Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84289 |
| ensemblid | ENSG00000168395.16 |
| hgncid | 19421 |
| symbol | ING5 |
| name | inhibitor of growth family member 5 |
| refseq_nuc | NM_032329.6 |
| refseq_prot | NP_115705.2 |
| ensembl_nuc | ENST00000313552.11 |
| ensembl_prot | ENSP00000322142.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 241702039 |
| end | 241729478 |
| strand | + |
| ver | v1.2 |
| region | chr2:241702039-241729478 |
| region5000 | chr2:241697039-241734478 |
| regionname0 | ING5_chr2_241702039_241729478 |
| regionname5000 | ING5_chr2_241697039_241734478 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 240 | 393 | 96 | 64 | 175 | 14 | 42 | 131 | ING5_chr2_241697039_241734478 | ING5 | MATAM others(235): Show |
chr2 | 241697039 | 241734478 |
| a0002 | 0/0 | 240 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | MATAM others(235): Show |
chr2 | 241697039 | 241734478 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 720 | 386 | 94 | 59 | 175 | 14 | 42 | ING5_chr2_241697039_241734478 | ING5 | ATGGC others(715): Show |
chr2 | 241697039 | 241734478 | ||
| a0001c0002 | 0/0 | 720 | 2 | 1 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | ATGGC others(715): Show |
chr2 | 241697039 | 241734478 | ||
| a0001c0003 | 0/0 | 720 | 2 | 0 | 2 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | ATGGC others(715): Show |
chr2 | 241697039 | 241734478 | ||
| a0001c0004 | 0/0 | 720 | 2 | 0 | 2 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | ATGGC others(715): Show |
chr2 | 241697039 | 241734478 | ||
| a0001c0006 | 0/0 | 720 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | ATGGC others(715): Show |
chr2 | 241697039 | 241734478 | ||
| a0002c0005 | 0/0 | 720 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | ATGGC others(715): Show |
chr2 | 241697039 | 241734478 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5197 | 68 | 3 | 27 | 30 | 4 | 3 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0002 | 0/0 | 5199 | 54 | 0 | 5 | 46 | 2 | 1 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0003 | 0/0 | 5197 | 52 | 14 | 7 | 22 | 0 | 9 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0004 | 0/0 | 5197 | 28 | 3 | 2 | 16 | 1 | 6 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0005 | 0/0 | 5195 | 25 | 1 | 2 | 14 | 2 | 6 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0006 | 0/0 | 5197 | 16 | 3 | 0 | 7 | 0 | 6 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0007 | 0/0 | 5197 | 12 | 11 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0008 | 0/0 | 5197 | 10 | 10 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0009 | 0/1 | 5197 | 6 | 0 | 2 | 0 | 1 | 2 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0010 | 0/0 | 5189 | 8 | 0 | 0 | 8 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5184): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0011 | 0/0 | 5197 | 8 | 2 | 2 | 0 | 2 | 2 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0012 | 0/0 | 5197 | 7 | 0 | 0 | 7 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0013 | 0/0 | 5197 | 5 | 5 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0014 | 0/0 | 5197 | 5 | 5 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0015 | 0/0 | 5201 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5196): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0016 | 0/0 | 5197 | 4 | 0 | 1 | 0 | 0 | 3 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0017 | 0/0 | 5199 | 4 | 4 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0018 | 0/0 | 5197 | 4 | 1 | 3 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0019 | 0/0 | 5199 | 3 | 0 | 0 | 3 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0020 | 0/0 | 5201 | 3 | 2 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5196): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0021 | 0/0 | 5197 | 3 | 0 | 0 | 1 | 0 | 2 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0022 | 0/0 | 5197 | 3 | 2 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0023 | 0/0 | 5197 | 3 | 0 | 0 | 3 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0024 | 0/0 | 5195 | 3 | 3 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0025 | 0/0 | 5197 | 3 | 3 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0026 | 0/0 | 5197 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0027 | 0/0 | 5195 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0028 | 0/0 | 5197 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0029 | 0/0 | 5197 | 2 | 0 | 1 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0030 | 0/0 | 5197 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0031 | 0/0 | 5197 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0032 | 0/0 | 5199 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0033 | 0/0 | 5197 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0034 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0035 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0036 | 0/0 | 5199 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0037 | 0/0 | 5199 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0038 | 0/0 | 5199 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0039 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0040 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0041 | 0/0 | 5197 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0042 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0043 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0044 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0045 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0046 | 0/0 | 5197 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0047 | 0/0 | 5197 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0048 | 0/0 | 5199 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0049 | 0/0 | 5197 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0050 | 0/0 | 5197 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0051 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0052 | 0/0 | 5197 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0053 | 0/0 | 5197 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0054 | 0/0 | 5199 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0055 | 0/0 | 5197 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0056 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0057 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0058 | 0/0 | 5199 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5194): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0059 | 0/0 | 5197 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0060 | 0/0 | 5197 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0061 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0062 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0063 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0064 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0065 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0001t0066 | 0/0 | 5197 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0002t0015 | 0/0 | 5201 | 2 | 1 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5196): Show |
chr2 | 241697039 | 241734478 |
| a0001c0003t0009 | 0/0 | 5197 | 2 | 0 | 2 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0004t0004 | 0/0 | 5197 | 2 | 0 | 2 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0001c0006t0003 | 0/0 | 5197 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5192): Show |
chr2 | 241697039 | 241734478 |
| a0002c0005t0005 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | AGACC others(5190): Show |
chr2 | 241697039 | 241734478 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0001 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0003 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0006 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0008g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0008g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0008g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0009g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0009g0045 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0009g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0010g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0010g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0010g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0010g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0011g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0011g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0011g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0011g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0012g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0012g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0012g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0013g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0013g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0013g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0013g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0014g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0014g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0015g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0016g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0016g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0016g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0017g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0017g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0018g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0018g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0018g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0019g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0019g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0020g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0020g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0021g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0021g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0022g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0022g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0022g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0023g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0023g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0023g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0024g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0024g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0024g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0025g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0025g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0026g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0026g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0027g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0027g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0028g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0028g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0029g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0029g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0030g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0031g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0031g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0032g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0033g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0034g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0035g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0036g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0037g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0038g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0039g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0040g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0041g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0042g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0043g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0044g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0045g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0046g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0047g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0048g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0049g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0050g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0051g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0052g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0053g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0054g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0055g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0056g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0057g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0058g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0059g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0060g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0061g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0062g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0063g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0064g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0065g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0001t0066g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0002t0015g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0002t0015g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0003t0009g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0004t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0004t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0001c0006t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| a0002c0005t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0029 | g0086 | EUR | GBR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0099 | EUR | GBR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | FIN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | FIN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0006 | EUR | FIN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00408 | hp1 | a0001 | c0001 | t0021 | g0003 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00408 | hp2 | a0001 | c0001 | t0042 | g0006 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0264 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00438 | hp2 | a0001 | c0001 | t0019 | g0251 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0051 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00558 | hp1 | a0001 | c0001 | t0010 | g0019 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00597 | hp2 | a0001 | c0001 | t0045 | g0278 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0277 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00639 | hp1 | a0001 | c0001 | t0058 | g0183 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00642 | hp1 | a0001 | c0001 | t0059 | g0004 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00642 | hp2 | a0001 | c0001 | t0011 | g0069 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00673 | hp1 | a0001 | c0001 | t0055 | g0053 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00673 | hp2 | a0001 | c0001 | t0019 | g0001 | EAS | CHS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0260 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00741 | hp1 | a0001 | c0001 | t0018 | g0070 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG00741 | hp2 | a0001 | c0001 | t0016 | g0043 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01069 | hp1 | a0001 | c0001 | t0018 | g0022 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0261 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01071 | hp1 | a0001 | c0001 | t0018 | g0022 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01074 | hp2 | a0001 | c0003 | t0009 | g0018 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01099 | hp1 | a0001 | c0001 | t0011 | g0028 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01099 | hp2 | a0001 | c0001 | t0022 | g0169 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01106 | hp2 | a0001 | c0001 | t0009 | g0164 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0045 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01109 | hp2 | a0001 | c0001 | t0020 | g0046 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01167 | hp1 | a0001 | c0001 | t0029 | g0089 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0074 