Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 166968 |
| ensemblid | ENSG00000155545.20 |
| hgncid | 26678 |
| symbol | MIER3 |
| name | MIER family member 3 |
| refseq_nuc | NM_001297599.2 |
| refseq_prot | NP_001284528.1 |
| ensembl_nuc | ENST00000381199.8 |
| ensembl_prot | ENSP00000370596.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 56919603 |
| end | 56952123 |
| strand | - |
| ver | v1.2 |
| region | chr5:56919603-56952123 |
| region5000 | chr5:56914603-56957123 |
| regionname0 | MIER3_chr5_56919603_56952123 |
| regionname5000 | MIER3_chr5_56914603_56957123 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 550 | 373 | 62 | 67 | 186 | 10 | 46 | 144 | MIER3_chr5_56914603_56957123 | MIER3 | MAEAS others(545): Show |
chr5 | 56914603 | 56957123 |
| a0002 | 0/0 | 550 | 21 | 20 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | MAEAS others(545): Show |
chr5 | 56914603 | 56957123 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1650 | 176 | 25 | 36 | 84 | 6 | 23 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 | ||
| a0001c0002 | 0/0 | 1650 | 174 | 23 | 26 | 100 | 4 | 21 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 | ||
| a0001c0004 | 0/0 | 1650 | 7 | 7 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 | ||
| a0001c0005 | 0/0 | 1650 | 6 | 1 | 4 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 | ||
| a0001c0006 | 0/0 | 1650 | 5 | 4 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 | ||
| a0001c0007 | 0/0 | 1650 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 | ||
| a0001c0008 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 | ||
| a0001c0009 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 | ||
| a0001c0010 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 | ||
| a0002c0003 | 0/0 | 1650 | 21 | 20 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | ATGGC others(1645): Show |
chr5 | 56914603 | 56957123 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5199 | 72 | 1 | 9 | 52 | 2 | 8 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0001t0002 | 0/1 | 5199 | 94 | 19 | 26 | 31 | 4 | 13 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0001t0004 | 1/0 | 5199 | 1 | 0 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0001t0005 | 0/0 | 5195 | 3 | 3 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5190): Show |
chr5 | 56914603 | 56957123 |
| a0001c0001t0006 | 0/0 | 5199 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0001t0009 | 0/0 | 5199 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0001t0015 | 0/0 | 5195 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5190): Show |
chr5 | 56914603 | 56957123 |
| a0001c0001t0017 | 0/0 | 5199 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0001t0019 | 0/0 | 5199 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0002t0001 | 0/0 | 5199 | 111 | 19 | 20 | 55 | 2 | 15 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0002t0003 | 0/0 | 5199 | 47 | 3 | 5 | 32 | 2 | 5 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0002t0004 | 0/0 | 5199 | 10 | 0 | 0 | 10 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0002t0007 | 0/0 | 5199 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0002t0010 | 0/0 | 5199 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0002t0011 | 0/0 | 5199 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0002t0012 | 0/0 | 5199 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0002t0013 | 0/0 | 5199 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0002t0020 | 0/0 | 5199 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0004t0002 | 0/0 | 5199 | 7 | 7 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0005t0002 | 0/0 | 5199 | 6 | 1 | 4 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0006t0002 | 0/0 | 5199 | 4 | 3 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0006t0008 | 0/0 | 5199 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0007t0001 | 0/0 | 5199 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0008t0016 | 0/0 | 5199 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0009t0002 | 0/0 | 5199 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0001c0010t0001 | 0/0 | 5199 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0002c0003t0001 | 0/0 | 5199 | 19 | 18 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0002c0003t0014 | 0/0 | 5199 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| a0002c0003t0018 | 0/0 | 5199 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | GTTCG others(5194): Show |
chr5 | 56914603 | 56957123 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 31 | 0 | 2 | 29 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0004 | 0/0 | 13 | 0 | 3 | 6 | 2 | 2 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0005 | 0/0 | 13 | 2 | 3 | 7 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0010 | 0/0 | 8 | 0 | 3 | 3 | 1 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0011 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0012 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0004g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0005g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0009g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0015g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0017g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0001t0019g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0002 | 0/0 | 30 | 5 | 8 | 13 | 1 | 3 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0003 | 0/0 | 22 | 0 | 5 | 13 | 0 | 4 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0007 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0008 | 0/0 | 9 | 0 | 0 | 7 | 2 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0015 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0004g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0011g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0012g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0013g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0002t0020g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0004t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0004t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0004t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0004t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0004t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0005t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0005t0002g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0005t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0005t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0006t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0006t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0006t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0006t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0006t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0007t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0008t0016g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0009t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0001c0010t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0009 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0014g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| a0002c0003t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | FIN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | FIN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00408 | hp2 | a0001 | c0001 | t0017 | g0115 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0084 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00558 | hp2 | a0001 | c0002 | t0012 | g0067 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0031 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01081 | hp2 | a0001 | c0001 | t0015 | g0118 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01109 | hp1 | a0001 | c0006 | t0002 | g0185 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01257 | hp2 | a0001 | c0005 | t0002 | g0037 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01346 | hp1 | a0001 | c0005 | t0002 | g0037 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0031 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01361 | hp2 | a0001 | c0005 | t0002 | g0134 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0170 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0146 | EUR | IBS | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01891 | hp1 | a0001 | c0006 | t0002 | g0183 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01943 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01952 | hp1 | a0001 | c0005 | t0002 | g0045 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02056 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02155 | hp1 | a0001 | c0007 | t0001 | g0112 | EAS | CDX | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | CDX | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02300 | hp2 | a0001 | c0002 | t0013 | g0065 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02523 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0173 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02622 | hp1 | a0001 | c0010 | t0001 | g0052 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02622 | hp2 | a0001 | c0006 | t0002 | g0184 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0171 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02698 | hp1 | a0001 | c0001 | t0019 | g0144 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02698 | hp2 | a0001 | c0002 | t0020 | g0093 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02723 | hp2 | a0001 | c0004 | t0002 | g0122 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02809 | hp1 | a0001 | c0004 | t0002 | g0119 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0102 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02896 | hp2 | a0001 | c0006 | t0008 | g0182 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0124 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0172 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03098 | hp2 | a0002 | c0003 | t0018 | g0169 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0044 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03195 | hp2 | a0002 | c0003 | t0014 | g0104 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0103 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03453 | hp2 | a0001 | c0006 | t0002 | g0181 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0179 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03491 | hp2 | a0001 | c0009 | t0002 | g0140 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03540 | hp1 | a0001 | c0004 | t0002 | g0024 