g0227 | EAS | CHB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | YRI | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18943 | hp1 | a0001 | c0002 | t0005 | g0078 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18977 | hp2 | a0001 | c0002 | t0005 | g0083 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18981 | hp1 | a0001 | c0001 | t0007 | g0228 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18999 | hp1 | a0001 | c0002 | t0005 | g0082 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19002 | hp1 | a0001 | c0002 | t0005 | g0079 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19011 | hp1 | a0001 | c0002 | t0005 | g0084 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | LWK | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0238 | AFR | LWK | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19043 | hp1 | a0001 | c0002 | t0005 | g0018 | AFR | LWK | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0221 | AFR | LWK | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19084 | hp1 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | YRI | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | YRI | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | ASW | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0217 | EUR | TSI | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA20905 | hp1 | a0001 | c0002 | t0005 | g0086 | SAS | GIH | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | GIH | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0214 | AMR | CLM | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0247 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0009 | AFR | ACB | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0181 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG03471 | hp2 | a0001 | c0002 | t0005 | g0075 | AFR | MSL | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | USA | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | USA | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | USA | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA21309 | hp1 | a0001 | c0002 | t0016 | g0182 | AFR | LWK | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | LWK | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0114 | REF | REF | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0005 | REF | REF | FAM177A1_chr14_35041272_35088378 | FAM177A1 | chr14 | 35041272 | 35088378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:35046510 | G | A | 1 | a0002 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.47G>A | p.Ser16Asn | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/5 | 239/3053 | 47/711 | 16/236 | chr14 | 35046510 | |||
| chr14:35079019 | A | G | 1 | a0003 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.499A>G | p.Lys167Glu | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/5 | 691/3053 | 499/711 | 167/236 | chr14 | 35079019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:35046601 | C | G | 1 | a0001c0005 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.138C>G | p.Ala46Ala | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/5 | 330/3053 | 138/711 | 46/236 | chr14 | 35046601 | |||
| chr14:35077167 | T | C | 2 | a0001c0002 a0001c0005 |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
synonymous_variant | LOW | c.357T>C | p.Gly119Gly | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/5 | 549/3053 | 357/711 | 119/236 | chr14 | 35077167 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:35046276 | T | A | 1 | a0001c0001t0010 | 6 | HG01109.hp2 HG02257.hp2 HG02572.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-188T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/5 | 188 | chr14 | 35046276 | ||||||
| chr14:35046287 | A | C | 1 | a0001c0002t0019 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-177A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/5 | 177 | chr14 | 35046287 | ||||||
| chr14:35046288 | G | C | 1 | a0001c0002t0019 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-176G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/5 | 176 | chr14 | 35046288 | ||||||
| chr14:35046325 | G | A | 1 | a0001c0002t0013 | 1 | HG03453.hp2 | 5_prime_UTR_variant | MODIFIER | c.-139G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/5 | 139 | chr14 | 35046325 | ||||||
| chr14:35046400 | TGG | T | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(13): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
5_prime_UTR_variant | MODIFIER | c.-62_-61delGG | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/5 | 61 | INFO_REALIGN_3_PRIME | chr14 | 35046400 | |||||
| chr14:35046435 | C | T | 1 | a0001c0001t0018 | 1 | HG03927.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/5 | chr14 | 35046435 | |||||||
| chr14:35081258 | TAA | T | 5 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0017 others(2): Show |
42 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*31_*32delAA | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 31 | chr14 | 35081258 | ||||||
| chr14:35081261 | GT | G | 2 | a0001c0001t0007 a0001c0001t0014 |
10 | HG00408.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*45delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 45 | INFO_REALIGN_3_PRIME | chr14 | 35081261 | |||||
| chr14:35081265 | T | C | 1 | a0001c0002t0019 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 37 | chr14 | 35081265 | ||||||
| chr14:35081322 | T | C | 1 | a0001c0001t0015 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*94T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 94 | chr14 | 35081322 | ||||||
| chr14:35081846 | T | C | 1 | a0001c0001t0011 | 2 | HG02258.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*618T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 618 | chr14 | 35081846 | ||||||
| chr14:35081949 | GGTTAT | G | 2 | a0001c0001t0001 a0001c0002t0017 |
111 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*727_*731delGTTAT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 727 | INFO_REALIGN_3_PRIME | chr14 | 35081949 | |||||
| chr14:35082057 | A | G | 1 | a0001c0001t0012 | 2 | HG01496.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 829 | chr14 | 35082057 | ||||||
| chr14:35082265 | G | A | 3 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 |
27 | HG00735.hp1 HG01081.hp1 HG01109.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1037G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 1037 | chr14 | 35082265 | ||||||
| chr14:35082506 | C | T | 1 | a0001c0002t0016 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1278C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 1278 | chr14 | 35082506 | ||||||
| chr14:35082519 | A | G | 1 | a0001c0001t0012 | 2 | HG01496.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1291A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 1291 | chr14 | 35082519 | ||||||
| chr14:35082564 | CAT | C | 5 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0017 others(2): Show |
42 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1341_*1342delAT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 1341 | INFO_REALIGN_3_PRIME | chr14 | 35082564 | |||||
| chr14:35082669 | T | C | 1 | a0001c0001t0004 | 34 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1441T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 1441 | chr14 | 35082669 | ||||||
| chr14:35083020 | T | C | 1 | a0001c0001t0014 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1792T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 1792 | chr14 | 35083020 | ||||||
| chr14:35083190 | T | A | 1 | a0001c0001t0006 | 12 | HG00735.hp1 HG01081.hp1 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1962T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 5/5 | 1962 | chr14 | 35083190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:35046699 | T | C | 5 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0027 others(2): Show |
8 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+71T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35046699 | |||||||
| chr14:35046714 | C | G | 49 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(46): Show |
72 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.165+86C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35046714 | |||||||
| chr14:35046751 | C | A | 8 | a0001c0001t0001g0030 a0001c0002t0009g0017 a0001c0002t0009g0031 others(5): Show |
9 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+123C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35046751 | |||||||
| chr14:35046786 | G | C | 1 | a0001c0001t0002g0243 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.165+158G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35046786 | |||||||
| chr14:35046893 | C | G | 112 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(109): Show |
140 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.165+265C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35046893 | |||||||
| chr14:35046999 | G | C | 4 | a0001c0001t0006g0183 a0001c0001t0006g0184 a0001c0001t0006g0185 others(1): Show |
4 | HG01081.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+371G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35046999 | |||||||
| chr14:35047007 | G | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.165+379G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047007 | |||||||
| chr14:35047061 | G | A | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.165+433G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047061 | |||||||
| chr14:35047145 | A | T | 7 | a0001c0001t0003g0010 a0001c0001t0003g0020 a0001c0001t0003g0104 others(4): Show |
10 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+517A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047145 | |||||||
| chr14:35047369 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.165+741T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047369 | |||||||
| chr14:35047384 | C | G | 1 | a0001c0001t0003g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165+756C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047384 | |||||||
| chr14:35047415 | C | G | 1 | a0001c0001t0003g0103 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.165+787C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047415 | |||||||
| chr14:35047415 | C | T | 2 | a0001c0001t0010g0241 a0001c0001t0010g0242 |
2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.165+787C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047415 | |||||||
| chr14:35047602 | A | G | 2 | a0001c0001t0010g0239 a0001c0001t0010g0240 |
2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.165+974A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047602 | |||||||
| chr14:35047616 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.165+988G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047616 | |||||||
| chr14:35047743 | G | A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.165+1115G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047743 | |||||||
| chr14:35047754 | GCAACAA | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02056.hp2 NA18978.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.165+1151_165+1156d others(8): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35047754 | ||||||
| chr14:35047754 | GCAACAAC others(2): Show |
G | 96 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(93): Show |
123 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.165+1148_165+1156d others(11): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35047754 | ||||||
| chr14:35047754 | GCAACAAC others(5): Show |
G | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.165+1145_165+1156d others(14): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35047754 | ||||||
| chr14:35047773 | CAACAACA others(3): Show |
C | 5 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(2): Show |
6 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1148_165+1157d others(12): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35047773 | ||||||
| chr14:35047773 | CAACAACA others(5): Show |
C | 1 | a0001c0002t0019g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+1148_165+1159d others(14): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35047773 | ||||||
| chr14:35047775 | ACAACAAC | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0150 |
3 | HG02965.hp1 NA18973.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.165+1148_165+1154d others(9): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047775 | |||||||
| chr14:35047776 | CAACAACA | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(70): Show |
105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.165+1151_165+1157d others(9): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35047776 | ||||||
