Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55109 |
| ensemblid | ENSG00000164252.13 |
| hgncid | 24684 |
| symbol | AGGF1 |
| name | angiogenic factor with G-patch and FHA domains 1 |
| refseq_nuc | NM_018046.5 |
| refseq_prot | NP_060516.2 |
| ensembl_nuc | ENST00000312916.12 |
| ensembl_prot | ENSP00000316109.7 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 77030404 |
| end | 77065234 |
| strand | + |
| ver | v1.2 |
| region | chr5:77030404-77065234 |
| region5000 | chr5:77025404-77070234 |
| regionname0 | AGGF1_chr5_77030404_77065234 |
| regionname5000 | AGGF1_chr5_77025404_77070234 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 714 | 335 | 81 | 56 | 150 | 10 | 36 | 113 | AGGF1_chr5_77025404_77070234 | AGGF1 | MASEA others(709): Show |
chr5 | 77025404 | 77070234 |
| a0002 | 0/0 | 714 | 96 | 7 | 25 | 51 | 6 | 7 | 43 | AGGF1_chr5_77025404_77070234 | AGGF1 | MASEA others(709): Show |
chr5 | 77025404 | 77070234 |
| a0003 | 0/0 | 714 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | MASEA others(709): Show |
chr5 | 77025404 | 77070234 |
| a0004 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | MASEA others(709): Show |
chr5 | 77025404 | 77070234 |
| a0005 | 0/0 | 718 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | MASEA others(713): Show |
chr5 | 77025404 | 77070234 |
| a0006 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | MASEA others(709): Show |
chr5 | 77025404 | 77070234 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2142 | 233 | 48 | 35 | 120 | 7 | 21 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2137): Show |
chr5 | 77025404 | 77070234 | ||
| a0001c0002 | 0/0 | 2142 | 95 | 29 | 20 | 30 | 3 | 13 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2137): Show |
chr5 | 77025404 | 77070234 | ||
| a0001c0004 | 0/0 | 2142 | 6 | 4 | 0 | 0 | 0 | 2 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2137): Show |
chr5 | 77025404 | 77070234 | ||
| a0001c0007 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2137): Show |
chr5 | 77025404 | 77070234 | ||
| a0002c0003 | 0/0 | 2142 | 95 | 7 | 25 | 50 | 6 | 7 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2137): Show |
chr5 | 77025404 | 77070234 | ||
| a0002c0008 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2137): Show |
chr5 | 77025404 | 77070234 | ||
| a0003c0005 | 0/0 | 2142 | 4 | 3 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2137): Show |
chr5 | 77025404 | 77070234 | ||
| a0004c0010 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2137): Show |
chr5 | 77025404 | 77070234 | ||
| a0005c0006 | 0/0 | 2154 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2149): Show |
chr5 | 77025404 | 77070234 | ||
| a0006c0009 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | ATGGC others(2137): Show |
chr5 | 77025404 | 77070234 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4490 | 166 | 28 | 17 | 100 | 4 | 16 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0004 | 0/1 | 4490 | 36 | 3 | 16 | 8 | 3 | 5 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0008 | 0/0 | 4490 | 6 | 6 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0009 | 0/0 | 4490 | 4 | 3 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0010 | 0/0 | 4490 | 4 | 0 | 0 | 4 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0012 | 0/0 | 4490 | 4 | 3 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0013 | 0/0 | 4490 | 4 | 0 | 0 | 4 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0017 | 0/0 | 4491 | 2 | 2 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4486): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0018 | 0/0 | 4490 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0021 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0022 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0023 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0024 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0001t0026 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0002t0001 | 0/0 | 4490 | 6 | 6 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0002t0003 | 0/0 | 4491 | 71 | 21 | 15 | 21 | 3 | 11 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4486): Show |
chr5 | 77025404 | 77070234 |
| a0001c0002t0005 | 0/0 | 4491 | 10 | 0 | 2 | 8 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4486): Show |
chr5 | 77025404 | 77070234 |
| a0001c0002t0006 | 0/0 | 4491 | 7 | 2 | 3 | 0 | 0 | 2 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4486): Show |
chr5 | 77025404 | 77070234 |
| a0001c0002t0020 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4486): Show |
chr5 | 77025404 | 77070234 |
| a0001c0004t0007 | 0/0 | 4490 | 6 | 4 | 0 | 0 | 0 | 2 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0001c0007t0004 | 0/0 | 4490 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0002c0003t0002 | 0/0 | 4490 | 85 | 5 | 22 | 47 | 5 | 6 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0002c0003t0014 | 0/0 | 4489 | 3 | 1 | 2 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4484): Show |
chr5 | 77025404 | 77070234 |
| a0002c0003t0015 | 0/0 | 4490 | 3 | 0 | 1 | 0 | 1 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0002c0003t0016 | 0/0 | 4490 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0002c0003t0019 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4486): Show |
chr5 | 77025404 | 77070234 |
| a0002c0003t0025 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0002c0008t0002 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0003c0005t0011 | 0/0 | 4490 | 4 | 3 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0004c0010t0001 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| a0005c0006t0004 | 0/0 | 4502 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4497): Show |
chr5 | 77025404 | 77070234 |
| a0006c0009t0001 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | GCCGT others(4485): Show |
chr5 | 77025404 | 77070234 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0008g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0008g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0009g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0010g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0010g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0010g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0012g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0012g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0013g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0013g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0013g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0013g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0017g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0017g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0018g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0018g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0021g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0022g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0023g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0024g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0001t0026g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0005g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0006g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0006g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0006g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0006g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0002t0020g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0004t0007g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0004t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0004t0007g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0004t0007g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0004t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0001c0007t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0001 | 0/0 | 14 | 2 | 1 | 7 | 0 | 4 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0010 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0017 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0014g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0014g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0015g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0015g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0016g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0019g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0003t0025g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0002c0008t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0003c0005t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0003c0005t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0003c0005t0011g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0003c0005t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0004c0010t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0005c0006t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| a0006c0009t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0002 | g0017 | EUR | GBR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | GBR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00140 | hp1 | a0002 | c0003 | t0015 | g0007 | EUR | GBR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0022 | EUR | GBR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00280 | hp1 | a0002 | c0003 | t0002 | g0010 | EUR | FIN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0321 | EUR | FIN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0285 | EUR | FIN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0094 | EUR | FIN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00423 | hp2 | a0001 | c0001 | t0023 | g0012 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00438 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00558 | hp2 | a0002 | c0003 | t0002 | g0017 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0295 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00639 | hp1 | a0002 | c0003 | t0002 | g0010 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0354 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00673 | hp2 | a0001 | c0002 | t0005 | g0282 | EAS | CHS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0115 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00733 | hp2 | a0002 | c0003 | t0002 | g0079 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0229 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00741 | hp1 | a0002 | c0003 | t0002 | g0009 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0039 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0039 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0284 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01074 | hp2 | a0002 | c0003 | t0002 | g0017 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01081 | hp2 | a0002 | c0003 | t0002 | g0055 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01099 | hp2 | a0001 | c0002 | t0006 | g0331 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0190 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01109 | hp2 | a0001 | c0007 | t0004 | g0004 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01167 | hp1 | a0003 | c0005 | t0011 | g0181 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01167 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01168 | hp1 | a0002 | c0003 | t0002 | g0001 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0264 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0185 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01255 | hp1 | a0002 | c0003 | t0014 | g0006 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0037 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01256 | hp2 | a0001 | c0002 | t0006 | g0332 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01257 | hp1 | a0002 | c0003 | t0002 | g0061 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0036 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01258 | hp1 | a0001 | c0002 | t0006 | g0042 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01258 | hp2 | a0002 | c0003 | t0002 | g0066 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01261 | hp2 | a0002 | c0003 | t0002 | g0075 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01346 | hp2 | a0002 | c0003 | t0015 | g0072 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01358 | hp2 | a0002 | c0003 | t0014 | g0046 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0009 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01496 | hp1 | a0002 | c0003 | t0002 | g0063 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01496 | hp2 | a0001 | c0001 | t0012 | g0119 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0301 | EUR | IBS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01515 | hp2 | a0002 | c0003 | t0002 | g0086 | EUR | IBS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0290 | EUR | IBS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01517 | hp2 | a0002 | c0003 | t0002 | g0007 | EUR | IBS | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01928 | hp1 | a0002 | c0003 | t0002 | g0064 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0283 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0281 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01934 | hp2 | a0002 | c0003 | t0002 | g0065 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01952 | hp1 | a0002 | c0003 | t0002 | g0050 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01975 | hp1 | a0001 | c0002 | t0005 | g0225 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01975 | hp2 | a0002 | c0003 | t0002 | g0060 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01978 | hp2 | a0002 | c0003 | t0002 | g0051 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01981 | hp1 | a0002 | c0003 | t0002 | g0049 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0270 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01993 | hp2 | a0002 | c0003 | t0002 | g0009 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02004 | hp1 | a0002 | c0003 | t0002 | g0308 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02004 | hp2 | a0002 | c0003 | t0002 | g0018 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02015 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02027 | hp1 | a0002 | c0003 | t0002 | g0056 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02055 | hp1 | a0001 | c0002 | t0003 | g0232 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0277 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02056 | hp2 | a0002 | c0003 | t0002 | g0084 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0262 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0261 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02074 | hp2 | a0004 | c0010 | t0001 | g0245 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0286 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0263 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02132 | hp1 | a0001 | c0002 | t0020 | g0276 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02135 | hp1 | a0001 | c0001 | t0013 | g0342 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02135 | hp2 | a0002 | c0003 | t0002 | g0082 | EAS | KHV | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0272 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0289 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0273 | EAS | CDX | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CDX | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0278 | EAS | CDX | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0120 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0267 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02273 | hp2 | a0002 | c0003 | t0002 | g0018 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0287 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02280 | hp2 | a0003 | c0005 | t0011 | g0183 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | PEL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0251 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0121 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0288 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0118 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02615 | hp2 | a0002 | c0003 | t0002 | g0074 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0024 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02630 | hp1 | a0002 | c0003 | t0002 | g0001 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0141 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0107 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0268 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02698 | hp1 | a0005 | c0006 | t0004 | g0113 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0271 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0142 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02717 | hp2 | a0001 | c0004 | t0007 | g0208 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02735 | hp1 | a0002 | c0003 | t0002 | g0001 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0016 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02738 | hp1 | a0001 | c0004 | t0007 | g0209 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0192 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02818 | hp1 | a0001 | c0004 | t0007 | g0211 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02886 | hp2 | a0001 | c0004 | t0007 | g0030 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0353 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02896 | hp1 | a0001 | c0002 | t0006 | g0227 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0233 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02897 | hp2 | a0001 | c0002 | t0006 | g0228 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0122 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02922 | hp2 | a0006 | c0009 | t0001 | g0218 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02976 | hp1 | a0001 | c0001 | t0026 | g0189 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02976 | hp2 | a0002 | c0003 | t0025 | g0073 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03017 | hp1 | a0001 | c0002 | t0006 | g0330 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0230 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0231 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0214 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0350 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03209 | hp1 | a0001 | c0001 | t0022 | g0204 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0216 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0352 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0106 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0182 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0133 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0212 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03486 | hp2 | a0001 | c0004 | t0007 | g0030 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0299 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0111 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0298 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0104 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03540 | hp1 | a0002 | c0003 | t0002 | g0006 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0024 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03669 | hp2 | a0002 | c0003 | t0002 | g0001 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03688 | hp2 | a0001 | c0004 | t0007 | g0210 | SAS | STU | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0037 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03710 | hp1 | a0001 | c0002 | t0006 | g0042 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0036 | SAS | PJL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0348 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03834 | hp2 | a0002 | c0003 | t0015 | g0007 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03927 | hp2 | a0002 | c0003 | t0002 | g0076 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0093 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG04115 | hp1 | a0002 | c0003 | t0002 | g0307 | SAS | STU | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0297 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG04199 | hp1 | a0002 | c0003 | t0002 | g0001 | SAS | STU | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0269 | SAS | STU | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG04204 | hp2 | a0002 | c0003 | t0002 | g0001 | SAS | STU | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0194 | AFR | YRI | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18522 | hp2 | a0001 | c0001 | t0024 | g0221 | AFR | YRI | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | CHB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18747 | hp1 | a0001 | c0001 | t0010 | g0165 | EAS | CHB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18747 | hp2 | a0002 | c0003 | t0002 | g0069 | EAS | CHB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0123 | AFR | YRI | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | YRI | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0274 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18940 | hp2 | a0001 | c0002 | t0003 | g0294 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0292 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18942 | hp1 | a0001 | c0002 | t0005 | g0300 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18943 | hp2 | a0001 | c0001 | t0013 | g0341 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0293 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18946 | hp1 | a0002 | c0003 | t0002 | g0068 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18949 | hp1 | a0001 | c0002 | t0003 | g0224 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18953 | hp1 | a0002 | c0003 | t0002 | g0081 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0349 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18959 | hp1 | a0001 | c0001 | t0010 | g0206 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18959 | hp2 | a0002 | c0008 | t0002 | g0305 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18960 | hp1 | a0002 | c0003 | t0002 | g0077 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18960 | hp2 | a0001 | c0002 | t0005 | g0038 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18963 | hp1 | a0001 | c0001 | t0010 | g0163 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18963 | hp2 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18965 | hp1 | a0002 | c0003 | t0002 | g0044 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18965 | hp2 | a0001 | c0002 | t0005 | g0275 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18966 | hp1 | a0002 | c0003 | t0002 | g0054 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18966 | hp2 | a0001 | c0002 | t0003 | g0279 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18967 | hp1 | a0002 | c0003 | t0002 | g0048 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18968 | hp2 | a0002 | c0003 | t0002 | g0085 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18969 | hp1 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18970 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18971 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18974 | hp2 | a0002 | c0003 | t0019 | g0008 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18975 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18975 | hp2 | a0001 | c0001 | t0013 | g0355 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18977 | hp2 | a0002 | c0003 | t0002 | g0083 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18978 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18979 | hp1 | a0001 | c0002 | t0005 | g0038 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18980 | hp1 | a0002 | c0003 | t0002 | g0078 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18981 | hp1 | a0002 | c0003 | t0002 | g0053 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18985 | hp2 | a0002 | c0003 | t0002 | g0052 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18986 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18987 | hp2 | a0001 | c0001 | t0018 | g0219 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18991 | hp1 | a0002 | c0003 | t0002 | g0304 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0265 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18992 | hp2 | a0002 | c0003 | t0016 | g0002 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18993 | hp2 | a0002 | c0003 | t0002 | g0019 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0005 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18997 | hp2 | a0001 | c0001 | t0018 | g0186 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0291 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19001 | hp1 | a0001 | c0002 | t0005 | g0302 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19004 | hp1 | a0002 | c0003 | t0002 | g0306 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19006 | hp2 | a0002 | c0003 | t0002 | g0020 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19007 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19007 | hp2 | a0001 | c0001 | t0021 | g0099 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19009 | hp1 | a0001 | c0002 | t0005 | g0090 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19009 | hp2 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19010 | hp1 | a0002 | c0003 | t0002 | g0058 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | LWK | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19030 | hp2 | a0003 | c0005 | t0011 | g0132 | AFR | LWK | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19043 | hp1 | a0002 | c0003 | t0002 | g0045 | AFR | LWK | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0215 | AFR | LWK | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0296 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19056 | hp1 | a0002 | c0003 | t0002 | g0020 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19058 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19060 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19062 | hp1 | a0001 | c0002 | t0005 | g0280 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19065 | hp2 | a0002 | c0003 | t0002 | g0057 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19068 | hp2 | a0002 | c0003 | t0002 | g0059 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19070 | hp2 | a0002 | c0003 | t0002 | g0080 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19072 | hp2 | a0002 | c0003 | t0002 | g0087 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19074 | hp1 | a0002 | c0003 | t0002 | g0006 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19076 | hp2 | a0002 | c0003 | t0016 | g0062 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19078 | hp1 | a0001 | c0001 | t0013 | g0315 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19078 | hp2 | a0001 | c0002 | t0003 | g0226 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19079 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19080 | hp2 | a0002 | c0003 | t0002 | g0047 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19081 | hp2 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19084 | hp1 | a0002 | c0003 | t0002 | g0019 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA20129 | hp1 | a0003 | c0005 | t0011 | g0180 | AFR | ASW | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ASW | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA20752 | hp2 | a0002 | c0003 | t0002 | g0010 | EUR | TSI | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0023 | EUR | TSI | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | TSI | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01123 | hp1 | a0002 | c0003 | t0002 | g0007 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | CLM | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02109 | hp1 | a0002 | c0003 | t0014 | g0006 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0351 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0193 | AFR | ACB | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0213 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | USA | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | USA | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18955 | hp1 | a0002 | c0003 | t0002 | g0070 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA18955 | hp2 | a0002 | c0003 | t0002 | g0089 | EAS | JPT | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA20300 | hp1 | a0001 | c0002 | t0003 | g0266 | AFR | USA | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | USA | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA21309 | hp1 | a0002 | c0003 | t0002 | g0001 | AFR | LWK | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0109 | REF | REF | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0252 | REF | REF | AGGF1_chr5_77025404_77070234 | AGGF1 | chr5 | 77025404 | 77070234 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:77030783 | C | CGTCCCCG others(5): Show |
1 | a0005 | 1 | HG02698.hp1 | disruptive_inframe_insertion | MODERATE | c.21_32dupCCCGCCGCGG others(2): Show |
p.Ser11_Pro12insProP others(8): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/14 | 396/4490 | 33/2145 | 11/714 | INFO_REALIGN_3_PRIME | chr5 | 77030783 | ||
| chr5:77035594 | G | A | 1 | a0006 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.367G>A | p.Glu123Lys | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/14 | 730/4490 | 367/2145 | 123/714 | chr5 | 77035594 | |||
| chr5:77035624 | G | A | 1 | a0004 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.397G>A | p.Glu133Lys | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/14 | 760/4490 | 397/2145 | 133/714 | chr5 | 77035624 | |||
| chr5:77063199 | C | A | 1 | a0002 | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
missense_variant | MODERATE | c.2092C>A | p.Pro698Thr | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 2455/4490 | 2092/2145 | 698/714 | chr5 | 77063199 | |||
| chr5:77063223 | A | T | 1 | a0003 | 4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
missense_variant | MODERATE | c.2116A>T | p.Met706Leu | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 2479/4490 | 2116/2145 | 706/714 | chr5 | 77063223 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:77030850 | G | A | 1 | a0001c0007 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.84G>A | p.Lys28Lys | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/14 | 447/4490 | 84/2145 | 28/714 | chr5 | 77030850 | |||
| chr5:77035557 | G | A | 1 | a0002c0008 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.330G>A | p.Thr110Thr | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/14 | 693/4490 | 330/2145 | 110/714 | chr5 | 77035557 | |||
| chr5:77048174 | T | C | 1 | a0001c0002 | 95 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(92): Show |
synonymous_variant | LOW | c.1215T>C | p.Ile405Ile | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/14 | 1578/4490 | 1215/2145 | 405/714 | chr5 | 77048174 | |||
| chr5:77054075 | T | C | 1 | a0001c0004 | 6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
synonymous_variant | LOW | c.1578T>C | p.Cys526Cys | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/14 | 1941/4490 | 1578/2145 | 526/714 | chr5 | 77054075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:77030439 | G | C | 1 | a0002c0003t0016 | 2 | NA18992.hp2 NA19076.hp2 |
5_prime_UTR_variant | MODIFIER | c.-328G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/14 | 328 | chr5 | 77030439 | ||||||
| chr5:77030473 | C | T | 1 | a0001c0001t0026 | 1 | HG02976.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-294C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/14 | chr5 | 77030473 | |||||||
| chr5:77030539 | G | T | 1 | a0002c0003t0025 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-228G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/14 | 228 | chr5 | 77030539 | ||||||
| chr5:77030719 | C | T | 2 | a0001c0001t0023 a0001c0001t0024 |
2 | HG00423.hp2 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-48C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/14 | 48 | chr5 | 77030719 | ||||||
| chr5:77063265 | G | GA | 6 | a0001c0001t0017 a0001c0002t0003 a0001c0002t0005 others(3): Show |
92 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*21dupA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 22 | INFO_REALIGN_3_PRIME | chr5 | 77063265 | |||||
| chr5:77063377 | A | C | 1 | a0001c0001t0022 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 125 | chr5 | 77063377 | ||||||
| chr5:77063519 | C | T | 5 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0024 others(2): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*267C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 267 | chr5 | 77063519 | ||||||
| chr5:77063638 | G | A | 2 | a0001c0001t0009 a0001c0001t0022 |
5 | HG01109.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*386G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 386 | chr5 | 77063638 | ||||||
| chr5:77063861 | C | T | 1 | a0001c0001t0021 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*609C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 609 | chr5 | 77063861 | ||||||
| chr5:77063871 | AT | A | 1 | a0002c0003t0014 | 3 | HG01255.hp1 HG01358.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*622delT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 622 | INFO_REALIGN_3_PRIME | chr5 | 77063871 | |||||
| chr5:77064089 | A | G | 1 | a0001c0002t0020 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*837A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 837 | chr5 | 77064089 | ||||||
| chr5:77064216 | A | G | 1 | a0001c0001t0018 | 2 | NA18987.hp2 NA18997.hp2 |
3_prime_UTR_variant | MODIFIER | c.*964A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 964 | chr5 | 77064216 | ||||||
| chr5:77064296 | G | C | 1 | a0001c0001t0010 | 4 | NA18747.hp1 NA18959.hp1 NA18963.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1044G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1044 | chr5 | 77064296 | ||||||
| chr5:77064297 | G | A | 7 | a0002c0003t0002 a0002c0003t0014 a0002c0003t0015 others(4): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1045G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1045 | chr5 | 77064297 | ||||||
| chr5:77064387 | C | T | 3 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0020 |
82 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1135C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1135 | chr5 | 77064387 | ||||||
| chr5:77064687 | C | T | 1 | a0001c0001t0013 | 4 | HG02135.hp1 NA18943.hp2 NA18975.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1435C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1435 | chr5 | 77064687 | ||||||
| chr5:77064835 | G | A | 1 | a0003c0005t0011 | 4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1583G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1583 | chr5 | 77064835 | ||||||
| chr5:77064880 | T | C | 1 | a0001c0004t0007 | 6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1628T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1628 | chr5 | 77064880 | ||||||
| chr5:77064953 | T | G | 2 | a0001c0001t0012 a0001c0004t0007 |
10 | HG01496.hp2 HG02615.hp1 HG02717.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1701T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1701 | chr5 | 77064953 | ||||||
| chr5:77064958 | G | A | 2 | a0001c0001t0008 a0001c0001t0017 |
8 | HG02486.hp2 HG02895.hp2 HG02970.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1706G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1706 | chr5 | 77064958 | ||||||
| chr5:77064991 | C | T | 1 | a0002c0003t0015 | 3 | HG00140.hp1 HG01346.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1739C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1739 | chr5 | 77064991 | ||||||
| chr5:77065080 | C | T | 1 | a0001c0002t0005 | 10 | HG00673.hp2 HG01928.hp2 HG01975.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1828C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 14/14 | 1828 | chr5 | 77065080 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:77031060 | G | A | 60 | a0001c0001t0001g0088 a0002c0003t0002g0001 a0002c0003t0002g0002 others(57): Show |
89 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.210+84G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031060 | |||||||
| chr5:77031250 | C | T | 2 | a0001c0001t0013g0355 a0001c0002t0003g0354 |
2 | HG00642.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.210+274C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031250 | |||||||
| chr5:77031277 | A | G | 4 | a0001c0001t0008g0351 a0001c0001t0008g0352 a0001c0001t0017g0350 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+301A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031277 | |||||||
| chr5:77031314 | A | C | 1 | a0001c0002t0003g0349 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.210+338A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031314 | |||||||
| chr5:77031398 | G | A | 1 | a0001c0002t0005g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.210+422G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031398 | |||||||
| chr5:77031487 | G | A | 31 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(28): Show |
37 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.210+511G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031487 | |||||||
| chr5:77031745 | A | G | 1 | a0001c0002t0003g0348 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.210+769A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031745 | |||||||
| chr5:77031961 | C | T | 1 | a0002c0003t0002g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.210+985C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031961 | |||||||
| chr5:77031972 | C | T | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.210+996C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031972 | |||||||
| chr5:77031993 | C | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0043 others(105): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.210+1017C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77031993 | |||||||
| chr5:77032135 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.210+1159A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032135 | |||||||
| chr5:77032249 | T | C | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.210+1273T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032249 | |||||||
| chr5:77032252 | T | TA | 50 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(47): Show |
56 | HG00438.hp1 HG00733.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.210+1298dupA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032252 | ||||||
| chr5:77032252 | T | TAA | 83 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.210+1297_210+1298d others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032252 | ||||||
| chr5:77032252 | T | TAAA | 21 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(18): Show |
22 | HG00323.hp2 HG01346.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.210+1296_210+1298d others(5): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032252 | ||||||
| chr5:77032252 | T | TAAAA | 11 | a0001c0001t0004g0091 a0001c0001t0012g0118 a0001c0001t0012g0119 others(8): Show |
15 | HG00438.hp2 HG01496.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.210+1295_210+1298d others(6): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032252 | ||||||
| chr5:77032252 | T | TAAAAA | 30 | a0002c0003t0002g0001 a0002c0003t0002g0007 a0002c0003t0002g0009 others(27): Show |
52 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.210+1294_210+1298d others(7): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032252 | ||||||
| chr5:77032252 | T | TAAAAAA | 20 | a0002c0003t0002g0006 a0002c0003t0002g0008 a0002c0003t0002g0017 others(17): Show |
25 | HG00099.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.210+1293_210+1298d others(8): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032252 | ||||||
| chr5:77032252 | T | TAAAAAAA | 6 | a0002c0003t0002g0044 a0002c0003t0002g0045 a0002c0003t0002g0047 others(3): Show |
6 | HG01358.hp2 NA18959.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+1292_210+1298d others(9): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032252 | ||||||
| chr5:77032252 | TA | T | 11 | a0001c0001t0001g0253 a0001c0001t0001g0258 a0001c0001t0001g0259 others(8): Show |
11 | HG00642.hp2 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.210+1298delA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032252 | ||||||
| chr5:77032252 | TAAAAAA | T | 51 | a0001c0002t0003g0016 a0001c0002t0003g0036 a0001c0002t0003g0037 others(48): Show |
58 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.210+1293_210+1298d others(8): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032252 | ||||||
| chr5:77032274 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0260 |
3 | HG00741.hp2 HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.210+1298A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032274 | |||||||
| chr5:77032344 | A | G | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.210+1368A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032344 | |||||||
| chr5:77032430 | G | A | 64 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(61): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.210+1454G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032430 | |||||||
| chr5:77032482 | T | G | 3 | a0001c0002t0003g0261 a0001c0002t0003g0262 a0001c0002t0003g0263 |
3 | HG02071.hp2 HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.210+1506T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032482 | |||||||