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01496 | hp2 | a0001 | c0002 | t0015 | g0220 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01515 | hp1 | a0001 | c0001 | t0011 | g0023 | EUR | IBS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01517 | hp2 | a0001 | c0001 | t0054 | g0096 | EUR | IBS | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01928 | hp1 | a0001 | c0004 | t0004 | g0133 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01928 | hp2 | a0001 | c0001 | t0036 | g0013 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01934 | hp2 | a0001 | c0001 | t0033 | g0203 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01943 | hp1 | a0001 | c0003 | t0009 | g0018 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01952 | hp1 | a0001 | c0004 | t0004 | g0002 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02055 | hp2 | a0001 | c0006 | t0003 | g0056 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02083 | hp1 | a0001 | c0001 | t0049 | g0003 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0161 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02145 | hp2 | a0001 | c0001 | t0028 | g0097 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | CDX | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02155 | hp2 | a0001 | c0001 | t0048 | g0113 | EAS | CDX | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | CDX | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | CDX | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02257 | hp1 | a0001 | c0001 | t0017 | g0016 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0219 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02258 | hp2 | a0001 | c0001 | t0065 | g0079 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02280 | hp1 | a0001 | c0001 | t0017 | g0016 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02451 | hp1 | a0001 | c0001 | t0022 | g0170 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02451 | hp2 | a0001 | c0001 | t0063 | g0085 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02523 | hp1 | a0001 | c0001 | t0032 | g0067 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0268 | EAS | KHV | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02572 | hp1 | a0001 | c0001 | t0018 | g0064 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0068 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0109 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02615 | hp2 | a0001 | c0002 | t0015 | g0221 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02622 | hp1 | a0001 | c0001 | t0014 | g0148 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02622 | hp2 | a0001 | c0001 | t0020 | g0046 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02683 | hp2 | a0001 | c0001 | t0052 | g0142 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02717 | hp1 | a0001 | c0001 | t0064 | g0023 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02723 | hp1 | a0001 | c0001 | t0062 | g0198 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0018 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0100 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02809 | hp1 | a0001 | c0001 | t0026 | g0032 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0105 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0163 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0153 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0027 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0025 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02895 | hp1 | a0001 | c0001 | t0025 | g0020 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02895 | hp2 | a0001 | c0001 | t0057 | g0165 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02897 | hp1 | a0001 | c0001 | t0025 | g0057 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0162 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0060 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02965 | hp1 | a0001 | c0001 | t0039 | g0216 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02970 | hp1 | a0001 | c0001 | t0014 | g0150 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0147 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02976 | hp1 | a0001 | c0001 | t0024 | g0145 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02976 | hp2 | a0001 | c0001 | t0028 | g0093 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0137 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03041 | hp2 | a0001 | c0001 | t0020 | g0218 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03098 | hp1 | a0001 | c0001 | t0022 | g0212 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03098 | hp2 | a0001 | c0001 | t0031 | g0151 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03130 | hp1 | a0001 | c0001 | t0051 | g0082 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0066 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03195 | hp1 | a0001 | c0001 | t0035 | g0015 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03209 | hp1 | a0001 | c0001 | t0034 | g0199 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03225 | hp1 | a0001 | c0001 | t0031 | g0038 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03225 | hp2 | a0001 | c0001 | t0056 | g0040 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03453 | hp1 | a0001 | c0001 | t0027 | g0155 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03453 | hp2 | a0001 | c0001 | t0026 | g0136 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0037 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03491 | hp2 | a0001 | c0001 | t0011 | g0024 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0037 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0222 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03516 | hp2 | a0001 | c0001 | t0061 | g0166 | AFR | ESN | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0065 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03579 | hp1 | a0001 | c0001 | t0014 | g0149 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03654 | hp1 | a0001 | c0001 | t0021 | g0036 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03669 | hp1 | a0001 | c0001 | t0016 | g0043 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0270 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0281 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0129 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0101 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0269 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03834 | hp2 | a0001 | c0001 | t0050 | g0003 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0117 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03927 | hp2 | a0001 | c0001 | t0016 | g0201 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0225 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03942 | hp2 | a0001 | c0001 | t0011 | g0028 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG04184 | hp1 | a0001 | c0001 | t0021 | g0036 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0116 | SAS | BEB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG04199 | hp1 | a0001 | c0001 | t0009 | g0202 | SAS | STU | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | STU | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG04204 | hp1 | a0001 | c0001 | t0016 | g0167 | SAS | STU | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | STU | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0271 | SAS | STU | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0259 | SAS | STU | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | YRI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0071 | AFR | YRI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | CHB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | YRI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18906 | hp2 | a0001 | c0001 | t0017 | g0016 | AFR | YRI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18945 | hp1 | a0001 | c0001 | t0038 | g0246 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18946 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18948 | hp2 | a0001 | c0001 | t0066 | g0180 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18949 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0267 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18957 | hp1 | a0001 | c0001 | t0012 | g0098 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18959 | hp1 | a0002 | c0005 | t0005 | g0274 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18964 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18964 | hp2 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18965 | hp2 | a0001 | c0001 | t0012 | g0083 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18969 | hp2 | a0001 | c0001 | t0030 | g0052 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18973 | hp1 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18977 | hp1 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18980 | hp1 | a0001 | c0001 | t0010 | g0262 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18980 | hp2 | a0001 | c0001 | t0023 | g0185 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18985 | hp2 | a0001 | c0001 | t0046 | g0031 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18990 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0265 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18998 | hp2 | a0001 | c0001 | t0041 | g0158 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18999 | hp2 | a0001 | c0001 | t0053 | g0090 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19001 | hp1 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19001 | hp2 | a0001 | c0001 | t0043 | g0273 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19002 | hp1 | a0001 | c0001 | t0023 | g0181 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0275 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19011 | hp1 | a0001 | c0001 | t0047 | g0140 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0027 | AFR | LWK | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | LWK | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0061 | AFR | LWK | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19054 | hp1 | a0001 | c0001 | t0023 | g0208 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19057 | hp2 | a0001 | c0001 | t0044 | g0266 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19064 | hp1 | a0001 | c0001 | t0019 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19064 | hp2 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19068 | hp1 | a0001 | c0001 | t0030 | g0052 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19084 | hp1 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19088 | hp1 | a0001 | c0001 | t0060 | g0118 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19088 | hp2 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19090 | hp2 | a0001 | c0001 | t0010 | g0263 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0160 | AFR | YRI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA19240 | hp2 | a0001 | c0001 | t0025 | g0020 | AFR | YRI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | ASW | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | ASW | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0272 | EUR | TSI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20752 | hp2 | a0001 | c0001 | t0011 | g0024 | EUR | TSI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20805 | hp1 | a0001 | c0001 | t0009 | g0205 | EUR | TSI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | GIH | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | CLM | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0159 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0025 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG02559 | hp2 | a0001 | c0001 | t0014 | g0038 | AFR | ACB | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03471 | hp1 | a0001 | c0001 | t0024 | g0081 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG03471 | hp2 | a0001 | c0001 | t0027 | g0154 | AFR | MSL | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | USA | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| HG06807 | hp2 | a0001 | c0001 | t0017 | g0124 | AFR | USA | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA20300 | hp2 | a0001 | c0001 | t0024 | g0146 | AFR | USA | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0063 | AFR | LWK | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| NA21309 | hp2 | a0001 | c0001 | t0040 | g0078 | AFR | LWK | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0045 | REF | REF | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0080 | REF | REF | ING5_chr2_241697039_241734478 | ING5 | chr2 | 241697039 | 241734478 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241711984 | G | A | 1 | a0002 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.395G>A | p.Arg132Gln | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/8 | 422/5197 | 395/723 | 132/240 | chr2 | 241711984 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241704702 | A | G | 1 | a0001c0006 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.87A>G | p.Arg29Arg | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/8 | 114/5197 | 87/723 | 29/240 | chr2 | 241704702 | |||
| chr2:241709304 | G | A | 1 | a0001c0002 | 2 | HG01496.hp2 HG02615.hp2 |
synonymous_variant | LOW | c.198G>A | p.Gln66Gln | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/8 | 225/5197 | 198/723 | 66/240 | chr2 | 241709304 | |||
| chr2:241709346 | C | T | 1 | a0001c0004 | 2 | HG01928.hp1 HG01952.hp1 |
synonymous_variant | LOW | c.240C>T | p.Asp80Asp | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/8 | 267/5197 | 240/723 | 80/240 | chr2 | 241709346 | |||
| chr2:241711469 | C | T | 1 | a0001c0003 | 2 | HG01074.hp2 HG01943.hp1 |
synonymous_variant | LOW | c.369C>T | p.Ser123Ser | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 4/8 | 396/5197 | 369/723 | 123/240 | chr2 | 241711469 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241725173 | G | C | 1 | a0001c0001t0032 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*142G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 142 | chr2 | 241725173 | ||||||
| chr2:241725213 | C | T | 1 | a0001c0001t0066 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*182C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 182 | chr2 | 241725213 | ||||||
| chr2:241725317 | C | T | 7 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0017 others(4): Show |
29 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*286C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 286 | chr2 | 241725317 | ||||||
| chr2:241725362 | G | A | 4 | a0001c0001t0009 a0001c0001t0033 a0001c0001t0034 others(1): Show |
9 | HG01074.hp2 HG01106.hp2 HG01109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 331 | chr2 | 241725362 | ||||||
| chr2:241725369 | G | A | 2 | a0001c0001t0006 a0001c0001t0035 |
17 | HG02165.hp1 HG02559.hp1 HG02602.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*338G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 338 | chr2 | 241725369 | ||||||
| chr2:241725380 | T | C | 1 | a0001c0001t0026 | 2 | HG02809.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*349T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 349 | chr2 | 241725380 | ||||||
| chr2:241725444 | C | T | 1 | a0001c0001t0025 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*413C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 413 | chr2 | 241725444 | ||||||
| chr2:241725451 | G | GCA | 6 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0032 others(3): Show |
61 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*422_*423dupAC | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 424 | INFO_REALIGN_3_PRIME | chr2 | 241725451 | |||||
| chr2:241725462 | C | G | 2 | a0001c0001t0014 a0001c0001t0031 |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*431C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 431 | chr2 | 241725462 | ||||||
| chr2:241725538 | T | C | 2 | a0001c0001t0014 a0001c0001t0031 |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*507T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 507 | chr2 | 241725538 | ||||||
| chr2:241725555 | C | T | 2 | a0001c0001t0024 a0001c0001t0063 |
4 | HG02451.hp2 HG02976.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*524C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 524 | chr2 | 241725555 | ||||||