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03579 | hp1 | a0001 | c0002 | t0010 | g0100 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0086 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03831 | hp1 | a0001 | c0001 | t0009 | g0141 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0094 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0126 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0088 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0087 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0174 | AFR | YRI | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CHB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CHB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18953 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18976 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18976 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18979 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18981 | hp1 | a0001 | c0002 | t0007 | g0090 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18985 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19001 | hp2 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19005 | hp2 | a0001 | c0007 | t0001 | g0113 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19006 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0024 | AFR | LWK | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0123 | AFR | LWK | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19059 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19076 | hp1 | a0001 | c0002 | t0011 | g0098 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0095 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19240 | hp1 | a0001 | c0008 | t0016 | g0168 | AFR | YRI | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA19240 | hp2 | a0002 | c0003 | t0001 | g0180 | AFR | YRI | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | GIH | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA20905 | hp2 | a0001 | c0005 | t0002 | g0045 | SAS | GIH | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0030 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0125 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0044 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0024 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0030 | AFR | USA | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | USA | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA20300 | hp1 | a0001 | c0005 | t0002 | g0175 | AFR | USA | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | USA | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | LWK | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | LWK | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0137 | REF | REF | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0130 | REF | REF | MIER3_chr5_56914603_56957123 | MIER3 | chr5 | 56914603 | 56957123 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56923192 | T | C | 1 | a0002 | 21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
missense_variant | MODERATE | c.1589A>G | p.Asn530Ser | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1610/5199 | 1589/1653 | 530/550 | chr5 | 56923192 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56923227 | A | T | 1 | a0001c0004 | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
synonymous_variant | LOW | c.1554T>A | p.Ala518Ala | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1575/5199 | 1554/1653 | 518/550 | chr5 | 56923227 | |||
| chr5:56923266 | A | G | 1 | a0001c0009 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.1515T>C | p.Phe505Phe | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1536/5199 | 1515/1653 | 505/550 | chr5 | 56923266 | |||
| chr5:56923827 | A | G | 1 | a0001c0010 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1059T>C | p.Tyr353Tyr | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 12/13 | 1080/5199 | 1059/1653 | 353/550 | chr5 | 56923827 | |||
| chr5:56930698 | G | T | 1 | a0001c0007 | 2 | HG02155.hp1 NA19005.hp2 |
synonymous_variant | LOW | c.795C>A | p.Ile265Ile | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/13 | 816/5199 | 795/1653 | 265/550 | chr5 | 56930698 | |||
| chr5:56935714 | A | G | 2 | a0001c0006 a0001c0008 |
6 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.474T>C | p.Val158Val | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 6/13 | 495/5199 | 474/1653 | 158/550 | chr5 | 56935714 | |||
| chr5:56937663 | G | A | 1 | a0001c0005 | 6 | HG01257.hp2 HG01346.hp1 HG01361.hp2 others(3): Show |
synonymous_variant | LOW | c.351C>T | p.Asp117Asp | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/13 | 372/5199 | 351/1653 | 117/550 | chr5 | 56937663 | |||
| chr5:56946947 | T | C | 3 | a0001c0002 a0001c0006 a0001c0010 |
180 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(177): Show |
synonymous_variant | LOW | c.159A>G | p.Ser53Ser | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/13 | 180/5199 | 159/1653 | 53/550 | chr5 | 56946947 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56919926 | G | A | 5 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0010 others(2): Show |
51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3202C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 3202 | chr5 | 56919926 | ||||||
| chr5:56920049 | T | G | 1 | a0001c0002t0010 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3079A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 3079 | chr5 | 56920049 | ||||||
| chr5:56920083 | G | T | 1 | a0001c0002t0011 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3045C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 3045 | chr5 | 56920083 | ||||||
| chr5:56920282 | A | G | 1 | a0001c0002t0010 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2846T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2846 | chr5 | 56920282 | ||||||
| chr5:56920448 | G | A | 1 | a0001c0001t0015 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2680C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2680 | chr5 | 56920448 | ||||||
| chr5:56920547 | C | T | 1 | a0001c0002t0013 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2581G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2581 | chr5 | 56920547 | ||||||
| chr5:56920610 | T | C | 1 | a0002c0003t0014 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2518A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2518 | chr5 | 56920610 | ||||||
| chr5:56920762 | A | G | 1 | a0001c0008t0016 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2366T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2366 | chr5 | 56920762 | ||||||
| chr5:56920940 | AATTT | A | 2 | a0001c0001t0005 a0001c0001t0015 |
4 | HG01081.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2184_*2187delAAAT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2184 | chr5 | 56920940 | ||||||
| chr5:56921265 | T | C | 1 | a0001c0008t0016 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1863A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1863 | chr5 | 56921265 | ||||||
| chr5:56921362 | A | C | 1 | a0001c0001t0009 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1766T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1766 | chr5 | 56921362 | ||||||
| chr5:56921369 | A | G | 5 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0010 others(2): Show |
51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1759T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1759 | chr5 | 56921369 | ||||||
| chr5:56921418 | A | C | 1 | a0001c0006t0008 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1710T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1710 | chr5 | 56921418 | ||||||
| chr5:56921514 | C | T | 1 | a0001c0006t0008 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1614G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1614 | chr5 | 56921514 | ||||||
| chr5:56921663 | A | G | 1 | a0001c0002t0012 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1465 | chr5 | 56921663 | ||||||
| chr5:56921702 | T | C | 5 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0010 others(2): Show |
51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1426A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1426 | chr5 | 56921702 | ||||||
| chr5:56921756 | G | C | 1 | a0001c0001t0006 | 2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1372C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1372 | chr5 | 56921756 | ||||||
| chr5:56922037 | T | C | 1 | a0001c0001t0017 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1091A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1091 | chr5 | 56922037 | ||||||
| chr5:56922202 | C | T | 14 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(11): Show |
167 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*926G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 926 | chr5 | 56922202 | ||||||
| chr5:56922297 | G | A | 1 | a0002c0003t0018 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*831C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 831 | chr5 | 56922297 | ||||||
| chr5:56922340 | T | C | 1 | a0001c0001t0019 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 788 | chr5 | 56922340 | ||||||
| chr5:56922452 | C | T | 1 | a0001c0002t0007 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*676G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 676 | chr5 | 56922452 | ||||||
| chr5:56922453 | G | A | 1 | a0001c0002t0020 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 675 | chr5 | 56922453 | ||||||
| chr5:56922724 | C | G | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(24): Show |
382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
3_prime_UTR_variant | MODIFIER | c.*404G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 404 | chr5 | 56922724 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56923871 | T | C | 32 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(29): Show |
51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1053-38A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 11/12 | chr5 | 56923871 | |||||||
| chr5:56924211 | T | C | 1 | a0001c0005t0002g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.925-169A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924211 | |||||||
| chr5:56924253 | G | GT | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.925-212dupA | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924253 | |||||||
| chr5:56924263 | T | A | 4 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(1): Show |
4 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.925-221A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924263 | |||||||