| chr14:35047776 | CAACAACA others(2): Show |
C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(14): Show |
18 | HG00408.hp1 HG00735.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+1151_165+1159d others(11): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35047776 | ||||||
| chr14:35047776 | CAACAACA others(3): Show |
C | 1 | a0001c0002t0009g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.165+1151_165+1160d others(12): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35047776 | ||||||
| chr14:35047782 | C | A | 4 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0063 others(1): Show |
5 | HG01074.hp1 HG02015.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+1154C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047782 | |||||||
| chr14:35047785 | A | C | 3 | a0001c0002t0005g0100 a0001c0002t0005g0102 a0001c0005t0005g0101 |
3 | HG01106.hp1 HG01346.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.165+1157A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047785 | |||||||
| chr14:35047811 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.165+1183A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047811 | |||||||
| chr14:35047851 | A | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0002g0179 |
3 | NA18961.hp2 NA18974.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.165+1223A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047851 | |||||||
| chr14:35047903 | C | T | 9 | a0001c0001t0003g0091 a0001c0001t0003g0092 a0001c0001t0003g0093 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+1275C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35047903 | |||||||
| chr14:35048164 | A | G | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.165+1536A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35048164 | |||||||
| chr14:35048404 | G | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.165+1776G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35048404 | |||||||
| chr14:35048408 | T | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0248 a0001c0001t0011g0246 others(1): Show |
6 | HG00738.hp1 HG01496.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+1780T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35048408 | |||||||
| chr14:35048412 | C | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.165+1784C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35048412 | |||||||
| chr14:35048447 | T | A | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+1819T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35048447 | |||||||
| chr14:35048551 | A | G | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165+1923A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35048551 | |||||||
| chr14:35048786 | G | A | 1 | a0001c0001t0008g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.165+2158G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35048786 | |||||||
| chr14:35048891 | C | CT | 9 | a0001c0001t0001g0176 a0001c0001t0003g0090 a0001c0001t0014g0238 others(6): Show |
10 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+2280dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35048891 | ||||||
| chr14:35048891 | CT | C | 16 | a0001c0001t0001g0111 a0001c0001t0001g0177 a0001c0001t0002g0249 others(13): Show |
16 | HG00408.hp1 HG01167.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+2280delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35048891 | ||||||
| chr14:35048914 | G | A | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165+2286G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35048914 | |||||||
| chr14:35048992 | G | A | 1 | a0001c0002t0009g0031 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.165+2364G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35048992 | |||||||
| chr14:35049187 | C | T | 10 | a0001c0001t0001g0030 a0001c0002t0009g0017 a0001c0002t0009g0031 others(7): Show |
11 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+2559C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35049187 | |||||||
| chr14:35049425 | A | C | 1 | a0001c0001t0012g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165+2797A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35049425 | |||||||
| chr14:35049466 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.165+2838G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35049466 | |||||||
| chr14:35050006 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.166-3272T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050006 | |||||||
| chr14:35050034 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.166-3244A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050034 | |||||||
| chr14:35050069 | C | T | 1 | a0001c0002t0005g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.166-3209C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050069 | |||||||
| chr14:35050076 | G | A | 1 | a0001c0001t0010g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.166-3202G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050076 | |||||||
| chr14:35050161 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(75): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.166-3117C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050161 | |||||||
| chr14:35050207 | C | A | 1 | a0001c0001t0003g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.166-3071C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050207 | |||||||
| chr14:35050255 | C | T | 3 | a0001c0001t0003g0040 a0001c0001t0003g0087 a0001c0001t0003g0088 |
3 | HG02922.hp1 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.166-3023C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050255 | |||||||
| chr14:35050305 | A | G | 1 | a0001c0001t0007g0230 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.166-2973A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050305 | |||||||
| chr14:35050444 | T | A | 2 | a0001c0002t0005g0041 a0001c0002t0005g0089 |
2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.166-2834T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050444 | |||||||
| chr14:35050460 | G | GC | 13 | a0001c0002t0005g0019 a0001c0002t0005g0078 a0001c0002t0005g0079 others(10): Show |
14 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-2812dupC | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 35050460 | ||||||
| chr14:35050505 | C | A | 10 | a0001c0001t0001g0030 a0001c0002t0009g0017 a0001c0002t0009g0031 others(7): Show |
11 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-2773C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050505 | |||||||
| chr14:35050520 | A | G | 1 | a0001c0002t0019g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.166-2758A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050520 | |||||||
| chr14:35050653 | G | A | 1 | a0001c0001t0004g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.166-2625G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050653 | |||||||
| chr14:35050782 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-2496A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050782 | |||||||
| chr14:35050797 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-2481C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050797 | |||||||
| chr14:35050921 | C | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.166-2357C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050921 | |||||||
| chr14:35050921 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.166-2357C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35050921 | |||||||
| chr14:35051054 | T | C | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-2224T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051054 | |||||||
| chr14:35051080 | T | C | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-2198T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051080 | |||||||
| chr14:35051144 | G | T | 1 | a0001c0002t0019g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.166-2134G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051144 | |||||||
| chr14:35051147 | T | C | 3 | a0001c0001t0006g0024 a0001c0001t0006g0189 a0001c0001t0006g0231 |
4 | HG00735.hp1 HG01255.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-2131T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051147 | |||||||
| chr14:35051154 | G | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.166-2124G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051154 | |||||||
| chr14:35051194 | A | G | 1 | a0001c0001t0007g0118 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.166-2084A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051194 | |||||||
| chr14:35051244 | C | T | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-2034C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051244 | |||||||
| chr14:35051348 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.166-1930G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051348 | |||||||
| chr14:35051476 | G | T | 1 | a0001c0001t0002g0284 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.166-1802G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051476 | |||||||
| chr14:35051610 | G | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG00408.hp1 HG01175.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1668G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051610 | |||||||
| chr14:35051632 | C | T | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1646C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051632 | |||||||
| chr14:35051711 | C | T | 45 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0025 others(42): Show |
66 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.166-1567C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051711 | |||||||
| chr14:35051755 | T | C | 1 | a0001c0001t0002g0252 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.166-1523T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051755 | |||||||
| chr14:35051841 | A | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0248 a0001c0001t0011g0246 others(1): Show |
6 | HG00738.hp1 HG01496.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-1437A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051841 | |||||||
| chr14:35051882 | G | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG00408.hp1 HG01175.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1396G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35051882 | |||||||
| chr14:35052267 | T | C | 11 | a0001c0001t0001g0030 a0001c0001t0014g0238 a0001c0002t0009g0017 others(8): Show |
12 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-1011T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35052267 | |||||||
| chr14:35052377 | G | C | 1 | a0001c0001t0002g0253 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.166-901G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35052377 | |||||||
| chr14:35052451 | C | A | 5 | a0001c0001t0008g0190 a0001c0001t0008g0191 a0001c0001t0008g0192 others(2): Show |
5 | HG02723.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-827C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35052451 | |||||||
| chr14:35052509 | A | G | 1 | a0001c0001t0002g0283 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.166-769A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35052509 | |||||||
| chr14:35052659 | G | A | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-619G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35052659 | |||||||
| chr14:35052688 | G | A | 1 | a0001c0001t0004g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.166-590G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35052688 | |||||||
| chr14:35052725 | G | A | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-553G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35052725 | |||||||
| chr14:35052867 | A | G | 11 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(8): Show |
12 | HG00735.hp1 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-411A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35052867 | |||||||
| chr14:35053001 | A | G | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-277A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35053001 | |||||||
| chr14:35053061 | A | T | 1 | a0001c0001t0008g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.166-217A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35053061 | |||||||
| chr14:35053144 | A | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.166-134A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35053144 | |||||||
| chr14:35053251 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.166-27C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35053251 | |||||||