| chr5:77032510 | G | A | 1 | a0001c0002t0003g0264 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.210+1534G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032510 | |||||||
| chr5:77032563 | C | CA | 157 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(154): Show |
183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.210+1610dupA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032563 | ||||||
| chr5:77032563 | C | CAA | 14 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0187 others(11): Show |
15 | HG01071.hp2 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.210+1609_210+1610d others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032563 | ||||||
| chr5:77032563 | CA | C | 17 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(14): Show |
17 | HG01167.hp1 HG01256.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.210+1610delA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032563 | ||||||
| chr5:77032563 | CAAAAA | C | 61 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(58): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.210+1606_210+1610d others(7): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032563 | ||||||
| chr5:77032588 | G | T | 1 | a0001c0002t0005g0302 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.210+1612G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032588 | |||||||
| chr5:77032606 | TATAACAG others(10): Show |
T | 2 | a0001c0001t0009g0215 a0001c0001t0009g0216 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.210+1633_210+1649d others(19): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 77032606 | ||||||
| chr5:77032947 | C | T | 3 | a0001c0002t0003g0297 a0001c0002t0003g0298 a0001c0002t0003g0299 |
3 | HG03490.hp2 HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.211-1471C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032947 | |||||||
| chr5:77032957 | C | A | 1 | a0001c0001t0001g0319 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.211-1461C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77032957 | |||||||
| chr5:77033120 | A | G | 2 | a0001c0001t0009g0214 a0001c0001t0022g0204 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.211-1298A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77033120 | |||||||
| chr5:77033141 | C | G | 1 | a0001c0001t0004g0114 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.211-1277C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77033141 | |||||||
| chr5:77033325 | T | C | 11 | a0002c0003t0002g0009 a0002c0003t0002g0018 a0002c0003t0002g0049 others(8): Show |
14 | HG00741.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.211-1093T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77033325 | |||||||
| chr5:77033338 | TTG | T | 4 | a0002c0003t0002g0045 a0002c0003t0002g0055 a0002c0003t0002g0074 others(1): Show |
4 | HG00733.hp2 HG01081.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1079_211-1078d others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77033338 | |||||||
| chr5:77033558 | G | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.211-860G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77033558 | |||||||
| chr5:77033737 | G | A | 32 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(29): Show |
38 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.211-681G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77033737 | |||||||
| chr5:77033919 | C | T | 2 | a0002c0003t0002g0061 a0002c0003t0002g0066 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.211-499C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77033919 | |||||||
| chr5:77033925 | C | T | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.211-493C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77033925 | |||||||
| chr5:77034034 | C | T | 6 | a0001c0001t0001g0131 a0001c0001t0001g0140 a0001c0001t0001g0173 others(3): Show |
6 | HG03927.hp1 HG04199.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-384C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77034034 | |||||||
| chr5:77034382 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.211-36A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 1/13 | chr5 | 77034382 | |||||||
| chr5:77034526 | T | C | 7 | a0001c0001t0001g0253 a0001c0002t0001g0222 a0001c0002t0001g0223 others(4): Show |
7 | HG00642.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.313+6T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77034526 | |||||||
| chr5:77034531 | T | C | 8 | a0001c0002t0003g0016 a0001c0002t0003g0036 a0001c0002t0003g0267 others(5): Show |
11 | HG01167.hp2 HG01169.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.313+11T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77034531 | |||||||
| chr5:77034576 | G | A | 55 | a0001c0002t0003g0016 a0001c0002t0003g0036 a0001c0002t0003g0037 others(52): Show |
62 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.313+56G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77034576 | |||||||
| chr5:77034643 | G | A | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.313+123G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77034643 | |||||||
| chr5:77034771 | A | G | 1 | a0001c0001t0017g0353 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.313+251A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77034771 | |||||||
| chr5:77034948 | A | G | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313+428A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77034948 | |||||||
| chr5:77034985 | CAAG | C | 8 | a0001c0002t0003g0016 a0001c0002t0003g0036 a0001c0002t0003g0267 others(5): Show |
11 | HG01167.hp2 HG01169.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.313+471_313+473del others(3): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 77034985 | ||||||
| chr5:77035115 | G | A | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-426G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77035115 | |||||||
| chr5:77035156 | C | A | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.314-385C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77035156 | |||||||
| chr5:77035317 | C | T | 1 | a0003c0005t0011g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.314-224C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77035317 | |||||||
| chr5:77035369 | C | T | 1 | a0001c0001t0001g0015 | 3 | HG02630.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.314-172C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77035369 | |||||||
| chr5:77035442 | A | G | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.314-99A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 2/13 | chr5 | 77035442 | |||||||
| chr5:77035806 | A | T | 1 | a0001c0001t0017g0350 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.516+63A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/13 | chr5 | 77035806 | |||||||
| chr5:77036089 | C | T | 4 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+346C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/13 | chr5 | 77036089 | |||||||
| chr5:77036153 | A | G | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.517-403A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/13 | chr5 | 77036153 | |||||||
| chr5:77036211 | A | T | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-345A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/13 | chr5 | 77036211 | |||||||
| chr5:77036460 | G | A | 1 | a0001c0001t0004g0115 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.517-96G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/13 | chr5 | 77036460 | |||||||
| chr5:77036510 | T | TA | 9 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0191 others(6): Show |
10 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-45dupA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr5 | 77036510 | ||||||
| chr5:77036532 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0205 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.517-24T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 3/13 | chr5 | 77036532 | |||||||
| chr5:77036781 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.681+61C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77036781 | |||||||
| chr5:77036881 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.681+161G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77036881 | |||||||
| chr5:77036943 | C | T | 1 | a0001c0002t0003g0272 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.681+223C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77036943 | |||||||
| chr5:77037292 | G | A | 264 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(261): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.681+572G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77037292 | |||||||
| chr5:77037343 | A | G | 1 | a0001c0004t0007g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.681+623A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77037343 | |||||||
| chr5:77037376 | T | C | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.681+656T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77037376 | |||||||
| chr5:77037430 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
6 | HG00423.hp2 HG00558.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+710G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77037430 | |||||||
| chr5:77037467 | T | C | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.681+747T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77037467 | |||||||
| chr5:77037472 | A | G | 1 | a0002c0003t0002g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.681+752A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77037472 | |||||||
| chr5:77037532 | G | T | 75 | a0001c0002t0003g0016 a0001c0002t0003g0024 a0001c0002t0003g0032 others(72): Show |
84 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.681+812G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77037532 | |||||||
| chr5:77037941 | A | G | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.681+1221A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77037941 | |||||||
| chr5:77038064 | C | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0333 others(12): Show |
21 | HG01943.hp1 HG02135.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.681+1344C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77038064 | |||||||
| chr5:77038332 | CCTGT | C | 4 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 others(1): Show |
5 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-1196_682-1193d others(6): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr5 | 77038332 | ||||||
| chr5:77038387 | G | T | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-1144G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77038387 | |||||||
| chr5:77038575 | C | G | 1 | a0001c0001t0004g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.682-956C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77038575 | |||||||
| chr5:77038604 | G | GAAATCTA others(89): Show |
1 | a0002c0003t0002g0052 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.682-926_682-831dup others(96): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr5 | 77038604 | ||||||
| chr5:77038725 | C | A | 1 | a0001c0002t0003g0273 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.682-806C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77038725 | |||||||
| chr5:77038951 | C | T | 2 | a0001c0002t0003g0298 a0001c0002t0003g0299 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.682-580C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77038951 | |||||||
| chr5:77039033 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.682-498G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77039033 | |||||||
| chr5:77039040 | A | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0172 |
3 | NA18943.hp1 NA18968.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.682-491A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77039040 | |||||||
| chr5:77039146 | C | T | 1 | a0001c0002t0003g0233 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.682-385C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77039146 | |||||||
| chr5:77039349 | A | G | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.682-182A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77039349 | |||||||
| chr5:77039438 | G | T | 1 | a0001c0002t0003g0040 | 2 | HG00544.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.682-93G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77039438 | |||||||
| chr5:77039489 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.682-42A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 4/13 | chr5 | 77039489 | |||||||
| chr5:77039798 | A | C | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.870+79A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77039798 | |||||||
| chr5:77039807 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0258 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.870+88A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77039807 | |||||||
| chr5:77040014 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(1): Show |
7 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.870+295G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040014 | |||||||
| chr5:77040100 | C | T | 278 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(275): Show |
340 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.870+381C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040100 | |||||||
| chr5:77040108 | A | AT | 8 | a0001c0001t0001g0188 a0001c0001t0001g0203 a0001c0001t0001g0220 others(5): Show |
8 | HG02055.hp1 HG02135.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+406dupT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77040108 | ||||||
| chr5:77040108 | AT | A | 173 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(170): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.870+406delT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77040108 | ||||||
| chr5:77040108 | ATT | A | 6 | a0001c0001t0001g0134 a0001c0001t0001g0145 a0003c0005t0011g0132 others(3): Show |
6 | HG00609.hp2 HG01167.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+405_870+406del others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77040108 | ||||||
| chr5:77040128 | G | C | 79 | a0001c0002t0003g0016 a0001c0002t0003g0024 a0001c0002t0003g0032 others(76): Show |
89 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.870+409G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040128 | |||||||
| chr5:77040151 | C | T | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.870+432C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040151 | |||||||
| chr5:77040190 | C | G | 2 | a0001c0001t0013g0315 a0001c0001t0013g0341 |
2 | NA18943.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.870+471C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040190 | |||||||
| chr5:77040228 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(1): Show |
7 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.870+509C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040228 | |||||||
| chr5:77040233 | C | T | 2 | a0001c0004t0007g0209 a0001c0004t0007g0210 |
2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.870+514C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040233 | |||||||
| chr5:77040234 | G | A | 9 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0191 others(6): Show |
10 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.870+515G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040234 | |||||||
| chr5:77040236 | G | A | 1 | a0001c0001t0017g0350 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.870+517G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040236 | |||||||
| chr5:77040244 | G | A | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.870+525G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040244 | |||||||
| chr5:77040271 | G | T | 1 | a0001c0001t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.870+552G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040271 | |||||||
| chr5:77040309 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.870+590C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040309 | |||||||
| chr5:77040420 | T | TA | 62 | a0001c0001t0013g0342 a0001c0002t0003g0274 a0002c0003t0002g0001 others(59): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.870+717dupA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77040420 | ||||||
| chr5:77040420 | TA | T | 66 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(63): Show |
75 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.870+717delA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77040420 | ||||||
| chr5:77040421 | A | T | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870+702A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040421 | |||||||
| chr5:77040521 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.870+802C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040521 | |||||||
| chr5:77040651 | A | T | 180 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(177): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.870+932A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040651 | |||||||
| chr5:77040667 | C | A | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.870+948C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040667 | |||||||
| chr5:77040740 | G | T | 1 | a0002c0003t0002g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.870+1021G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040740 | |||||||
| chr5:77040782 | C | G | 1 | a0002c0003t0002g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.870+1063C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040782 | |||||||
| chr5:77040880 | T | C | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.870+1161T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77040880 | |||||||
| chr5:77041006 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.870+1287G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041006 | |||||||
| chr5:77041113 | C | G | 7 | a0001c0002t0003g0266 a0001c0002t0003g0291 a0001c0002t0003g0292 others(4): Show |
7 | HG00609.hp1 NA18940.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.870+1394C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041113 | |||||||
| chr5:77041119 | TC | T | 176 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(173): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.870+1402delC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77041119 | ||||||
| chr5:77041124 | T | G | 1 | a0002c0003t0002g0081 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.870+1405T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041124 | |||||||
| chr5:77041133 | C | T | 180 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(177): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.870+1414C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041133 | |||||||
| chr5:77041148 | T | C | 1 | a0002c0003t0002g0081 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.870+1429T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041148 | |||||||
| chr5:77041169 | T | C | 1 | a0002c0003t0002g0081 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.870+1450T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041169 | |||||||
| chr5:77041218 | C | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.870+1499C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041218 | |||||||
| chr5:77041403 | C | T | 102 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
117 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.870+1684C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041403 | |||||||
| chr5:77041566 | C | CA | 93 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
108 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.870+1867dupA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77041566 | ||||||
| chr5:77041566 | CA | C | 15 | a0001c0001t0001g0088 a0001c0001t0001g0202 a0001c0001t0001g0303 others(12): Show |
15 | HG01169.hp2 HG01256.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.870+1867delA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77041566 | ||||||
| chr5:77041584 | A | AG | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+1865_870+1866i others(3): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041584 | |||||||
| chr5:77041586 | A | AG | 4 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0210 others(1): Show |
5 | HG02717.hp2 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.870+1868dupG | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77041586 | ||||||
| chr5:77041761 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.870+2042T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041761 | |||||||
| chr5:77041780 | A | C | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.870+2061A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041780 | |||||||
| chr5:77041785 | T | A | 5 | a0001c0001t0001g0196 a0001c0001t0001g0236 a0001c0001t0001g0321 others(2): Show |