| chr5:56924264 | A | T | 4 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0164 others(1): Show |
6 | HG01256.hp2 HG01258.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.925-222T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924264 | |||||||
| chr5:56924320 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.925-278G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924320 | |||||||
| chr5:56924376 | G | A | 1 | a0001c0002t0001g0057 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.925-334C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924376 | |||||||
| chr5:56924555 | T | C | 60 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(57): Show |
105 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.925-513A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924555 | |||||||
| chr5:56924577 | A | G | 1 | a0001c0002t0003g0099 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.925-535T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924577 | |||||||
| chr5:56924635 | A | G | 6 | a0002c0003t0001g0044 a0002c0003t0001g0170 a0002c0003t0001g0171 others(3): Show |
7 | HG01433.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.925-593T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924635 | |||||||
| chr5:56924887 | T | C | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.925-845A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924887 | |||||||
| chr5:56924975 | T | G | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.925-933A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924975 | |||||||
| chr5:56924990 | T | G | 6 | a0002c0003t0001g0009 a0002c0003t0001g0102 a0002c0003t0001g0103 others(3): Show |
13 | HG02145.hp1 HG02572.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.925-948A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924990 | |||||||
| chr5:56925171 | C | T | 13 | a0002c0003t0001g0009 a0002c0003t0001g0044 a0002c0003t0001g0102 others(10): Show |
21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.925-1129G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925171 | |||||||
| chr5:56925172 | G | A | 32 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(29): Show |
51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.925-1130C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925172 | |||||||
| chr5:56925216 | A | C | 2 | a0001c0002t0001g0072 a0001c0002t0001g0074 |
2 | HG00621.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.925-1174T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925216 | |||||||
| chr5:56925350 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.925-1308C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925350 | |||||||
| chr5:56925369 | C | G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.925-1327G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925369 | |||||||
| chr5:56925501 | A | G | 70 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(67): Show |
117 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.925-1459T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925501 | |||||||
| chr5:56925579 | T | C | 1 | a0001c0002t0003g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.925-1537A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925579 | |||||||
| chr5:56925710 | A | G | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.925-1668T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925710 | |||||||
| chr5:56925857 | T | C | 1 | a0002c0003t0001g0173 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.925-1815A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925857 | |||||||
| chr5:56925961 | T | A | 1 | a0001c0001t0015g0118 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.925-1919A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925961 | |||||||
| chr5:56926017 | G | T | 2 | a0001c0002t0003g0089 a0001c0002t0003g0092 |
2 | NA18981.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.925-1975C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926017 | |||||||
| chr5:56926053 | G | A | 2 | a0001c0002t0003g0015 a0002c0003t0001g0180 |
5 | HG01928.hp1 HG01943.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.925-2011C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926053 | |||||||
| chr5:56926065 | T | A | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.925-2023A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926065 | |||||||
| chr5:56926111 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(140): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.925-2069A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926111 | |||||||
| chr5:56926260 | TA | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(19): Show |
70 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.925-2219delT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926260 | |||||||
| chr5:56926293 | G | A | 19 | a0001c0001t0001g0152 a0001c0001t0002g0010 a0001c0001t0002g0011 others(16): Show |
37 | HG00280.hp1 HG00609.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.925-2251C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926293 | |||||||
| chr5:56926317 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.925-2275A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926317 | |||||||
| chr5:56926413 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.924+2354T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926413 | |||||||
| chr5:56926413 | A | T | 1 | a0001c0002t0001g0053 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.924+2354T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926413 | |||||||
| chr5:56926478 | A | G | 1 | a0001c0001t0002g0011 | 7 | HG01257.hp1 HG01258.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.924+2289T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926478 | |||||||
| chr5:56926531 | A | T | 65 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(62): Show |
112 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.924+2236T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926531 | |||||||
| chr5:56926626 | T | C | 1 | a0001c0002t0001g0059 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.924+2141A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926626 | |||||||
| chr5:56926645 | A | ATGGTACA others(7): Show |
5 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(2): Show |
7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.924+2121_924+2122i others(16): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926645 | |||||||
| chr5:56926718 | C | T | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.924+2049G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926718 | |||||||
| chr5:56926719 | G | A | 7 | a0001c0002t0001g0066 a0002c0003t0001g0044 a0002c0003t0001g0170 others(4): Show |
8 | HG01433.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.924+2048C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926719 | |||||||
| chr5:56926859 | C | A | 2 | a0001c0001t0005g0023 a0001c0001t0015g0118 |
4 | HG01081.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.924+1908G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926859 | |||||||
| chr5:56926884 | A | AT | 18 | a0001c0001t0002g0005 a0001c0001t0002g0127 a0001c0001t0002g0128 others(15): Show |
32 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.924+1882dupA | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926884 | |||||||
| chr5:56926912 | C | T | 36 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(33): Show |
55 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.924+1855G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926912 | |||||||
| chr5:56926938 | C | A | 1 | a0002c0003t0001g0044 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.924+1829G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926938 | |||||||
| chr5:56927040 | C | T | 3 | a0001c0002t0001g0050 a0001c0002t0001g0055 a0001c0010t0001g0052 |
3 | HG02572.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.924+1727G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927040 | |||||||
| chr5:56927118 | CAT | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(21): Show |
72 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+1647_924+1648d others(4): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927118 | |||||||
| chr5:56927173 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(107): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.924+1594C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927173 | |||||||
| chr5:56927296 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.924+1471G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927296 | |||||||
| chr5:56927478 | T | G | 1 | a0001c0002t0003g0096 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.924+1289A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927478 | |||||||
| chr5:56927607 | G | C | 2 | a0001c0004t0002g0024 a0001c0004t0002g0119 |
4 | HG02809.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.924+1160C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927607 | |||||||
| chr5:56927671 | G | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(26): Show |
79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.924+1096C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927671 | |||||||
| chr5:56927678 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(180): Show |
379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.924+1089C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927678 | |||||||
| chr5:56927965 | C | G | 1 | a0001c0002t0003g0085 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.924+802G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927965 | |||||||
| chr5:56928051 | A | AT | 30 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(27): Show |
49 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.924+715dupA | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928051 | |||||||
| chr5:56928234 | A | T | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.924+533T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928234 | |||||||
| chr5:56928297 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(159): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.924+470T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928297 | |||||||
| chr5:56928351 | C | T | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.924+416G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928351 | |||||||
| chr5:56928365 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.924+402C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928365 | |||||||