| chr14:35053275 | T | C | 1 | a0001c0001t0004g0232 | 1 | HG01255.hp1 | splice_region_variant&intron_variant | LOW | c.166-3T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 1/4 | chr14 | 35053275 | |||||||
| chr14:35053501 | A | T | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+50A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35053501 | |||||||
| chr14:35053686 | G | A | 1 | a0001c0002t0019g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.339+235G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35053686 | |||||||
| chr14:35053717 | C | T | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+266C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35053717 | |||||||
| chr14:35053719 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.339+268C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35053719 | |||||||
| chr14:35053757 | T | A | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.339+306T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35053757 | |||||||
| chr14:35053992 | C | G | 1 | a0001c0001t0003g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.339+541C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35053992 | |||||||
| chr14:35054011 | A | G | 37 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(34): Show |
43 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.339+560A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054011 | |||||||
| chr14:35054060 | G | A | 39 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(36): Show |
45 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.339+609G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054060 | |||||||
| chr14:35054121 | A | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | NA18984.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.339+670A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054121 | |||||||
| chr14:35054195 | A | T | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+744A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054195 | |||||||
| chr14:35054281 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0171 |
6 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+830C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054281 | |||||||
| chr14:35054342 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.339+891G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054342 | |||||||
| chr14:35054501 | T | C | 8 | a0001c0001t0002g0254 a0001c0001t0007g0225 a0001c0001t0007g0226 others(5): Show |
8 | HG00408.hp1 HG00423.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.339+1050T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054501 | |||||||
| chr14:35054520 | A | G | 1 | a0001c0001t0003g0068 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.339+1069A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054520 | |||||||
| chr14:35054577 | G | A | 38 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(35): Show |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.339+1126G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054577 | |||||||
| chr14:35054870 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(229): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.339+1419A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35054870 | |||||||
| chr14:35054985 | A | AAAAAAAT | 39 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(36): Show |
45 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.339+1546_339+1552d others(9): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35054985 | ||||||
| chr14:35055039 | C | T | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+1588C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055039 | |||||||
| chr14:35055049 | C | T | 1 | a0001c0001t0007g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.339+1598C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055049 | |||||||
| chr14:35055100 | G | A | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+1649G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055100 | |||||||
| chr14:35055135 | C | G | 1 | a0001c0001t0003g0103 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.339+1684C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055135 | |||||||
| chr14:35055175 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.339+1724C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055175 | |||||||
| chr14:35055203 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(75): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.339+1752T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055203 | |||||||
| chr14:35055251 | C | T | 4 | a0001c0001t0002g0014 a0001c0001t0002g0248 a0001c0001t0011g0246 others(1): Show |
6 | HG00738.hp1 HG01496.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+1800C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055251 | |||||||
| chr14:35055258 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.339+1807G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055258 | |||||||
| chr14:35055263 | A | ATT | 39 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(36): Show |
45 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.339+1813_339+1814d others(4): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35055263 | ||||||
| chr14:35055347 | A | AG | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(229): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.339+1897dupG | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35055347 | ||||||
| chr14:35055364 | T | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.339+1913T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055364 | |||||||
| chr14:35055435 | A | T | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.339+1984A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055435 | |||||||
| chr14:35055441 | G | GT | 19 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(16): Show |
19 | HG00544.hp2 HG00639.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.339+2006dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35055441 | ||||||
| chr14:35055449 | T | A | 1 | a0001c0001t0002g0255 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.339+1998T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055449 | |||||||
| chr14:35055594 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0164 others(1): Show |
4 | HG03225.hp1 NA18950.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+2143C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055594 | |||||||
| chr14:35055656 | C | T | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+2205C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055656 | |||||||
| chr14:35055919 | T | C | 2 | a0001c0001t0012g0180 a0001c0001t0012g0181 |
2 | HG01496.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.339+2468T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055919 | |||||||
| chr14:35055952 | T | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0110 a0001c0001t0001g0116 others(11): Show |
22 | HG00423.hp1 NA18612.hp1 NA18945.hp1 others(19): Show |
intron_variant | MODIFIER | c.339+2501T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35055952 | |||||||
| chr14:35056159 | T | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.339+2708T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35056159 | |||||||
| chr14:35056253 | T | C | 1 | a0001c0001t0002g0256 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.339+2802T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35056253 | |||||||
| chr14:35056261 | C | G | 1 | a0001c0001t0002g0256 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.339+2810C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35056261 | |||||||
| chr14:35056327 | G | A | 4 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(1): Show |
5 | HG00099.hp1 HG00741.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+2876G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35056327 | |||||||
| chr14:35056409 | G | T | 1 | a0001c0001t0004g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.339+2958G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35056409 | |||||||
| chr14:35057026 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
8 | HG00280.hp2 HG01123.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.339+3575C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35057026 | |||||||
| chr14:35057046 | C | G | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+3595C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35057046 | |||||||
| chr14:35057225 | G | A | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+3774G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35057225 | |||||||
| chr14:35057344 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.339+3893C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35057344 | |||||||
| chr14:35057632 | G | A | 1 | a0001c0002t0005g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.339+4181G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35057632 | |||||||
| chr14:35057689 | A | G | 4 | a0001c0001t0006g0184 a0001c0001t0006g0185 a0001c0001t0006g0186 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+4238A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35057689 | |||||||
| chr14:35058032 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.339+4581C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058032 | |||||||
| chr14:35058033 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.339+4582A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058033 | |||||||
| chr14:35058048 | C | T | 11 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(8): Show |
12 | HG00735.hp1 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+4597C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058048 | |||||||
| chr14:35058051 | C | T | 38 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(35): Show |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.339+4600C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058051 | |||||||
| chr14:35058140 | T | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0248 a0001c0001t0011g0246 others(1): Show |
6 | HG00738.hp1 HG01496.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+4689T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058140 | |||||||
| chr14:35058185 | T | C | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+4734T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058185 | |||||||
| chr14:35058262 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.339+4811C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058262 | |||||||
| chr14:35058525 | A | G | 4 | a0001c0001t0006g0184 a0001c0001t0006g0185 a0001c0001t0006g0186 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+5074A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058525 | |||||||
| chr14:35058684 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.339+5233G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058684 | |||||||
| chr14:35058725 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.339+5274C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058725 | |||||||
| chr14:35058732 | C | T | 1 | a0001c0002t0005g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.339+5281C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058732 | |||||||
| chr14:35058742 | G | C | 1 | a0001c0001t0008g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.339+5291G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058742 | |||||||
| chr14:35058817 | A | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(103): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.339+5366A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058817 | |||||||
| chr14:35058836 | A | T | 1 | a0001c0001t0003g0066 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.339+5385A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058836 | |||||||
| chr14:35058876 | A | C | 1 | a0001c0001t0004g0222 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.339+5425A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058876 | |||||||
| chr14:35058987 | C | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.339+5536C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35058987 | |||||||
| chr14:35059010 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.339+5559A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059010 | |||||||
| chr14:35059021 | C | T | 11 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(8): Show |
12 | HG00735.hp1 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+5570C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059021 | |||||||
