Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57708 |
| ensemblid | ENSG00000198160.15 |
| hgncid | 29657 |
| symbol | MIER1 |
| name | MIER1 transcriptional regulator |
| refseq_nuc | NM_001077700.3 |
| refseq_prot | NP_001071168.2 |
| ensembl_nuc | ENST00000401041.6 |
| ensembl_prot | ENSP00000383820.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 66924990 |
| end | 66988619 |
| strand | + |
| ver | v1.2 |
| region | chr1:66924990-66988619 |
| region5000 | chr1:66919990-66993619 |
| regionname0 | MIER1_chr1_66924990_66988619 |
| regionname5000 | MIER1_chr1_66919990_66993619 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 565 | 245 | 84 | 39 | 80 | 12 | 28 | 58 | MIER1_chr1_66919990_66993619 | MIER1 | MDGAS others(560): Show |
chr1 | 66919990 | 66993619 |
| a0002 | 0/0 | 565 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | MDGAS others(560): Show |
chr1 | 66919990 | 66993619 |
| a0003 | 0/0 | 565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | MDGAS others(560): Show |
chr1 | 66919990 | 66993619 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1695 | 240 | 79 | 39 | 80 | 12 | 28 | MIER1_chr1_66919990_66993619 | MIER1 | ATGGA others(1690): Show |
chr1 | 66919990 | 66993619 | ||
| a0001c0002 | 0/0 | 1695 | 3 | 3 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | ATGGA others(1690): Show |
chr1 | 66919990 | 66993619 | ||
| a0001c0004 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | ATGGA others(1690): Show |
chr1 | 66919990 | 66993619 | ||
| a0001c0005 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | ATGGA others(1690): Show |
chr1 | 66919990 | 66993619 | ||
| a0002c0003 | 0/0 | 1695 | 2 | 0 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | ATGGA others(1690): Show |
chr1 | 66919990 | 66993619 | ||
| a0003c0006 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | ATGGA others(1690): Show |
chr1 | 66919990 | 66993619 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5456 | 84 | 13 | 10 | 45 | 3 | 12 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0002 | 0/0 | 5473 | 50 | 9 | 8 | 23 | 4 | 6 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5468): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0003 | 0/0 | 5454 | 26 | 22 | 4 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5449): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0004 | 0/0 | 5458 | 23 | 12 | 5 | 2 | 2 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5453): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0005 | 0/0 | 5458 | 22 | 11 | 2 | 5 | 1 | 3 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5453): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0006 | 1/0 | 5456 | 8 | 0 | 4 | 0 | 1 | 2 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0007 | 0/0 | 5474 | 6 | 3 | 3 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5469): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0008 | 0/0 | 5458 | 3 | 3 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5453): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0009 | 0/0 | 5456 | 3 | 0 | 0 | 0 | 0 | 3 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0011 | 0/0 | 5456 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0012 | 0/0 | 5456 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0013 | 0/0 | 5456 | 2 | 0 | 1 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0014 | 0/0 | 5473 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5468): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0015 | 0/0 | 5456 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0016 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0017 | 0/0 | 5456 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0018 | 0/0 | 5456 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0019 | 0/0 | 5473 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5468): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0020 | 0/0 | 5473 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5468): Show |
chr1 | 66919990 | 66993619 |
| a0001c0001t0021 | 0/0 | 5473 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5468): Show |
chr1 | 66919990 | 66993619 |
| a0001c0002t0010 | 0/0 | 5456 | 3 | 3 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0004t0001 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0001c0005t0001 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0002c0003t0001 | 0/0 | 5456 | 2 | 0 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5451): Show |
chr1 | 66919990 | 66993619 |
| a0003c0006t0003 | 0/0 | 5454 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | AGGCC others(5449): Show |
chr1 | 66919990 | 66993619 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0006g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0006g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0006g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0008g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0009g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0009g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0012g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0012g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0013g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0013g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0014g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0014g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0015g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0016g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0017g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0018g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0020g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0001t0021g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0002t0010g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0002t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0001c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0002c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0002c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| a0003c0006t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | GBR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0065 | EUR | GBR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0188 | EUR | FIN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00621 | hp2 | a0001 | c0001 | t0015 | g0144 | EAS | CHS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00639 | hp2 | a0001 | c0001 | t0021 | g0178 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00738 | hp1 | a0003 | c0006 | t0003 | g0057 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0119 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0126 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0081 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01109 | hp2 | a0001 | c0001 | t0017 | g0148 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0169 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0170 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0168 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01256 | hp1 | a0001 | c0001 | t0013 | g0105 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0134 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0187 | EUR | IBS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0208 | EUR | IBS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01517 | hp2 | a0001 | c0001 | t0013 | g0102 | EUR | IBS | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02132 | hp1 | a0001 | c0001 | t0020 | g0217 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CDX | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0223 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0069 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0173 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0124 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0095 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0141 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0172 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02723 | hp2 | a0001 | c0001 | t0014 | g0222 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02738 | hp2 | a0001 | c0001 | t0009 | g0090 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02818 | hp2 | a0001 | c0002 | t0010 | g0008 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03209 | hp1 | a0001 | c0002 | t0010 | g0008 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03225 | hp2 | a0001 | c0001 | t0016 | g0068 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0092 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0175 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03669 | hp1 | a0001 | c0001 | t0009 | g0084 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0003 | SAS | STU | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0046 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0080 | SAS | BEB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | BEB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | STU | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0041 | SAS | STU | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | YRI | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18960 | hp1 | a0001 | c0001 | t0012 | g0100 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18979 | hp1 | a0001 | c0001 | t0012 | g0101 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19079 | hp1 | a0001 | c0001 | t0018 | g0135 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | YRI | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | YRI | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ASW | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20129 | hp2 | a0001 | c0002 | t0010 | g0050 | AFR | ASW | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0048 | EUR | TSI | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0192 | EUR | TSI | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0060 | EUR | TSI | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | GIH | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | GIH | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0070 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | USA | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | USA | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | USA | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | USA | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0174 | AFR | LWK | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0088 | REF | REF | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0190 | REF | REF | MIER1_chr1_66919990_66993619 | MIER1 | chr1 | 66919990 | 66993619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:66958089 | A | T | 1 | a0003 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.370A>T | p.Ser124Cys | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/14 | 409/5456 | 370/1698 | 124/565 | chr1 | 66958089 | |||
| chr1:66984748 | A | G | 1 | a0002 | 2 | HG00738.hp2 HG01256.hp2 |
missense_variant | MODERATE | c.1546A>G | p.Arg516Gly | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1585/5456 | 1546/1698 | 516/565 | chr1 | 66984748 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:66926188 | G | A | 1 | a0001c0004 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.114G>A | p.Thr38Thr | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/14 | 153/5456 | 114/1698 | 38/565 | chr1 | 66926188 | |||
| chr1:66970935 | A | C | 1 | a0001c0002 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.900A>C | p.Gly300Gly | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/14 | 939/5456 | 900/1698 | 300/565 | chr1 | 66970935 | |||
| chr1:66984612 | G | A | 1 | a0001c0005 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1410G>A | p.Glu470Glu | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1449/5456 | 1410/1698 | 470/565 | chr1 | 66984612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:66985804 | G | A | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(1): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*904G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 904 | chr1 | 66985804 | ||||||
| chr1:66985814 | A | AT | 1 | a0001c0001t0001 | 5 | HG01934.hp2 HG02293.hp1 HG02300.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*937dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 938 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | |||||
| chr1:66985814 | AT | A | 5 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(2): Show |
17 | HG00423.hp1 HG01106.hp1 HG01256.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*937delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 937 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | |||||
| chr1:66985814 | ATT | A | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(4): Show |
27 | HG00140.hp1 HG01106.hp2 HG01255.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*936_*937delTT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 936 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | |||||
| chr1:66985814 | ATTT | A | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
66 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*935_*937delTTT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 935 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | |||||
| chr1:66985814 | ATTTT | A | 4 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(1): Show |
29 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*934_*937delTTTT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 934 | INFO_REALIGN_3_PRIME | chr1 | 66985814 | |||||
| chr1:66985835 | TTTA | T | 1 | a0001c0001t0004 | 11 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*936_*938delTTA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 936 | chr1 | 66985835 | ||||||
| chr1:66985919 | A | C | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0014 others(3): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1019A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1019 | chr1 | 66985919 | ||||||
| chr1:66986047 | T | C | 1 | a0001c0001t0015 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1147T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1147 | chr1 | 66986047 | ||||||
| chr1:66986215 | A | G | 1 | a0001c0001t0008 | 3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1315A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1315 | chr1 | 66986215 | ||||||
| chr1:66986239 | C | T | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0019 others(2): Show |
59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1339C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1339 | chr1 | 66986239 | ||||||
| chr1:66986241 | G | T | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0019 others(2): Show |
59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1341G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1341 | chr1 | 66986241 | ||||||
| chr1:66986254 | T | C | 1 | a0001c0001t0019 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1354 | chr1 | 66986254 | ||||||