5 | HG00280.hp2 HG03139.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+2066T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041785 | |||||||
| chr5:77041785 | TTTTA | T | 8 | a0001c0001t0012g0182 a0001c0001t0013g0315 a0001c0002t0003g0193 others(5): Show |
8 | HG02148.hp2 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.870+2094_870+2097d others(6): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77041785 | ||||||
| chr5:77041786 | TTTATTTA | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 |
6 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.870+2070_870+2076d others(9): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77041786 | ||||||
| chr5:77041787 | TTA | T | 12 | a0001c0001t0001g0143 a0001c0001t0001g0205 a0001c0001t0004g0022 others(9): Show |
13 | HG01123.hp2 HG01993.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.870+2070_870+2071d others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77041787 | ||||||
| chr5:77041788 | TA | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(51): Show |
64 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.870+2070delA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041788 | |||||||
| chr5:77041788 | TATTTA | T | 14 | a0001c0001t0001g0124 a0001c0001t0001g0150 a0001c0001t0001g0151 others(11): Show |
15 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.870+2070_870+2074d others(7): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041788 | |||||||
| chr5:77041789 | A | T | 164 | a0001c0001t0001g0025 a0001c0001t0001g0135 a0001c0001t0001g0155 others(161): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.870+2070A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041789 | |||||||
| chr5:77041792 | T | A | 1 | a0001c0002t0005g0275 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.870+2073T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041792 | |||||||
| chr5:77041793 | A | T | 174 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(171): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.870+2074A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041793 | |||||||
| chr5:77041797 | A | T | 188 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(185): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.870+2078A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041797 | |||||||
| chr5:77041800 | T | A | 25 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0023 others(22): Show |
30 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.870+2081T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041800 | |||||||
| chr5:77041801 | A | T | 98 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0124 others(95): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.870+2082A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041801 | |||||||
| chr5:77041801 | ATT | A | 6 | a0001c0001t0004g0022 a0001c0001t0004g0097 a0001c0001t0004g0106 others(3): Show |
7 | HG00140.hp2 HG01069.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.870+2084_870+2085d others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77041801 | ||||||
| chr5:77041801 | ATTT | A | 82 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
96 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.870+2083_870+2085d others(5): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041801 | |||||||
| chr5:77041804 | T | A | 15 | a0001c0001t0001g0124 a0001c0001t0001g0143 a0001c0001t0001g0150 others(12): Show |
16 | HG00140.hp2 HG01069.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.870+2085T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041804 | |||||||
| chr5:77041805 | A | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(14): Show |
21 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.870+2086A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041805 | |||||||
| chr5:77041809 | A | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 |
6 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.870+2090A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041809 | |||||||
| chr5:77041939 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0247 |
2 | HG04184.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.870+2220C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041939 | |||||||
| chr5:77041982 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.870+2263T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77041982 | |||||||
| chr5:77042033 | TCAAGCAT others(9): Show |
T | 4 | a0001c0002t0003g0277 a0001c0002t0003g0278 a0001c0002t0003g0279 others(1): Show |
4 | HG02056.hp1 HG02132.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2315_870+2330d others(18): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042033 | |||||||
| chr5:77042088 | G | C | 5 | a0001c0001t0004g0098 a0001c0001t0004g0100 a0001c0001t0004g0110 others(2): Show |
5 | HG00621.hp1 NA18964.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+2369G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042088 | |||||||
| chr5:77042109 | C | T | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.870+2390C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042109 | |||||||
| chr5:77042253 | C | T | 7 | a0001c0001t0008g0031 a0001c0001t0008g0212 a0001c0001t0008g0213 others(4): Show |
8 | HG02486.hp2 HG02895.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+2534C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042253 | |||||||
| chr5:77042264 | C | T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
111 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.870+2545C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042264 | |||||||
| chr5:77042288 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(1): Show |
7 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.870+2569C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042288 | |||||||
| chr5:77042351 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(1): Show |
7 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.870+2632C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042351 | |||||||
| chr5:77042369 | ACTTCCCA others(81): Show |
A | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.870+2652_870+2739d others(90): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042369 | ||||||
| chr5:77042384 | CGGCCGGG others(135): Show |
C | 4 | a0001c0001t0001g0014 a0001c0002t0003g0024 a0001c0002t0003g0122 others(1): Show |
4 | HG02155.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+2698_870+2839d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042384 | ||||||
| chr5:77042388 | C | T | 1 | a0001c0001t0026g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.870+2669C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042388 | |||||||
| chr5:77042412 | C | T | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.870+2693C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042412 | |||||||
| chr5:77042417 | A | C | 1 | a0001c0001t0001g0005 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.870+2698A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042417 | |||||||
| chr5:77042429 | T | C | 2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.870+2710T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042429 | |||||||
| chr5:77042434 | G | A | 68 | a0001c0001t0004g0097 a0001c0001t0004g0101 a0001c0001t0017g0353 others(65): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.870+2715G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042434 | |||||||
| chr5:77042446 | C | G | 1 | a0001c0001t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.870+2727C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042446 | |||||||
| chr5:77042467 | C | T | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.870+2748C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042467 | |||||||
| chr5:77042473 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.870+2754G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042473 | |||||||
| chr5:77042480 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0303 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.870+2761C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042480 | |||||||
| chr5:77042480 | CGGGCGGG others(185): Show |
C | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.870+2766_870+2957d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042480 | ||||||
| chr5:77042484 | C | CA | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2765_870+2766i others(3): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042484 | |||||||
| chr5:77042486 | G | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2767G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042486 | |||||||
| chr5:77042490 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870+2771G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042490 | |||||||
| chr5:77042491 | C | A | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870+2772C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042491 | |||||||
| chr5:77042492 | T | C | 2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.870+2773T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042492 | |||||||
| chr5:77042492 | TGACCCC | T | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2774_870+2779d others(8): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042492 | |||||||
| chr5:77042494 | AC | A | 263 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(260): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.870+2783delC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042494 | ||||||
| chr5:77042494 | ACCCCCCC others(87): Show |
A | 2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.870+2783_870+2876d others(96): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042494 | ||||||
| chr5:77042501 | C | T | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2782C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042501 | |||||||
| chr5:77042503 | ACCTC | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2791_870+2794d others(6): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042503 | ||||||
| chr5:77042509 | C | T | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2790C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042509 | |||||||
| chr5:77042514 | G | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2795G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042514 | |||||||
| chr5:77042516 | A | T | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2797A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042516 | |||||||
| chr5:77042517 | C | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2798C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042517 | |||||||
| chr5:77042517 | C | T | 2 | a0001c0002t0003g0231 a0001c0002t0003g0233 |
2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870+2798C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042517 | |||||||
| chr5:77042522 | CGGCT | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2807_870+2810d others(6): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042522 | ||||||
| chr5:77042525 | C | CTGGCCGG others(30): Show |
1 | a0002c0003t0015g0007 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.870+2820_870+2821i others(39): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042525 | ||||||
| chr5:77042526 | T | TGGCCGGG others(30): Show |
157 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(154): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.870+2820_870+2821i others(39): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042526 | ||||||
| chr5:77042530 | CGGGCAGA others(135): Show |
C | 4 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+2821_870+2962d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042530 | ||||||
| chr5:77042531 | G | GGGCAGAG others(30): Show |
1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.870+2820_870+2821i others(39): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042531 | ||||||
| chr5:77042540 | C | G | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2821C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042540 | |||||||
| chr5:77042543 | C | T | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2824C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042543 | |||||||
| chr5:77042550 | C | T | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2831C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042550 | |||||||
| chr5:77042554 | C | T | 2 | a0001c0001t0008g0351 a0001c0001t0008g0352 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.870+2835C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042554 | |||||||
| chr5:77042555 | G | A | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2836G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042555 | |||||||
| chr5:77042557 | A | T | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2838A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042557 | |||||||
| chr5:77042558 | C | A | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2839C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042558 | |||||||
| chr5:77042564 | G | A | 1 | a0001c0001t0001g0344 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.870+2845G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042564 | |||||||
| chr5:77042567 | T | C | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2848T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042567 | |||||||
| chr5:77042569 | G | GGCAGAGG others(13): Show |
4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2850_870+2851i others(22): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042569 | |||||||
| chr5:77042574 | G | A | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2855G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042574 | |||||||
| chr5:77042576 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0205 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.870+2857G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042576 | |||||||
| chr5:77042580 | G | C | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2861G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042580 | |||||||
| chr5:77042586 | A | AC | 35 | a0001c0001t0001g0033 a0001c0001t0001g0124 a0001c0001t0001g0134 others(32): Show |
36 | HG00609.hp2 HG00738.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.870+2876dupC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042586 | ||||||
| chr5:77042586 | A | ACCCCCCC others(314): Show |
1 | a0001c0001t0001g0303 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870+2876_870+2877i others(323): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042586 | ||||||
| chr5:77042602 | CTCCCGGA others(42): Show |
C | 1 | a0001c0001t0001g0323 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.870+2893_870+2941d others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042602 | ||||||
| chr5:77042606 | C | T | 79 | a0001c0002t0003g0016 a0001c0002t0003g0024 a0001c0002t0003g0032 others(76): Show |
89 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.870+2887C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042606 | |||||||
| chr5:77042612 | T | G | 167 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(164): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.870+2893T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042612 | |||||||
| chr5:77042623 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0043 others(34): Show |
44 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.870+2904C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042623 | |||||||
| chr5:77042635 | T | C | 2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.870+2916T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042635 | |||||||
| chr5:77042644 | C | T | 1 | a0001c0002t0003g0348 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.870+2925C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042644 | |||||||
| chr5:77042651 | A | C | 2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.870+2932A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042651 | |||||||
| chr5:77042651 | ATCCCGGA others(542): Show |
A | 1 | a0001c0001t0001g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.870+3015_871-3065d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042651 | ||||||
| chr5:77042655 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.870+2936C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042655 | |||||||
| chr5:77042664 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.870+2945C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042664 | |||||||
| chr5:77042672 | T | C | 259 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(256): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.870+2953T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042672 | |||||||
| chr5:77042684 | C | T | 1 | a0001c0001t0012g0182 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.870+2965C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042684 | |||||||
| chr5:77042690 | A | G | 1 | a0002c0003t0002g0044 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.870+2971A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042690 | |||||||
| chr5:77042705 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.870+2986C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042705 | |||||||
| chr5:77042733 | C | T | 6 | a0001c0001t0012g0182 a0002c0003t0002g0008 a0002c0003t0002g0047 others(3): Show |
7 | HG03453.hp1 NA18963.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.870+3014C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042733 | |||||||
| chr5:77042734 | G | A | 2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.870+3015G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042734 | |||||||
| chr5:77042736 | ACGGGGCG others(190): Show |
A | 2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.870+3036_870+3232d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042736 | ||||||
| chr5:77042760 | G | A | 1 | a0001c0002t0003g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870+3041G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042760 | |||||||
| chr5:77042765 | A | AC | 75 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0131 others(72): Show |
104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.870+3054dupC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042765 | ||||||
| chr5:77042767 | CCCCCCCA others(40): Show |
C | 2 | a0002c0003t0002g0057 a0002c0003t0016g0002 |
2 | NA18992.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.870+3055_870+3101d others(49): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042767 | ||||||
| chr5:77042768 | CCCCCCAC others(39): Show |
C | 2 | a0001c0001t0024g0221 a0002c0003t0016g0062 |
2 | NA18522.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.870+3055_870+3100d others(48): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042768 | ||||||
| chr5:77042769 | CCCCCACC others(138): Show |
C | 1 | a0001c0001t0004g0106 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.870+3055_870+3199d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042769 | ||||||
| chr5:77042787 | ACGGGGCG others(41): Show |
A | 1 | a0001c0004t0007g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.870+3092_870+3139d others(50): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042787 | ||||||
| chr5:77042787 | ACGGGGCG others(139): Show |
A | 30 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(27): Show |
36 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.870+3092_870+3237d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042787 | ||||||
| chr5:77042789 | G | GGGGCGGC others(364): Show |
1 | a0001c0001t0001g0253 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.870+3092_871-3166d others(373): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042789 | ||||||
| chr5:77042805 | C | CG | 139 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(136): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.870+3091dupG | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042805 | ||||||
| chr5:77042806 | GGGGGCTG others(187): Show |
G | 1 | a0001c0004t0007g0210 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.870+3092_870+3285d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042806 | ||||||
| chr5:77042812 | T | C | 76 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0001t0001g0174 others(73): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.870+3093T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042812 | |||||||
| chr5:77042814 | A | AC | 11 | a0001c0001t0001g0169 a0001c0001t0001g0244 a0001c0001t0012g0119 others(8): Show |
12 | HG00597.hp2 HG00642.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+3102dupC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042814 | ||||||
| chr5:77042815 | CCCCCCCA others(188): Show |