| chr14:35059036 | C | T | 1 | a0001c0001t0010g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.339+5585C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059036 | |||||||
| chr14:35059037 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.339+5586G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059037 | |||||||
| chr14:35059061 | G | T | 30 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0188 others(27): Show |
34 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+5610G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059061 | |||||||
| chr14:35059216 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.339+5765C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059216 | |||||||
| chr14:35059216 | C | T | 1 | a0001c0001t0003g0065 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.339+5765C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059216 | |||||||
| chr14:35059217 | G | C | 1 | a0001c0001t0001g0130 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.339+5766G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059217 | |||||||
| chr14:35059349 | A | C | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+5898A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059349 | |||||||
| chr14:35059535 | C | CT | 29 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(26): Show |
29 | HG00408.hp1 HG01109.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.339+6103dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35059535 | ||||||
| chr14:35059535 | CT | C | 9 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0176 others(6): Show |
9 | HG02083.hp1 HG02486.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.339+6103delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35059535 | ||||||
| chr14:35059595 | C | T | 3 | a0001c0002t0005g0100 a0001c0002t0005g0102 a0001c0005t0005g0101 |
3 | HG01106.hp1 HG01346.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.339+6144C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059595 | |||||||
| chr14:35059613 | C | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(75): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.339+6162C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059613 | |||||||
| chr14:35059628 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.339+6177A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059628 | |||||||
| chr14:35059629 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.339+6178G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059629 | |||||||
| chr14:35059738 | G | T | 1 | a0001c0001t0010g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.339+6287G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059738 | |||||||
| chr14:35059746 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.339+6295A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059746 | |||||||
| chr14:35059957 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(76): Show |
114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.339+6506G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35059957 | |||||||
| chr14:35060396 | T | C | 1 | a0001c0001t0014g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.339+6945T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35060396 | |||||||
| chr14:35060635 | T | G | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+7184T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35060635 | |||||||
| chr14:35060637 | T | G | 13 | a0001c0002t0005g0019 a0001c0002t0005g0078 a0001c0002t0005g0079 others(10): Show |
14 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.339+7186T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35060637 | |||||||
| chr14:35060707 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.339+7256G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35060707 | |||||||
| chr14:35060795 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.339+7344G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35060795 | |||||||
| chr14:35060869 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0155 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.339+7418G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35060869 | |||||||
| chr14:35061025 | T | C | 6 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(3): Show |
6 | HG00408.hp1 HG01175.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+7574T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061025 | |||||||
| chr14:35061030 | T | C | 49 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(46): Show |
72 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.339+7579T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061030 | |||||||
| chr14:35061068 | G | A | 1 | a0001c0001t0008g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.339+7617G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061068 | |||||||
| chr14:35061085 | C | CAT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.339+7635_339+7636i others(4): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35061085 | ||||||
| chr14:35061108 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.339+7657G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061108 | |||||||
| chr14:35061262 | A | G | 30 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0188 others(27): Show |
34 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+7811A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061262 | |||||||
| chr14:35061358 | AGGTTTTG others(7): Show |
A | 1 | a0001c0001t0001g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.339+7910_339+7923d others(16): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35061358 | ||||||
| chr14:35061364 | T | G | 2 | a0001c0001t0012g0180 a0001c0001t0012g0181 |
2 | HG01496.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.339+7913T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061364 | |||||||
| chr14:35061412 | T | G | 38 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(35): Show |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.339+7961T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061412 | |||||||
| chr14:35061422 | A | G | 30 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0188 others(27): Show |
34 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+7971A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061422 | |||||||
| chr14:35061462 | A | AT | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(78): Show |
116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.339+8026dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35061462 | ||||||
| chr14:35061462 | AT | A | 28 | a0001c0001t0003g0037 a0001c0001t0004g0012 a0001c0001t0004g0013 others(25): Show |
32 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.339+8026delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35061462 | ||||||
| chr14:35061519 | CT | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(73): Show |
111 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.339+8083delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35061519 | ||||||
| chr14:35061625 | A | AG | 7 | a0001c0001t0001g0153 a0001c0001t0002g0281 a0001c0001t0003g0064 others(4): Show |
7 | HG00544.hp2 HG00741.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+8180dupG | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35061625 | ||||||
| chr14:35061632 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.339+8181A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061632 | |||||||
| chr14:35061743 | C | T | 2 | a0001c0001t0008g0196 a0001c0001t0008g0197 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.339+8292C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061743 | |||||||
| chr14:35061769 | TA | T | 37 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(34): Show |
43 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.339+8328delA | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35061769 | ||||||
| chr14:35061851 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(75): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.339+8400C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35061851 | |||||||
| chr14:35062307 | T | C | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+8856T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062307 | |||||||
| chr14:35062548 | C | T | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG02165.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.339+9097C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062548 | |||||||
| chr14:35062607 | T | G | 2 | a0001c0001t0010g0241 a0001c0001t0010g0242 |
2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.339+9156T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062607 | |||||||
| chr14:35062660 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.339+9209G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062660 | |||||||
| chr14:35062725 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0154 |
3 | NA18941.hp1 NA18962.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.339+9274T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062725 | |||||||
| chr14:35062792 | T | C | 1 | a0001c0001t0014g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.339+9341T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062792 | |||||||
| chr14:35062793 | CA | C | 25 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(22): Show |
26 | HG00735.hp1 HG01081.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.339+9356delA | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35062793 | ||||||
| chr14:35062878 | C | CA | 5 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | NA18906.hp1 NA18939.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+9427_339+9428i others(3): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062878 | |||||||
| chr14:35062879 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(70): Show |
108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.339+9428G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062879 | |||||||
| chr14:35062880 | G | GT | 24 | a0001c0001t0002g0251 a0001c0001t0002g0255 a0001c0001t0002g0259 others(21): Show |
24 | HG01123.hp2 HG01175.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.339+9445dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35062880 | ||||||
| chr14:35062880 | G | T | 5 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | NA18906.hp1 NA18939.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+9429G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062880 | |||||||
| chr14:35062985 | T | A | 13 | a0001c0002t0005g0019 a0001c0002t0005g0078 a0001c0002t0005g0079 others(10): Show |
14 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.339+9534T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062985 | |||||||
| chr14:35062997 | A | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.339+9546A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35062997 | |||||||
| chr14:35063016 | C | T | 1 | a0001c0001t0002g0257 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.339+9565C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063016 | |||||||
| chr14:35063055 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.339+9604C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063055 | |||||||
| chr14:35063056 | G | T | 11 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(8): Show |
12 | HG00735.hp1 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+9605G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063056 | |||||||
| chr14:35063086 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.339+9635G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063086 | |||||||
| chr14:35063141 | C | G | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+9690C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063141 | |||||||
| chr14:35063159 | C | CA | 7 | a0001c0001t0001g0124 a0001c0001t0001g0136 a0001c0001t0002g0260 others(4): Show |
7 | HG02004.hp2 HG03942.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+9727dupA | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35063159 | ||||||
| chr14:35063159 | CA | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0152 a0001c0001t0001g0171 others(19): Show |
27 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.339+9727delA | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35063159 | ||||||
| chr14:35063204 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.339+9753G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063204 | |||||||
| chr14:35063300 | T | TG | 38 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(35): Show |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.339+9851dupG | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35063300 | ||||||