| chr5:56928512 | G | T | 52 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(49): Show |
95 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.924+255C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928512 | |||||||
| chr5:56928581 | T | C | 1 | a0001c0002t0003g0091 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.924+186A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928581 | |||||||
| chr5:56928621 | G | A | 1 | a0001c0002t0003g0083 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.924+146C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928621 | |||||||
| chr5:56928623 | A | C | 3 | a0001c0004t0002g0122 a0001c0004t0002g0123 a0001c0004t0002g0124 |
3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.924+144T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928623 | |||||||
| chr5:56928658 | T | TTGGC | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(108): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.924+108_924+109ins others(4): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928658 | |||||||
| chr5:56928887 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(108): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.830-26A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928887 | |||||||
| chr5:56928893 | C | T | 12 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0030 others(9): Show |
24 | HG00423.hp1 HG01516.hp2 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.830-32G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928893 | |||||||
| chr5:56928932 | G | T | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-71C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928932 | |||||||
| chr5:56928955 | ACTCT | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(40): Show |
102 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.830-98_830-95delAG others(2): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928955 | |||||||
| chr5:56928967 | T | A | 68 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(65): Show |
115 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.830-106A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928967 | |||||||
| chr5:56928969 | T | A | 68 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(65): Show |
115 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.830-108A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928969 | |||||||
| chr5:56928979 | A | T | 9 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(6): Show |
11 | HG01109.hp1 HG02723.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.830-118T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928979 | |||||||
| chr5:56928981 | A | T | 68 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(65): Show |
115 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.830-120T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928981 | |||||||
| chr5:56928982 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.830-121G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928982 | |||||||
| chr5:56928989 | T | TCACACA | 5 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(2): Show |
7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.830-129_830-128ins others(6): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928989 | |||||||
| chr5:56928991 | T | A | 9 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(6): Show |
11 | HG01109.hp1 HG02723.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.830-130A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | |||||||
| chr5:56928991 | T | TCACACA | 30 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(27): Show |
48 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.830-136_830-131dup others(6): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | |||||||
| chr5:56928991 | T | TCACACAC others(1): Show |
59 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(56): Show |
104 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.830-138_830-131dup others(8): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | |||||||
| chr5:56928991 | T | TCACACAC others(3): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0107 others(8): Show |
30 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.830-140_830-131dup others(10): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | |||||||
| chr5:56928991 | T | TCACACAC others(5): Show |
26 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0034 others(23): Show |
63 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.830-142_830-131dup others(12): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | |||||||
| chr5:56928991 | T | TCACACAC others(7): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0078 others(1): Show |
7 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.830-144_830-131dup others(14): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | |||||||
| chr5:56929005 | A | ACACACAC others(7): Show |
2 | a0001c0006t0002g0184 a0002c0003t0018g0169 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.830-145_830-144ins others(14): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929005 | |||||||
| chr5:56929005 | A | ACACACAC others(5): Show |
1 | a0001c0006t0002g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.830-145_830-144ins others(12): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929005 | |||||||
| chr5:56929005 | A | ACACACAC others(3): Show |
1 | a0001c0006t0008g0182 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.830-145_830-144ins others(10): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929005 | |||||||
| chr5:56929005 | A | ACACACAC others(1): Show |
3 | a0001c0006t0002g0181 a0001c0006t0002g0185 a0001c0008t0016g0168 |
3 | HG01109.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.830-145_830-144ins others(8): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929005 | |||||||
| chr5:56929007 | T | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(93): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.830-146A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929007 | |||||||
| chr5:56929009 | T | A | 2 | a0001c0002t0003g0032 a0002c0003t0001g0174 |
3 | NA18522.hp1 NA18960.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.830-148A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929009 | |||||||
| chr5:56929172 | T | TA | 17 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0032 others(14): Show |
23 | HG00673.hp1 HG02080.hp1 HG02698.hp2 others(20): Show |
intron_variant | MODIFIER | c.830-312dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929172 | |||||||
| chr5:56929181 | T | A | 2 | a0001c0002t0003g0079 a0001c0002t0003g0096 |
2 | NA18968.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.830-320A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929181 | |||||||
| chr5:56929198 | C | T | 2 | a0001c0001t0005g0023 a0001c0001t0015g0118 |
4 | HG01081.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.830-337G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929198 | |||||||
| chr5:56929449 | C | T | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.830-588G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929449 | |||||||
| chr5:56929462 | A | C | 1 | a0001c0008t0016g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.830-601T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929462 | |||||||
| chr5:56929591 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(108): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.830-730C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929591 | |||||||
| chr5:56929760 | T | C | 1 | a0001c0008t0016g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.830-899A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929760 | |||||||
| chr5:56929942 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(108): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.829+722A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929942 | |||||||
| chr5:56930060 | A | T | 1 | a0001c0001t0002g0038 | 2 | HG00609.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.829+604T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930060 | |||||||
| chr5:56930281 | C | T | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.829+383G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930281 | |||||||
| chr5:56930384 | A | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(38): Show |
99 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.829+280T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930384 | |||||||
| chr5:56930502 | A | G | 1 | a0001c0002t0001g0062 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.829+162T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930502 | |||||||
| chr5:56930583 | T | C | 65 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(62): Show |
112 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.829+81A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930583 | |||||||
| chr5:56930778 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(36): Show |
97 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.748-33C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56930778 | |||||||
| chr5:56930816 | G | A | 1 | a0001c0001t0002g0039 | 2 | HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.748-71C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56930816 | |||||||
| chr5:56930962 | A | G | 1 | a0001c0008t0016g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.748-217T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56930962 | |||||||
| chr5:56930997 | CT | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(140): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.748-253delA | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56930997 | |||||||
| chr5:56931053 | A | C | 1 | a0001c0002t0001g0051 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.748-308T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931053 | |||||||
| chr5:56931150 | C | T | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-405G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931150 | |||||||
| chr5:56931201 | G | C | 5 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(2): Show |
7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-456C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931201 | |||||||
| chr5:56931242 | C | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(108): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.748-497G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931242 | |||||||
| chr5:56931463 | T | G | 1 | a0001c0002t0003g0084 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-718A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931463 | |||||||