| chr1:66986457 | A | G | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1557A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1557 | chr1 | 66986457 | ||||||
| chr1:66986639 | G | A | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0019 others(2): Show |
59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1739G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1739 | chr1 | 66986639 | ||||||
| chr1:66986731 | G | T | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(1): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1831G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1831 | chr1 | 66986731 | ||||||
| chr1:66986799 | G | A | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(1): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1899G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1899 | chr1 | 66986799 | ||||||
| chr1:66986864 | G | T | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1964 | chr1 | 66986864 | ||||||
| chr1:66986866 | A | T | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1966A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1966 | chr1 | 66986866 | ||||||
| chr1:66986868 | C | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1968C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1968 | chr1 | 66986868 | ||||||
| chr1:66986869 | C | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1969C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1969 | chr1 | 66986869 | ||||||
| chr1:66986870 | T | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1970T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1970 | chr1 | 66986870 | ||||||
| chr1:66986872 | G | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1972G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1972 | chr1 | 66986872 | ||||||
| chr1:66986875 | C | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1975 | chr1 | 66986875 | ||||||
| chr1:66986879 | G | T | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1979G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1979 | chr1 | 66986879 | ||||||
| chr1:66986880 | T | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1980T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1980 | chr1 | 66986880 | ||||||
| chr1:66986890 | T | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1990T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1990 | chr1 | 66986890 | ||||||
| chr1:66986893 | G | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1993G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1993 | chr1 | 66986893 | ||||||
| chr1:66986894 | T | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1994T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1994 | chr1 | 66986894 | ||||||
| chr1:66986898 | A | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1998A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 1998 | chr1 | 66986898 | ||||||
| chr1:66986903 | T | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2003T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2003 | chr1 | 66986903 | ||||||
| chr1:66986904 | T | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2004T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2004 | chr1 | 66986904 | ||||||
| chr1:66986905 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2005T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2005 | chr1 | 66986905 | ||||||
| chr1:66986909 | A | T | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2009A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2009 | chr1 | 66986909 | ||||||
| chr1:66986916 | G | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2016G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2016 | chr1 | 66986916 | ||||||
| chr1:66986918 | A | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2018 | chr1 | 66986918 | ||||||
| chr1:66986924 | T | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2024T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2024 | chr1 | 66986924 | ||||||
| chr1:66986925 | A | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2025A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2025 | chr1 | 66986925 | ||||||
| chr1:66986935 | T | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2035T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2035 | chr1 | 66986935 | ||||||
| chr1:66986936 | T | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2036T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2036 | chr1 | 66986936 | ||||||
| chr1:66986938 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2038T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2038 | chr1 | 66986938 | ||||||
| chr1:66986939 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2039T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2039 | chr1 | 66986939 | ||||||
| chr1:66986940 | G | T | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2040G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2040 | chr1 | 66986940 | ||||||
| chr1:66986945 | G | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2045G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2045 | chr1 | 66986945 | ||||||
| chr1:66986951 | G | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2051 | chr1 | 66986951 | ||||||
| chr1:66986952 | A | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2052A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2052 | chr1 | 66986952 | ||||||
| chr1:66986953 | T | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2053T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2053 | chr1 | 66986953 | ||||||
| chr1:66986955 | C | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2055C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2055 | chr1 | 66986955 | ||||||
| chr1:66986956 | C | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2056C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2056 | chr1 | 66986956 | ||||||
| chr1:66986960 | T | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2060T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2060 | chr1 | 66986960 | ||||||
| chr1:66986961 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2061T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2061 | chr1 | 66986961 | ||||||
| chr1:66986963 | A | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2063A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2063 | chr1 | 66986963 | ||||||
| chr1:66986964 | C | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2064C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2064 | chr1 | 66986964 | ||||||
| chr1:66986965 | C | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2065C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2065 | chr1 | 66986965 | ||||||
| chr1:66986974 | A | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2074A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2074 | chr1 | 66986974 | ||||||
| chr1:66986975 | A | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2075A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2075 | chr1 | 66986975 | ||||||
| chr1:66986976 | G | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2076G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2076 | chr1 | 66986976 | ||||||
| chr1:66986981 | A | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2081A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2081 | chr1 | 66986981 | ||||||
| chr1:66986982 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2082T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2082 | chr1 | 66986982 | ||||||
| chr1:66986984 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2084T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2084 | chr1 | 66986984 | ||||||
| chr1:66986985 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2085T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2085 | chr1 | 66986985 | ||||||
| chr1:66986986 | A | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2086A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2086 | chr1 | 66986986 | ||||||
| chr1:66986988 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2088 | chr1 | 66986988 | ||||||
| chr1:66986991 | C | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2091C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2091 | chr1 | 66986991 | ||||||
| chr1:66986992 | A | T | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2092A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2092 | chr1 | 66986992 | ||||||
| chr1:66986996 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2096T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2096 | chr1 | 66986996 | ||||||
| chr1:66987001 | A | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2101A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2101 | chr1 | 66987001 | ||||||
| chr1:66987004 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2104T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2104 | chr1 | 66987004 | ||||||
| chr1:66987008 | T | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2108T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2108 | chr1 | 66987008 | ||||||
| chr1:66987009 | G | C | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2109 | chr1 | 66987009 | ||||||
| chr1:66987011 | A | G | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2111A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2111 | chr1 | 66987011 | ||||||
| chr1:66987023 | C | T | 1 | a0001c0001t0017 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2123C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2123 | chr1 | 66987023 | ||||||
| chr1:66987034 | T | A | 1 | a0001c0001t0021 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2134T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2134 | chr1 | 66987034 | ||||||
| chr1:66987037 | A | G | 1 | a0001c0001t0020 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2137A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2137 | chr1 | 66987037 | ||||||
| chr1:66987146 | T | A | 1 | a0001c0001t0011 | 2 | HG02109.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2246T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2246 | chr1 | 66987146 | ||||||
| chr1:66987352 | A | G | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*2452A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2452 | chr1 | 66987352 | ||||||
| chr1:66987417 | C | A | 1 | a0001c0001t0014 | 2 | HG02257.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2517C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2517 | chr1 | 66987417 | ||||||
| chr1:66987437 | A | AT | 1 | a0001c0001t0007 | 6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2541dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2542 | INFO_REALIGN_3_PRIME | chr1 | 66987437 | |||||
| chr1:66987762 | A | AAT | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 |
48 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2874_*2875dupTA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 2876 | INFO_REALIGN_3_PRIME | chr1 | 66987762 | |||||
| chr1:66987907 | G | C | 1 | a0001c0001t0014 | 2 | HG02257.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3007G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3007 | chr1 | 66987907 | ||||||
| chr1:66987918 | ACT | A | 2 | a0001c0001t0003 a0003c0006t0003 |
27 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3021_*3022delCT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3021 | INFO_REALIGN_3_PRIME | chr1 | 66987918 | |||||
| chr1:66987947 | A | C | 1 | a0001c0001t0013 | 2 | HG01256.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3047A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3047 | chr1 | 66987947 | ||||||
| chr1:66987968 | G | A | 1 | a0001c0001t0009 | 3 | HG02738.hp2 HG03491.hp2 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3068G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3068 | chr1 | 66987968 | ||||||
| chr1:66988113 | T | TGTGTGCT others(10): Show |
6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0014 others(3): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3214_*3215insTGTG others(13): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3215 | INFO_REALIGN_3_PRIME | chr1 | 66988113 | |||||
| chr1:66988408 | A | T | 1 | a0001c0001t0014 | 2 | HG02257.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3508A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3508 | chr1 | 66988408 | ||||||
| chr1:66988450 | A | G | 1 | a0001c0001t0012 | 2 | NA18960.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3550A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3550 | chr1 | 66988450 | ||||||
| chr1:66988513 | C | T | 1 | a0001c0002t0010 | 3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3613C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3613 | chr1 | 66988513 | ||||||
| chr1:66988554 | A | G | 2 | a0001c0001t0011 a0001c0001t0016 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3654A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3654 | chr1 | 66988554 | ||||||
| chr1:66988604 | A | G | 1 | a0001c0001t0004 | 23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3704A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 14/14 | 3704 | chr1 | 66988604 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:66925175 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.67+80C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925175 | |||||||
| chr1:66925316 | G | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.67+221G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925316 | |||||||
| chr1:66925320 | G | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.67+225G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925320 | |||||||
| chr1:66925324 | C | T | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.67+229C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925324 | |||||||
| chr1:66925520 | A | G | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.67+425A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925520 | |||||||
| chr1:66925642 | G | C | 16 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0018 others(13): Show |
17 | HG01192.hp1 HG01934.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-500G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 1/13 | chr1 | 66925642 | |||||||
| chr1:66926813 | T | C | 3 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 |
3 | HG01167.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.168+571T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66926813 | |||||||
| chr1:66926931 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.168+689A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66926931 | |||||||
| chr1:66926963 | A | G | 1 | a0001c0001t0002g0221 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.168+721A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66926963 | |||||||
| chr1:66927031 | A | G | 11 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(8): Show |
11 | HG00423.hp2 HG01243.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+789A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66927031 | |||||||