C | 1 | a0001c0004t0007g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.870+3103_870+3297d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042815 | ||||||
| chr5:77042816 | C | A | 4 | a0001c0002t0006g0042 a0001c0002t0006g0330 a0001c0002t0006g0331 others(1): Show |
5 | HG01099.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+3097C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042816 | |||||||
| chr5:77042816 | CCCCCCAC others(42): Show |
C | 1 | a0001c0001t0001g0344 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.870+3195_870+3243d others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042816 | ||||||
| chr5:77042826 | C | T | 6 | a0002c0003t0002g0001 a0002c0003t0002g0048 a0002c0003t0002g0068 others(3): Show |
7 | NA18747.hp2 NA18946.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.870+3107C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042826 | |||||||
| chr5:77042827 | C | T | 1 | a0001c0001t0001g0343 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.870+3108C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042827 | |||||||
| chr5:77042828 | C | A | 3 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0211 |
3 | HG02717.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.870+3109C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042828 | |||||||
| chr5:77042835 | G | A | 2 | a0001c0001t0024g0221 a0002c0003t0002g0057 |
2 | NA18522.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.870+3116G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042835 | |||||||
| chr5:77042836 | C | T | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+3117C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042836 | |||||||
| chr5:77042847 | GCCGGGCG others(25): Show |
G | 1 | a0002c0003t0002g0056 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.870+3139_870+3170d others(34): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042847 | ||||||
| chr5:77042849 | C | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0135 a0001c0001t0001g0143 others(11): Show |
14 | HG01081.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.870+3130C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042849 | |||||||
| chr5:77042850 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.870+3131G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042850 | |||||||
| chr5:77042853 | C | CG | 17 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0001t0001g0203 others(14): Show |
17 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.870+3140dupG | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042853 | ||||||
| chr5:77042865 | A | C | 6 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(3): Show |
6 | HG01496.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+3146A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042865 | |||||||
| chr5:77042876 | C | T | 1 | a0001c0002t0003g0348 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.870+3157C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042876 | |||||||
| chr5:77042877 | C | A | 1 | a0001c0004t0007g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.870+3158C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042877 | |||||||
| chr5:77042881 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.870+3162C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042881 | |||||||
| chr5:77042884 | G | C | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+3165G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042884 | |||||||
| chr5:77042885 | C | T | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.870+3166C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042885 | |||||||
| chr5:77042902 | C | CG | 25 | a0001c0001t0001g0014 a0001c0001t0001g0088 a0001c0001t0001g0140 others(22): Show |
25 | HG00621.hp2 HG01192.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.870+3189dupG | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042902 | ||||||
| chr5:77042914 | A | AC | 6 | a0001c0001t0001g0320 a0001c0001t0001g0338 a0002c0003t0002g0001 others(3): Show |
6 | HG04115.hp1 HG04199.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+3200dupC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042914 | ||||||
| chr5:77042914 | A | C | 3 | a0001c0002t0006g0042 a0001c0002t0006g0330 a0001c0002t0006g0332 |
4 | HG01256.hp2 HG01258.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+3195A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042914 | |||||||
| chr5:77042930 | C | T | 7 | a0001c0001t0008g0031 a0001c0001t0008g0212 a0001c0001t0008g0213 others(4): Show |
8 | HG02486.hp2 HG02895.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+3211C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042930 | |||||||
| chr5:77042933 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0004g0106 a0001c0002t0006g0042 others(4): Show |
8 | HG01099.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.870+3214G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042933 | |||||||
| chr5:77042933 | G | C | 221 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(218): Show |
273 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.870+3214G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042933 | |||||||
| chr5:77042933 | GCGGGGCG others(42): Show |
G | 1 | a0001c0001t0001g0033 | 2 | HG00738.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.870+3282_871-3298d others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042933 | ||||||
| chr5:77042951 | C | CG | 15 | a0001c0001t0001g0131 a0001c0001t0001g0139 a0001c0001t0001g0170 others(12): Show |
15 | HG00597.hp1 HG00621.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.870+3238dupG | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042951 | ||||||
| chr5:77042954 | G | A | 2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.870+3235G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042954 | |||||||
| chr5:77042959 | C | T | 3 | a0001c0001t0004g0097 a0001c0001t0004g0101 a0006c0009t0001g0218 |
3 | HG01993.hp1 HG02293.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.870+3240C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042959 | |||||||
| chr5:77042961 | A | AC | 20 | a0001c0001t0001g0124 a0001c0001t0001g0131 a0001c0001t0001g0169 others(17): Show |
20 | HG00621.hp2 HG01192.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.870+3249dupC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042961 | ||||||
| chr5:77042963 | C | A | 1 | a0002c0003t0002g0057 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.870+3244C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042963 | |||||||
| chr5:77042974 | C | T | 1 | a0001c0002t0003g0354 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.870+3255C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042974 | |||||||
| chr5:77042982 | A | C | 1 | a0002c0003t0002g0057 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.870+3263A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042982 | |||||||
| chr5:77042982 | A | G | 11 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0191 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+3263A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042982 | |||||||
| chr5:77042984 | G | A | 2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.870+3265G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042984 | |||||||
| chr5:77042984 | G | GGGGCGGC others(296): Show |
4 | a0001c0002t0006g0042 a0001c0002t0006g0330 a0001c0002t0006g0331 others(1): Show |
5 | HG01099.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+3281_870+3282i others(305): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042984 | ||||||
| chr5:77042988 | C | T | 1 | a0002c0003t0002g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.870+3269C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042988 | |||||||
| chr5:77042996 | C | G | 1 | a0001c0002t0003g0274 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.870+3277C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77042996 | |||||||
| chr5:77042996 | CGGGCGGG others(218): Show |
C | 1 | a0001c0001t0001g0329 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.870+3282_871-3122d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77042996 | ||||||
| chr5:77043000 | C | CG | 19 | a0001c0001t0001g0188 a0001c0001t0001g0195 a0001c0001t0001g0203 others(16): Show |
19 | HG00597.hp2 HG01192.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.870+3287dupG | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043000 | ||||||
| chr5:77043006 | G | T | 4 | a0001c0002t0006g0042 a0001c0002t0006g0330 a0001c0002t0006g0331 others(1): Show |
5 | HG01099.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+3287G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043006 | |||||||
| chr5:77043008 | C | T | 7 | a0001c0001t0004g0097 a0001c0001t0004g0101 a0001c0002t0006g0042 others(4): Show |
8 | HG01099.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.870+3289C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043008 | |||||||
| chr5:77043010 | A | AC | 11 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0140 others(8): Show |
11 | HG00597.hp1 HG00597.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.870+3298dupC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043010 | ||||||
| chr5:77043029 | GGACGGGG others(71): Show |
G | 1 | a0001c0002t0003g0268 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.871-3297_871-3220d others(80): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043029 | ||||||
| chr5:77043045 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0149 others(2): Show |
8 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.871-3302C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043045 | |||||||
| chr5:77043110 | C | T | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.871-3237C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043110 | |||||||
| chr5:77043118 | C | T | 2 | a0001c0001t0012g0119 a0001c0001t0012g0133 |
2 | HG01496.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.871-3229C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043118 | |||||||
| chr5:77043123 | C | T | 2 | a0001c0004t0007g0209 a0001c0004t0007g0210 |
2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.871-3224C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043123 | |||||||
| chr5:77043130 | A | G | 1 | a0001c0002t0003g0268 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.871-3217A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043130 | |||||||
| chr5:77043135 | T | C | 1 | a0001c0002t0003g0268 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.871-3212T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043135 | |||||||
| chr5:77043139 | C | A | 1 | a0001c0002t0003g0268 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.871-3208C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043139 | |||||||
| chr5:77043141 | C | T | 3 | a0001c0001t0012g0119 a0001c0001t0012g0133 a0006c0009t0001g0218 |
3 | HG01496.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.871-3206C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043141 | |||||||
| chr5:77043160 | A | G | 2 | a0001c0001t0012g0119 a0001c0001t0012g0133 |
2 | HG01496.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.871-3187A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043160 | |||||||
| chr5:77043173 | G | A | 2 | a0001c0001t0012g0119 a0001c0001t0012g0133 |
2 | HG01496.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.871-3174G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043173 | |||||||
| chr5:77043177 | G | A | 9 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0191 others(6): Show |
10 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.871-3170G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043177 | |||||||
| chr5:77043179 | GGGGCTGA others(296): Show |
G | 2 | a0001c0001t0012g0119 a0001c0001t0012g0133 |
2 | HG01496.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.871-3126_871-2824d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043179 | ||||||
| chr5:77043182 | G | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0035 others(10): Show |
16 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.871-3165G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043182 | |||||||
| chr5:77043187 | C | CCCCCCCA others(217): Show |
1 | a0001c0001t0001g0258 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.871-2946_871-2945i others(226): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043187 | ||||||
| chr5:77043187 | C | T | 2 | a0001c0001t0001g0201 a0002c0003t0002g0048 |
2 | HG02572.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.871-3160C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043187 | |||||||
| chr5:77043204 | C | CGGACGGG others(6): Show |
2 | a0001c0001t0004g0097 a0001c0001t0004g0101 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.871-3140_871-3128d others(15): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043204 | ||||||
| chr5:77043214 | G | A | 1 | a0002c0003t0002g0020 | 2 | NA19006.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.871-3133G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043214 | |||||||
| chr5:77043221 | T | C | 177 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(174): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.871-3126T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043221 | |||||||
| chr5:77043238 | C | A | 1 | a0002c0003t0002g0304 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.871-3109C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043238 | |||||||
| chr5:77043287 | G | T | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.871-3060G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043287 | |||||||
| chr5:77043291 | C | T | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.871-3056C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043291 | |||||||
| chr5:77043292 | G | A | 12 | a0001c0002t0003g0224 a0001c0002t0003g0274 a0001c0002t0003g0296 others(9): Show |
13 | HG00673.hp2 HG01928.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.871-3055G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043292 | |||||||
| chr5:77043294 | C | T | 14 | a0001c0001t0004g0097 a0001c0001t0004g0101 a0001c0001t0008g0031 others(11): Show |
15 | HG00609.hp1 HG01167.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.871-3053C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043294 | |||||||
| chr5:77043298 | C | G | 2 | a0001c0004t0007g0209 a0001c0004t0007g0210 |
2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.871-3049C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043298 | |||||||
| chr5:77043299 | C | T | 5 | a0001c0001t0012g0118 a0001c0001t0012g0182 a0001c0004t0007g0030 others(2): Show |
6 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-3048C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043299 | |||||||
| chr5:77043313 | A | AC | 13 | a0001c0001t0001g0129 a0001c0001t0001g0195 a0001c0001t0004g0101 others(10): Show |
13 | HG00544.hp2 HG01978.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.871-3027dupC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043313 | ||||||
| chr5:77043331 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0326 a0001c0001t0001g0328 |
3 | HG01168.hp2 HG01169.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.871-3016C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043331 | |||||||
| chr5:77043336 | A | G | 14 | a0001c0001t0004g0097 a0001c0001t0004g0101 a0001c0001t0008g0031 others(11): Show |
15 | HG00609.hp1 HG01167.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.871-3011A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043336 | |||||||
| chr5:77043349 | G | A | 14 | a0001c0001t0004g0097 a0001c0001t0004g0101 a0001c0001t0008g0031 others(11): Show |
15 | HG00609.hp1 HG01167.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.871-2998G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043349 | |||||||
| chr5:77043355 | GGGTCTGA others(120): Show |
G | 13 | a0001c0001t0004g0097 a0001c0001t0004g0101 a0001c0001t0008g0031 others(10): Show |
14 | HG00609.hp1 HG01167.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-2989_871-2863d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043355 | ||||||
| chr5:77043356 | GGTCTGAC others(119): Show |
G | 1 | a0001c0004t0007g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.871-2989_871-2864d others(2): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043356 | ||||||
| chr5:77043358 | T | G | 1 | a0002c0003t0002g0010 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.871-2989T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043358 | |||||||
| chr5:77043380 | C | CGGACGGG others(6): Show |
30 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(27): Show |
36 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.871-2964_871-2952d others(15): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043380 | ||||||
| chr5:77043397 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0333 others(12): Show |
21 | HG01943.hp1 HG02135.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.871-2950C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043397 | |||||||
| chr5:77043434 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(1): Show |
7 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-2913C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043434 | |||||||
| chr5:77043460 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.871-2887G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043460 | |||||||
| chr5:77043463 | G | GGGGCGGC others(42): Show |
2 | a0001c0001t0001g0220 a0001c0001t0001g0238 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.871-2878_871-2877i others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043463 | ||||||
| chr5:77043467 | C | T | 1 | a0001c0002t0003g0040 | 2 | HG00544.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.871-2880C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043467 | |||||||
| chr5:77043470 | T | C | 2 | a0001c0001t0004g0106 a0001c0002t0003g0273 |
2 | HG02155.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.871-2877T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043470 | |||||||
| chr5:77043474 | C | G | 3 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0211 |
4 | HG02717.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2873C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043474 | |||||||
| chr5:77043482 | A | AGGGCTGA others(42): Show |
44 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0303 others(41): Show |
55 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.871-2823_871-2822i others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043482 | ||||||
| chr5:77043482 | A | AGGGCTGA others(43): Show |
7 | a0001c0002t0005g0302 a0002c0003t0002g0044 a0002c0003t0002g0051 others(4): Show |
7 | HG01261.hp2 HG01978.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-2851_871-2850i others(52): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043482 | ||||||
| chr5:77043482 | A | AGGGCTGA others(44): Show |
1 | a0001c0001t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.871-2851_871-2850i others(53): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043482 | ||||||
| chr5:77043482 | A | AGGGCTGA others(42): Show |
2 | a0001c0001t0012g0118 a0001c0001t0012g0182 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.871-2855_871-2854i others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043482 | ||||||
| chr5:77043482 | AGGGCTGA others(42): Show |
A | 1 | a0001c0001t0001g0334 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.871-2833_871-2785d others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043482 | ||||||
| chr5:77043507 | C | A | 1 | a0002c0003t0002g0304 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.871-2840C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043507 | |||||||
| chr5:77043507 | C | CGGACAGG others(218): Show |
1 | a0001c0002t0003g0273 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.871-2836_871-2835i others(227): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043507 | ||||||
| chr5:77043507 | C | CGGACGGG others(42): Show |
68 | a0001c0002t0003g0016 a0001c0002t0003g0024 a0001c0002t0003g0032 others(65): Show |
77 | HG00323.hp1 HG00544.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.871-2823_871-2822i others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043507 | ||||||
| chr5:77043507 | C | T | 2 | a0001c0002t0003g0295 a0001c0002t0005g0302 |
2 | HG00609.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.871-2840C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043507 | |||||||
| chr5:77043511 | C | CGGGGCGG others(42): Show |
57 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(54): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.871-2823_871-2822i others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043511 | ||||||