| chr5:56931466 | G | A | 1 | a0001c0002t0003g0084 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-721C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931466 | |||||||
| chr5:56931467 | T | C | 1 | a0001c0002t0003g0084 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-722A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931467 | |||||||
| chr5:56931499 | T | A | 53 | a0001c0001t0001g0152 a0001c0001t0002g0005 a0001c0001t0002g0010 others(50): Show |
96 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.748-754A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931499 | |||||||
| chr5:56931552 | G | GATAA | 32 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(29): Show |
51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.748-808_748-807ins others(4): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931552 | |||||||
| chr5:56931630 | C | T | 1 | a0001c0004t0002g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.748-885G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931630 | |||||||
| chr5:56931632 | G | A | 2 | a0002c0003t0001g0171 a0002c0003t0001g0172 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.748-887C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931632 | |||||||
| chr5:56931642 | G | A | 1 | a0001c0002t0003g0088 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.748-897C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931642 | |||||||
| chr5:56931744 | T | C | 5 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(2): Show |
7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-999A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931744 | |||||||
| chr5:56931797 | A | G | 13 | a0002c0003t0001g0009 a0002c0003t0001g0044 a0002c0003t0001g0102 others(10): Show |
21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.748-1052T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931797 | |||||||
| chr5:56932006 | T | C | 1 | a0001c0001t0002g0147 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.747+1241A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932006 | |||||||
| chr5:56932074 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.747+1173G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932074 | |||||||
| chr5:56932164 | G | A | 1 | a0001c0002t0003g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.747+1083C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932164 | |||||||
| chr5:56932173 | G | A | 3 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0153 |
3 | NA18963.hp1 NA19078.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.747+1074C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932173 | |||||||
| chr5:56932213 | T | C | 14 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0030 others(11): Show |
27 | HG00423.hp1 HG00642.hp1 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.747+1034A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932213 | |||||||
| chr5:56932344 | A | G | 1 | a0001c0001t0002g0036 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.747+903T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932344 | |||||||
| chr5:56932482 | G | A | 1 | a0001c0001t0002g0040 | 2 | HG01106.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.747+765C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932482 | |||||||
| chr5:56932574 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(108): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.747+673T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932574 | |||||||
| chr5:56932618 | G | A | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.747+629C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932618 | |||||||
| chr5:56932640 | G | A | 32 | a0001c0001t0002g0150 a0001c0002t0003g0008 a0001c0002t0003g0015 others(29): Show |
51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.747+607C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932640 | |||||||
| chr5:56932644 | T | C | 1 | a0001c0004t0002g0119 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.747+603A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932644 | |||||||
| chr5:56932668 | T | C | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.747+579A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932668 | |||||||
| chr5:56932678 | A | T | 1 | a0001c0002t0001g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.747+569T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932678 | |||||||
| chr5:56932686 | G | A | 1 | a0001c0008t0016g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.747+561C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932686 | |||||||
| chr5:56932780 | T | C | 1 | a0001c0001t0002g0151 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.747+467A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932780 | |||||||
| chr5:56933151 | A | G | 5 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(2): Show |
7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.747+96T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56933151 | |||||||
| chr5:56933461 | C | T | 64 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(61): Show |
111 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.596-63G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933461 | |||||||
| chr5:56933826 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(38): Show |
99 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.596-428T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933826 | |||||||
| chr5:56933841 | T | C | 1 | a0001c0002t0001g0074 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.596-443A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933841 | |||||||
| chr5:56933913 | T | C | 1 | a0001c0002t0003g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.596-515A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933913 | |||||||
| chr5:56933953 | GGA | G | 59 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(56): Show |
104 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.596-557_596-556del others(2): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933953 | |||||||
| chr5:56934142 | G | C | 6 | a0002c0003t0001g0009 a0002c0003t0001g0102 a0002c0003t0001g0103 others(3): Show |
13 | HG02145.hp1 HG02572.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.596-744C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934142 | |||||||
| chr5:56934269 | T | C | 1 | a0001c0001t0002g0153 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.596-871A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934269 | |||||||
| chr5:56934343 | A | G | 2 | a0002c0003t0001g0179 a0002c0003t0001g0180 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.596-945T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934343 | |||||||
| chr5:56934408 | A | C | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-1010T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934408 | |||||||
| chr5:56934461 | T | C | 1 | a0001c0005t0002g0134 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.595+967A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934461 | |||||||
| chr5:56934544 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0164 |
3 | HG02109.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.595+884C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934544 | |||||||
| chr5:56934724 | GA | G | 79 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(76): Show |
180 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.595+703delT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934724 | |||||||
| chr5:56934821 | T | C | 1 | a0001c0002t0003g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.595+607A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934821 | |||||||
| chr5:56934829 | T | C | 1 | a0001c0001t0002g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.595+599A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934829 | |||||||
| chr5:56934895 | T | C | 1 | a0001c0002t0003g0085 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.595+533A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934895 | |||||||
| chr5:56935207 | C | A | 2 | a0001c0002t0001g0013 a0001c0002t0012g0067 |
6 | HG00558.hp2 NA18991.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+221G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56935207 | |||||||
| chr5:56935227 | G | T | 3 | a0001c0002t0003g0020 a0001c0002t0003g0091 a0001c0002t0007g0090 |
5 | HG00673.hp1 NA18959.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+201C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56935227 | |||||||
| chr5:56935309 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.595+119G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56935309 | |||||||
| chr5:56935593 | A | G | 1 | a0001c0002t0001g0071 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.522+73T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 6/12 | chr5 | 56935593 | |||||||
| chr5:56935782 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0186 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.437-31G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56935782 | |||||||
| chr5:56935855 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.437-104T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56935855 | |||||||
| chr5:56936216 | CA | C | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.437-466delT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56936216 | |||||||
| chr5:56936721 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.436+857A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56936721 | |||||||
| chr5:56936768 | T | C | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.436+810A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56936768 | |||||||
| chr5:56937149 | G | A | 2 | a0001c0002t0001g0014 a0001c0002t0001g0060 |
6 | HG01884.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+429C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56937149 | |||||||
| chr5:56937201 | A | T | 1 | a0001c0002t0001g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.436+377T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56937201 | |||||||
| chr5:56937329 | G | A | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.436+249C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56937329 | |||||||
| chr5:56937400 | A | G | 1 | a0001c0002t0001g0049 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.436+178T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56937400 | |||||||