| chr1:66927206 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.168+964G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66927206 | |||||||
| chr1:66927730 | G | T | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.168+1488G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66927730 | |||||||
| chr1:66928145 | G | A | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG00140.hp1 HG02080.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.168+1903G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66928145 | |||||||
| chr1:66928217 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.168+1975A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66928217 | |||||||
| chr1:66928960 | C | T | 1 | a0001c0001t0004g0081 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.168+2718C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66928960 | |||||||
| chr1:66929024 | AG | A | 21 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0032 others(18): Show |
24 | HG01106.hp2 HG01255.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.168+2783delG | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929024 | |||||||
| chr1:66929235 | A | G | 5 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(2): Show |
5 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+2993A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929235 | |||||||
| chr1:66929548 | T | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0096 a0001c0004t0001g0095 |
4 | HG02572.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+3306T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929548 | |||||||
| chr1:66929636 | G | A | 1 | a0001c0001t0003g0017 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.168+3394G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929636 | |||||||
| chr1:66929652 | A | C | 16 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0018 others(13): Show |
17 | HG01192.hp1 HG01934.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.168+3410A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929652 | |||||||
| chr1:66929960 | G | A | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+3718G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66929960 | |||||||
| chr1:66930224 | G | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02027.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.168+3982G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930224 | |||||||
| chr1:66930539 | T | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(172): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.168+4297T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930539 | |||||||
| chr1:66930544 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.168+4302G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930544 | |||||||
| chr1:66930748 | C | T | 1 | a0001c0001t0004g0076 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.168+4506C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930748 | |||||||
| chr1:66930811 | C | T | 3 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 |
3 | HG01106.hp2 NA20300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.168+4569C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930811 | |||||||
| chr1:66930876 | C | G | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+4634C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66930876 | |||||||
| chr1:66931010 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.168+4768C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931010 | |||||||
| chr1:66931056 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.168+4814C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931056 | |||||||
| chr1:66931069 | C | A | 6 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(3): Show |
7 | HG01255.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+4827C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931069 | |||||||
| chr1:66931221 | G | T | 4 | a0001c0001t0002g0016 a0001c0001t0002g0210 a0001c0001t0002g0211 others(1): Show |
5 | NA18954.hp1 NA18965.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+4979G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931221 | |||||||
| chr1:66931491 | T | G | 1 | a0001c0001t0009g0084 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+5249T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931491 | |||||||
| chr1:66931525 | G | A | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.168+5283G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931525 | |||||||
| chr1:66931593 | A | G | 5 | a0001c0001t0004g0010 a0001c0001t0004g0072 a0001c0001t0004g0073 others(2): Show |
6 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+5351A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931593 | |||||||
| chr1:66931597 | C | A | 1 | a0001c0001t0003g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.168+5355C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931597 | |||||||
| chr1:66931641 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168+5399C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931641 | |||||||
| chr1:66931728 | G | A | 2 | a0001c0001t0004g0051 a0001c0001t0004g0052 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.168+5486G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931728 | |||||||
| chr1:66931970 | G | A | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | NA18980.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.168+5728G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931970 | |||||||
| chr1:66931974 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.168+5732T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66931974 | |||||||
| chr1:66932182 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.168+5940T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932182 | |||||||
| chr1:66932340 | T | A | 1 | a0001c0001t0002g0176 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168+6098T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932340 | |||||||
| chr1:66932435 | G | C | 24 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(21): Show |
26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.168+6193G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932435 | |||||||
| chr1:66932436 | A | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.168+6194A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932436 | |||||||
| chr1:66932501 | T | A | 2 | a0001c0001t0012g0100 a0001c0001t0012g0101 |
2 | NA18960.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.168+6259T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932501 | |||||||
| chr1:66932751 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.168+6509C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932751 | |||||||
| chr1:66932816 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168+6574A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932816 | |||||||
| chr1:66932870 | A | G | 1 | a0001c0001t0006g0014 | 2 | HG01099.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.168+6628A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932870 | |||||||
| chr1:66932924 | G | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.168+6682G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932924 | |||||||
| chr1:66932950 | A | G | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.168+6708A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66932950 | |||||||
| chr1:66933035 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0096 a0001c0004t0001g0095 |
4 | HG02572.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+6793C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933035 | |||||||
| chr1:66933233 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.169-6795G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933233 | |||||||
| chr1:66933355 | A | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02486.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.169-6673A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933355 | |||||||
| chr1:66933364 | T | C | 2 | a0001c0001t0001g0096 a0001c0004t0001g0095 |
2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.169-6664T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933364 | |||||||
| chr1:66933754 | A | G | 8 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(5): Show |
9 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-6274A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933754 | |||||||
| chr1:66933783 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(172): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.169-6245T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66933783 | |||||||
| chr1:66934143 | A | G | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-5885A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934143 | |||||||
| chr1:66934247 | A | G | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-5781A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934247 | |||||||
| chr1:66934391 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.169-5637C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934391 | |||||||
| chr1:66934405 | C | CT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(134): Show |
155 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.169-5607dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66934405 | ||||||
| chr1:66934405 | C | CTT | 9 | a0001c0001t0001g0161 a0001c0001t0007g0168 a0001c0001t0007g0169 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-5608_169-5607d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66934405 | ||||||
| chr1:66934414 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-5614T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934414 | |||||||
| chr1:66934472 | A | G | 1 | a0001c0001t0014g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169-5556A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934472 | |||||||
| chr1:66934572 | C | CT | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(155): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.169-5442dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66934572 | ||||||
| chr1:66934572 | C | CTT | 5 | a0001c0001t0001g0160 a0001c0001t0003g0030 a0001c0001t0003g0031 others(2): Show |
5 | HG01192.hp1 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-5443_169-5442d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66934572 | ||||||
| chr1:66934626 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.169-5402G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934626 | |||||||
| chr1:66934844 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.169-5184G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66934844 | |||||||
| chr1:66935118 | A | T | 26 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(23): Show |
28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.169-4910A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935118 | |||||||
| chr1:66935448 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.169-4580C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935448 | |||||||
| chr1:66935552 | T | G | 1 | a0001c0001t0004g0076 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.169-4476T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935552 | |||||||
| chr1:66935899 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.169-4129A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935899 | |||||||
| chr1:66935940 | ACT | A | 14 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(11): Show |
14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4087_169-4086d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935940 | |||||||
| chr1:66935943 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.169-4085T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935943 | |||||||
| chr1:66935946 | A | G | 14 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(11): Show |
14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4082A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935946 | |||||||
| chr1:66935947 | A | C | 14 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(11): Show |
14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4081A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935947 | |||||||
| chr1:66935979 | T | C | 1 | a0001c0001t0013g0105 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.169-4049T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66935979 | |||||||
| chr1:66936278 | G | A | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.169-3750G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936278 | |||||||
| chr1:66936283 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0002g0207 |
2 | NA18990.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.169-3745C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936283 | |||||||
| chr1:66936722 | C | T | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.169-3306C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936722 | |||||||
| chr1:66936771 | C | T | 1 | a0001c0001t0019g0175 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.169-3257C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936771 | |||||||
| chr1:66936913 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.169-3115T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936913 | |||||||
| chr1:66936985 | C | T | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-3043C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66936985 | |||||||
| chr1:66936998 | C | CA | 7 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
7 | HG00558.hp1 HG00639.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-3008dupA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66936998 | ||||||
| chr1:66936998 | CA | C | 89 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0085 others(86): Show |
96 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.169-3008delA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66936998 | ||||||
| chr1:66936998 | CAA | C | 36 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0002g0015 others(33): Show |
37 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.169-3009_169-3008d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66936998 | ||||||
| chr1:66936998 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0005g0038 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.169-3020_169-3008d others(15): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66936998 | ||||||
| chr1:66937021 | G | A | 1 | a0001c0001t0011g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.169-3007G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937021 | |||||||
| chr1:66937023 | G | A | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-3005G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937023 | |||||||
| chr1:66937149 | C | T | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.169-2879C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937149 | |||||||