| chr2:241725556 | G | A | 1 | a0001c0001t0020 | 3 | HG01109.hp2 HG02622.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*525G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 525 | chr2 | 241725556 | ||||||
| chr2:241725564 | T | C | 54 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(51): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*533T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 533 | chr2 | 241725564 | ||||||
| chr2:241725593 | T | C | 20 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(17): Show |
113 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*562T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 562 | chr2 | 241725593 | ||||||
| chr2:241725614 | C | T | 1 | a0001c0001t0038 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 583 | chr2 | 241725614 | ||||||
| chr2:241725627 | T | C | 1 | a0001c0001t0023 | 3 | NA18980.hp2 NA19002.hp1 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*596T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 596 | chr2 | 241725627 | ||||||
| chr2:241725827 | T | C | 1 | a0001c0001t0042 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 796 | chr2 | 241725827 | ||||||
| chr2:241725828 | CTG | C | 15 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0015 others(12): Show |
53 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*803_*804delGT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 803 | INFO_REALIGN_3_PRIME | chr2 | 241725828 | |||||
| chr2:241725883 | T | C | 2 | a0001c0001t0046 a0001c0001t0047 |
2 | NA18985.hp2 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*852T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 852 | chr2 | 241725883 | ||||||
| chr2:241725905 | A | G | 57 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(54): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*874A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 874 | chr2 | 241725905 | ||||||
| chr2:241726040 | G | A | 15 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0015 others(12): Show |
56 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1009G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1009 | chr2 | 241726040 | ||||||
| chr2:241726187 | G | C | 47 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(44): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*1156G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1156 | chr2 | 241726187 | ||||||
| chr2:241726295 | T | C | 1 | a0001c0001t0046 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1264T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1264 | chr2 | 241726295 | ||||||
| chr2:241726432 | C | T | 10 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0029 others(7): Show |
46 | HG00140.hp1 HG00140.hp2 HG00673.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1401C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1401 | chr2 | 241726432 | ||||||
| chr2:241726521 | T | C | 2 | a0001c0001t0014 a0001c0001t0031 |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1490T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1490 | chr2 | 241726521 | ||||||
| chr2:241726573 | G | A | 1 | a0001c0001t0029 | 2 | HG00140.hp1 HG01167.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1542G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1542 | chr2 | 241726573 | ||||||
| chr2:241726603 | C | G | 1 | a0001c0001t0036 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1572C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1572 | chr2 | 241726603 | ||||||
| chr2:241726692 | C | T | 3 | a0001c0001t0015 a0001c0001t0020 a0001c0002t0015 |
7 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1661C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1661 | chr2 | 241726692 | ||||||
| chr2:241726705 | C | T | 9 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0011 others(6): Show |
42 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1674C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1674 | chr2 | 241726705 | ||||||
| chr2:241726723 | G | A | 2 | a0001c0001t0012 a0001c0001t0053 |
8 | NA18946.hp2 NA18949.hp2 NA18957.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1692G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1692 | chr2 | 241726723 | ||||||
| chr2:241726757 | T | C | 51 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(48): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*1726T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1726 | chr2 | 241726757 | ||||||
| chr2:241726763 | C | T | 1 | a0001c0001t0064 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1732C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1732 | chr2 | 241726763 | ||||||
| chr2:241726779 | G | A | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(47): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*1748G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1748 | chr2 | 241726779 | ||||||
| chr2:241726809 | T | G | 1 | a0001c0001t0057 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1778T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1778 | chr2 | 241726809 | ||||||
| chr2:241726870 | C | G | 1 | a0001c0001t0035 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1839C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1839 | chr2 | 241726870 | ||||||
| chr2:241726914 | C | T | 1 | a0001c0001t0033 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1883C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1883 | chr2 | 241726914 | ||||||
| chr2:241726920 | C | G | 1 | a0001c0001t0051 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1889C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1889 | chr2 | 241726920 | ||||||
| chr2:241726945 | G | A | 1 | a0001c0001t0022 | 3 | HG01099.hp2 HG02451.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1914G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 1914 | chr2 | 241726945 | ||||||
| chr2:241727229 | G | A | 5 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0015 others(2): Show |
17 | HG01109.hp2 HG01496.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2198G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 2198 | chr2 | 241727229 | ||||||
| chr2:241727277 | C | T | 1 | a0001c0001t0053 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2246C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 2246 | chr2 | 241727277 | ||||||
| chr2:241727285 | T | TTG | 5 | a0001c0001t0017 a0001c0001t0048 a0001c0001t0054 others(2): Show |
8 | HG00639.hp1 HG01517.hp2 HG02155.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2276_*2277dupGT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 2278 | INFO_REALIGN_3_PRIME | chr2 | 241727285 | |||||
| chr2:241727285 | T | TTGTGTG | 3 | a0001c0001t0015 a0001c0001t0020 a0001c0002t0015 |
7 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2272_*2277dupGTGT others(2): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 2278 | INFO_REALIGN_3_PRIME | chr2 | 241727285 | |||||
| chr2:241727618 | A | G | 1 | a0001c0001t0024 | 3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2587A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 2587 | chr2 | 241727618 | ||||||
| chr2:241727645 | C | A | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(33): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2614C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 2614 | chr2 | 241727645 | ||||||
| chr2:241727704 | A | G | 1 | a0001c0001t0062 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2673A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 2673 | chr2 | 241727704 | ||||||
| chr2:241727734 | A | G | 3 | a0001c0001t0011 a0001c0001t0064 a0001c0001t0065 |
10 | HG00642.hp2 HG01099.hp1 HG01515.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2703A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 2703 | chr2 | 241727734 | ||||||
| chr2:241728151 | G | A | 1 | a0001c0001t0049 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3120G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3120 | chr2 | 241728151 | ||||||
| chr2:241728210 | C | T | 1 | a0001c0001t0044 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3179C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3179 | chr2 | 241728210 | ||||||
| chr2:241728262 | G | A | 1 | a0001c0001t0030 | 2 | NA18969.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3231G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3231 | chr2 | 241728262 | ||||||
| chr2:241728347 | C | T | 3 | a0001c0001t0015 a0001c0001t0020 a0001c0002t0015 |
7 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3316C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3316 | chr2 | 241728347 | ||||||
| chr2:241728348 | G | A | 2 | a0001c0001t0039 a0001c0001t0055 |
2 | HG00673.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3317G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3317 | chr2 | 241728348 | ||||||
| chr2:241728428 | G | T | 1 | a0001c0001t0043 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3397G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3397 | chr2 | 241728428 | ||||||
| chr2:241728455 | G | C | 7 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0033 others(4): Show |
16 | HG01074.hp2 HG01106.hp2 HG01109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3424G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3424 | chr2 | 241728455 | ||||||
| chr2:241728478 | T | G | 22 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(19): Show |
128 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*3447T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3447 | chr2 | 241728478 | ||||||
| chr2:241728479 | A | G | 52 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(49): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*3448A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3448 | chr2 | 241728479 | ||||||
| chr2:241728567 | G | C | 1 | a0001c0001t0028 | 2 | HG02145.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3536G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3536 | chr2 | 241728567 | ||||||
| chr2:241728635 | A | G | 60 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(57): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*3604A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3604 | chr2 | 241728635 | ||||||
| chr2:241728652 | G | A | 4 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0027 others(1): Show |
9 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3621G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3621 | chr2 | 241728652 | ||||||
| chr2:241728655 | T | G | 9 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0024 others(6): Show |
42 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3624T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3624 | chr2 | 241728655 | ||||||
| chr2:241728673 | C | T | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*3642C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3642 | chr2 | 241728673 | ||||||
| chr2:241728674 | G | A | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(45): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3643G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3643 | chr2 | 241728674 | ||||||
| chr2:241728674 | GCCCGT | G | 1 | a0001c0001t0010 | 8 | HG00558.hp1 NA18973.hp1 NA18977.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3645_*3649delCCGT others(1): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3645 | INFO_REALIGN_3_PRIME | chr2 | 241728674 | |||||
| chr2:241728683 | A | C | 5 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0036 others(2): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3652A>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3652 | chr2 | 241728683 | ||||||
| chr2:241728683 | AT | A | 1 | a0001c0001t0010 | 8 | HG00558.hp1 NA18973.hp1 NA18977.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3653delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3653 | chr2 | 241728683 | ||||||
| chr2:241728739 | C | T | 9 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0024 others(6): Show |
42 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3708C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3708 | chr2 | 241728739 | ||||||
| chr2:241728740 | G | A | 1 | a0001c0001t0039 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3709G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3709 | chr2 | 241728740 | ||||||
| chr2:241728778 | C | T | 1 | a0001c0001t0018 | 4 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3747C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3747 | chr2 | 241728778 | ||||||
| chr2:241728898 | A | G | 1 | a0001c0001t0059 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3867A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3867 | chr2 | 241728898 | ||||||
| chr2:241728957 | T | C | 4 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0027 others(1): Show |
9 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3926T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 3926 | chr2 | 241728957 | ||||||
| chr2:241729120 | T | C | 52 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(49): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*4089T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 4089 | chr2 | 241729120 | ||||||
| chr2:241729178 | C | G | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4147C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 4147 | chr2 | 241729178 | ||||||
| chr2:241729344 | A | G | 1 | a0001c0001t0019 | 3 | HG00438.hp2 HG00673.hp2 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4313A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 4313 | chr2 | 241729344 | ||||||
| chr2:241729424 | C | A | 1 | a0001c0001t0054 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4393C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 8/8 | 4393 | chr2 | 241729424 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241702134 | G | T | 1 | a0001c0001t0030g0052 | 2 | NA18969.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.37+32G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702134 | |||||||
| chr2:241702151 | C | T | 80 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(77): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.37+49C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702151 | |||||||
| chr2:241702199 | C | T | 1 | a0001c0001t0005g0281 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.37+97C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702199 | |||||||
| chr2:241702275 | AGGGCGCG others(6): Show |
A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.37+186_37+198delCG others(11): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 241702275 | ||||||
| chr2:241702289 | G | A | 6 | a0001c0001t0015g0219 a0001c0001t0015g0222 a0001c0001t0020g0046 others(3): Show |
7 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.37+187G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702289 | |||||||
| chr2:241702294 | C | CG | 7 | a0001c0001t0001g0055 a0001c0001t0002g0223 a0001c0001t0002g0224 others(4): Show |
7 | HG00673.hp1 HG02055.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.37+198dupG | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 241702294 | ||||||
| chr2:241702380 | T | G | 5 | a0001c0001t0007g0058 a0001c0001t0007g0059 a0001c0001t0007g0060 others(2): Show |
6 | HG01884.hp1 HG02109.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+278T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702380 | |||||||
| chr2:241702388 | G | T | 2 | a0001c0001t0039g0216 a0001c0006t0003g0056 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.37+286G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702388 | |||||||
| chr2:241702449 | C | T | 36 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(33): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.37+347C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702449 | |||||||
| chr2:241702510 | CGGGGCTC others(9): Show |
C | 36 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(33): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.37+420_37+435delCC others(14): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 241702510 | ||||||
| chr2:241702556 | CTGTGCGC others(3): Show |
C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG00733.hp2 HG01496.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.37+463_37+472delCG others(8): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 241702556 | ||||||