| chr5:77043511 | C | CGGGGCGG others(42): Show |
1 | a0001c0002t0003g0194 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.871-2823_871-2822i others(51): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043511 | ||||||
| chr5:77043511 | C | T | 6 | a0002c0003t0002g0044 a0002c0003t0002g0051 a0002c0003t0002g0052 others(3): Show |
6 | HG01261.hp2 HG01978.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-2836C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043511 | |||||||
| chr5:77043515 | G | GCGGCCTG others(45): Show |
1 | a0002c0003t0002g0304 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.871-2828_871-2827i others(54): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043515 | ||||||
| chr5:77043525 | G | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
76 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.871-2822G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043525 | |||||||
| chr5:77043538 | A | ACCCCCCC others(43): Show |
1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.871-2785_871-2784i others(52): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043538 | ||||||
| chr5:77043538 | A | ACCCCCCC others(43): Show |
2 | a0001c0002t0003g0226 a0001c0002t0003g0264 |
2 | HG01192.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.871-2792_871-2791i others(52): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043538 | ||||||
| chr5:77043538 | A | ACCCCCCC others(44): Show |
1 | a0001c0002t0003g0288 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.871-2802_871-2801i others(53): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043538 | ||||||
| chr5:77043547 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.871-2800C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043547 | |||||||
| chr5:77043574 | A | G | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.871-2773A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043574 | |||||||
| chr5:77043577 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.871-2770C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043577 | |||||||
| chr5:77043577 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
57 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.871-2770C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043577 | |||||||
| chr5:77043587 | A | AC | 45 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
58 | HG00438.hp1 HG00597.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.871-2747dupC | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043587 | ||||||
| chr5:77043587 | A | ACC | 19 | a0001c0001t0001g0088 a0001c0001t0001g0195 a0001c0001t0001g0197 others(16): Show |
19 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.871-2748_871-2747d others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043587 | ||||||
| chr5:77043592 | C | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0149 a0001c0001t0001g0172 |
4 | NA18943.hp1 NA18968.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2755C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043592 | |||||||
| chr5:77043593 | C | CCT | 62 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(59): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.871-2753_871-2752i others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043593 | ||||||
| chr5:77043597 | C | CCCT | 38 | a0001c0002t0003g0036 a0001c0002t0003g0040 a0001c0002t0003g0120 others(35): Show |
40 | HG00544.hp2 HG00673.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.871-2748_871-2747i others(5): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043597 | ||||||
| chr5:77043597 | C | CCT | 54 | a0001c0001t0001g0260 a0001c0001t0001g0303 a0001c0001t0004g0023 others(51): Show |
61 | HG00323.hp1 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.871-2749_871-2748i others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043597 | ||||||
| chr5:77043597 | C | CT | 46 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0124 others(43): Show |
56 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.871-2750_871-2749i others(3): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043597 | |||||||
| chr5:77043597 | C | T | 119 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.871-2750C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043597 | |||||||
| chr5:77043601 | G | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0041 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.871-2746G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043601 | |||||||
| chr5:77043602 | G | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0323 |
3 | HG00738.hp2 HG01070.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.871-2745G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043602 | |||||||
| chr5:77043623 | G | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0238 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.871-2724G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043623 | |||||||
| chr5:77043632 | ACCCCCCA others(43): Show |
A | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.871-2694_871-2645d others(52): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77043632 | ||||||
| chr5:77043644 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(1): Show |
7 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-2703C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043644 | |||||||
| chr5:77043649 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0034 others(2): Show |
6 | HG00597.hp2 HG01943.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-2698C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043649 | |||||||
| chr5:77043706 | G | A | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.871-2641G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043706 | |||||||
| chr5:77043716 | G | C | 1 | a0002c0003t0002g0018 | 2 | HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.871-2631G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043716 | |||||||
| chr5:77043719 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0135 a0001c0001t0001g0155 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.871-2628C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043719 | |||||||
| chr5:77043744 | G | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0191 others(6): Show |
10 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.871-2603G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043744 | |||||||
| chr5:77043760 | G | A | 1 | a0001c0001t0004g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.871-2587G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043760 | |||||||
| chr5:77043784 | T | C | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-2563T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043784 | |||||||
| chr5:77043784 | T | G | 182 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(179): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.871-2563T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043784 | |||||||
| chr5:77043796 | G | A | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2551G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043796 | |||||||
| chr5:77043801 | G | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 |
6 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-2546G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043801 | |||||||
| chr5:77043842 | A | G | 1 | a0002c0003t0002g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.871-2505A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043842 | |||||||
| chr5:77043868 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.871-2479C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043868 | |||||||
| chr5:77043872 | C | T | 3 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0004g0111 |
3 | HG01261.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.871-2475C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043872 | |||||||
| chr5:77043882 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.871-2465C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043882 | |||||||
| chr5:77043887 | G | A | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2460G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043887 | |||||||
| chr5:77043887 | G | C | 3 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0004g0111 |
3 | HG01261.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.871-2460G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043887 | |||||||
| chr5:77043900 | C | T | 2 | a0001c0001t0001g0312 a0001c0001t0001g0314 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.871-2447C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043900 | |||||||
| chr5:77043908 | C | T | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.871-2439C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043908 | |||||||
| chr5:77043914 | G | A | 1 | a0001c0002t0005g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.871-2433G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043914 | |||||||
| chr5:77043922 | C | T | 32 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(29): Show |
38 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-2425C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77043922 | |||||||
| chr5:77044037 | A | G | 329 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(326): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.871-2310A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044037 | |||||||
| chr5:77044061 | TGGCGGCC others(69): Show |
T | 1 | a0002c0003t0002g0085 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.871-2278_871-2203d others(78): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77044061 | ||||||
| chr5:77044068 | C | T | 1 | a0001c0002t0003g0349 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.871-2279C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044068 | |||||||
| chr5:77044073 | G | A | 2 | a0001c0002t0003g0289 a0001c0002t0003g0354 |
2 | HG00642.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.871-2274G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044073 | |||||||
| chr5:77044076 | G | C | 1 | a0001c0001t0004g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.871-2271G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044076 | |||||||
| chr5:77044184 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.871-2163C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044184 | |||||||
| chr5:77044221 | G | A | 278 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(275): Show |
340 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.871-2126G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044221 | |||||||
| chr5:77044300 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-2047C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044300 | |||||||
| chr5:77044348 | G | T | 102 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
117 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.871-1999G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044348 | |||||||
| chr5:77044413 | A | G | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.871-1934A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044413 | |||||||
| chr5:77044588 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.871-1759A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044588 | |||||||
| chr5:77044739 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.871-1608T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044739 | |||||||
| chr5:77044855 | G | C | 1 | a0001c0002t0003g0291 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.871-1492G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044855 | |||||||
| chr5:77044934 | G | A | 1 | a0001c0002t0003g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.871-1413G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044934 | |||||||
| chr5:77044983 | T | C | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-1364T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044983 | |||||||
| chr5:77044986 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.871-1361A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77044986 | |||||||
| chr5:77045064 | C | CA | 12 | a0001c0001t0001g0188 a0001c0001t0008g0031 a0001c0001t0008g0212 others(9): Show |
13 | HG02486.hp2 HG02738.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.871-1268dupA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77045064 | ||||||
| chr5:77045064 | CA | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.871-1268delA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77045064 | ||||||
| chr5:77045122 | C | CAGAAGAG others(2): Show |
3 | a0001c0002t0003g0297 a0001c0002t0003g0298 a0001c0002t0003g0299 |
3 | HG03490.hp2 HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.871-1224_871-1216d others(11): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 77045122 | ||||||
| chr5:77045352 | G | C | 102 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
117 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.871-995G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045352 | |||||||
| chr5:77045379 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 |
6 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-968A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045379 | |||||||
| chr5:77045403 | G | A | 274 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(271): Show |
335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.871-944G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045403 | |||||||
| chr5:77045417 | C | A | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-930C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045417 | |||||||
| chr5:77045462 | TGTTC | T | 33 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(30): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.871-884_871-881del others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045462 | |||||||
| chr5:77045463 | G | A | 146 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(143): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.871-884G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045463 | |||||||
| chr5:77045464 | T | A | 1 | a0002c0003t0002g0085 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.871-883T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045464 | |||||||
| chr5:77045725 | C | T | 32 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(29): Show |
38 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-622C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045725 | |||||||
| chr5:77045756 | C | T | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.871-591C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045756 | |||||||
| chr5:77045762 | G | A | 3 | a0001c0002t0003g0185 a0001c0002t0003g0193 a0001c0002t0003g0194 |
3 | HG01243.hp1 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.871-585G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045762 | |||||||
| chr5:77045844 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.871-503C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045844 | |||||||
| chr5:77045870 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.871-477T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045870 | |||||||
| chr5:77045882 | T | C | 1 | a0002c0003t0002g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.871-465T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77045882 | |||||||
| chr5:77046021 | G | A | 5 | a0001c0002t0003g0032 a0001c0002t0003g0229 a0001c0002t0003g0232 others(2): Show |
6 | HG00735.hp1 HG02055.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-326G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77046021 | |||||||
| chr5:77046119 | G | A | 33 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(30): Show |
39 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.871-228G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77046119 | |||||||
| chr5:77046148 | T | C | 32 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(29): Show |
38 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-199T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77046148 | |||||||
| chr5:77046163 | G | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 |
6 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-184G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77046163 | |||||||
| chr5:77046203 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.871-144A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77046203 | |||||||
| chr5:77046247 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.871-100A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77046247 | |||||||
| chr5:77046328 | T | A | 2 | a0001c0001t0004g0094 a0001c0001t0004g0095 |
2 | HG00323.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.871-19T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 5/13 | chr5 | 77046328 | |||||||
| chr5:77046801 | TATTGAAA others(9): Show |
T | 1 | a0001c0001t0013g0315 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1201+125_1201+140d others(18): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77046801 | |||||||
| chr5:77046818 | G | A | 2 | a0001c0001t0018g0186 a0001c0001t0018g0219 |
2 | NA18987.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1201+141G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77046818 | |||||||
| chr5:77046864 | A | G | 1 | a0002c0003t0002g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1201+187A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77046864 | |||||||
| chr5:77046949 | A | G | 1 | a0001c0002t0003g0284 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1201+272A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77046949 | |||||||
| chr5:77047004 | C | T | 176 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(173): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1201+327C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047004 | |||||||
| chr5:77047181 | C | G | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201+504C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047181 | |||||||
| chr5:77047213 | A | AG | 4 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(1): Show |
7 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1201+536_1201+537i others(3): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047213 | |||||||
| chr5:77047321 | A | G | 1 | a0002c0003t0015g0072 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1201+644A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047321 | |||||||
| chr5:77047359 | TAA | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1201+683_1201+684d others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047359 | |||||||
| chr5:77047400 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18988.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1201+723A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047400 | |||||||
| chr5:77047468 | C | A | 1 | a0001c0001t0001g0172 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1202-693C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047468 | |||||||
| chr5:77047483 | G | A | 1 | a0002c0003t0002g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1202-678G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047483 | |||||||
| chr5:77047511 | C | T | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1202-650C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047511 | |||||||
| chr5:77047558 | G | T | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202-603G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047558 | |||||||
| chr5:77047605 | C | CT | 101 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): Show |
116 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1202-555dupT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 77047605 | ||||||
| chr5:77047607 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1202-554G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047607 | |||||||
| chr5:77047645 | C | G | 3 | a0001c0001t0008g0031 a0001c0001t0008g0212 a0001c0001t0008g0213 |
4 | HG02970.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202-516C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047645 | |||||||
| chr5:77047658 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0336 |
3 | NA18942.hp2 NA18946.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1202-503C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047658 | |||||||
| chr5:77047770 | G | A | 1 | a0001c0001t0009g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1202-391G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047770 | |||||||
| chr5:77047817 | C | CT | 15 | a0001c0001t0001g0139 a0001c0001t0001g0188 a0001c0001t0001g0239 others(12): Show |
19 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.1202-327dupT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 77047817 | ||||||