| chr1:66937155 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(166): Show |
189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.169-2873T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937155 | |||||||
| chr1:66937156 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.169-2872G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937156 | |||||||
| chr1:66937270 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.169-2758G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937270 | |||||||
| chr1:66937335 | C | G | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-2693C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937335 | |||||||
| chr1:66937588 | AAAAAG | A | 26 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(23): Show |
28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.169-2425_169-2421d others(7): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 66937588 | ||||||
| chr1:66937632 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.169-2396C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66937632 | |||||||
| chr1:66938104 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.169-1924G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938104 | |||||||
| chr1:66938235 | A | G | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.169-1793A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938235 | |||||||
| chr1:66938290 | A | G | 2 | a0001c0001t0004g0064 a0001c0001t0004g0065 |
2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.169-1738A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938290 | |||||||
| chr1:66938817 | A | C | 1 | a0001c0001t0002g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.169-1211A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938817 | |||||||
| chr1:66938836 | T | G | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0158 |
3 | HG00621.hp1 NA18953.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.169-1192T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66938836 | |||||||
| chr1:66939195 | A | G | 2 | a0001c0001t0003g0066 a0001c0001t0003g0067 |
2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.169-833A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939195 | |||||||
| chr1:66939227 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(166): Show |
189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.169-801T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939227 | |||||||
| chr1:66939367 | G | A | 25 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(22): Show |
26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.169-661G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939367 | |||||||
| chr1:66939374 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(164): Show |
187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.169-654G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939374 | |||||||
| chr1:66939509 | A | G | 3 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 |
3 | HG01167.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.169-519A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939509 | |||||||
| chr1:66939781 | C | G | 1 | a0001c0001t0002g0171 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.169-247C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939781 | |||||||
| chr1:66939919 | A | G | 1 | a0002c0003t0001g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.169-109A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939919 | |||||||
| chr1:66939963 | C | T | 2 | a0001c0001t0011g0069 a0001c0001t0011g0070 |
2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.169-65C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 2/13 | chr1 | 66939963 | |||||||
| chr1:66940270 | CT | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(144): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.193+239delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66940270 | ||||||
| chr1:66940270 | CTT | C | 5 | a0001c0001t0001g0085 a0001c0001t0001g0111 a0001c0001t0002g0209 others(2): Show |
5 | HG02976.hp2 NA18954.hp2 NA19079.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+238_193+239del others(2): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66940270 | ||||||
| chr1:66940273 | T | TC | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+221_193+222ins others(1): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940273 | |||||||
| chr1:66940462 | G | A | 2 | a0001c0001t0003g0009 a0001c0001t0003g0053 |
3 | HG02630.hp1 HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193+410G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940462 | |||||||
| chr1:66940482 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.193+430C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940482 | |||||||
| chr1:66940854 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.193+802G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940854 | |||||||
| chr1:66940908 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.193+856G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66940908 | |||||||
| chr1:66941279 | G | A | 26 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(23): Show |
28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.193+1227G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941279 | |||||||
| chr1:66941323 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193+1271C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941323 | |||||||
| chr1:66941451 | T | G | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+1399T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941451 | |||||||
| chr1:66941550 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.193+1498C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941550 | |||||||
| chr1:66941821 | A | G | 2 | a0001c0001t0003g0066 a0001c0001t0003g0067 |
2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.193+1769A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941821 | |||||||
| chr1:66941863 | G | A | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.193+1811G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66941863 | |||||||
| chr1:66941970 | C | CA | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(133): Show |
153 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.193+1935dupA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66941970 | ||||||
| chr1:66941970 | C | CAA | 11 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0003g0009 others(8): Show |
13 | HG02074.hp2 HG02257.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.193+1934_193+1935d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66941970 | ||||||
| chr1:66941970 | C | CAAA | 13 | a0001c0001t0004g0051 a0001c0001t0004g0060 a0001c0001t0004g0061 others(10): Show |
13 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.193+1933_193+1935d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66941970 | ||||||
| chr1:66941970 | C | CAAAA | 5 | a0001c0001t0004g0010 a0001c0001t0004g0072 a0001c0001t0004g0073 others(2): Show |
6 | HG01243.hp1 HG02615.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+1932_193+1935d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66941970 | ||||||
| chr1:66942046 | T | G | 1 | a0001c0001t0004g0076 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.193+1994T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942046 | |||||||
| chr1:66942158 | A | G | 1 | a0001c0001t0004g0063 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193+2106A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942158 | |||||||
| chr1:66942218 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.193+2166G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942218 | |||||||
| chr1:66942232 | A | G | 1 | a0001c0001t0018g0135 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.193+2180A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942232 | |||||||
| chr1:66942671 | A | C | 1 | a0001c0001t0002g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.193+2619A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942671 | |||||||
| chr1:66942763 | G | A | 1 | a0001c0001t0005g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.193+2711G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942763 | |||||||
| chr1:66942771 | G | A | 2 | a0001c0001t0003g0020 a0001c0001t0003g0028 |
2 | HG01934.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.193+2719G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942771 | |||||||
| chr1:66942990 | T | C | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+2938T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66942990 | |||||||
| chr1:66943145 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.194-3005A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943145 | |||||||
| chr1:66943224 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.194-2926A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943224 | |||||||
| chr1:66943614 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.194-2536C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943614 | |||||||
| chr1:66943633 | T | A | 2 | a0001c0001t0003g0066 a0001c0001t0003g0067 |
2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.194-2517T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943633 | |||||||
| chr1:66943662 | C | T | 2 | a0001c0001t0003g0066 a0001c0001t0003g0067 |
2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.194-2488C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943662 | |||||||
| chr1:66943876 | A | G | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-2274A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66943876 | |||||||
| chr1:66943990 | AT | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.194-2148delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66943990 | ||||||
| chr1:66944131 | AATT | A | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 |
3 | HG01243.hp2 HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.194-2015_194-2013d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66944131 | ||||||
| chr1:66944303 | TA | T | 21 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0032 others(18): Show |
24 | HG01106.hp2 HG01255.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.194-1842delA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66944303 | ||||||
| chr1:66944355 | C | T | 26 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(23): Show |
28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.194-1795C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66944355 | |||||||
| chr1:66944371 | CTAGGTCC others(35): Show |
C | 1 | a0001c0001t0001g0133 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.194-1775_194-1734d others(44): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66944371 | ||||||
| chr1:66944488 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.194-1662A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66944488 | |||||||
| chr1:66944590 | A | AT | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.194-1558dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66944590 | ||||||
| chr1:66944721 | T | A | 3 | a0001c0001t0002g0194 a0001c0002t0010g0008 a0001c0002t0010g0050 |
4 | HG02486.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-1429T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66944721 | |||||||
| chr1:66945260 | G | GGT | 6 | a0001c0001t0002g0182 a0001c0001t0002g0199 a0001c0001t0002g0215 others(3): Show |
6 | HG00423.hp2 HG01943.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-883_194-882dup others(2): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945260 | ||||||
| chr1:66945267 | G | GTGTATAT others(1): Show |
3 | a0001c0001t0002g0206 a0001c0001t0002g0224 a0001c0001t0002g0225 |
3 | NA18967.hp1 NA19003.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.194-882_194-881ins others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | G | GTGTATAT others(3): Show |
1 | a0001c0001t0020g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.194-882_194-881ins others(10): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATA | G | 5 | a0001c0001t0002g0188 a0001c0001t0002g0204 a0001c0001t0002g0205 others(2): Show |
5 | HG00323.hp2 HG01261.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-836_194-833del others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATA | G | 8 | a0001c0001t0002g0176 a0001c0001t0002g0186 a0001c0001t0002g0187 others(5): Show |
8 | HG01516.hp2 HG01517.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-838_194-833del others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(1): Show |
G | 4 | a0001c0001t0002g0016 a0001c0001t0002g0184 a0001c0001t0002g0185 others(1): Show |
5 | HG01496.hp1 NA18954.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-840_194-833del others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(3): Show |
G | 5 | a0001c0001t0002g0015 a0001c0001t0002g0171 a0001c0001t0002g0183 others(2): Show |
6 | HG00558.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-842_194-833del others(10): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0002g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.194-844_194-833del others(12): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(7): Show |
G | 3 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0021g0178 |
3 | HG00639.hp2 HG02300.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.194-846_194-833del others(14): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(13): Show |
G | 3 | a0001c0001t0003g0019 a0001c0001t0003g0027 a0001c0001t0003g0029 |
3 | HG02559.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.194-852_194-833del others(20): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(15): Show |
G | 17 | a0001c0001t0001g0151 a0001c0001t0003g0017 a0001c0001t0003g0024 others(14): Show |
20 | HG01255.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.194-854_194-833del others(22): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(17): Show |
G | 11 | a0001c0001t0001g0136 a0001c0001t0001g0155 a0001c0001t0005g0037 others(8): Show |
11 | HG01106.hp2 HG02027.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.194-856_194-833del others(24): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(19): Show |
G | 26 | a0001c0001t0001g0150 a0001c0001t0002g0177 a0001c0001t0002g0195 others(23): Show |
28 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.194-858_194-833del others(26): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(21): Show |
G | 5 | a0001c0001t0001g0132 a0001c0001t0001g0149 a0001c0001t0017g0148 others(2): Show |
6 | HG01109.hp2 HG02129.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-860_194-833del others(28): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945267 | GTATATAT others(23): Show |
G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(106): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-862_194-833del others(30): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945267 | ||||||