| chr2:241702602 | G | C | 1 | a0001c0001t0005g0281 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.37+500G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702602 | |||||||
| chr2:241702616 | C | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(76): Show |
105 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.37+514C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702616 | |||||||
| chr2:241702704 | T | C | 1 | a0001c0001t0041g0158 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.37+602T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702704 | |||||||
| chr2:241702707 | A | T | 2 | a0001c0001t0004g0039 a0001c0001t0004g0157 |
3 | NA18955.hp2 NA18997.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.37+605A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702707 | |||||||
| chr2:241702747 | G | A | 2 | a0001c0001t0005g0225 a0001c0001t0005g0259 |
2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.37+645G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702747 | |||||||
| chr2:241702779 | T | C | 80 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(77): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.37+677T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702779 | |||||||
| chr2:241702817 | C | T | 1 | a0001c0001t0003g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.37+715C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702817 | |||||||
| chr2:241702862 | A | T | 80 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(77): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.37+760A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241702862 | |||||||
| chr2:241703071 | G | C | 1 | a0001c0001t0008g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.37+969G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703071 | |||||||
| chr2:241703395 | G | C | 28 | a0001c0001t0003g0062 a0001c0001t0007g0021 a0001c0001t0007g0071 others(25): Show |
35 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.38-1258G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703395 | |||||||
| chr2:241703400 | C | T | 44 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(41): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.38-1253C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703400 | |||||||
| chr2:241703438 | C | G | 202 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(199): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.38-1215C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703438 | |||||||
| chr2:241703587 | C | CAG | 299 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(296): Show |
390 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.38-1060_38-1059dup others(2): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 241703587 | ||||||
| chr2:241703612 | C | G | 1 | a0001c0001t0015g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.38-1041C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703612 | |||||||
| chr2:241703693 | C | T | 1 | a0001c0001t0065g0079 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.38-960C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703693 | |||||||
| chr2:241703806 | A | G | 3 | a0001c0001t0003g0017 a0001c0001t0003g0143 a0001c0001t0003g0144 |
5 | HG01081.hp1 HG01123.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.38-847A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703806 | |||||||
| chr2:241703904 | C | A | 5 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.38-749C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703904 | |||||||
| chr2:241703939 | C | G | 1 | a0001c0001t0022g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.38-714C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703939 | |||||||
| chr2:241703966 | A | G | 198 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(195): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.38-687A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241703966 | |||||||
| chr2:241704038 | A | G | 111 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0013 others(108): Show |
143 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.38-615A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704038 | |||||||
| chr2:241704055 | G | A | 3 | a0001c0001t0024g0081 a0001c0001t0024g0145 a0001c0001t0024g0146 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.38-598G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704055 | |||||||
| chr2:241704056 | G | C | 28 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(25): Show |
35 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.38-597G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704056 | |||||||
| chr2:241704080 | A | G | 1 | a0001c0001t0003g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.38-573A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704080 | |||||||
| chr2:241704150 | C | T | 81 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0013 others(78): Show |
106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.38-503C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704150 | |||||||
| chr2:241704189 | C | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG01070.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.38-464C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704189 | |||||||
| chr2:241704194 | A | G | 81 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0013 others(78): Show |
106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.38-459A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704194 | |||||||
| chr2:241704220 | C | T | 28 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(25): Show |
35 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.38-433C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704220 | |||||||
| chr2:241704225 | C | T | 1 | a0001c0001t0023g0208 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.38-428C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704225 | |||||||
| chr2:241704402 | A | T | 80 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(77): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.38-251A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704402 | |||||||
| chr2:241704476 | G | A | 1 | a0001c0001t0009g0164 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.38-177G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704476 | |||||||
| chr2:241704519 | G | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18963.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.38-134G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704519 | |||||||
| chr2:241704583 | G | A | 110 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(107): Show |
142 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.38-70G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 1/7 | chr2 | 241704583 | |||||||
| chr2:241704758 | A | G | 80 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(77): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.109+34A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241704758 | |||||||
| chr2:241704894 | T | C | 80 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(77): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.109+170T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241704894 | |||||||
| chr2:241704937 | T | C | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(198): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.109+213T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241704937 | |||||||
| chr2:241705027 | G | T | 1 | a0001c0001t0047g0140 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.109+303G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705027 | |||||||
| chr2:241705032 | G | A | 1 | a0001c0001t0051g0082 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.109+308G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705032 | |||||||
| chr2:241705079 | G | A | 30 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(27): Show |
37 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.109+355G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705079 | |||||||
| chr2:241705083 | C | G | 1 | a0001c0001t0015g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.109+359C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705083 | |||||||
| chr2:241705098 | G | A | 1 | a0001c0001t0014g0147 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.109+374G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705098 | |||||||
| chr2:241705113 | C | T | 3 | a0001c0001t0015g0222 a0001c0001t0027g0154 a0001c0001t0027g0155 |
3 | HG03453.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+389C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705113 | |||||||
| chr2:241705290 | G | A | 1 | a0001c0001t0030g0052 | 2 | NA18969.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.109+566G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705290 | |||||||
| chr2:241705310 | C | T | 8 | a0001c0001t0003g0204 a0001c0001t0009g0018 a0001c0001t0009g0045 others(5): Show |
9 | HG01074.hp2 HG01106.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+586C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705310 | |||||||
| chr2:241705313 | C | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(77): Show |
106 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.109+589C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705313 | |||||||
| chr2:241705317 | A | G | 1 | a0001c0001t0016g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.109+593A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705317 | |||||||
| chr2:241705346 | G | A | 30 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(27): Show |
37 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.109+622G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705346 | |||||||
| chr2:241705358 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.109+634G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705358 | |||||||
| chr2:241705366 | C | T | 1 | a0001c0001t0040g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109+642C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705366 | |||||||
| chr2:241705386 | G | GTTTC | 46 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(43): Show |
63 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.109+665_109+666ins others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241705386 | ||||||
| chr2:241705386 | G | T | 30 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(27): Show |
37 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.109+662G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705386 | |||||||
| chr2:241705388 | T | TTCTTTTT others(3): Show |
8 | a0001c0001t0002g0224 a0001c0001t0005g0014 a0001c0001t0005g0276 others(5): Show |
10 | HG00597.hp2 HG00621.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+665_109+666ins others(10): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241705388 | ||||||
| chr2:241705389 | T | TCTTTTTT others(2): Show |
26 | a0001c0001t0002g0223 a0001c0001t0002g0255 a0001c0001t0002g0256 others(23): Show |
32 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.109+665_109+666ins others(9): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705389 | |||||||
| chr2:241705394 | C | CT | 11 | a0001c0001t0003g0137 a0001c0001t0003g0138 a0001c0001t0004g0132 others(8): Show |
12 | HG00735.hp1 HG01099.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+691dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241705394 | ||||||
| chr2:241705394 | C | CTTTT | 28 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0048 others(25): Show |
44 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.109+688_109+691dup others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241705394 | ||||||
| chr2:241705394 | C | T | 34 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0255 others(31): Show |
42 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.109+670C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705394 | |||||||
| chr2:241705394 | CT | C | 10 | a0001c0001t0004g0084 a0001c0001t0007g0021 a0001c0001t0012g0083 others(7): Show |
11 | HG00673.hp1 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+691delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241705394 | ||||||
| chr2:241705398 | T | TC | 4 | a0001c0001t0001g0044 a0001c0001t0001g0200 a0001c0001t0013g0162 others(1): Show |
5 | HG02818.hp1 HG02897.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+674_109+675ins others(1): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705398 | |||||||
| chr2:241705399 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(78): Show |
106 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.109+675T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705399 | |||||||
| chr2:241705400 | T | C | 2 | a0001c0001t0025g0057 a0001c0001t0057g0165 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.109+676T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705400 | |||||||
| chr2:241705401 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0143 a0001c0001t0003g0144 |
5 | HG01081.hp1 HG01123.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+677T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705401 | |||||||
| chr2:241705408 | T | TTTTC | 13 | a0001c0001t0002g0047 a0001c0001t0002g0227 a0001c0001t0002g0228 others(10): Show |
14 | HG01952.hp2 HG01981.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.109+687_109+688ins others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241705408 | ||||||
| chr2:241705436 | T | C | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(163): Show |
217 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.109+712T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705436 | |||||||
| chr2:241705527 | A | T | 1 | a0001c0001t0003g0131 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.109+803A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705527 | |||||||
| chr2:241705636 | G | A | 1 | a0001c0001t0029g0086 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.109+912G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705636 | |||||||
| chr2:241705693 | A | C | 80 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(77): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.109+969A>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705693 | |||||||
| chr2:241705828 | C | T | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.109+1104C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241705828 | |||||||
| chr2:241705982 | T | TAACTTTG others(316): Show |
2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.109+1275_109+1276i others(325): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241705982 | ||||||
| chr2:241705982 | T | TAACTTTG others(316): Show |
1 | a0001c0001t0039g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.109+1275_109+1276i others(325): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241705982 | ||||||
| chr2:241706051 | G | A | 184 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(181): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.109+1327G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706051 | |||||||
| chr2:241706173 | A | G | 8 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(5): Show |
9 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+1449A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706173 | |||||||
| chr2:241706174 | C | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.109+1450C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706174 | |||||||
| chr2:241706220 | C | T | 2 | a0001c0001t0008g0026 a0001c0001t0008g0027 |
4 | HG02647.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+1496C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706220 | |||||||
| chr2:241706222 | C | A | 1 | a0001c0001t0014g0147 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.109+1498C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706222 | |||||||
| chr2:241706445 | C | T | 1 | a0001c0001t0002g0238 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.109+1721C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706445 | |||||||
| chr2:241706477 | A | C | 43 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(40): Show |
52 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.109+1753A>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706477 | |||||||
| chr2:241706496 | G | A | 37 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(34): Show |