| chr14:35063401 | G | A | 11 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(8): Show |
12 | HG00735.hp1 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+9950G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063401 | |||||||
| chr14:35063441 | G | C | 1 | a0001c0001t0003g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+9990G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063441 | |||||||
| chr14:35063492 | C | T | 2 | a0001c0001t0002g0258 a0003c0004t0002g0274 |
2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.339+10041C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063492 | |||||||
| chr14:35063514 | G | C | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+10063G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063514 | |||||||
| chr14:35063764 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.339+10313A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063764 | |||||||
| chr14:35063823 | T | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0154 |
3 | NA18941.hp1 NA18962.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.339+10372T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063823 | |||||||
| chr14:35063927 | A | G | 1 | a0001c0001t0007g0227 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.339+10476A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35063927 | |||||||
| chr14:35064047 | C | CA | 33 | a0001c0001t0001g0134 a0001c0001t0002g0015 a0001c0001t0002g0243 others(30): Show |
38 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.339+10618dupA | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35064047 | ||||||
| chr14:35064047 | CA | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(73): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.339+10618delA | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35064047 | ||||||
| chr14:35064066 | A | G | 1 | a0001c0001t0004g0200 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.339+10615A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064066 | |||||||
| chr14:35064103 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.339+10652A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064103 | |||||||
| chr14:35064146 | G | A | 1 | a0001c0002t0005g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.339+10695G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064146 | |||||||
| chr14:35064346 | G | A | 3 | a0001c0001t0002g0256 a0001c0001t0002g0265 a0001c0001t0002g0279 |
3 | NA18968.hp1 NA18975.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.339+10895G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064346 | |||||||
| chr14:35064441 | C | G | 30 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0188 others(27): Show |
34 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+10990C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064441 | |||||||
| chr14:35064446 | C | T | 4 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(1): Show |
5 | HG00099.hp1 HG00741.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+10995C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064446 | |||||||
| chr14:35064542 | A | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.339+11091A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064542 | |||||||
| chr14:35064553 | G | T | 1 | a0001c0001t0003g0045 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.339+11102G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064553 | |||||||
| chr14:35064583 | T | C | 39 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(36): Show |
45 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.339+11132T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064583 | |||||||
| chr14:35064634 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.339+11183A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064634 | |||||||
| chr14:35064658 | AT | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(47): Show |
73 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.339+11217delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35064658 | ||||||
| chr14:35064673 | T | C | 39 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(36): Show |
45 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.339+11222T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064673 | |||||||
| chr14:35064674 | G | A | 38 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(35): Show |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.339+11223G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064674 | |||||||
| chr14:35064682 | G | C | 37 | a0001c0001t0001g0030 a0001c0002t0005g0009 a0001c0002t0005g0016 others(34): Show |
43 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.339+11231G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064682 | |||||||
| chr14:35064743 | C | T | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+11292C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064743 | |||||||
| chr14:35064744 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.339+11293A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064744 | |||||||
| chr14:35064803 | C | A | 1 | a0001c0001t0003g0104 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.339+11352C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064803 | |||||||
| chr14:35064867 | T | C | 30 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0188 others(27): Show |
34 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+11416T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064867 | |||||||
| chr14:35064895 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(75): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.339+11444G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064895 | |||||||
| chr14:35064963 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.339+11512C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064963 | |||||||
| chr14:35064978 | G | C | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+11527G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35064978 | |||||||
| chr14:35065050 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.339+11599T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35065050 | |||||||
| chr14:35065065 | AT | A | 41 | a0001c0001t0001g0030 a0001c0001t0001g0123 a0001c0001t0004g0215 others(38): Show |
47 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.339+11623delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35065065 | ||||||
| chr14:35065229 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.339+11778G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35065229 | |||||||
| chr14:35065356 | TC | T | 28 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(25): Show |
33 | HG01106.hp1 HG01346.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.340-11793delC | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35065356 | |||||||
| chr14:35065357 | C | CT | 32 | a0001c0001t0001g0030 a0001c0001t0001g0130 a0001c0001t0001g0134 others(29): Show |
34 | HG00738.hp1 HG01109.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.340-11773dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35065357 | ||||||
| chr14:35065357 | C | T | 1 | a0001c0002t0005g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.340-11793C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35065357 | |||||||
| chr14:35065357 | CT | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0124 others(17): Show |
22 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-11773delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35065357 | ||||||
| chr14:35065696 | A | AT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.340-11437dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35065696 | ||||||
| chr14:35065696 | A | ATT | 21 | a0001c0001t0001g0134 a0001c0001t0001g0151 a0001c0001t0001g0163 others(18): Show |
22 | HG00280.hp2 HG00735.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-11438_340-1143 others(6): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35065696 | ||||||
| chr14:35065696 | A | ATTT | 32 | a0001c0001t0001g0030 a0001c0001t0006g0236 a0001c0002t0005g0009 others(29): Show |
38 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.340-11439_340-1143 others(7): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35065696 | ||||||
| chr14:35065696 | A | ATTTT | 6 | a0001c0002t0005g0027 a0001c0002t0005g0039 a0001c0002t0005g0082 others(3): Show |
6 | HG01099.hp1 HG02055.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-11440_340-1143 others(8): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35065696 | ||||||
| chr14:35065770 | C | T | 2 | a0001c0002t0005g0009 a0001c0002t0005g0027 |
4 | HG02055.hp2 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-11380C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35065770 | |||||||
| chr14:35065816 | C | T | 1 | a0001c0001t0012g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-11334C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35065816 | |||||||
| chr14:35065954 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.340-11196G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35065954 | |||||||
| chr14:35065995 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(75): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.340-11155C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35065995 | |||||||
| chr14:35066009 | A | G | 1 | a0001c0001t0012g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.340-11141A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066009 | |||||||
| chr14:35066088 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.340-11062A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066088 | |||||||
| chr14:35066406 | C | CT | 37 | a0001c0001t0001g0030 a0001c0001t0003g0090 a0001c0002t0005g0009 others(34): Show |
43 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.340-10727dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35066406 | ||||||
| chr14:35066406 | CT | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0128 a0001c0001t0001g0143 others(9): Show |
13 | HG00597.hp1 HG01081.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.340-10727delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35066406 | ||||||
| chr14:35066467 | G | A | 49 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(46): Show |
72 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.340-10683G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066467 | |||||||
| chr14:35066507 | C | G | 30 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(27): Show |
35 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.340-10643C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066507 | |||||||
| chr14:35066553 | C | T | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340-10597C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066553 | |||||||
| chr14:35066639 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.340-10511A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066639 | |||||||
| chr14:35066652 | G | A | 30 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(27): Show |
35 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.340-10498G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066652 | |||||||
| chr14:35066779 | A | T | 30 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(27): Show |
35 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.340-10371A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066779 | |||||||
| chr14:35066791 | T | A | 1 | a0001c0001t0010g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.340-10359T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066791 | |||||||
| chr14:35066803 | C | CT | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.340-10337dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35066803 | ||||||
| chr14:35066846 | C | T | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.340-10304C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066846 | |||||||
| chr14:35066875 | C | T | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340-10275C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35066875 | |||||||
| chr14:35067110 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.340-10040A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067110 | |||||||
| chr14:35067232 | C | CT | 7 | a0001c0001t0008g0187 a0001c0001t0008g0190 a0001c0001t0008g0191 others(4): Show |
7 | HG02723.hp2 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.340-9917dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35067232 | ||||||
| chr14:35067300 | T | C | 1 | a0001c0001t0008g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.340-9850T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067300 | |||||||