| chr5:56937714 | G | A | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.316-16C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56937714 | |||||||
| chr5:56937724 | C | G | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.316-26G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56937724 | |||||||
| chr5:56937861 | T | G | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.316-163A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56937861 | |||||||
| chr5:56937910 | C | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(36): Show |
97 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.316-212G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56937910 | |||||||
| chr5:56938104 | A | G | 1 | a0001c0002t0003g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.316-406T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56938104 | |||||||
| chr5:56938186 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.316-488C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56938186 | |||||||
| chr5:56938206 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.316-508A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56938206 | |||||||
| chr5:56938631 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.315+252A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56938631 | |||||||
| chr5:56939251 | G | C | 1 | a0001c0001t0002g0154 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.181-234C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939251 | |||||||
| chr5:56939477 | C | T | 1 | a0001c0002t0003g0030 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.181-460G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939477 | |||||||
| chr5:56939615 | T | G | 5 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(2): Show |
7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-598A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939615 | |||||||
| chr5:56939685 | C | T | 5 | a0001c0001t0002g0133 a0001c0005t0002g0037 a0001c0005t0002g0045 others(2): Show |
7 | HG00735.hp2 HG01257.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-668G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939685 | |||||||
| chr5:56939721 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(122): Show |
287 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.181-704G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939721 | |||||||
| chr5:56939794 | C | A | 1 | a0001c0002t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.181-777G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939794 | |||||||
| chr5:56939860 | T | A | 1 | a0001c0001t0006g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.181-843A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939860 | |||||||
| chr5:56939863 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.181-846A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939863 | |||||||
| chr5:56939992 | A | G | 3 | a0001c0001t0002g0036 a0001c0001t0002g0131 a0001c0001t0002g0163 |
4 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-975T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939992 | |||||||
| chr5:56940149 | G | A | 1 | a0002c0003t0001g0172 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.181-1132C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940149 | |||||||
| chr5:56940186 | C | T | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.181-1169G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940186 | |||||||
| chr5:56940240 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.181-1223A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940240 | |||||||
| chr5:56940301 | T | C | 6 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-1284A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940301 | |||||||
| chr5:56940349 | T | C | 80 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(77): Show |
181 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.181-1332A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940349 | |||||||
| chr5:56940540 | T | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.181-1523A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940540 | |||||||
| chr5:56940724 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.181-1707C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940724 | |||||||
| chr5:56940828 | G | C | 1 | a0001c0002t0003g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.181-1811C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940828 | |||||||
| chr5:56940901 | C | G | 1 | a0001c0008t0016g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.181-1884G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940901 | |||||||
| chr5:56941073 | T | G | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.181-2056A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941073 | |||||||
| chr5:56941108 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.181-2091A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941108 | |||||||
| chr5:56941151 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.181-2134C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941151 | |||||||
| chr5:56941203 | T | C | 3 | a0001c0004t0002g0122 a0001c0004t0002g0123 a0001c0004t0002g0124 |
3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.181-2186A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941203 | |||||||
| chr5:56941239 | A | G | 1 | a0001c0001t0001g0016 | 4 | NA18979.hp2 NA18982.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-2222T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941239 | |||||||
| chr5:56941267 | T | C | 1 | a0001c0002t0003g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.181-2250A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941267 | |||||||
| chr5:56941308 | T | A | 42 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(39): Show |
124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.181-2291A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941308 | |||||||
| chr5:56941328 | G | A | 42 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(39): Show |
124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.181-2311C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941328 | |||||||
| chr5:56941467 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.181-2450G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941467 | |||||||
| chr5:56941838 | C | A | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.181-2821G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941838 | |||||||
| chr5:56941870 | A | G | 1 | a0001c0001t0002g0017 | 4 | HG00438.hp1 HG03239.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-2853T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941870 | |||||||
| chr5:56941880 | T | G | 1 | a0001c0001t0002g0157 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.181-2863A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941880 | |||||||
| chr5:56941932 | T | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0107 others(2): Show |
17 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.181-2915A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941932 | |||||||
| chr5:56941973 | C | G | 6 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-2956G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941973 | |||||||
| chr5:56942000 | G | T | 3 | a0001c0001t0002g0036 a0001c0001t0002g0131 a0001c0001t0002g0163 |
4 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-2983C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942000 | |||||||
| chr5:56942018 | G | GA | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-3002dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942018 | |||||||
| chr5:56942055 | CAGTTAAG others(4): Show |
C | 9 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0080 others(6): Show |
20 | HG00423.hp1 HG01516.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.181-3049_181-3039d others(13): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942055 | |||||||
| chr5:56942299 | G | C | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-3282C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942299 | |||||||
| chr5:56942313 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.181-3296T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942313 | |||||||
| chr5:56942335 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0186 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.181-3318A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942335 | |||||||
| chr5:56942377 | G | A | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.181-3360C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942377 | |||||||
| chr5:56942578 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.181-3561A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942578 | |||||||
| chr5:56942712 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.181-3695A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942712 | |||||||
| chr5:56942770 | A | G | 79 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(76): Show |
180 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.181-3753T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942770 | |||||||
| chr5:56942812 | G | C | 2 | a0001c0002t0001g0027 a0001c0002t0001g0068 |
3 | HG02559.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.181-3795C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942812 | |||||||
| chr5:56942984 | A | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(65): Show |
199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.180+3942T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942984 | |||||||
| chr5:56943335 | T | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(20): Show |
71 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.180+3591A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943335 | |||||||
| chr5:56943335 | T | TA | 68 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(65): Show |
169 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.180+3590dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943335 | |||||||
| chr5:56943350 | TAGA | T | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+3573_180+3575d others(5): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943350 | |||||||
| chr5:56943500 | C | T | 1 | a0001c0002t0003g0089 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.180+3426G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943500 | |||||||
| chr5:56943542 | C | G | 73 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(70): Show |
174 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.180+3384G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943542 | |||||||