| chr1:66945269 | A | G | 4 | a0001c0001t0002g0213 a0001c0001t0002g0221 a0001c0001t0003g0058 others(1): Show |
4 | HG01167.hp1 HG03139.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-881A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945269 | |||||||
| chr1:66945271 | A | G | 2 | a0001c0001t0002g0202 a0001c0001t0002g0218 |
2 | HG01243.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.194-879A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945271 | |||||||
| chr1:66945273 | A | G | 4 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0214 others(1): Show |
4 | HG01261.hp1 HG02129.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-877A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945273 | |||||||
| chr1:66945279 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0203 |
3 | HG00558.hp2 NA18995.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.194-871A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945279 | |||||||
| chr1:66945289 | A | G | 3 | a0001c0001t0003g0019 a0001c0001t0003g0027 a0001c0001t0003g0029 |
3 | HG02559.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.194-861A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945289 | |||||||
| chr1:66945291 | A | G | 17 | a0001c0001t0001g0151 a0001c0001t0003g0017 a0001c0001t0003g0024 others(14): Show |
20 | HG01255.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.194-859A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945291 | |||||||
| chr1:66945291 | ATATATAT others(23): Show |
A | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.194-858_194-829del others(30): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945291 | |||||||
| chr1:66945292 | TATATATA others(19): Show |
T | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.194-856_194-831del others(26): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945292 | ||||||
| chr1:66945293 | A | G | 11 | a0001c0001t0001g0136 a0001c0001t0001g0155 a0001c0001t0005g0037 others(8): Show |
11 | HG01106.hp2 HG02027.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.194-857A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945293 | |||||||
| chr1:66945295 | A | G | 19 | a0001c0001t0001g0150 a0001c0001t0003g0004 a0001c0001t0003g0009 others(16): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.194-855A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945295 | |||||||
| chr1:66945297 | A | G | 5 | a0001c0001t0001g0132 a0001c0001t0001g0149 a0001c0001t0017g0148 others(2): Show |
6 | HG01109.hp2 HG02129.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-853A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945297 | |||||||
| chr1:66945299 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(106): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-851A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945299 | |||||||
| chr1:66945308 | TATATATA others(3): Show |
T | 2 | a0001c0001t0007g0168 a0001c0001t0007g0172 |
2 | HG01192.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.194-840_194-831del others(10): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 66945308 | ||||||
| chr1:66945316 | T | A | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0020g0217 |
3 | HG00423.hp2 HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.194-834T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945316 | |||||||
| chr1:66945318 | A | T | 1 | a0001c0001t0007g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194-832A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945318 | |||||||
| chr1:66945323 | C | A | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.194-827C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945323 | |||||||
| chr1:66945324 | C | A | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.194-826C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945324 | |||||||
| chr1:66945374 | T | G | 14 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(11): Show |
14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.194-776T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945374 | |||||||
| chr1:66945478 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.194-672C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945478 | |||||||
| chr1:66945501 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.194-649T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945501 | |||||||
| chr1:66945545 | G | A | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.194-605G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945545 | |||||||
| chr1:66945641 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.194-509T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945641 | |||||||
| chr1:66945909 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
7 | HG00423.hp1 HG01106.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-241T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945909 | |||||||
| chr1:66945973 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0154 |
2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.194-177C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66945973 | |||||||
| chr1:66946017 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02027.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.194-133A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 3/13 | chr1 | 66946017 | |||||||
| chr1:66946402 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.339+107T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946402 | |||||||
| chr1:66946436 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.339+141G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946436 | |||||||
| chr1:66946552 | G | A | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.339+257G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946552 | |||||||
| chr1:66946578 | G | T | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(44): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.339+283G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946578 | |||||||
| chr1:66946584 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02080.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.339+289A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946584 | |||||||
| chr1:66946685 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.339+390A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946685 | |||||||
| chr1:66946828 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.339+533A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946828 | |||||||
| chr1:66946936 | TC | T | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.339+643delC | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66946936 | ||||||
| chr1:66946967 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.339+672T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66946967 | |||||||
| chr1:66947040 | T | A | 1 | a0001c0001t0017g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.339+745T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947040 | |||||||
| chr1:66947139 | T | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(164): Show |
187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.339+844T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947139 | |||||||
| chr1:66947231 | G | T | 1 | a0003c0006t0003g0057 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.339+936G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947231 | |||||||
| chr1:66947235 | G | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.339+940G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947235 | |||||||
| chr1:66947270 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.339+975C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947270 | |||||||
| chr1:66947308 | C | G | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.339+1013C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947308 | |||||||
| chr1:66947368 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.339+1073A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947368 | |||||||
| chr1:66947489 | A | G | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.339+1194A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947489 | |||||||
| chr1:66947792 | C | T | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.339+1497C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947792 | |||||||
| chr1:66947794 | C | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0162 |
3 | HG01891.hp1 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.339+1499C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947794 | |||||||
| chr1:66947795 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.339+1500A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947795 | |||||||
| chr1:66947902 | G | T | 1 | a0001c0001t0001g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.339+1607G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947902 | |||||||
| chr1:66947935 | C | T | 24 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(21): Show |
26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+1640C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66947935 | |||||||
| chr1:66948038 | A | G | 26 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0096 others(23): Show |
28 | HG00597.hp2 HG00621.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.339+1743A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66948038 | |||||||
| chr1:66948067 | G | A | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.339+1772G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66948067 | |||||||
| chr1:66948431 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.339+2136A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66948431 | |||||||
| chr1:66948685 | G | C | 3 | a0001c0001t0001g0118 a0002c0003t0001g0119 a0002c0003t0001g0134 |
3 | HG00323.hp1 HG00738.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.339+2390G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66948685 | |||||||
| chr1:66949108 | G | T | 3 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 |
3 | HG01106.hp2 NA20300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.339+2813G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949108 | |||||||
| chr1:66949187 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.339+2892G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949187 | |||||||
| chr1:66949334 | G | T | 1 | a0001c0001t0005g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+3039G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949334 | |||||||
| chr1:66949335 | C | G | 1 | a0001c0001t0005g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339+3040C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949335 | |||||||
| chr1:66949546 | C | A | 1 | a0001c0001t0003g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.339+3251C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949546 | |||||||
| chr1:66949936 | AC | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.339+3642delC | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66949936 | |||||||
| chr1:66949963 | ATTG | A | 6 | a0001c0001t0004g0010 a0001c0001t0004g0071 a0001c0001t0004g0072 others(3): Show |
7 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+3671_339+3673d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66949963 | ||||||
| chr1:66950004 | T | C | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.339+3709T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950004 | |||||||
| chr1:66950094 | A | T | 2 | a0001c0001t0001g0149 a0001c0001t0017g0148 |
2 | HG01109.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.339+3799A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950094 | |||||||
| chr1:66950213 | A | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0072 a0001c0001t0004g0073 others(2): Show |
6 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+3918A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950213 | |||||||
| chr1:66950389 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.339+4094G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950389 | |||||||
| chr1:66950407 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.339+4112C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950407 | |||||||
| chr1:66950418 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(215): Show |
240 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.339+4123T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950418 | |||||||
| chr1:66950709 | A | AC | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(171): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.339+4414_339+4415i others(3): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950709 | |||||||
| chr1:66950713 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.339+4418A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950713 | |||||||
| chr1:66950749 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.339+4454T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950749 | |||||||
| chr1:66950838 | ATC | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.339+4549_339+4550d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66950838 | ||||||
| chr1:66950910 | A | G | 1 | a0001c0001t0007g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.339+4615A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66950910 | |||||||
| chr1:66951256 | G | A | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+4961G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951256 | |||||||
| chr1:66951294 | A | G | 1 | a0001c0001t0002g0221 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.339+4999A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951294 | |||||||
| chr1:66951418 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(164): Show |
187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.339+5123T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951418 | |||||||
| chr1:66951428 | C | T | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.339+5133C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951428 | |||||||
| chr1:66951494 | A | G | 2 | a0001c0001t0009g0084 a0001c0001t0009g0092 |
2 | HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.339+5199A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951494 | |||||||
| chr1:66951558 | T | C | 1 | a0001c0001t0019g0175 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.339+5263T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951558 | |||||||
| chr1:66951572 | GT | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(165): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.339+5289delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66951572 | ||||||
| chr1:66951767 | C | T | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.339+5472C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951767 | |||||||
| chr1:66951838 | T | C | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.339+5543T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951838 | |||||||