| chr14:35067324 | C | T | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0146 others(1): Show |
4 | NA18941.hp1 NA18962.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-9826C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067324 | |||||||
| chr14:35067597 | A | T | 1 | a0001c0001t0010g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.340-9553A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067597 | |||||||
| chr14:35067637 | T | A | 1 | a0001c0002t0019g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.340-9513T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067637 | |||||||
| chr14:35067671 | A | G | 37 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(34): Show |
43 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.340-9479A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067671 | |||||||
| chr14:35067672 | C | A | 49 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(46): Show |
72 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.340-9478C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067672 | |||||||
| chr14:35067700 | T | C | 1 | a0001c0001t0003g0065 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.340-9450T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067700 | |||||||
| chr14:35067714 | T | C | 1 | a0001c0001t0007g0225 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.340-9436T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067714 | |||||||
| chr14:35067771 | A | G | 3 | a0001c0001t0003g0077 a0001c0001t0012g0180 a0001c0001t0012g0181 |
3 | HG01496.hp2 HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.340-9379A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067771 | |||||||
| chr14:35067909 | A | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(75): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.340-9241A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35067909 | |||||||
| chr14:35068342 | A | G | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-8808A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068342 | |||||||
| chr14:35068489 | C | T | 2 | a0001c0001t0003g0037 a0001c0001t0003g0095 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.340-8661C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068489 | |||||||
| chr14:35068595 | T | G | 3 | a0001c0001t0006g0024 a0001c0001t0006g0189 a0001c0001t0006g0231 |
4 | HG00735.hp1 HG01255.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-8555T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068595 | |||||||
| chr14:35068737 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.340-8413C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068737 | |||||||
| chr14:35068778 | C | T | 30 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(27): Show |
35 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.340-8372C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068778 | |||||||
| chr14:35068792 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.340-8358G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068792 | |||||||
| chr14:35068799 | C | T | 1 | a0001c0001t0006g0231 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.340-8351C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068799 | |||||||
| chr14:35068872 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340-8278G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068872 | |||||||
| chr14:35068873 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340-8277A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068873 | |||||||
| chr14:35068929 | C | T | 6 | a0001c0001t0004g0013 a0001c0001t0004g0200 a0001c0001t0004g0211 others(3): Show |
8 | HG01109.hp1 HG01175.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-8221C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35068929 | |||||||
| chr14:35069048 | C | T | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.340-8102C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069048 | |||||||
| chr14:35069070 | T | G | 1 | a0001c0001t0011g0247 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.340-8080T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069070 | |||||||
| chr14:35069134 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.340-8016C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069134 | |||||||
| chr14:35069153 | C | T | 1 | a0001c0001t0014g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.340-7997C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069153 | |||||||
| chr14:35069174 | A | T | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.340-7976A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069174 | |||||||
| chr14:35069175 | T | A | 1 | a0001c0001t0003g0047 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.340-7975T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069175 | |||||||
| chr14:35069285 | G | GT | 88 | a0001c0001t0001g0113 a0001c0001t0001g0134 a0001c0001t0001g0142 others(85): Show |
115 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.340-7848dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35069285 | ||||||
| chr14:35069285 | G | GTT | 7 | a0001c0001t0002g0257 a0001c0001t0002g0260 a0001c0001t0002g0272 others(4): Show |
7 | HG01433.hp2 HG04115.hp1 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-7849_340-7848d others(4): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35069285 | ||||||
| chr14:35069289 | T | G | 3 | a0001c0001t0010g0198 a0001c0001t0010g0239 a0001c0001t0010g0240 |
3 | HG02257.hp2 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.340-7861T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069289 | |||||||
| chr14:35069431 | A | G | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-7719A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069431 | |||||||
| chr14:35069488 | T | G | 1 | a0001c0002t0005g0083 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.340-7662T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069488 | |||||||
| chr14:35069575 | G | A | 3 | a0001c0001t0004g0188 a0001c0001t0004g0195 a0001c0001t0004g0201 |
3 | HG02074.hp2 HG03831.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.340-7575G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069575 | |||||||
| chr14:35069587 | A | G | 11 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(8): Show |
12 | HG00735.hp1 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-7563A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069587 | |||||||
| chr14:35069588 | T | C | 9 | a0001c0001t0007g0115 a0001c0001t0007g0117 a0001c0001t0007g0118 others(6): Show |
9 | HG00408.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-7562T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069588 | |||||||
| chr14:35069686 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.340-7464A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069686 | |||||||
| chr14:35069808 | C | T | 1 | a0001c0002t0005g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.340-7342C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069808 | |||||||
| chr14:35069844 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.340-7306G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069844 | |||||||
| chr14:35069848 | T | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(72): Show |
110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.340-7302T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069848 | |||||||
| chr14:35069883 | C | T | 6 | a0001c0001t0001g0119 a0001c0001t0001g0133 a0001c0001t0001g0141 others(3): Show |
6 | HG02135.hp2 NA18943.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-7267C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069883 | |||||||
| chr14:35069916 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.340-7234G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069916 | |||||||
| chr14:35069925 | T | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(72): Show |
110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.340-7225T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069925 | |||||||
| chr14:35069939 | A | G | 4 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0001t0004g0210 others(1): Show |
4 | HG00140.hp1 HG01123.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-7211A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069939 | |||||||
| chr14:35069989 | G | C | 29 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(26): Show |
34 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.340-7161G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35069989 | |||||||
| chr14:35070029 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.340-7121T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070029 | |||||||
| chr14:35070032 | T | C | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340-7118T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070032 | |||||||
| chr14:35070093 | C | T | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-7057C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070093 | |||||||
| chr14:35070114 | C | CA | 31 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0040 others(28): Show |
38 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.340-7000dupA | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | C | CAA | 7 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0047 others(4): Show |
7 | HG00438.hp2 HG02109.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.340-7001_340-7000d others(4): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0006g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.340-7010_340-7000d others(13): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CA | C | 8 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0065 others(5): Show |
8 | HG01346.hp2 HG02083.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-7000delA | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAA | C | 11 | a0001c0001t0004g0013 a0001c0001t0004g0188 a0001c0001t0004g0195 others(8): Show |
13 | HG01243.hp1 HG01255.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.340-7002_340-7000d others(5): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAA | C | 12 | a0001c0001t0004g0012 a0001c0001t0004g0200 a0001c0001t0004g0202 others(9): Show |
14 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.340-7003_340-7000d others(6): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAA | C | 11 | a0001c0001t0004g0201 a0001c0001t0004g0204 a0001c0001t0004g0205 others(8): Show |
11 | HG01106.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-7004_340-7000d others(7): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAA | C | 12 | a0001c0001t0008g0187 a0001c0001t0008g0196 a0001c0001t0008g0197 others(9): Show |
12 | HG00741.hp2 HG01109.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.340-7005_340-7000d others(8): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA | C | 19 | a0001c0002t0005g0019 a0001c0002t0005g0027 a0001c0002t0005g0071 others(16): Show |
21 | HG00099.hp1 HG00639.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.340-7006_340-7000d others(9): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA others(1): Show |
C | 10 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(7): Show |
14 | HG01099.hp1 HG02559.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.340-7007_340-7000d others(10): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0004g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.340-7009_340-7000d others(12): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0004g0207 a0001c0001t0004g0233 |
2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.340-7010_340-7000d others(13): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0002g0260 a0001c0001t0002g0264 a0001c0001t0002g0267 others(2): Show |
5 | HG04199.hp2 NA18965.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-7014_340-7000d others(17): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA others(9): Show |
C | 44 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(41): Show |
67 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.340-7015_340-7000d others(18): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0157 a0001c0001t0002g0266 |
2 | HG01081.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.340-7016_340-7000d others(19): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA others(11): Show |
C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(69): Show |
107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.340-7017_340-7000d others(20): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01975.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.340-7018_340-7000d others(21): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070114 | CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.340-7024_340-7000d others(27): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070114 | ||||||