46 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.109+1772G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706496 | |||||||
| chr2:241706497 | C | T | 1 | a0001c0001t0003g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.109+1773C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706497 | |||||||
| chr2:241706508 | A | G | 37 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(34): Show |
46 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.109+1784A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706508 | |||||||
| chr2:241706527 | G | C | 1 | a0001c0001t0008g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.109+1803G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706527 | |||||||
| chr2:241706559 | C | T | 3 | a0001c0001t0024g0081 a0001c0001t0024g0145 a0001c0001t0024g0146 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.109+1835C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706559 | |||||||
| chr2:241706625 | C | CA | 63 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(60): Show |
88 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.109+1919dupA | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241706625 | ||||||
| chr2:241706625 | C | CAA | 6 | a0001c0001t0001g0168 a0001c0001t0001g0209 a0001c0001t0007g0058 others(3): Show |
6 | HG01433.hp1 HG01981.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+1918_109+1919d others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241706625 | ||||||
| chr2:241706625 | CA | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(117): Show |
152 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.109+1919delA | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241706625 | ||||||
| chr2:241706625 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0015g0219 a0001c0001t0015g0222 a0001c0001t0020g0046 others(3): Show |
7 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+1911_109+1919d others(11): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241706625 | ||||||
| chr2:241706683 | C | T | 1 | a0001c0001t0006g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.109+1959C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706683 | |||||||
| chr2:241706776 | C | T | 1 | a0001c0001t0055g0053 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.109+2052C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706776 | |||||||
| chr2:241706863 | A | AT | 31 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(28): Show |
38 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.109+2149dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241706863 | ||||||
| chr2:241706935 | A | G | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(198): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.109+2211A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241706935 | |||||||
| chr2:241706956 | A | AT | 122 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(119): Show |
160 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.110-2240dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241706956 | ||||||
| chr2:241706956 | A | ATT | 10 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(7): Show |
10 | HG00741.hp1 HG03098.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-2241_110-2240d others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241706956 | ||||||
| chr2:241707051 | C | T | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(65): Show |
93 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.110-2165C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707051 | |||||||
| chr2:241707072 | G | C | 1 | a0001c0001t0062g0198 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.110-2144G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707072 | |||||||
| chr2:241707084 | C | T | 2 | a0001c0001t0003g0131 a0001c0001t0003g0217 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.110-2132C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707084 | |||||||
| chr2:241707109 | A | G | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(198): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.110-2107A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707109 | |||||||
| chr2:241707158 | C | T | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.110-2058C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707158 | |||||||
| chr2:241707227 | G | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(68): Show |
96 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.110-1989G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707227 | |||||||
| chr2:241707294 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.110-1922G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707294 | |||||||
| chr2:241707295 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.110-1921T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707295 | |||||||
| chr2:241707539 | C | A | 1 | a0001c0001t0014g0147 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.110-1677C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707539 | |||||||
| chr2:241707763 | G | T | 47 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(44): Show |
63 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.110-1453G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707763 | |||||||
| chr2:241707782 | A | G | 27 | a0001c0001t0005g0006 a0001c0001t0005g0051 a0001c0001t0005g0225 others(24): Show |
32 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.110-1434A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707782 | |||||||
| chr2:241707929 | C | T | 1 | a0001c0001t0039g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-1287C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707929 | |||||||
| chr2:241707966 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.110-1250C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707966 | |||||||
| chr2:241707989 | C | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
47 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.110-1227C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241707989 | |||||||
| chr2:241708036 | C | T | 46 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(43): Show |
62 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.110-1180C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708036 | |||||||
| chr2:241708057 | C | T | 3 | a0001c0001t0003g0017 a0001c0001t0003g0143 a0001c0001t0003g0144 |
5 | HG01081.hp1 HG01123.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-1159C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708057 | |||||||
| chr2:241708120 | T | C | 4 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0076 others(1): Show |
5 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1096T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708120 | |||||||
| chr2:241708131 | C | T | 1 | a0001c0001t0063g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.110-1085C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708131 | |||||||
| chr2:241708150 | C | G | 5 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-1066C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708150 | |||||||
| chr2:241708185 | C | T | 1 | a0001c0001t0052g0142 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.110-1031C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708185 | |||||||
| chr2:241708213 | GT | G | 6 | a0001c0001t0001g0187 a0001c0001t0002g0227 a0001c0001t0008g0063 others(3): Show |
7 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-991delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 241708213 | ||||||
| chr2:241708245 | T | C | 1 | a0001c0006t0003g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.110-971T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708245 | |||||||
| chr2:241708299 | C | G | 2 | a0001c0001t0011g0068 a0001c0001t0011g0069 |
2 | HG00642.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.110-917C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708299 | |||||||
| chr2:241708308 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.110-908C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708308 | |||||||
| chr2:241708353 | A | G | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(198): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.110-863A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708353 | |||||||
| chr2:241708369 | G | A | 2 | a0001c0001t0022g0169 a0001c0001t0022g0212 |
2 | HG01099.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110-847G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708369 | |||||||
| chr2:241708420 | G | A | 1 | a0001c0001t0040g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.110-796G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708420 | |||||||
| chr2:241708458 | C | T | 1 | a0001c0001t0040g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.110-758C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708458 | |||||||
| chr2:241708564 | A | G | 1 | a0001c0001t0014g0147 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.110-652A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708564 | |||||||
| chr2:241708645 | G | A | 4 | a0001c0001t0002g0047 a0001c0001t0002g0228 a0001c0001t0002g0229 others(1): Show |
5 | HG02132.hp1 NA18957.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-571G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708645 | |||||||
| chr2:241708691 | C | T | 1 | a0001c0001t0039g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-525C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708691 | |||||||
| chr2:241708770 | T | C | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.110-446T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708770 | |||||||
| chr2:241708787 | G | A | 1 | a0001c0006t0003g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.110-429G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708787 | |||||||
| chr2:241708869 | A | G | 2 | a0001c0001t0009g0045 a0001c0001t0009g0164 |
2 | HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.110-347A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708869 | |||||||
| chr2:241708919 | C | A | 2 | a0001c0001t0003g0030 a0001c0001t0003g0087 |
3 | HG01167.hp2 HG01169.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.110-297C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241708919 | |||||||
| chr2:241709007 | C | T | 1 | a0001c0001t0019g0251 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.110-209C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241709007 | |||||||
| chr2:241709012 | C | G | 1 | a0001c0001t0007g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.110-204C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241709012 | |||||||
| chr2:241709130 | C | T | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(72): Show |
101 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.110-86C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241709130 | |||||||
| chr2:241709131 | G | A | 44 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(41): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.110-85G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241709131 | |||||||
| chr2:241709134 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(72): Show |
101 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.110-82G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241709134 | |||||||
| chr2:241709140 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.110-76C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 2/7 | chr2 | 241709140 | |||||||
| chr2:241709461 | C | T | 3 | a0001c0001t0024g0081 a0001c0001t0024g0145 a0001c0001t0024g0146 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.276+79C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241709461 | |||||||
| chr2:241709555 | G | GT | 109 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0030 others(106): Show |
144 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.276+191dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 241709555 | ||||||
| chr2:241709555 | G | GTT | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(86): Show |
115 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.276+190_276+191dup others(2): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 241709555 | ||||||
| chr2:241709562 | T | TTG | 46 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(43): Show |
62 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.276+181_276+182ins others(2): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 241709562 | ||||||
| chr2:241709640 | T | C | 1 | a0001c0001t0034g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276+258T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241709640 | |||||||
| chr2:241709692 | C | T | 44 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(41): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.276+310C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241709692 | |||||||
| chr2:241709832 | C | T | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+450C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241709832 | |||||||
| chr2:241709896 | C | T | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.276+514C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241709896 | |||||||
| chr2:241709921 | TTTTATTT others(6): Show |
T | 1 | a0001c0001t0005g0267 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.276+560_276+572del others(13): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 241709921 | ||||||
| chr2:241709938 | A | T | 6 | a0001c0001t0003g0122 a0001c0001t0013g0159 a0001c0001t0013g0160 others(3): Show |
6 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+556A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241709938 | |||||||
| chr2:241709939 | T | A | 6 | a0001c0001t0003g0122 a0001c0001t0013g0159 a0001c0001t0013g0160 others(3): Show |
6 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+557T>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241709939 | |||||||
| chr2:241709982 | G | A | 66 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(63): Show |
91 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.276+600G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241709982 | |||||||
| chr2:241710020 | G | T | 28 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(25): Show |
35 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.276+638G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710020 | |||||||
| chr2:241710103 | T | TTTA | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
101 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.276+736_276+738dup others(3): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 241710103 | ||||||
| chr2:241710116 | T | TTAG | 8 | a0001c0001t0003g0204 a0001c0001t0009g0018 a0001c0001t0009g0045 others(5): Show |
9 | HG01074.hp2 HG01106.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.276+736_276+737ins others(3): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 241710116 | ||||||
| chr2:241710216 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.276+834C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710216 | |||||||
| chr2:241710261 | G | A | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+879G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710261 | |||||||
| chr2:241710342 | G | A | 47 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(44): Show |
63 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.276+960G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710342 | |||||||
| chr2:241710351 | A | G | 4 | a0001c0001t0003g0033 a0001c0001t0003g0103 a0001c0001t0003g0104 others(1): Show |
5 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+969A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710351 | |||||||
| chr2:241710378 | G | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(237): Show |
317 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.276+996G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710378 | |||||||
| chr2:241710379 | T | G | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+997T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710379 | |||||||
| chr2:241710587 | C | T | 1 | a0001c0001t0005g0261 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.277-790C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710587 | |||||||
| chr2:241710689 | G | C | 3 | a0001c0001t0006g0015 a0001c0001t0006g0105 a0001c0001t0035g0015 |
4 | HG02559.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-688G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710689 | |||||||