| chr5:77047883 | T | G | 32 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(29): Show |
38 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1202-278T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047883 | |||||||
| chr5:77047916 | G | A | 2 | a0003c0005t0011g0132 a0003c0005t0011g0180 |
2 | NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202-245G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047916 | |||||||
| chr5:77047920 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 |
6 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1202-241A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77047920 | |||||||
| chr5:77048008 | C | T | 3 | a0001c0002t0005g0090 a0001c0002t0005g0225 a0001c0002t0005g0283 |
3 | HG01928.hp2 HG01975.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1202-153C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 6/13 | chr5 | 77048008 | |||||||
| chr5:77048317 | A | C | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313+45A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048317 | |||||||
| chr5:77048318 | A | G | 1 | a0001c0001t0004g0093 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1313+46A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048318 | |||||||
| chr5:77048402 | A | C | 3 | a0001c0002t0003g0231 a0001c0002t0003g0233 a0001c0002t0003g0251 |
3 | HG02451.hp1 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1313+130A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048402 | |||||||
| chr5:77048520 | T | G | 1 | a0001c0001t0012g0182 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1313+248T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048520 | |||||||
| chr5:77048541 | G | A | 2 | a0001c0002t0003g0261 a0001c0002t0003g0262 |
2 | HG02071.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1313+269G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048541 | |||||||
| chr5:77048710 | C | G | 1 | a0001c0001t0004g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1314-226C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048710 | |||||||
| chr5:77048734 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0160 a0001c0001t0001g0250 |
3 | HG02257.hp1 HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1314-202G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048734 | |||||||
| chr5:77048761 | G | A | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314-175G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048761 | |||||||
| chr5:77048838 | C | T | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314-98C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048838 | |||||||
| chr5:77048925 | T | A | 1 | a0001c0001t0018g0219 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1314-11T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 7/13 | chr5 | 77048925 | |||||||
| chr5:77049063 | G | A | 1 | a0001c0002t0003g0231 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1365+76G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049063 | |||||||
| chr5:77049084 | A | T | 1 | a0001c0001t0013g0315 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1365+97A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049084 | |||||||
| chr5:77049112 | T | G | 1 | a0001c0001t0018g0219 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1365+125T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049112 | |||||||
| chr5:77049149 | A | G | 2 | a0003c0005t0011g0132 a0003c0005t0011g0180 |
2 | NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1365+162A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049149 | |||||||
| chr5:77049393 | A | C | 1 | a0001c0001t0012g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1365+406A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049393 | |||||||
| chr5:77049511 | T | C | 2 | a0003c0005t0011g0132 a0003c0005t0011g0180 |
2 | NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1365+524T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049511 | |||||||
| chr5:77049548 | C | CT | 15 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0203 others(12): Show |
15 | HG00438.hp1 HG00735.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1365+580dupT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77049548 | ||||||
| chr5:77049548 | CT | C | 77 | a0001c0001t0001g0088 a0001c0001t0001g0129 a0001c0001t0001g0146 others(74): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1365+580delT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77049548 | ||||||
| chr5:77049618 | C | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
71 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1365+631C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049618 | |||||||
| chr5:77049700 | C | G | 4 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+713C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049700 | |||||||
| chr5:77049700 | C | T | 2 | a0001c0002t0003g0273 a0001c0002t0003g0286 |
2 | HG02080.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1365+713C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049700 | |||||||
| chr5:77049834 | G | A | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1365+847G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77049834 | |||||||
| chr5:77050048 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1365+1061C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050048 | |||||||
| chr5:77050114 | T | C | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1365+1127T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050114 | |||||||
| chr5:77050197 | A | G | 2 | a0002c0003t0002g0069 a0002c0003t0002g0071 |
2 | NA18747.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1365+1210A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050197 | |||||||
| chr5:77050306 | C | CT | 23 | a0001c0001t0001g0029 a0001c0001t0001g0184 a0001c0001t0001g0187 others(20): Show |
24 | HG00423.hp1 HG00438.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1365+1348dupT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77050306 | ||||||
| chr5:77050306 | CT | C | 70 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0311 others(67): Show |
83 | HG00544.hp2 HG00609.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1365+1348delT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77050306 | ||||||
| chr5:77050306 | CTT | C | 8 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0250 others(5): Show |
8 | HG00323.hp1 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1365+1347_1365+134 others(6): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77050306 | ||||||
| chr5:77050306 | CTTT | C | 20 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0124 others(17): Show |
22 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1365+1346_1365+134 others(7): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77050306 | ||||||
| chr5:77050306 | CTTTT | C | 81 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
95 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1365+1345_1365+134 others(8): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77050306 | ||||||
| chr5:77050306 | CTTTTTTT others(2): Show |
C | 55 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(52): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1365+1340_1365+134 others(13): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77050306 | ||||||
| chr5:77050306 | CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0012g0119 a0002c0003t0002g0045 a0002c0003t0002g0055 others(5): Show |
8 | HG00733.hp2 HG01081.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1365+1339_1365+134 others(14): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77050306 | ||||||
| chr5:77050306 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0012g0118 a0001c0001t0012g0133 a0001c0001t0012g0182 |
3 | HG02615.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1365+1338_1365+134 others(15): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77050306 | ||||||
| chr5:77050334 | T | A | 1 | a0002c0003t0002g0052 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1365+1347T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050334 | |||||||
| chr5:77050425 | C | T | 1 | a0001c0001t0004g0021 | 2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1365+1438C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050425 | |||||||
| chr5:77050586 | A | G | 1 | a0001c0002t0003g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1365+1599A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050586 | |||||||
| chr5:77050678 | G | A | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1365+1691G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050678 | |||||||
| chr5:77050705 | C | G | 1 | a0001c0001t0001g0346 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1365+1718C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050705 | |||||||
| chr5:77050899 | A | G | 32 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(29): Show |
38 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1366-1807A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050899 | |||||||
| chr5:77050993 | T | C | 1 | a0001c0001t0013g0315 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1366-1713T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77050993 | |||||||
| chr5:77051029 | G | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
59 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1366-1677G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051029 | |||||||
| chr5:77051128 | CTAA | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1366-1574_1366-157 others(7): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77051128 | ||||||
| chr5:77051162 | G | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1366-1544G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051162 | |||||||
| chr5:77051163 | G | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1366-1543G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051163 | |||||||
| chr5:77051249 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1366-1457C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051249 | |||||||
| chr5:77051355 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0167 |
2 | NA18971.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1366-1351C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051355 | |||||||
| chr5:77051392 | C | T | 6 | a0002c0003t0002g0017 a0002c0003t0002g0304 a0002c0003t0002g0306 others(3): Show |
8 | HG00099.hp1 HG00558.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366-1314C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051392 | |||||||
| chr5:77051400 | T | A | 1 | a0001c0001t0013g0315 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1366-1306T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051400 | |||||||
| chr5:77051432 | C | CA | 67 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
76 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1366-1259dupA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77051432 | ||||||
| chr5:77051432 | CA | C | 67 | a0001c0001t0001g0317 a0001c0001t0018g0219 a0001c0002t0006g0227 others(64): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1366-1259delA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77051432 | ||||||
| chr5:77051447 | A | G | 1 | a0002c0003t0002g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1366-1259A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051447 | |||||||
| chr5:77051454 | T | A | 1 | a0001c0002t0003g0122 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1366-1252T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051454 | |||||||
| chr5:77051466 | A | G | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1366-1240A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051466 | |||||||
| chr5:77051519 | A | G | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1366-1187A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051519 | |||||||
| chr5:77051638 | T | C | 38 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(35): Show |
44 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1366-1068T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051638 | |||||||
| chr5:77051785 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1366-921G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77051785 | |||||||
| chr5:77052095 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1366-611G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052095 | |||||||
| chr5:77052123 | C | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0154 a0001c0001t0001g0310 |
3 | NA18945.hp2 NA18978.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1366-583C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052123 | |||||||
| chr5:77052130 | A | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0191 others(6): Show |
10 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1366-576A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052130 | |||||||
| chr5:77052162 | G | C | 4 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-544G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052162 | |||||||
| chr5:77052268 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1366-438G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052268 | |||||||
| chr5:77052301 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0136 a0001c0001t0008g0212 |
4 | HG03486.hp1 NA18949.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-405G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052301 | |||||||
| chr5:77052345 | C | CCTGT | 4 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-358_1366-355d others(6): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 77052345 | ||||||
| chr5:77052362 | A | G | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1366-344A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052362 | |||||||
| chr5:77052375 | A | G | 1 | a0001c0004t0007g0208 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1366-331A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052375 | |||||||
| chr5:77052481 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1366-225T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052481 | |||||||
| chr5:77052534 | A | G | 4 | a0002c0003t0002g0019 a0002c0003t0002g0052 a0002c0003t0002g0053 others(1): Show |
5 | NA18981.hp1 NA18985.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1366-172A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052534 | |||||||
| chr5:77052552 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1366-154A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 8/13 | chr5 | 77052552 | |||||||
| chr5:77053062 | T | C | 4 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+255T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 9/13 | chr5 | 77053062 | |||||||
| chr5:77053137 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1467+330T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 9/13 | chr5 | 77053137 | |||||||
| chr5:77053243 | G | A | 77 | a0001c0002t0003g0016 a0001c0002t0003g0024 a0001c0002t0003g0032 others(74): Show |
87 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1467+436G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 9/13 | chr5 | 77053243 | |||||||
| chr5:77053380 | G | A | 1 | a0001c0002t0003g0286 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1467+573G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 9/13 | chr5 | 77053380 | |||||||
| chr5:77053434 | G | A | 4 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-531G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 9/13 | chr5 | 77053434 | |||||||
| chr5:77053438 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1468-527G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 9/13 | chr5 | 77053438 | |||||||
| chr5:77053664 | T | A | 1 | a0001c0002t0001g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1468-301T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 9/13 | chr5 | 77053664 | |||||||
| chr5:77054271 | G | A | 7 | a0001c0001t0008g0031 a0001c0001t0008g0212 a0001c0001t0008g0213 others(4): Show |
8 | HG02486.hp2 HG02895.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1633+141G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054271 | |||||||
| chr5:77054314 | G | A | 102 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
117 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1633+184G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054314 | |||||||
| chr5:77054329 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1633+199T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054329 | |||||||
| chr5:77054800 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+670A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054800 | |||||||
| chr5:77054802 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+672G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054802 | |||||||
| chr5:77054804 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+674C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054804 | |||||||
| chr5:77054808 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+678C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054808 | |||||||
| chr5:77054809 | A | C | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+679A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054809 | |||||||
| chr5:77054810 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+680C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054810 | |||||||
| chr5:77054812 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+682G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054812 | |||||||
| chr5:77054815 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+685G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054815 | |||||||
| chr5:77054820 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+690C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054820 | |||||||
| chr5:77054821 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+691T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054821 | |||||||
| chr5:77054822 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1633+692G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054822 | |||||||
| chr5:77054825 | A | C | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-689A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054825 | |||||||
| chr5:77054826 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-688T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054826 | |||||||
| chr5:77054829 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-685A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054829 | |||||||
| chr5:77054831 | T | G | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-683T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054831 | |||||||
| chr5:77054833 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-681T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054833 | |||||||
| chr5:77054835 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-679A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054835 | |||||||
| chr5:77054837 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-677C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054837 | |||||||
| chr5:77054838 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-676G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054838 | |||||||
| chr5:77054840 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-674A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054840 | |||||||
| chr5:77054848 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-666A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054848 | |||||||
| chr5:77054850 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-664A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054850 | |||||||
| chr5:77054852 | G | C | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-662G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054852 | |||||||
| chr5:77054854 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-660C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054854 | |||||||
| chr5:77054857 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-657G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054857 | |||||||
| chr5:77054858 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-656G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054858 | |||||||
| chr5:77054859 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-655C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054859 | |||||||
| chr5:77054862 | G | C | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-652G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054862 | |||||||
| chr5:77054863 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-651A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054863 | |||||||
| chr5:77054870 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-644A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054870 | |||||||