| chr14:35070182 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340-6968A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070182 | |||||||
| chr14:35070193 | C | G | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-6957C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070193 | |||||||
| chr14:35070212 | G | T | 49 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(46): Show |
72 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.340-6938G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070212 | |||||||
| chr14:35070216 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.340-6934C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070216 | |||||||
| chr14:35070237 | G | A | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340-6913G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070237 | |||||||
| chr14:35070239 | T | C | 5 | a0001c0001t0006g0183 a0001c0001t0006g0184 a0001c0001t0006g0185 others(2): Show |
5 | HG01081.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-6911T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070239 | |||||||
| chr14:35070307 | A | G | 1 | a0001c0001t0014g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.340-6843A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070307 | |||||||
| chr14:35070353 | G | A | 1 | a0001c0001t0002g0279 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.340-6797G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070353 | |||||||
| chr14:35070667 | C | A | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.340-6483C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070667 | |||||||
| chr14:35070676 | A | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(111): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.340-6474A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070676 | |||||||
| chr14:35070943 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.340-6207G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35070943 | |||||||
| chr14:35070983 | T | TTTTC | 36 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(33): Show |
42 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.340-6147_340-6144d others(6): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35070983 | ||||||
| chr14:35071019 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(87): Show |
125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.340-6131C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071019 | |||||||
| chr14:35071037 | C | T | 11 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(8): Show |
12 | HG00735.hp1 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-6113C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071037 | |||||||
| chr14:35071198 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.340-5952C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071198 | |||||||
| chr14:35071202 | T | C | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.340-5948T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071202 | |||||||
| chr14:35071205 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.340-5945G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071205 | |||||||
| chr14:35071293 | G | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(73): Show |
111 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.340-5857G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071293 | |||||||
| chr14:35071296 | C | T | 1 | a0001c0002t0005g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.340-5854C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071296 | |||||||
| chr14:35071380 | T | G | 1 | a0001c0001t0003g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.340-5770T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071380 | |||||||
| chr14:35071383 | G | A | 3 | a0001c0001t0010g0198 a0001c0001t0010g0239 a0001c0001t0010g0240 |
3 | HG02257.hp2 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.340-5767G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071383 | |||||||
| chr14:35071498 | A | G | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.340-5652A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071498 | |||||||
| chr14:35071558 | G | T | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-5592G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071558 | |||||||
| chr14:35071591 | C | CT | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(73): Show |
111 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.340-5558dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35071591 | ||||||
| chr14:35071721 | G | A | 1 | a0001c0001t0002g0269 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.340-5429G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071721 | |||||||
| chr14:35071857 | C | T | 30 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(27): Show |
35 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.340-5293C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071857 | |||||||
| chr14:35071935 | T | G | 1 | a0001c0002t0005g0016 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.340-5215T>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071935 | |||||||
| chr14:35071964 | C | T | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340-5186C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35071964 | |||||||
| chr14:35072088 | A | C | 1 | a0001c0001t0003g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.340-5062A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072088 | |||||||
| chr14:35072131 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.340-5019C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072131 | |||||||
| chr14:35072146 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(72): Show |
110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.340-5004G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072146 | |||||||
| chr14:35072199 | T | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(230): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.340-4951T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072199 | |||||||
| chr14:35072296 | A | G | 37 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(34): Show |
43 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.340-4854A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072296 | |||||||
| chr14:35072313 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0176 |
2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.340-4837T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072313 | |||||||
| chr14:35072314 | A | G | 1 | a0001c0001t0006g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.340-4836A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072314 | |||||||
| chr14:35072361 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.340-4789C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072361 | |||||||
| chr14:35072605 | G | C | 1 | a0001c0001t0004g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.340-4545G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072605 | |||||||
| chr14:35072785 | T | C | 1 | a0001c0001t0003g0047 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.340-4365T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072785 | |||||||
| chr14:35072836 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340-4314C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072836 | |||||||
| chr14:35072850 | C | A | 1 | a0001c0001t0008g0199 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.340-4300C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072850 | |||||||
| chr14:35072940 | G | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(111): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.340-4210G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072940 | |||||||
| chr14:35072970 | G | A | 1 | a0001c0001t0004g0217 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.340-4180G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35072970 | |||||||
| chr14:35073057 | G | C | 1 | a0001c0001t0003g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.340-4093G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073057 | |||||||
| chr14:35073062 | C | CTCT | 38 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(35): Show |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.340-4068_340-4066d others(5): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 35073062 | ||||||
| chr14:35073077 | T | A | 1 | a0001c0001t0014g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.340-4073T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073077 | |||||||
| chr14:35073131 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.340-4019C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073131 | |||||||
| chr14:35073218 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.340-3932C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073218 | |||||||
| chr14:35073279 | A | C | 4 | a0001c0001t0002g0250 a0001c0001t0002g0271 a0001c0001t0002g0280 others(1): Show |
4 | HG02723.hp1 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-3871A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073279 | |||||||
| chr14:35073287 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(72): Show |
110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.340-3863C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073287 | |||||||
| chr14:35073295 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.340-3855C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073295 | |||||||
| chr14:35073317 | G | A | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340-3833G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073317 | |||||||
| chr14:35073318 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
4 | HG01884.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-3832C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073318 | |||||||
| chr14:35073497 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.340-3653T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073497 | |||||||
| chr14:35073504 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.340-3646C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073504 | |||||||
| chr14:35073521 | G | C | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340-3629G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073521 | |||||||
| chr14:35073553 | A | G | 37 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(34): Show |
43 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.340-3597A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073553 | |||||||
| chr14:35073817 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.340-3333T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073817 | |||||||
| chr14:35073819 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.340-3331C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35073819 | |||||||
| chr14:35074290 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.340-2860G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35074290 | |||||||
| chr14:35074394 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(12): Show |
27 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.340-2756C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35074394 | |||||||
| chr14:35074411 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340-2739C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35074411 | |||||||
| chr14:35074496 | T | C | 11 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(8): Show |
12 | HG00735.hp1 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-2654T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35074496 | |||||||
| chr14:35074684 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340-2466A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35074684 | |||||||
| chr14:35074885 | AC | A | 3 | a0001c0001t0003g0052 a0001c0001t0003g0056 a0001c0001t0003g0065 |
3 | HG02083.hp2 NA18961.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.340-2264delC | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35074885 | |||||||
| chr14:35074928 | T | C | 2 | a0001c0001t0002g0251 a0001c0001t0002g0261 |
2 | NA18950.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.340-2222T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35074928 | |||||||
| chr14:35075094 | G | A | 38 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(35): Show |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.340-2056G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075094 | |||||||