| chr1:66951872 | G | T | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+5577G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951872 | |||||||
| chr1:66951951 | C | T | 5 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+5656C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66951951 | |||||||
| chr1:66952059 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.339+5764A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952059 | |||||||
| chr1:66952074 | CTTAG | C | 2 | a0001c0001t0008g0007 a0001c0001t0008g0042 |
3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.339+5783_339+5786d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66952074 | ||||||
| chr1:66952344 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.340-5715C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952344 | |||||||
| chr1:66952432 | A | G | 24 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(21): Show |
26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-5627A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952432 | |||||||
| chr1:66952637 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.340-5422A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952637 | |||||||
| chr1:66952758 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.340-5301C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952758 | |||||||
| chr1:66952779 | C | T | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.340-5280C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66952779 | |||||||
| chr1:66953122 | T | G | 1 | a0001c0001t0004g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.340-4937T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953122 | |||||||
| chr1:66953184 | G | A | 1 | a0001c0001t0004g0078 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.340-4875G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953184 | |||||||
| chr1:66953406 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.340-4653G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953406 | |||||||
| chr1:66953596 | C | CT | 13 | a0001c0001t0001g0112 a0001c0001t0002g0213 a0001c0001t0002g0214 others(10): Show |
13 | HG00423.hp2 HG01243.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.340-4447dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66953596 | ||||||
| chr1:66953612 | T | TA | 24 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(21): Show |
26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-4445dupA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66953612 | ||||||
| chr1:66953777 | T | A | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340-4282T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953777 | |||||||
| chr1:66953818 | G | A | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.340-4241G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953818 | |||||||
| chr1:66953834 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(194): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.340-4225T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66953834 | |||||||
| chr1:66954238 | G | A | 1 | a0001c0001t0007g0173 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340-3821G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954238 | |||||||
| chr1:66954483 | G | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.340-3576G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954483 | |||||||
| chr1:66954548 | C | T | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(44): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.340-3511C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954548 | |||||||
| chr1:66954553 | C | G | 1 | a0001c0001t0002g0199 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.340-3506C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954553 | |||||||
| chr1:66954852 | G | A | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.340-3207G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954852 | |||||||
| chr1:66954908 | C | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.340-3151C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954908 | |||||||
| chr1:66954995 | C | T | 25 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(22): Show |
26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.340-3064C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66954995 | |||||||
| chr1:66955336 | G | GT | 51 | a0001c0001t0001g0103 a0001c0001t0001g0118 a0001c0001t0001g0120 others(48): Show |
53 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.340-2695dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | ||||||
| chr1:66955336 | G | GTT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(91): Show |
108 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.340-2696_340-2695d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | ||||||
| chr1:66955336 | G | GTTT | 36 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0096 others(33): Show |
40 | HG00140.hp1 HG00621.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.340-2697_340-2695d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | ||||||
| chr1:66955336 | GT | G | 5 | a0001c0001t0002g0177 a0001c0001t0002g0184 a0001c0001t0002g0188 others(2): Show |
5 | HG00323.hp2 HG02895.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-2695delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | ||||||
| chr1:66955336 | GTTTTTTT others(5): Show |
G | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340-2706_340-2695d others(14): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66955336 | ||||||
| chr1:66955546 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.340-2513A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955546 | |||||||
| chr1:66955628 | A | G | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.340-2431A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955628 | |||||||
| chr1:66955707 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.340-2352C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955707 | |||||||
| chr1:66955769 | G | A | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(44): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.340-2290G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955769 | |||||||
| chr1:66955795 | G | T | 1 | a0001c0001t0002g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.340-2264G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66955795 | |||||||
| chr1:66956031 | G | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(172): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.340-2028G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956031 | |||||||
| chr1:66956236 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.340-1823A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956236 | |||||||
| chr1:66956324 | G | T | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-1735G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956324 | |||||||
| chr1:66956618 | T | C | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(44): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.340-1441T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956618 | |||||||
| chr1:66956830 | A | G | 1 | a0001c0001t0004g0078 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.340-1229A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956830 | |||||||
| chr1:66956867 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.340-1192C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66956867 | |||||||
| chr1:66957217 | A | G | 1 | a0001c0001t0006g0126 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.340-842A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66957217 | |||||||
| chr1:66957307 | C | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(194): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.340-752C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66957307 | |||||||
| chr1:66957405 | ATGCTTAA others(2): Show |
A | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.340-651_340-643del others(9): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66957405 | ||||||
| chr1:66957557 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.340-502A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | chr1 | 66957557 | |||||||
| chr1:66957587 | G | GT | 38 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0087 others(35): Show |
41 | HG00597.hp1 HG00621.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.340-452dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66957587 | ||||||
| chr1:66957631 | AT | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.340-424delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 66957631 | ||||||
| chr1:66958314 | T | TTTCTC | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.501+97_501+98insTC others(3): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 66958314 | ||||||
| chr1:66958447 | T | TATTCTTT others(314): Show |
1 | a0001c0001t0004g0063 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.501+232_501+233ins others(321): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 66958447 | ||||||
| chr1:66958474 | TA | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(166): Show |
189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.501+261delA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 66958474 | ||||||
| chr1:66958589 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0156 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.502-262C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | chr1 | 66958589 | |||||||
| chr1:66958805 | A | G | 21 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0032 others(18): Show |
24 | HG01106.hp2 HG01255.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.502-46A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | chr1 | 66958805 | |||||||
| chr1:66958835 | A | G | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.502-16A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 5/13 | chr1 | 66958835 | |||||||
| chr1:66959335 | A | C | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.635-344A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 6/13 | chr1 | 66959335 | |||||||
| chr1:66959628 | T | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.635-51T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 6/13 | chr1 | 66959628 | |||||||
| chr1:66959793 | A | T | 3 | a0001c0001t0001g0118 a0002c0003t0001g0119 a0002c0003t0001g0134 |
3 | HG00323.hp1 HG00738.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.699+50A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66959793 | |||||||
| chr1:66959811 | A | AT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(161): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.699+79dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 66959811 | ||||||
| chr1:66959976 | T | G | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.699+233T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66959976 | |||||||
| chr1:66960087 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.699+344G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960087 | |||||||
| chr1:66960356 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.699+613G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960356 | |||||||
| chr1:66960540 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(164): Show |
187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.699+797A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960540 | |||||||
| chr1:66960657 | A | T | 14 | a0001c0001t0004g0060 a0001c0001t0004g0061 a0001c0001t0004g0062 others(11): Show |
14 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.699+914A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960657 | |||||||
| chr1:66960804 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.699+1061A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960804 | |||||||
| chr1:66960912 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.699+1169A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66960912 | |||||||
| chr1:66961033 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.699+1290T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961033 | |||||||
| chr1:66961227 | T | G | 2 | a0001c0001t0002g0187 a0001c0001t0002g0208 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.699+1484T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961227 | |||||||
| chr1:66961256 | C | T | 1 | a0001c0001t0009g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.699+1513C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961256 | |||||||
| chr1:66961509 | T | C | 1 | a0001c0001t0015g0144 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.700-1579T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961509 | |||||||
| chr1:66961623 | G | T | 25 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(22): Show |
26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.700-1465G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961623 | |||||||
| chr1:66961710 | G | T | 1 | a0001c0001t0007g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.700-1378G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961710 | |||||||
| chr1:66961725 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0029 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.700-1363A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961725 | |||||||
| chr1:66961864 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.700-1224A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961864 | |||||||
| chr1:66961995 | G | A | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.700-1093G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66961995 | |||||||
| chr1:66962086 | C | T | 17 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(14): Show |
18 | HG01106.hp2 HG01255.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.700-1002C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962086 | |||||||
| chr1:66962319 | C | CT | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.700-768dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 66962319 | ||||||
| chr1:66962319 | C | G | 2 | a0001c0001t0004g0061 a0001c0001t0004g0062 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.700-769C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962319 | |||||||
| chr1:66962353 | A | G | 6 | a0001c0001t0004g0010 a0001c0001t0004g0071 a0001c0001t0004g0072 others(3): Show |
7 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.700-735A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962353 | |||||||
| chr1:66962457 | A | G | 6 | a0001c0001t0006g0003 a0001c0001t0006g0014 a0001c0001t0006g0126 others(3): Show |
9 | HG01069.hp1 HG01099.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.700-631A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962457 | |||||||
| chr1:66962829 | CTTCT | C | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.700-256_700-253del others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 66962829 | ||||||