| chr2:241710711 | C | T | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.277-666C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710711 | |||||||
| chr2:241710764 | A | G | 1 | a0001c0001t0007g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.277-613A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710764 | |||||||
| chr2:241710773 | C | T | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.277-604C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710773 | |||||||
| chr2:241710858 | C | T | 3 | a0001c0001t0003g0032 a0001c0001t0026g0032 a0001c0001t0026g0136 |
3 | HG02647.hp1 HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.277-519C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241710858 | |||||||
| chr2:241711008 | C | A | 44 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(41): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.277-369C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241711008 | |||||||
| chr2:241711082 | G | A | 1 | a0001c0001t0040g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.277-295G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241711082 | |||||||
| chr2:241711132 | T | A | 1 | a0001c0006t0003g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.277-245T>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241711132 | |||||||
| chr2:241711219 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(69): Show |
97 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.277-158G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241711219 | |||||||
| chr2:241711345 | T | C | 1 | a0001c0001t0002g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.277-32T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 3/7 | chr2 | 241711345 | |||||||
| chr2:241711708 | CTGGGCAA others(9): Show |
C | 1 | a0001c0001t0062g0198 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.388+221_388+236del others(16): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 4/7 | chr2 | 241711708 | |||||||
| chr2:241711714 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.388+226A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 4/7 | chr2 | 241711714 | |||||||
| chr2:241711715 | A | G | 1 | a0001c0001t0002g0231 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.388+227A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 4/7 | chr2 | 241711715 | |||||||
| chr2:241711785 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18963.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.389-193C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 4/7 | chr2 | 241711785 | |||||||
| chr2:241711829 | A | G | 1 | a0001c0001t0008g0153 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.389-149A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 4/7 | chr2 | 241711829 | |||||||
| chr2:241711916 | A | C | 36 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(33): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.389-62A>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 4/7 | chr2 | 241711916 | |||||||
| chr2:241712174 | G | A | 2 | a0001c0001t0018g0022 a0001c0001t0018g0070 |
3 | HG00741.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.482+103G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712174 | |||||||
| chr2:241712180 | C | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(48): Show |
67 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.482+109C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712180 | |||||||
| chr2:241712200 | A | C | 1 | a0001c0001t0002g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.482+129A>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712200 | |||||||
| chr2:241712206 | C | T | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+135C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712206 | |||||||
| chr2:241712209 | G | A | 1 | a0001c0001t0003g0106 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.482+138G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712209 | |||||||
| chr2:241712227 | C | T | 3 | a0001c0001t0022g0169 a0001c0001t0022g0170 a0001c0001t0022g0212 |
3 | HG01099.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.482+156C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712227 | |||||||
| chr2:241712263 | GC | G | 46 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(43): Show |
62 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.482+193delC | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712263 | |||||||
| chr2:241712313 | C | T | 1 | a0001c0001t0003g0138 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.482+242C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712313 | |||||||
| chr2:241712411 | T | C | 1 | a0001c0001t0039g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.482+340T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712411 | |||||||
| chr2:241712425 | T | C | 1 | a0001c0001t0011g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.482+354T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712425 | |||||||
| chr2:241712467 | AGTTATTT others(47): Show |
A | 1 | a0001c0001t0002g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.482+397_482+450del others(54): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712467 | |||||||
| chr2:241712581 | G | A | 46 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(43): Show |
62 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.482+510G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712581 | |||||||
| chr2:241712592 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.482+521C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712592 | |||||||
| chr2:241712595 | A | T | 1 | a0001c0001t0003g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.482+524A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712595 | |||||||
| chr2:241712700 | C | T | 29 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0048 others(26): Show |
44 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.482+629C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712700 | |||||||
| chr2:241712935 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.482+864G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712935 | |||||||
| chr2:241712957 | C | T | 2 | a0001c0001t0017g0016 a0001c0001t0017g0124 |
4 | HG02257.hp1 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+886C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241712957 | |||||||
| chr2:241713000 | C | CA | 141 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(138): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.482+941dupA | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241713000 | ||||||
| chr2:241713002 | A | G | 28 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(25): Show |
35 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.482+931A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713002 | |||||||
| chr2:241713058 | C | CT | 42 | a0001c0001t0002g0254 a0001c0001t0002g0258 a0001c0001t0003g0119 others(39): Show |
49 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.482+1002dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241713058 | ||||||
| chr2:241713159 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.482+1088C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713159 | |||||||
| chr2:241713354 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482+1283G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713354 | |||||||
| chr2:241713367 | G | GT | 44 | a0001c0001t0001g0186 a0001c0001t0002g0252 a0001c0001t0002g0253 others(41): Show |
53 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.482+1317dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241713367 | ||||||
| chr2:241713367 | G | GTT | 8 | a0001c0001t0001g0207 a0001c0001t0005g0264 a0001c0001t0005g0275 others(5): Show |
8 | HG00423.hp2 HG00621.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.482+1316_482+1317d others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241713367 | ||||||
| chr2:241713367 | G | GTTTT | 6 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.482+1314_482+1317d others(6): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241713367 | ||||||
| chr2:241713367 | GT | G | 11 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0002g0243 others(8): Show |
11 | HG01261.hp2 HG01517.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+1317delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241713367 | ||||||
| chr2:241713410 | C | A | 235 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(232): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.482+1339C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713410 | |||||||
| chr2:241713433 | C | T | 99 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(96): Show |
133 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.482+1362C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713433 | |||||||
| chr2:241713455 | C | T | 3 | a0001c0001t0004g0084 a0001c0001t0004g0099 a0001c0001t0004g0100 |
3 | HG00140.hp2 HG02738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.482+1384C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713455 | |||||||
| chr2:241713472 | G | A | 1 | a0001c0001t0007g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.482+1401G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713472 | |||||||
| chr2:241713852 | A | G | 1 | a0001c0001t0010g0262 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.482+1781A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713852 | |||||||
| chr2:241713883 | G | A | 98 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(95): Show |
132 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.482+1812G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713883 | |||||||
| chr2:241713893 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.482+1822C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241713893 | |||||||
| chr2:241713989 | C | CA | 8 | a0001c0001t0001g0174 a0001c0001t0002g0240 a0001c0001t0002g0242 others(5): Show |
8 | HG00741.hp1 HG03831.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.482+1934dupA | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241713989 | ||||||
| chr2:241713989 | CA | C | 9 | a0001c0001t0003g0104 a0001c0001t0012g0098 a0001c0001t0013g0159 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.482+1934delA | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241713989 | ||||||
| chr2:241714005 | AT | A | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1935delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714005 | |||||||
| chr2:241714019 | G | A | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.482+1948G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714019 | |||||||
| chr2:241714033 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0143 a0001c0001t0003g0144 |
5 | HG01081.hp1 HG01123.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.482+1962T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714033 | |||||||
| chr2:241714100 | G | C | 1 | a0001c0001t0002g0243 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.482+2029G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714100 | |||||||
| chr2:241714171 | C | T | 3 | a0001c0001t0006g0037 a0001c0001t0006g0116 a0001c0001t0006g0117 |
4 | HG03490.hp2 HG03492.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+2100C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714171 | |||||||
| chr2:241714346 | T | C | 15 | a0001c0001t0003g0204 a0001c0001t0009g0018 a0001c0001t0009g0045 others(12): Show |
16 | HG01074.hp2 HG01106.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.482+2275T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714346 | |||||||
| chr2:241714376 | C | T | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+2305C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714376 | |||||||
| chr2:241714410 | T | G | 1 | a0001c0001t0002g0258 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.482+2339T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714410 | |||||||
| chr2:241714461 | T | G | 1 | a0001c0001t0002g0048 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.482+2390T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714461 | |||||||
| chr2:241714598 | C | CT | 8 | a0001c0001t0001g0206 a0001c0001t0006g0117 a0001c0001t0014g0038 others(5): Show |
8 | HG02559.hp2 HG02622.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.482+2539dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241714598 | ||||||
| chr2:241714646 | G | A | 3 | a0001c0001t0024g0081 a0001c0001t0024g0145 a0001c0001t0024g0146 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.482+2575G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714646 | |||||||
| chr2:241714680 | C | T | 19 | a0001c0001t0008g0025 a0001c0001t0008g0026 a0001c0001t0008g0027 others(16): Show |
25 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.482+2609C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714680 | |||||||
| chr2:241714694 | C | G | 1 | a0001c0001t0004g0135 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.482+2623C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714694 | |||||||
| chr2:241714787 | G | A | 3 | a0001c0001t0022g0169 a0001c0001t0022g0170 a0001c0001t0022g0212 |
3 | HG01099.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.482+2716G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714787 | |||||||
| chr2:241714796 | A | T | 36 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(33): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.482+2725A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714796 | |||||||
| chr2:241714805 | A | ATTTTATT others(81): Show |
1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2734_482+2735i others(90): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714805 | |||||||
| chr2:241714806 | G | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2735G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714806 | |||||||
| chr2:241714808 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2737C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714808 | |||||||
| chr2:241714810 | G | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2739G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714810 | |||||||
| chr2:241714812 | TCTCAAAC others(77): Show |
T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2742_482+2825d others(86): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714812 | |||||||
| chr2:241714898 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2827C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714898 | |||||||
| chr2:241714901 | G | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2830G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714901 | |||||||
| chr2:241714902 | A | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2831A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714902 | |||||||
| chr2:241714904 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2833C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714904 | |||||||
| chr2:241714910 | A | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2839A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714910 | |||||||
| chr2:241714916 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2845C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714916 | |||||||
| chr2:241714918 | A | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2847A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714918 | |||||||
| chr2:241714919 | G | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2848G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714919 | |||||||
| chr2:241714920 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2849C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714920 | |||||||
| chr2:241714925 | A | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2854A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714925 | |||||||
| chr2:241714926 | G | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2855G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714926 | |||||||
| chr2:241714930 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2859C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714930 | |||||||
| chr2:241714931 | A | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2860A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714931 | |||||||