| chr5:77054875 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-639T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054875 | |||||||
| chr5:77054881 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-633C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054881 | |||||||
| chr5:77054882 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-632G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054882 | |||||||
| chr5:77054889 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-625G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054889 | |||||||
| chr5:77054891 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-623C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054891 | |||||||
| chr5:77054892 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-622C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054892 | |||||||
| chr5:77054895 | T | C | 1 | a0001c0002t0003g0289 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1634-619T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054895 | |||||||
| chr5:77054895 | T | G | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-619T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054895 | |||||||
| chr5:77054897 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-617G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054897 | |||||||
| chr5:77054901 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-613G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054901 | |||||||
| chr5:77054902 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-612C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054902 | |||||||
| chr5:77054904 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-610C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054904 | |||||||
| chr5:77054905 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-609G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054905 | |||||||
| chr5:77054907 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-607G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054907 | |||||||
| chr5:77054910 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-604G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054910 | |||||||
| chr5:77054918 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-596T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054918 | |||||||
| chr5:77054921 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-593A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054921 | |||||||
| chr5:77054922 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-592T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054922 | |||||||
| chr5:77054927 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-587C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054927 | |||||||
| chr5:77054929 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-585T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054929 | |||||||
| chr5:77054930 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-584T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054930 | |||||||
| chr5:77054931 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-583A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054931 | |||||||
| chr5:77054933 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-581T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054933 | |||||||
| chr5:77054936 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-578T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054936 | |||||||
| chr5:77054937 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-577T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054937 | |||||||
| chr5:77054938 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1634-576A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054938 | |||||||
| chr5:77054983 | C | G | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1634-531C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054983 | |||||||
| chr5:77054987 | C | T | 4 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-527C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77054987 | |||||||
| chr5:77055176 | A | G | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1634-338A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77055176 | |||||||
| chr5:77055245 | T | C | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1634-269T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77055245 | |||||||
| chr5:77055483 | C | A | 6 | a0002c0003t0002g0007 a0002c0003t0002g0010 a0002c0003t0002g0086 others(3): Show |
10 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1634-31C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 10/13 | chr5 | 77055483 | |||||||
| chr5:77055911 | G | A | 75 | a0001c0002t0003g0016 a0001c0002t0003g0024 a0001c0002t0003g0032 others(72): Show |
84 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1716+315G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77055911 | |||||||
| chr5:77055928 | C | G | 6 | a0001c0001t0001g0311 a0001c0001t0001g0318 a0001c0001t0001g0320 others(3): Show |
6 | NA18948.hp2 NA18979.hp2 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716+332C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77055928 | |||||||
| chr5:77056148 | A | G | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1716+552A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056148 | |||||||
| chr5:77056226 | C | CT | 174 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(171): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1716+650dupT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 77056226 | ||||||
| chr5:77056226 | C | CTT | 13 | a0001c0001t0001g0124 a0001c0001t0001g0140 a0001c0001t0001g0207 others(10): Show |
14 | HG01978.hp2 HG02027.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1716+649_1716+650d others(4): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 77056226 | ||||||
| chr5:77056309 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1716+713A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056309 | |||||||
| chr5:77056385 | C | T | 2 | a0001c0001t0017g0350 a0001c0001t0017g0353 |
2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1716+789C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056385 | |||||||
| chr5:77056386 | G | C | 1 | a0001c0001t0026g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1716+790G>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056386 | |||||||
| chr5:77056389 | C | A | 1 | a0001c0001t0004g0096 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1716+793C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056389 | |||||||
| chr5:77056410 | G | A | 9 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(6): Show |
10 | HG01496.hp2 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1716+814G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056410 | |||||||
| chr5:77056529 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1716+933A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056529 | |||||||
| chr5:77056544 | A | G | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1716+948A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056544 | |||||||
| chr5:77056548 | A | T | 1 | a0001c0001t0024g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1716+952A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056548 | |||||||
| chr5:77056639 | A | T | 1 | a0001c0001t0017g0350 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1716+1043A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056639 | |||||||
| chr5:77056796 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1716+1200A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056796 | |||||||
| chr5:77056814 | A | C | 35 | a0001c0001t0001g0179 a0001c0001t0001g0258 a0001c0001t0004g0004 others(32): Show |
41 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1716+1218A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056814 | |||||||
| chr5:77056891 | CA | C | 3 | a0001c0001t0008g0031 a0001c0001t0008g0212 a0001c0001t0008g0213 |
4 | HG02970.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+1301delA | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 77056891 | ||||||
| chr5:77056908 | TTAATAA | T | 9 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(6): Show |
10 | HG01496.hp2 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1716+1316_1716+132 others(10): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 77056908 | ||||||
| chr5:77056967 | C | T | 1 | a0001c0002t0003g0293 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1716+1371C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77056967 | |||||||
| chr5:77057062 | C | T | 1 | a0001c0002t0005g0282 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1716+1466C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77057062 | |||||||
| chr5:77057225 | A | C | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1716+1629A>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77057225 | |||||||
| chr5:77057427 | A | G | 1 | a0002c0003t0002g0063 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1716+1831A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77057427 | |||||||
| chr5:77057430 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0258 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1716+1834A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77057430 | |||||||
| chr5:77057437 | T | C | 1 | a0002c0003t0002g0020 | 2 | NA19006.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1716+1841T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77057437 | |||||||
| chr5:77057513 | T | G | 3 | a0001c0001t0008g0031 a0001c0001t0008g0212 a0001c0001t0008g0213 |
4 | HG02970.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+1917T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77057513 | |||||||
| chr5:77057622 | G | A | 1 | a0002c0003t0002g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1717-1994G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77057622 | |||||||
| chr5:77057989 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1717-1627A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77057989 | |||||||
| chr5:77058028 | G | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1717-1588G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77058028 | |||||||
| chr5:77058103 | A | T | 1 | a0001c0001t0001g0339 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1717-1513A>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77058103 | |||||||
| chr5:77058177 | C | G | 179 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(176): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1717-1439C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77058177 | |||||||
| chr5:77058268 | A | G | 1 | a0001c0002t0003g0123 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1717-1348A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77058268 | |||||||
| chr5:77058673 | G | A | 1 | a0002c0003t0002g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1717-943G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77058673 | |||||||
| chr5:77058762 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1717-854G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77058762 | |||||||
| chr5:77058777 | C | T | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1717-839C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77058777 | |||||||
| chr5:77059068 | A | G | 1 | a0002c0003t0002g0068 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1717-548A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059068 | |||||||
| chr5:77059070 | T | C | 5 | a0001c0004t0007g0030 a0001c0004t0007g0208 a0001c0004t0007g0209 others(2): Show |
6 | HG02717.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1717-546T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059070 | |||||||
| chr5:77059089 | T | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0043 others(39): Show |
50 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1717-527T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059089 | |||||||
| chr5:77059117 | AT | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0091 a0001c0001t0004g0092 |
4 | HG00639.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-492delT | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 77059117 | ||||||
| chr5:77059204 | C | T | 1 | a0006c0009t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1717-412C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059204 | |||||||
| chr5:77059229 | G | A | 176 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(173): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1717-387G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059229 | |||||||
| chr5:77059247 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0166 |
2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1717-369T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059247 | |||||||
| chr5:77059374 | G | T | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-242G>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059374 | |||||||
| chr5:77059392 | C | A | 1 | a0001c0001t0008g0351 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1717-224C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059392 | |||||||
| chr5:77059413 | C | T | 1 | a0001c0002t0003g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1717-203C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059413 | |||||||
| chr5:77059437 | T | C | 2 | a0001c0001t0009g0215 a0001c0001t0022g0204 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1717-179T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059437 | |||||||
| chr5:77059462 | A | G | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1717-154A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059462 | |||||||
| chr5:77059537 | C | T | 3 | a0001c0002t0006g0042 a0001c0002t0006g0331 a0001c0002t0006g0332 |
4 | HG01099.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1717-79C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 11/13 | chr5 | 77059537 | |||||||
| chr5:77059846 | ATTTG | A | 3 | a0001c0002t0003g0032 a0001c0002t0003g0229 a0001c0002t0003g0232 |
4 | HG00735.hp1 HG02055.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844+107_1844+110d others(6): Show |
AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr5 | 77059846 | ||||||
| chr5:77059881 | G | A | 1 | a0002c0003t0002g0056 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1844+138G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77059881 | |||||||
| chr5:77059914 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1844+171T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77059914 | |||||||
| chr5:77060030 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0164 a0001c0001t0001g0178 |
3 | NA19005.hp1 NA19057.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1844+287C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77060030 | |||||||
| chr5:77060280 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1844+537A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77060280 | |||||||
| chr5:77060299 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1844+556C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77060299 | |||||||
| chr5:77060395 | C | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1844+652C>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77060395 | |||||||
| chr5:77060590 | T | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0258 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1844+847T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77060590 | |||||||
| chr5:77060675 | C | G | 11 | a0002c0003t0002g0009 a0002c0003t0002g0018 a0002c0003t0002g0049 others(8): Show |
14 | HG00741.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1844+932C>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77060675 | |||||||
| chr5:77060900 | T | C | 65 | a0002c0003t0002g0001 a0002c0003t0002g0002 a0002c0003t0002g0006 others(62): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1845-803T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77060900 | |||||||
| chr5:77060934 | G | A | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1845-769G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77060934 | |||||||
| chr5:77061076 | A | G | 9 | a0001c0001t0012g0118 a0001c0001t0012g0119 a0001c0001t0012g0133 others(6): Show |
10 | HG01496.hp2 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1845-627A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061076 | |||||||
| chr5:77061115 | T | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1845-588T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061115 | |||||||
| chr5:77061122 | A | G | 1 | a0001c0002t0003g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1845-581A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061122 | |||||||
| chr5:77061148 | G | A | 4 | a0001c0002t0006g0042 a0001c0002t0006g0330 a0001c0002t0006g0331 others(1): Show |
5 | HG01099.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1845-555G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061148 | |||||||
| chr5:77061247 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1845-456C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061247 | |||||||
| chr5:77061313 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0258 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1845-390G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061313 | |||||||
| chr5:77061318 | A | G | 1 | a0001c0002t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1845-385A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061318 | |||||||
| chr5:77061468 | T | G | 1 | a0002c0003t0002g0049 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1845-235T>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061468 | |||||||
| chr5:77061523 | T | C | 4 | a0003c0005t0011g0132 a0003c0005t0011g0180 a0003c0005t0011g0181 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845-180T>C | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061523 | |||||||
| chr5:77061633 | C | T | 1 | a0001c0002t0003g0233 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1845-70C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061633 | |||||||
| chr5:77061699 | A | G | 7 | a0001c0001t0008g0031 a0001c0001t0008g0212 a0001c0001t0008g0213 others(4): Show |
8 | HG02486.hp2 HG02895.hp2 HG02970.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1845-4A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 12/13 | chr5 | 77061699 | |||||||
| chr5:77061875 | G | A | 2 | a0002c0003t0002g0010 a0002c0003t0002g0086 |
4 | HG00280.hp1 HG00639.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944+73G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77061875 | |||||||
| chr5:77061952 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(1): Show |
7 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1944+150A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77061952 | |||||||
| chr5:77062206 | A | G | 6 | a0001c0001t0001g0311 a0001c0001t0001g0318 a0001c0001t0001g0320 others(3): Show |
6 | NA18948.hp2 NA18979.hp2 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.1944+404A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77062206 | |||||||
| chr5:77062255 | C | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0191 others(6): Show |
10 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1944+453C>T | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77062255 | |||||||
| chr5:77062622 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 others(1): Show |
7 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1945-430A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77062622 | |||||||
| chr5:77062752 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0260 |
6 | HG00741.hp2 HG01106.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945-300A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77062752 | |||||||
| chr5:77062818 | A | G | 1 | a0002c0003t0002g0050 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1945-234A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77062818 | |||||||
| chr5:77062897 | A | G | 34 | a0001c0001t0004g0004 a0001c0001t0004g0021 a0001c0001t0004g0022 others(31): Show |
40 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1945-155A>G | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77062897 | |||||||
| chr5:77062962 | T | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1945-90T>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77062962 | |||||||
| chr5:77062972 | G | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0179 a0001c0001t0001g0184 others(10): Show |
14 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1945-80G>A | AGGF1 | ENSG00000164252.13 | transcript | ENST00000312916.12 | protein_coding | 13/13 | chr5 | 77062972 |