| chr5:56943558 | G | A | 3 | a0002c0003t0001g0044 a0002c0003t0001g0173 a0002c0003t0001g0174 |
4 | HG02559.hp1 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+3368C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943558 | |||||||
| chr5:56943644 | T | A | 2 | a0001c0002t0003g0033 a0001c0002t0011g0098 |
3 | NA18948.hp2 NA19060.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.180+3282A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943644 | |||||||
| chr5:56943745 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0121 |
2 | NA18955.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.180+3181T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943745 | |||||||
| chr5:56943771 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.180+3155C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943771 | |||||||
| chr5:56943800 | G | A | 13 | a0002c0003t0001g0009 a0002c0003t0001g0044 a0002c0003t0001g0102 others(10): Show |
21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.180+3126C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943800 | |||||||
| chr5:56943850 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.180+3076C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943850 | |||||||
| chr5:56943887 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.180+3039G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943887 | |||||||
| chr5:56944088 | C | T | 5 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(2): Show |
7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+2838G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944088 | |||||||
| chr5:56944099 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.180+2827T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944099 | |||||||
| chr5:56944117 | AG | A | 16 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0032 others(13): Show |
22 | HG00673.hp1 HG02080.hp1 HG02698.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+2808delC | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944117 | |||||||
| chr5:56944152 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0022 others(14): Show |
53 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.180+2774C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944152 | |||||||
| chr5:56944238 | G | A | 2 | a0002c0003t0001g0179 a0002c0003t0001g0180 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.180+2688C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944238 | |||||||
| chr5:56944253 | C | T | 1 | a0001c0002t0003g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.180+2673G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944253 | |||||||
| chr5:56944288 | G | A | 1 | a0001c0008t0016g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.180+2638C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944288 | |||||||
| chr5:56944425 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(118): Show |
282 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.180+2501T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944425 | |||||||
| chr5:56944460 | G | A | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.180+2466C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944460 | |||||||
| chr5:56944475 | C | G | 15 | a0001c0001t0005g0023 a0001c0001t0015g0118 a0002c0003t0001g0009 others(12): Show |
25 | HG01081.hp2 HG01433.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.180+2451G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944475 | |||||||
| chr5:56944480 | C | CA | 5 | a0001c0001t0002g0158 a0001c0001t0002g0178 a0001c0001t0005g0023 others(2): Show |
8 | HG01081.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+2445dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944480 | |||||||
| chr5:56944526 | C | T | 1 | a0001c0002t0003g0079 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.180+2400G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944526 | |||||||
| chr5:56944799 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.180+2127T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944799 | |||||||
| chr5:56944913 | T | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0159 |
3 | HG01256.hp2 HG01258.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.180+2013A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944913 | |||||||
| chr5:56944921 | T | TCC | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.180+2003_180+2004d others(4): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944921 | |||||||
| chr5:56944957 | A | G | 2 | a0001c0002t0001g0026 a0001c0002t0001g0069 |
3 | HG02280.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.180+1969T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944957 | |||||||
| chr5:56945174 | G | A | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+1752C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945174 | |||||||
| chr5:56945192 | G | A | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.180+1734C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945192 | |||||||
| chr5:56945457 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(21): Show |
72 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.180+1469G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945457 | |||||||
| chr5:56945492 | G | C | 1 | a0001c0001t0002g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.180+1434C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945492 | |||||||
| chr5:56945665 | C | T | 1 | a0001c0002t0001g0029 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.180+1261G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945665 | |||||||
| chr5:56945851 | T | A | 15 | a0001c0001t0005g0023 a0001c0001t0015g0118 a0002c0003t0001g0009 others(12): Show |
25 | HG01081.hp2 HG01433.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.180+1075A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945851 | |||||||
| chr5:56945862 | A | G | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.180+1064T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945862 | |||||||
| chr5:56945882 | T | C | 15 | a0001c0001t0005g0023 a0001c0001t0015g0118 a0002c0003t0001g0009 others(12): Show |
25 | HG01081.hp2 HG01433.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.180+1044A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945882 | |||||||
| chr5:56946041 | G | T | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+885C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946041 | |||||||
| chr5:56946132 | A | G | 5 | a0001c0002t0001g0007 a0001c0002t0001g0028 a0001c0002t0001g0056 others(2): Show |
23 | HG00544.hp1 HG00597.hp2 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.180+794T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946132 | |||||||
| chr5:56946206 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.180+720C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946206 | |||||||
| chr5:56946246 | T | A | 1 | a0001c0001t0002g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.180+680A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946246 | |||||||
| chr5:56946271 | T | C | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.180+655A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946271 | |||||||
| chr5:56946406 | C | G | 2 | a0001c0001t0002g0043 a0001c0001t0002g0164 |
3 | HG02109.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.180+520G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946406 | |||||||
| chr5:56946496 | C | T | 42 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(39): Show |
124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.180+430G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946496 | |||||||
| chr5:56946546 | C | A | 1 | a0001c0001t0002g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.180+380G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946546 | |||||||
| chr5:56946721 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(179): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.180+205A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946721 | |||||||
| chr5:56946787 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.180+139G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946787 | |||||||
| chr5:56946816 | G | GA | 7 | a0001c0001t0005g0023 a0001c0001t0015g0118 a0001c0006t0002g0181 others(4): Show |
9 | HG01081.hp2 HG01109.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+109dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946816 | |||||||
| chr5:56946838 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.180+88G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946838 | |||||||
| chr5:56947301 | T | C | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.35-230A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947301 | |||||||
| chr5:56947319 | A | T | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.35-248T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947319 | |||||||
| chr5:56947353 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.35-282C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947353 | |||||||
| chr5:56947427 | A | T | 1 | a0002c0003t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.35-356T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947427 | |||||||
| chr5:56947453 | T | C | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-382A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947453 | |||||||
| chr5:56947476 | C | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(36): Show |
97 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.35-405G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947476 | |||||||
| chr5:56947519 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.35-448T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947519 | |||||||
| chr5:56947735 | C | A | 1 | a0001c0008t0016g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.35-664G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947735 | |||||||
| chr5:56947858 | T | C | 42 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(39): Show |
124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.35-787A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947858 | |||||||
| chr5:56947939 | T | C | 5 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(2): Show |
7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-868A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947939 | |||||||
| chr5:56948138 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.35-1067G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948138 | |||||||