| chr2:241714934 | A | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2863A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714934 | |||||||
| chr2:241714950 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2879C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714950 | |||||||
| chr2:241714952 | A | T | 1 | a0001c0001t0002g0250 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.482+2881A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714952 | |||||||
| chr2:241714971 | C | T | 3 | a0001c0001t0008g0025 a0001c0001t0008g0061 a0001c0001t0008g0153 |
4 | HG02486.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+2900C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714971 | |||||||
| chr2:241714986 | T | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0055 others(10): Show |
20 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.482+2915T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241714986 | |||||||
| chr2:241715022 | A | G | 46 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(43): Show |
62 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.482+2951A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715022 | |||||||
| chr2:241715314 | C | G | 1 | a0001c0001t0002g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.482+3243C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715314 | |||||||
| chr2:241715321 | A | G | 1 | a0001c0001t0033g0203 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.482+3250A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715321 | |||||||
| chr2:241715352 | G | A | 1 | a0001c0001t0003g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.482+3281G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715352 | |||||||
| chr2:241715382 | G | A | 45 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(42): Show |
62 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.482+3311G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715382 | |||||||
| chr2:241715408 | G | A | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+3337G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715408 | |||||||
| chr2:241715445 | G | A | 99 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(96): Show |
132 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.482+3374G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715445 | |||||||
| chr2:241715470 | G | T | 42 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0034 others(39): Show |
58 | HG00408.hp1 HG02040.hp2 HG02074.hp1 others(55): Show |
intron_variant | MODIFIER | c.482+3399G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715470 | |||||||
| chr2:241715472 | A | AT | 73 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0178 others(70): Show |
94 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.482+3426dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241715472 | ||||||
| chr2:241715472 | A | ATT | 26 | a0001c0001t0001g0186 a0001c0001t0003g0054 a0001c0001t0004g0007 others(23): Show |
31 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.482+3425_482+3426d others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241715472 | ||||||
| chr2:241715472 | A | ATTT | 11 | a0001c0001t0008g0025 a0001c0001t0008g0027 a0001c0001t0011g0024 others(8): Show |
15 | HG00642.hp2 HG01099.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.482+3424_482+3426d others(5): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241715472 | ||||||
| chr2:241715472 | AT | A | 42 | a0001c0001t0001g0175 a0001c0001t0001g0194 a0001c0001t0002g0001 others(39): Show |
57 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.482+3426delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241715472 | ||||||
| chr2:241715472 | ATT | A | 10 | a0001c0001t0002g0231 a0001c0001t0002g0244 a0001c0001t0014g0038 others(7): Show |
10 | HG02040.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.482+3425_482+3426d others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241715472 | ||||||
| chr2:241715506 | G | A | 1 | a0001c0001t0002g0013 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.482+3435G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715506 | |||||||
| chr2:241715576 | A | G | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+3505A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715576 | |||||||
| chr2:241715629 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.482+3558C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715629 | |||||||
| chr2:241715642 | C | T | 1 | a0001c0001t0062g0198 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.482+3571C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715642 | |||||||
| chr2:241715767 | G | A | 1 | a0001c0001t0006g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.482+3696G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715767 | |||||||
| chr2:241715777 | G | A | 2 | a0001c0001t0003g0110 a0001c0001t0003g0141 |
2 | NA19080.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.482+3706G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715777 | |||||||
| chr2:241715791 | AT | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(31): Show |
48 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.482+3730delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241715791 | ||||||
| chr2:241715959 | A | G | 36 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(33): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.482+3888A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241715959 | |||||||
| chr2:241716137 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.482+4066A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716137 | |||||||
| chr2:241716247 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.482+4176C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716247 | |||||||
| chr2:241716252 | T | C | 6 | a0001c0001t0014g0038 a0001c0001t0014g0148 a0001c0001t0014g0149 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.482+4181T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716252 | |||||||
| chr2:241716281 | C | G | 1 | a0001c0001t0007g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.482+4210C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716281 | |||||||
| chr2:241716281 | CT | C | 146 | a0001c0001t0001g0175 a0001c0001t0002g0240 a0001c0001t0003g0002 others(143): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.482+4232delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241716281 | ||||||
| chr2:241716281 | CTT | C | 69 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(66): Show |
87 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.482+4231_482+4232d others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241716281 | ||||||
| chr2:241716281 | CTTT | C | 8 | a0001c0001t0002g0224 a0001c0001t0002g0231 a0001c0001t0014g0038 others(5): Show |
8 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.482+4230_482+4232d others(5): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241716281 | ||||||
| chr2:241716282 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.482+4211T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716282 | |||||||
| chr2:241716307 | A | G | 3 | a0001c0001t0024g0081 a0001c0001t0024g0145 a0001c0001t0024g0146 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.482+4236A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716307 | |||||||
| chr2:241716415 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.482+4344C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716415 | |||||||
| chr2:241716458 | A | G | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+4387A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716458 | |||||||
| chr2:241716476 | G | GTAGAGAC others(321): Show |
1 | a0001c0001t0002g0231 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.482+4419_482+4420i others(330): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241716476 | ||||||
| chr2:241716476 | G | GTAGAGAC others(322): Show |
29 | a0001c0001t0002g0001 a0001c0001t0002g0047 a0001c0001t0002g0048 others(26): Show |
42 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.482+4419_482+4420i others(331): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241716476 | ||||||
| chr2:241716476 | G | GTAGAGAC others(323): Show |
12 | a0001c0001t0002g0013 a0001c0001t0002g0050 a0001c0001t0002g0226 others(9): Show |
15 | HG00438.hp2 HG01928.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.482+4419_482+4420i others(332): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241716476 | ||||||
| chr2:241716476 | G | GTAGAGAC others(323): Show |
1 | a0001c0001t0002g0223 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.482+4419_482+4420i others(332): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241716476 | ||||||
| chr2:241716476 | G | GTAGAGAC others(327): Show |
2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.482+4419_482+4420i others(336): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241716476 | ||||||
| chr2:241716490 | T | TTTTTTTT others(329): Show |
1 | a0001c0001t0002g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.482+4419_482+4420i others(338): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716490 | |||||||
| chr2:241716491 | C | A | 1 | a0001c0001t0002g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.482+4420C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716491 | |||||||
| chr2:241716526 | C | A | 1 | a0001c0001t0002g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.482+4455C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716526 | |||||||
| chr2:241716590 | G | A | 3 | a0001c0001t0024g0081 a0001c0001t0024g0145 a0001c0001t0024g0146 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.482+4519G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716590 | |||||||
| chr2:241716604 | A | T | 1 | a0001c0001t0004g0157 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.482+4533A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716604 | |||||||
| chr2:241716698 | A | G | 1 | a0001c0001t0062g0198 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.482+4627A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716698 | |||||||
| chr2:241716786 | A | C | 1 | a0001c0001t0001g0012 | 4 | NA18966.hp2 NA18979.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+4715A>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241716786 | |||||||
| chr2:241717047 | C | G | 46 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(43): Show |
62 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.482+4976C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717047 | |||||||
| chr2:241717048 | T | C | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+4977T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717048 | |||||||
| chr2:241717077 | A | AT | 11 | a0001c0001t0001g0207 a0001c0001t0003g0204 a0001c0001t0009g0018 others(8): Show |
12 | HG01074.hp2 HG01106.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.482+5021dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241717077 | ||||||
| chr2:241717077 | A | ATT | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+5020_482+5021d others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241717077 | ||||||
| chr2:241717077 | AT | A | 5 | a0001c0001t0001g0175 a0001c0001t0002g0224 a0001c0001t0002g0238 others(2): Show |
6 | HG01515.hp2 HG02717.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+5021delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241717077 | ||||||
| chr2:241717267 | T | C | 53 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(50): Show |
69 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.482+5196T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717267 | |||||||
| chr2:241717317 | C | T | 1 | a0001c0001t0007g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.482+5246C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717317 | |||||||
| chr2:241717358 | A | G | 9 | a0001c0001t0003g0204 a0001c0001t0009g0018 a0001c0001t0009g0045 others(6): Show |
10 | HG01074.hp2 HG01106.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.482+5287A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717358 | |||||||
| chr2:241717360 | C | G | 1 | a0001c0001t0002g0049 | 2 | HG00423.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.482+5289C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717360 | |||||||
| chr2:241717410 | A | T | 1 | a0001c0001t0048g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.482+5339A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717410 | |||||||
| chr2:241717511 | C | T | 46 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(43): Show |
62 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.483-5428C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717511 | |||||||
| chr2:241717580 | G | A | 3 | a0001c0001t0024g0081 a0001c0001t0024g0145 a0001c0001t0024g0146 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.483-5359G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717580 | |||||||
| chr2:241717599 | CCTTTTTT | C | 19 | a0001c0001t0008g0025 a0001c0001t0008g0026 a0001c0001t0008g0027 others(16): Show |
25 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.483-5334_483-5328d others(9): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241717599 | ||||||
| chr2:241717696 | C | CT | 10 | a0001c0001t0003g0030 a0001c0001t0003g0087 a0001c0001t0006g0112 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.483-5230dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241717696 | ||||||
| chr2:241717696 | CT | C | 28 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(25): Show |
35 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.483-5230delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241717696 | ||||||
| chr2:241717746 | G | C | 3 | a0001c0001t0023g0181 a0001c0001t0023g0185 a0001c0001t0023g0208 |
3 | NA18980.hp2 NA19002.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.483-5193G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717746 | |||||||
| chr2:241717797 | A | T | 1 | a0001c0001t0006g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.483-5142A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241717797 | |||||||
| chr2:241718068 | G | A | 1 | a0001c0001t0004g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.483-4871G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718068 | |||||||
| chr2:241718082 | C | T | 7 | a0001c0001t0014g0038 a0001c0001t0014g0147 a0001c0001t0014g0148 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-4857C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718082 | |||||||
| chr2:241718173 | C | T | 31 | a0001c0001t0007g0021 a0001c0001t0007g0071 a0001c0001t0007g0072 others(28): Show |
38 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.483-4766C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718173 | |||||||
| chr2:241718248 | A | G | 1 | a0001c0001t0007g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.483-4691A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718248 | |||||||
| chr2:241718323 | TCCTC | T | 230 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(227): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.483-4603_483-4600d others(6): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241718323 | ||||||
| chr2:241718355 | CCCTCCCT others(9): Show |
C | 2 | a0001c0001t0005g0259 a0001c0001t0005g0271 |
2 | HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.483-4564_483-4549d others(18): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241718355 | ||||||
| chr2:241718416 | T | C | 2 | a0001c0001t0003g0088 a0001c0001t0003g0111 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.483-4523T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718416 | |||||||
| chr2:241718419 | C | CT | 59 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0048 others(56): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.483-4503dupT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241718419 | ||||||
| chr2:241718419 | C | CTT | 7 | a0001c0001t0002g0224 a0001c0001t0002g0247 a0001c0001t0002g0258 others(4): Show |
7 | HG01099.hp2 HG02451.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-4504_483-4503d others(4): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241718419 | ||||||
| chr2:241718621 | T | C | 3 | a0001c0001t0024g0081 a0001c0001t0024g0145 a0001c0001t0024g0146 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.483-4318T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718621 | |||||||