| chr1:66962892 | G | C | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.700-196G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 7/13 | chr1 | 66962892 | |||||||
| chr1:66963541 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.772+381G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66963541 | |||||||
| chr1:66963770 | T | G | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.772+610T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66963770 | |||||||
| chr1:66963776 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.772+616C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66963776 | |||||||
| chr1:66964009 | CCATTT | C | 3 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0046 |
3 | HG03654.hp2 HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.772+860_772+864del others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964009 | ||||||
| chr1:66964073 | A | AT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0087 a0001c0001t0001g0103 others(2): Show |
6 | HG02698.hp1 NA18972.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.772+928dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964073 | ||||||
| chr1:66964090 | A | G | 26 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(23): Show |
28 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.772+930A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964090 | |||||||
| chr1:66964179 | C | G | 1 | a0001c0001t0007g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.772+1019C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964179 | |||||||
| chr1:66964348 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0012g0100 others(1): Show |
4 | HG00597.hp2 NA18960.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.772+1188C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964348 | |||||||
| chr1:66964420 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.772+1260G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964420 | |||||||
| chr1:66964448 | CT | C | 8 | a0001c0001t0002g0171 a0001c0001t0002g0179 a0001c0001t0002g0182 others(5): Show |
8 | HG01167.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.772+1309delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964448 | ||||||
| chr1:66964448 | CTTTTTT | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(161): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.772+1304_772+1309d others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964448 | ||||||
| chr1:66964671 | T | TG | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.772+1512dupG | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66964671 | ||||||
| chr1:66964744 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.772+1584A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964744 | |||||||
| chr1:66964812 | A | G | 1 | a0001c0001t0007g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.772+1652A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66964812 | |||||||
| chr1:66965157 | G | A | 2 | a0001c0001t0005g0043 a0001c0001t0005g0044 |
2 | NA18988.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.772+1997G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965157 | |||||||
| chr1:66965206 | C | T | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.772+2046C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965206 | |||||||
| chr1:66965275 | A | G | 1 | a0001c0001t0005g0006 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.772+2115A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965275 | |||||||
| chr1:66965682 | A | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.772+2522A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965682 | |||||||
| chr1:66965691 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0089 |
2 | NA18971.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.772+2531T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965691 | |||||||
| chr1:66965816 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.772+2656T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66965816 | |||||||
| chr1:66966040 | A | T | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.772+2880A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966040 | |||||||
| chr1:66966225 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.772+3065C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966225 | |||||||
| chr1:66966261 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.772+3101C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966261 | |||||||
| chr1:66966304 | C | A | 1 | a0001c0001t0002g0221 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.772+3144C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966304 | |||||||
| chr1:66966312 | T | C | 1 | a0001c0001t0005g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.772+3152T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966312 | |||||||
| chr1:66966348 | C | T | 57 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(54): Show |
59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.772+3188C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966348 | |||||||
| chr1:66966385 | A | G | 3 | a0001c0001t0009g0084 a0001c0001t0009g0090 a0001c0001t0009g0092 |
3 | HG02738.hp2 HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.772+3225A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66966385 | |||||||
| chr1:66967200 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.773-3608G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967200 | |||||||
| chr1:66967302 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.773-3506T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967302 | |||||||
| chr1:66967402 | G | T | 3 | a0001c0001t0002g0201 a0001c0001t0002g0206 a0001c0001t0002g0207 |
3 | NA18990.hp1 NA18991.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.773-3406G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967402 | |||||||
| chr1:66967510 | CT | C | 5 | a0001c0001t0001g0136 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | NA18971.hp2 NA19003.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.773-3291delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66967510 | ||||||
| chr1:66967644 | AT | A | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.773-3150delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66967644 | ||||||
| chr1:66967685 | A | G | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.773-3123A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967685 | |||||||
| chr1:66967816 | A | G | 1 | a0001c0001t0002g0186 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.773-2992A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967816 | |||||||
| chr1:66967986 | A | C | 1 | a0001c0001t0002g0194 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.773-2822A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66967986 | |||||||
| chr1:66968100 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.773-2708C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968100 | |||||||
| chr1:66968591 | C | T | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.773-2217C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968591 | |||||||
| chr1:66968712 | A | G | 1 | a0001c0001t0004g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.773-2096A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968712 | |||||||
| chr1:66968728 | A | G | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.773-2080A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968728 | |||||||
| chr1:66968801 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02486.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.773-2007G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968801 | |||||||
| chr1:66968919 | C | T | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.773-1889C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66968919 | |||||||
| chr1:66969140 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.773-1668T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969140 | |||||||
| chr1:66969267 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.773-1541C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969267 | |||||||
| chr1:66969296 | A | G | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.773-1512A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969296 | |||||||
| chr1:66969312 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.773-1496G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969312 | |||||||
| chr1:66969479 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.773-1329A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969479 | |||||||
| chr1:66969495 | A | G | 2 | a0001c0001t0003g0066 a0001c0001t0003g0067 |
2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.773-1313A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969495 | |||||||
| chr1:66969502 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.773-1306G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969502 | |||||||
| chr1:66969545 | C | CA | 10 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(7): Show |
12 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.773-1233dupA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | ||||||
| chr1:66969545 | C | CAA | 17 | a0001c0001t0001g0089 a0001c0001t0001g0097 a0001c0001t0001g0098 others(14): Show |
17 | HG01934.hp2 HG02027.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.773-1234_773-1233d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | ||||||
| chr1:66969545 | CA | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0093 others(39): Show |
50 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.773-1233delA | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | ||||||
| chr1:66969545 | CAA | C | 35 | a0001c0001t0002g0016 a0001c0001t0002g0180 a0001c0001t0002g0182 others(32): Show |
36 | HG00323.hp2 HG00639.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.773-1234_773-1233d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | ||||||
| chr1:66969545 | CAAA | C | 30 | a0001c0001t0002g0015 a0001c0001t0002g0171 a0001c0001t0002g0176 others(27): Show |
33 | HG00423.hp2 HG00558.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.773-1235_773-1233d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | ||||||
| chr1:66969545 | CAAAA | C | 52 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0018 others(49): Show |
57 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.773-1236_773-1233d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | ||||||
| chr1:66969545 | CAAAAA | C | 6 | a0001c0001t0003g0067 a0001c0001t0007g0168 a0001c0001t0007g0169 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.773-1237_773-1233d others(7): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | ||||||
| chr1:66969545 | CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0137 a0001c0001t0001g0156 a0001c0001t0001g0163 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.773-1243_773-1233d others(13): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | ||||||
| chr1:66969545 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0002g0183 a0001c0001t0014g0222 a0001c0001t0014g0223 |
3 | HG02257.hp1 HG02723.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.773-1245_773-1233d others(15): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66969545 | ||||||
| chr1:66969581 | G | C | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.773-1227G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969581 | |||||||
| chr1:66969730 | A | G | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(44): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.773-1078A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969730 | |||||||
| chr1:66969928 | T | G | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.773-880T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969928 | |||||||
| chr1:66969934 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.773-874A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66969934 | |||||||
| chr1:66970089 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0121 |
2 | NA18953.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.773-719T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970089 | |||||||
| chr1:66970098 | AT | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02486.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.773-708delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 66970098 | ||||||
| chr1:66970223 | C | G | 1 | a0001c0001t0002g0188 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.773-585C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970223 | |||||||
| chr1:66970573 | A | G | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.773-235A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970573 | |||||||
| chr1:66970613 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.773-195A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970613 | |||||||
| chr1:66970763 | A | G | 31 | a0001c0001t0002g0016 a0001c0001t0002g0179 a0001c0001t0002g0180 others(28): Show |
32 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.773-45A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 8/13 | chr1 | 66970763 | |||||||
| chr1:66971262 | T | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.924+303T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971262 | |||||||
| chr1:66971351 | T | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.925-304T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971351 | |||||||
| chr1:66971360 | C | T | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.925-295C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971360 | |||||||
| chr1:66971404 | C | A | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(44): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.925-251C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971404 | |||||||
| chr1:66971467 | A | G | 3 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 |
3 | HG01167.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.925-188A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 9/13 | chr1 | 66971467 | |||||||
| chr1:66971890 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0004g0061 |
2 | HG02622.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1006+154C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66971890 | |||||||
| chr1:66972050 | GATA | G | 55 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0176 others(52): Show |
57 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1006+318_1006+320d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972050 | ||||||
| chr1:66972151 | C | A | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1006+415C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972151 | |||||||
| chr1:66972216 | C | CAT | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1006+492_1006+493d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972216 | ||||||
| chr1:66972228 | TACACTAC | T | 5 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0001t0002g0191 others(2): Show |