| chr14:35075095 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.340-2055T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075095 | |||||||
| chr14:35075112 | C | T | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.340-2038C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075112 | |||||||
| chr14:35075124 | A | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(71): Show |
109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.340-2026A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075124 | |||||||
| chr14:35075244 | A | G | 1 | a0001c0002t0019g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.340-1906A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075244 | |||||||
| chr14:35075305 | G | A | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.340-1845G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075305 | |||||||
| chr14:35075596 | A | T | 30 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(27): Show |
35 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.340-1554A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075596 | |||||||
| chr14:35075797 | A | G | 1 | a0001c0001t0003g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.340-1353A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075797 | |||||||
| chr14:35075813 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.340-1337A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075813 | |||||||
| chr14:35075838 | C | T | 36 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(33): Show |
42 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.340-1312C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075838 | |||||||
| chr14:35075954 | C | G | 38 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(35): Show |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.340-1196C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35075954 | |||||||
| chr14:35076073 | T | C | 1 | a0001c0001t0002g0025 | 2 | HG01106.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.340-1077T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35076073 | |||||||
| chr14:35076600 | A | T | 11 | a0001c0001t0007g0115 a0001c0001t0007g0117 a0001c0001t0007g0118 others(8): Show |
11 | HG00408.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-550A>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35076600 | |||||||
| chr14:35076624 | G | A | 1 | a0001c0001t0007g0230 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.340-526G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35076624 | |||||||
| chr14:35076732 | A | G | 30 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0188 others(27): Show |
34 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.340-418A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | chr14 | 35076732 | |||||||
| chr14:35077246 | A | G | 30 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(27): Show |
35 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.406+30A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077246 | |||||||
| chr14:35077292 | T | A | 36 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(33): Show |
42 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.406+76T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077292 | |||||||
| chr14:35077322 | T | C | 1 | a0001c0001t0002g0273 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.406+106T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077322 | |||||||
| chr14:35077468 | C | CT | 24 | a0001c0001t0002g0026 a0001c0001t0002g0253 a0001c0001t0002g0280 others(21): Show |
25 | HG01169.hp1 HG01175.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.406+277dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 35077468 | ||||||
| chr14:35077468 | CT | C | 27 | a0001c0001t0002g0252 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
31 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.406+277delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 35077468 | ||||||
| chr14:35077468 | CTTTTT | C | 33 | a0001c0001t0001g0116 a0001c0001t0001g0123 a0001c0002t0005g0009 others(30): Show |
39 | HG00099.hp1 HG00639.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.406+273_406+277del others(5): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 35077468 | ||||||
| chr14:35077468 | CTTTTTT | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(71): Show |
109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.406+272_406+277del others(6): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 35077468 | ||||||
| chr14:35077499 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.406+283G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077499 | |||||||
| chr14:35077506 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.406+290C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077506 | |||||||
| chr14:35077544 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(111): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.406+328A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077544 | |||||||
| chr14:35077551 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(232): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.406+335T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077551 | |||||||
| chr14:35077552 | G | A | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.406+336G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077552 | |||||||
| chr14:35077591 | G | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(111): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.406+375G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077591 | |||||||
| chr14:35077607 | C | T | 1 | a0001c0002t0005g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.406+391C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077607 | |||||||
| chr14:35077640 | G | A | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.406+424G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077640 | |||||||
| chr14:35077696 | A | G | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.406+480A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077696 | |||||||
| chr14:35077699 | G | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(50): Show |
74 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.406+483G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077699 | |||||||
| chr14:35077704 | G | T | 1 | a0001c0001t0003g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.406+488G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077704 | |||||||
| chr14:35077712 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.406+496G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077712 | |||||||
| chr14:35077734 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0155 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.406+518G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077734 | |||||||
| chr14:35077857 | A | G | 3 | a0001c0001t0012g0180 a0001c0001t0012g0181 a0001c0002t0016g0182 |
3 | HG01496.hp2 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.406+641A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35077857 | |||||||
| chr14:35078228 | G | T | 45 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0025 others(42): Show |
66 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.407-699G>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35078228 | |||||||
| chr14:35078555 | T | C | 6 | a0001c0002t0009g0017 a0001c0002t0009g0031 a0001c0002t0009g0032 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.407-372T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35078555 | |||||||
| chr14:35078621 | G | C | 5 | a0001c0001t0001g0110 a0001c0001t0001g0126 a0001c0001t0001g0128 others(2): Show |
5 | NA18968.hp2 NA18992.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-306G>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35078621 | |||||||
| chr14:35078691 | C | T | 38 | a0001c0002t0005g0009 a0001c0002t0005g0016 a0001c0002t0005g0018 others(35): Show |
44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.407-236C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35078691 | |||||||
| chr14:35078752 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.407-175C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 3/4 | chr14 | 35078752 | |||||||
| chr14:35079068 | A | C | 1 | a0001c0001t0003g0063 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.504+44A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35079068 | |||||||
| chr14:35079174 | A | G | 1 | a0001c0001t0003g0066 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.504+150A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35079174 | |||||||
| chr14:35079306 | C | T | 3 | a0001c0001t0003g0077 a0001c0001t0012g0180 a0001c0001t0012g0181 |
3 | HG01496.hp2 HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.504+282C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35079306 | |||||||
| chr14:35079548 | A | C | 1 | a0001c0001t0003g0054 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.504+524A>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35079548 | |||||||
| chr14:35079586 | C | T | 1 | a0001c0002t0013g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.504+562C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35079586 | |||||||
| chr14:35079693 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.504+669A>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35079693 | |||||||
| chr14:35079836 | T | C | 1 | a0001c0001t0004g0222 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.504+812T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35079836 | |||||||
| chr14:35079867 | T | C | 2 | a0001c0001t0004g0208 a0001c0001t0004g0210 |
2 | HG00140.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.504+843T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35079867 | |||||||
| chr14:35080053 | G | GTCTC | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(229): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.505-967_505-964dup others(4): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 35080053 | ||||||
| chr14:35080072 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.505-950C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35080072 | |||||||
| chr14:35080231 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.505-791T>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35080231 | |||||||
| chr14:35080355 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.505-667C>T | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35080355 | |||||||
| chr14:35080445 | C | A | 1 | a0001c0001t0014g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505-577C>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35080445 | |||||||
| chr14:35080567 | G | A | 26 | a0001c0001t0006g0024 a0001c0001t0006g0183 a0001c0001t0006g0184 others(23): Show |
27 | HG00735.hp1 HG01081.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.505-455G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35080567 | |||||||
| chr14:35080912 | C | CT | 14 | a0001c0001t0001g0134 a0001c0001t0001g0147 a0001c0001t0003g0049 others(11): Show |
14 | HG00408.hp1 HG00438.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.505-90dupT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 35080912 | ||||||
| chr14:35080912 | CT | C | 10 | a0001c0001t0001g0124 a0001c0001t0001g0140 a0001c0001t0001g0156 others(7): Show |
10 | HG01257.hp2 HG02280.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.505-90delT | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 35080912 | ||||||
| chr14:35080914 | T | TC | 4 | a0001c0001t0002g0014 a0001c0001t0002g0248 a0001c0001t0011g0246 others(1): Show |
6 | HG00738.hp1 HG01496.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-108_505-107ins others(1): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35080914 | |||||||
| chr14:35080915 | T | C | 43 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0025 others(40): Show |
64 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.505-107T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35080915 | |||||||
| chr14:35080916 | T | C | 2 | a0001c0001t0002g0245 a0001c0001t0002g0270 |
2 | HG01257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.505-106T>C | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35080916 | |||||||
| chr14:35080998 | C | G | 1 | a0001c0001t0007g0226 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.505-24C>G | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35080998 | |||||||
| chr14:35081001 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.505-21G>A | FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 4/4 | chr14 | 35081001 |