| chr2:241718622 | G | A | 2 | a0001c0001t0017g0016 a0001c0001t0017g0124 |
4 | HG02257.hp1 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-4317G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718622 | |||||||
| chr2:241718732 | T | A | 102 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(99): Show |
136 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.483-4207T>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718732 | |||||||
| chr2:241718847 | C | T | 235 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(232): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.483-4092C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718847 | |||||||
| chr2:241718870 | T | G | 37 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(34): Show |
46 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.483-4069T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718870 | |||||||
| chr2:241718928 | C | T | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.483-4011C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718928 | |||||||
| chr2:241718928 | CT | C | 2 | a0001c0001t0004g0092 a0001c0001t0030g0052 |
3 | HG02155.hp1 NA18969.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.483-4010delT | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718928 | |||||||
| chr2:241718930 | C | A | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.483-4009C>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241718930 | |||||||
| chr2:241719050 | G | A | 1 | a0001c0001t0017g0124 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.483-3889G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241719050 | |||||||
| chr2:241719100 | G | A | 234 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(231): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.483-3839G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241719100 | |||||||
| chr2:241719174 | G | A | 1 | a0001c0001t0039g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.483-3765G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241719174 | |||||||
| chr2:241719200 | G | A | 1 | a0001c0001t0063g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.483-3739G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241719200 | |||||||
| chr2:241719274 | G | A | 1 | a0001c0001t0004g0126 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.483-3665G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241719274 | |||||||
| chr2:241719364 | A | T | 98 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(95): Show |
132 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.483-3575A>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241719364 | |||||||
| chr2:241719405 | C | T | 9 | a0001c0001t0003g0204 a0001c0001t0009g0018 a0001c0001t0009g0045 others(6): Show |
10 | HG01074.hp2 HG01106.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.483-3534C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241719405 | |||||||
| chr2:241719652 | G | A | 29 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(26): Show |
37 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.483-3287G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241719652 | |||||||
| chr2:241720006 | C | T | 1 | a0001c0001t0038g0246 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.483-2933C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720006 | |||||||
| chr2:241720105 | G | A | 4 | a0001c0001t0016g0043 a0001c0001t0016g0167 a0001c0001t0016g0201 others(1): Show |
5 | HG00741.hp2 HG02683.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.483-2834G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720105 | |||||||
| chr2:241720139 | C | T | 42 | a0001c0001t0003g0002 a0001c0001t0003g0032 a0001c0001t0003g0054 others(39): Show |
54 | HG00140.hp1 HG00140.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.483-2800C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720139 | |||||||
| chr2:241720217 | C | T | 1 | a0001c0001t0038g0246 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.483-2722C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720217 | |||||||
| chr2:241720237 | A | C | 1 | a0001c0001t0004g0135 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.483-2702A>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720237 | |||||||
| chr2:241720283 | C | T | 7 | a0001c0001t0004g0084 a0001c0001t0004g0095 a0001c0001t0004g0099 others(4): Show |
7 | HG00140.hp1 HG00140.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.483-2656C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720283 | |||||||
| chr2:241720298 | C | T | 29 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0048 others(26): Show |
44 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.483-2641C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720298 | |||||||
| chr2:241720469 | G | T | 1 | a0001c0001t0040g0078 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.483-2470G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720469 | |||||||
| chr2:241720591 | G | A | 98 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(95): Show |
132 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.483-2348G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720591 | |||||||
| chr2:241720660 | C | T | 4 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0002g0236 others(1): Show |
4 | HG01952.hp2 HG01981.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2279C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720660 | |||||||
| chr2:241720673 | G | A | 1 | a0001c0001t0002g0245 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.483-2266G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720673 | |||||||
| chr2:241720688 | C | T | 1 | a0001c0001t0003g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.483-2251C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720688 | |||||||
| chr2:241720768 | G | A | 5 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.483-2171G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720768 | |||||||
| chr2:241720868 | G | A | 2 | a0001c0001t0005g0272 a0001c0001t0005g0280 |
2 | HG02055.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.483-2071G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241720868 | |||||||
| chr2:241721057 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.483-1882C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721057 | |||||||
| chr2:241721132 | G | T | 1 | a0001c0001t0039g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.483-1807G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721132 | |||||||
| chr2:241721167 | C | T | 1 | a0001c0001t0016g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.483-1772C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721167 | |||||||
| chr2:241721168 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.483-1771G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721168 | |||||||
| chr2:241721250 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0174 a0001c0001t0001g0178 |
4 | NA18747.hp2 NA18952.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-1689G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721250 | |||||||
| chr2:241721273 | C | T | 97 | a0001c0001t0001g0184 a0001c0001t0003g0002 a0001c0001t0003g0003 others(94): Show |
129 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.483-1666C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721273 | |||||||
| chr2:241721401 | G | A | 1 | a0001c0001t0002g0231 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.483-1538G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721401 | |||||||
| chr2:241721503 | C | G | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.483-1436C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721503 | |||||||
| chr2:241721602 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.483-1337C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721602 | |||||||
| chr2:241721672 | T | TA | 3 | a0001c0001t0024g0081 a0001c0001t0024g0145 a0001c0001t0024g0146 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.483-1266dupA | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241721672 | ||||||
| chr2:241721704 | T | C | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.483-1235T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721704 | |||||||
| chr2:241721946 | G | A | 96 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(93): Show |
128 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.483-993G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721946 | |||||||
| chr2:241721947 | T | A | 36 | a0001c0001t0007g0021 a0001c0001t0007g0058 a0001c0001t0007g0059 others(33): Show |
45 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.483-992T>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721947 | |||||||
| chr2:241721991 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.483-948C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241721991 | |||||||
| chr2:241722118 | G | A | 44 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(41): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.483-821G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722118 | |||||||
| chr2:241722130 | G | A | 44 | a0001c0001t0004g0091 a0001c0001t0005g0006 a0001c0001t0005g0014 others(41): Show |
53 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.483-809G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722130 | |||||||
| chr2:241722223 | G | A | 1 | a0001c0001t0007g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.483-716G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722223 | |||||||
| chr2:241722285 | G | A | 5 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.483-654G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722285 | |||||||
| chr2:241722349 | G | C | 1 | a0001c0001t0034g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.483-590G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722349 | |||||||
| chr2:241722477 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.483-462G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722477 | |||||||
| chr2:241722488 | C | T | 1 | a0001c0001t0003g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.483-451C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722488 | |||||||
| chr2:241722507 | C | T | 8 | a0001c0001t0008g0025 a0001c0001t0008g0061 a0001c0001t0008g0063 others(5): Show |
10 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-432C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722507 | |||||||
| chr2:241722615 | A | ATTGCGTG others(7): Show |
1 | a0001c0001t0003g0143 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.483-323_483-310dup others(14): Show |
ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 241722615 | ||||||
| chr2:241722620 | G | A | 1 | a0001c0001t0011g0069 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.483-319G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722620 | |||||||
| chr2:241722749 | G | T | 1 | a0001c0001t0039g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.483-190G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722749 | |||||||
| chr2:241722784 | G | A | 33 | a0001c0001t0007g0021 a0001c0001t0007g0058 a0001c0001t0007g0059 others(30): Show |
42 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.483-155G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 5/7 | chr2 | 241722784 | |||||||
| chr2:241723206 | G | T | 33 | a0001c0001t0007g0021 a0001c0001t0007g0058 a0001c0001t0007g0059 others(30): Show |
42 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.619-4G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 6/7 | chr2 | 241723206 | |||||||
| chr2:241723290 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.680+19G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241723290 | |||||||
| chr2:241723346 | T | C | 238 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(235): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.680+75T>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241723346 | |||||||
| chr2:241723377 | G | A | 1 | a0001c0001t0005g0268 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.680+106G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241723377 | |||||||
| chr2:241723447 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.680+176G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241723447 | |||||||
| chr2:241723647 | T | G | 2 | a0001c0001t0027g0154 a0001c0001t0027g0155 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.680+376T>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241723647 | |||||||
| chr2:241723991 | G | C | 1 | a0001c0001t0004g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.680+720G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241723991 | |||||||
| chr2:241724133 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.681-856C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724133 | |||||||
| chr2:241724190 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.681-799C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724190 | |||||||
| chr2:241724200 | C | T | 12 | a0001c0001t0006g0008 a0001c0001t0006g0015 a0001c0001t0006g0037 others(9): Show |
17 | HG02165.hp1 HG02559.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.681-789C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724200 | |||||||
| chr2:241724277 | G | C | 95 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(92): Show |
127 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.681-712G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724277 | |||||||
| chr2:241724325 | G | A | 33 | a0001c0001t0007g0021 a0001c0001t0007g0058 a0001c0001t0007g0059 others(30): Show |
42 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.681-664G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724325 | |||||||
| chr2:241724520 | G | C | 35 | a0001c0001t0005g0006 a0001c0001t0005g0014 a0001c0001t0005g0051 others(32): Show |
44 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.681-469G>C | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724520 | |||||||
| chr2:241724524 | A | G | 221 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(218): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.681-465A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724524 | |||||||
| chr2:241724582 | C | G | 2 | a0001c0001t0025g0020 a0001c0001t0025g0057 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.681-407C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724582 | |||||||
| chr2:241724610 | G | T | 1 | a0001c0006t0003g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.681-379G>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724610 | |||||||
| chr2:241724705 | C | T | 1 | a0001c0001t0039g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.681-284C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724705 | |||||||
| chr2:241724722 | C | G | 3 | a0001c0001t0005g0051 a0001c0001t0005g0276 a0001c0001t0043g0273 |
4 | HG00544.hp1 NA19001.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-267C>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724722 | |||||||
| chr2:241724750 | A | G | 37 | a0001c0001t0007g0021 a0001c0001t0007g0058 a0001c0001t0007g0059 others(34): Show |
46 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.681-239A>G | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724750 | |||||||
| chr2:241724769 | TG | T | 239 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(236): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.681-218delG | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 241724769 | ||||||
| chr2:241724783 | G | A | 236 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0047 others(233): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.681-206G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724783 | |||||||
| chr2:241724883 | C | T | 1 | a0001c0001t0032g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.681-106C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724883 | |||||||
| chr2:241724946 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.681-43C>T | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724946 | |||||||
| chr2:241724947 | G | A | 1 | a0001c0001t0058g0183 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.681-42G>A | ING5 | ENSG00000168395.16 | transcript | ENST00000313552.11 | protein_coding | 7/7 | chr2 | 241724947 |