| chr5:56948139 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(37): Show |
98 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.35-1068T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948139 | |||||||
| chr5:56948429 | C | T | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.35-1358G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948429 | |||||||
| chr5:56948464 | G | A | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.35-1393C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948464 | |||||||
| chr5:56948481 | T | G | 4 | a0001c0001t0002g0043 a0001c0001t0002g0164 a0001c0001t0002g0165 others(1): Show |
5 | HG02109.hp1 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-1410A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948481 | |||||||
| chr5:56948560 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0177 |
3 | HG02683.hp1 HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.35-1489C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948560 | |||||||
| chr5:56948565 | A | G | 1 | a0001c0002t0001g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.35-1494T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948565 | |||||||
| chr5:56948576 | G | A | 1 | a0001c0002t0003g0099 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.35-1505C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948576 | |||||||
| chr5:56948704 | A | G | 1 | a0001c0008t0016g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.35-1633T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948704 | |||||||
| chr5:56948777 | G | A | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.35-1706C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948777 | |||||||
| chr5:56948936 | T | C | 1 | a0001c0002t0001g0028 | 2 | HG03669.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.34+1692A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948936 | |||||||
| chr5:56948973 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.34+1655T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948973 | |||||||
| chr5:56949104 | C | T | 2 | a0001c0005t0002g0045 a0001c0005t0002g0175 |
3 | HG01952.hp1 NA20300.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.34+1524G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949104 | |||||||
| chr5:56949121 | C | T | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.34+1507G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949121 | |||||||
| chr5:56949148 | G | C | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.34+1480C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949148 | |||||||
| chr5:56949217 | G | C | 74 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(71): Show |
175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.34+1411C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949217 | |||||||
| chr5:56949268 | G | GAAC | 5 | a0001c0004t0002g0024 a0001c0004t0002g0119 a0001c0004t0002g0122 others(2): Show |
7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+1357_34+1359dup others(3): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949268 | |||||||
| chr5:56949313 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(21): Show |
72 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.34+1315T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949313 | |||||||
| chr5:56949351 | C | T | 13 | a0002c0003t0001g0009 a0002c0003t0001g0044 a0002c0003t0001g0102 others(10): Show |
21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.34+1277G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949351 | |||||||
| chr5:56949442 | C | G | 31 | a0001c0002t0003g0008 a0001c0002t0003g0015 a0001c0002t0003g0020 others(28): Show |
50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.34+1186G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949442 | |||||||
| chr5:56949501 | T | C | 1 | a0001c0001t0002g0018 | 4 | HG00735.hp1 HG01516.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+1127A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949501 | |||||||
| chr5:56949547 | G | A | 1 | a0001c0001t0002g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.34+1081C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949547 | |||||||
| chr5:56949556 | A | G | 1 | a0001c0002t0001g0019 | 3 | HG00423.hp2 NA18612.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.34+1072T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949556 | |||||||
| chr5:56949776 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.34+852A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949776 | |||||||
| chr5:56949816 | C | T | 1 | a0001c0002t0003g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.34+812G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949816 | |||||||
| chr5:56949838 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.34+790G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949838 | |||||||
| chr5:56949933 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.34+695C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949933 | |||||||
| chr5:56949976 | C | G | 75 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(72): Show |
176 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.34+652G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949976 | |||||||
| chr5:56950021 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.34+607C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950021 | |||||||
| chr5:56950265 | TACTC | T | 3 | a0001c0004t0002g0122 a0001c0004t0002g0123 a0001c0004t0002g0124 |
3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.34+359_34+362delGA others(2): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950265 | |||||||
| chr5:56950338 | C | G | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+290G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950338 | |||||||
| chr5:56950449 | A | AAAC | 79 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(76): Show |
180 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.34+176_34+178dupGT others(1): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950449 | |||||||
| chr5:56950516 | C | A | 1 | a0001c0006t0002g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.34+112G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950516 | |||||||
| chr5:56950551 | G | C | 3 | a0001c0004t0002g0122 a0001c0004t0002g0123 a0001c0004t0002g0124 |
3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.34+77C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950551 | |||||||
| chr5:56950663 | G | C | 1 | a0001c0002t0003g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.10-11C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950663 | |||||||
| chr5:56950758 | T | G | 1 | a0001c0002t0003g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.10-106A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950758 | |||||||
| chr5:56950763 | A | G | 1 | a0001c0002t0001g0048 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.10-111T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950763 | |||||||
| chr5:56950783 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(122): Show |
287 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.10-131T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950783 | |||||||
| chr5:56950893 | G | A | 1 | a0001c0008t0016g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.10-241C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950893 | |||||||
| chr5:56951008 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.10-356T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951008 | |||||||
| chr5:56951025 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.10-373C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951025 | |||||||
| chr5:56951075 | G | A | 1 | a0001c0001t0002g0043 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.10-423C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951075 | |||||||
| chr5:56951196 | C | A | 7 | a0002c0003t0001g0044 a0002c0003t0001g0170 a0002c0003t0001g0171 others(4): Show |
8 | HG01433.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-544G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951196 | |||||||
| chr5:56951209 | G | A | 2 | a0001c0005t0002g0045 a0001c0005t0002g0175 |
3 | HG01952.hp1 NA20300.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.10-557C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951209 | |||||||
| chr5:56951446 | T | G | 1 | a0001c0001t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.9+648A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951446 | |||||||
| chr5:56951516 | T | G | 1 | a0001c0001t0002g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.9+578A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951516 | |||||||
| chr5:56951552 | C | T | 23 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0013 others(20): Show |
82 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.9+542G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951552 | |||||||
| chr5:56951701 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.9+393C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951701 | |||||||
| chr5:56951701 | G | T | 42 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(39): Show |
124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.9+393C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951701 | |||||||
| chr5:56951702 | GGGGGCTC others(25): Show |
G | 9 | a0001c0002t0001g0025 a0001c0002t0001g0048 a0001c0002t0001g0049 others(6): Show |
10 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.9+360_9+391delGGGC others(28): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951702 | |||||||
| chr5:56951831 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.9+263G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951831 | |||||||
| chr5:56951931 | G | A | 2 | a0002c0003t0001g0179 a0002c0003t0001g0180 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.9+163C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951931 | |||||||
| chr5:56951981 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.9+113G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951981 | |||||||
| chr5:56951988 | G | A | 5 | a0001c0006t0002g0181 a0001c0006t0002g0183 a0001c0006t0002g0184 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+106C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951988 | |||||||
| chr5:56952075 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.9+19C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56952075 | |||||||
| chr5:56952080 | G | C | 1 | a0001c0001t0002g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.9+14C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56952080 |