5 | HG00323.hp2 HG00735.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+494_1006+500d others(9): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972228 | ||||||
| chr1:66972229 | ACAC | A | 49 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0176 others(46): Show |
51 | HG00558.hp2 HG00639.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.1006+494_1006+496d others(5): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972229 | |||||||
| chr1:66972232 | CTACATAT others(7): Show |
C | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1006+499_1006+512d others(16): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972232 | ||||||
| chr1:66972235 | C | CAT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0118 others(6): Show |
9 | HG00323.hp1 HG00597.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+525_1006+526d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972235 | ||||||
| chr1:66972235 | C | CATAT | 4 | a0001c0001t0001g0096 a0001c0001t0004g0078 a0001c0004t0001g0095 others(1): Show |
4 | HG00738.hp2 HG01069.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+523_1006+526d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972235 | ||||||
| chr1:66972235 | C | CATATATA others(3): Show |
1 | a0001c0002t0010g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1006+517_1006+526d others(12): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972235 | ||||||
| chr1:66972236 | ATATATAT | A | 43 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0177 others(40): Show |
45 | HG00558.hp2 HG00639.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006+501_1006+507d others(9): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972236 | |||||||
| chr1:66972236 | ATATATAT others(2): Show |
A | 3 | a0001c0001t0007g0173 a0001c0001t0007g0174 a0001c0001t0020g0217 |
3 | HG02132.hp1 HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1006+501_1006+509d others(11): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972236 | |||||||
| chr1:66972239 | T | TATATATA others(18): Show |
1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1006+522_1006+523i others(27): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972239 | ||||||
| chr1:66972240 | A | C | 1 | a0001c0001t0002g0214 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1006+504A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972240 | |||||||
| chr1:66972241 | T | C | 5 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0001t0002g0191 others(2): Show |
5 | HG00323.hp2 HG00735.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+505T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972241 | |||||||
| chr1:66972242 | A | C | 2 | a0001c0001t0002g0176 a0001c0001t0002g0184 |
2 | HG03017.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1006+506A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972242 | |||||||
| chr1:66972242 | AT | A | 5 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0001t0002g0191 others(2): Show |
5 | HG00323.hp2 HG00735.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+507delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972242 | |||||||
| chr1:66972243 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1006+507T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972243 | |||||||
| chr1:66972244 | A | C | 48 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0177 others(45): Show |
50 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1006+508A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972244 | |||||||
| chr1:66972245 | TATATATA others(11): Show |
T | 1 | a0001c0001t0005g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1006+514_1006+531d others(20): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972245 | ||||||
| chr1:66972246 | A | C | 4 | a0001c0001t0002g0216 a0001c0001t0007g0173 a0001c0001t0007g0174 others(1): Show |
4 | HG00423.hp2 HG02132.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+510A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972246 | |||||||
| chr1:66972257 | TATATAG | T | 10 | a0001c0001t0004g0010 a0001c0001t0004g0064 a0001c0001t0004g0072 others(7): Show |
11 | HG00735.hp2 HG02615.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1006+526_1006+531d others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972257 | ||||||
| chr1:66972259 | TATAG | T | 72 | a0001c0001t0001g0013 a0001c0001t0001g0085 a0001c0001t0001g0086 others(69): Show |
77 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1006+527_1006+530d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972259 | ||||||
| chr1:66972261 | TAG | T | 21 | a0001c0001t0001g0011 a0001c0001t0001g0091 a0001c0001t0001g0142 others(18): Show |
23 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1006+527_1006+528d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 66972261 | ||||||
| chr1:66972263 | G | T | 72 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0096 others(69): Show |
75 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1006+527G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972263 | |||||||
| chr1:66972455 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1007-442C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972455 | |||||||
| chr1:66972809 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1007-88C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972809 | |||||||
| chr1:66972852 | A | T | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1007-45A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 10/13 | chr1 | 66972852 | |||||||
| chr1:66973217 | G | A | 57 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(54): Show |
59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1101+226G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973217 | |||||||
| chr1:66973375 | T | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1101+384T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973375 | |||||||
| chr1:66973407 | G | C | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1101+416G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973407 | |||||||
| chr1:66973410 | G | C | 22 | a0001c0001t0002g0015 a0001c0001t0002g0176 a0001c0001t0002g0182 others(19): Show |
23 | HG00423.hp2 HG00558.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1101+419G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973410 | |||||||
| chr1:66973437 | C | T | 8 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(5): Show |
9 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101+446C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973437 | |||||||
| chr1:66973833 | T | C | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1101+842T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66973833 | |||||||
| chr1:66974002 | A | T | 1 | a0001c0001t0002g0186 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1101+1011A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974002 | |||||||
| chr1:66974067 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1101+1076C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974067 | |||||||
| chr1:66974385 | C | T | 8 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(5): Show |
9 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101+1394C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974385 | |||||||
| chr1:66974433 | T | G | 3 | a0001c0001t0002g0193 a0001c0002t0010g0008 a0001c0002t0010g0050 |
4 | HG02109.hp1 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+1442T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974433 | |||||||
| chr1:66974436 | G | T | 46 | a0001c0001t0001g0139 a0001c0001t0003g0004 a0001c0001t0003g0009 others(43): Show |
51 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.1101+1445G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974436 | |||||||
| chr1:66974439 | G | T | 1 | a0001c0001t0008g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1101+1448G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974439 | |||||||
| chr1:66974539 | T | C | 25 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(22): Show |
26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1101+1548T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974539 | |||||||
| chr1:66974540 | G | A | 2 | a0001c0001t0004g0064 a0001c0001t0004g0065 |
2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1101+1549G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974540 | |||||||
| chr1:66974779 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0154 |
2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1101+1788C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974779 | |||||||
| chr1:66974800 | C | A | 24 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(21): Show |
26 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1102-1795C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66974800 | |||||||
| chr1:66975019 | G | A | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1102-1576G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975019 | |||||||
| chr1:66975113 | C | T | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1102-1482C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975113 | |||||||
| chr1:66975164 | A | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0138 a0001c0001t0001g0161 others(1): Show |
4 | HG03669.hp2 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102-1431A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975164 | |||||||
| chr1:66975444 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1102-1151T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975444 | |||||||
| chr1:66975533 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1102-1062A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975533 | |||||||
| chr1:66975538 | AAAAG | A | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1102-1052_1102-104 others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66975538 | ||||||
| chr1:66975679 | C | T | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1102-916C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975679 | |||||||
| chr1:66975923 | A | G | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1102-672A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975923 | |||||||
| chr1:66975983 | C | CT | 6 | a0001c0001t0003g0058 a0001c0001t0003g0059 a0001c0001t0005g0006 others(3): Show |
8 | HG01167.hp1 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1102-604dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66975983 | ||||||
| chr1:66975988 | T | G | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1102-607T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975988 | |||||||
| chr1:66975988 | T | TTG | 53 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0177 others(50): Show |
55 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.1102-606_1102-605i others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66975988 | ||||||
| chr1:66975990 | T | G | 59 | a0001c0001t0001g0112 a0001c0001t0001g0131 a0001c0001t0002g0015 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1102-605T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975990 | |||||||
| chr1:66975992 | G | T | 70 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(67): Show |
76 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.1102-603G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66975992 | |||||||
| chr1:66976018 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1102-577C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976018 | |||||||
| chr1:66976032 | G | A | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1102-563G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976032 | |||||||
| chr1:66976245 | A | AC | 27 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(24): Show |
28 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1102-344dupC | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66976245 | ||||||
| chr1:66976527 | C | T | 49 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0176 others(46): Show |
51 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.1102-68C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976527 | |||||||
| chr1:66976539 | A | C | 1 | a0001c0001t0004g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1102-56A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976539 | |||||||
| chr1:66976567 | CT | C | 16 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0018 others(13): Show |
17 | HG01192.hp1 HG01934.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1102-26delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 66976567 | ||||||
| chr1:66976592 | C | T | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
splice_region_variant&intron_variant | LOW | c.1102-3C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 11/13 | chr1 | 66976592 | |||||||
| chr1:66976888 | C | G | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1229+166C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66976888 | |||||||
| chr1:66977060 | T | C | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(44): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.1229+338T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977060 | |||||||
| chr1:66977116 | T | C | 1 | a0001c0001t0017g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1229+394T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977116 | |||||||
| chr1:66977202 | C | T | 3 | a0001c0001t0011g0069 a0001c0001t0011g0070 a0001c0001t0016g0068 |
3 | HG02109.hp2 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1229+480C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977202 | |||||||
| chr1:66977213 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1229+491G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977213 | |||||||
| chr1:66977630 | T | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1229+908T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977630 | |||||||
| chr1:66977982 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1229+1260A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66977982 | |||||||
| chr1:66978068 | C | G | 55 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0176 others(52): Show |
57 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1229+1346C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978068 | |||||||
| chr1:66978209 | A | AAAAG | 55 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0176 others(52): Show |
57 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1229+1489_1229+149 others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66978209 | ||||||
| chr1:66978209 | A | G | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1229+1487A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978209 | |||||||
| chr1:66978286 | ATAGG | A | 58 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(55): Show |
60 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1229+1571_1229+157 others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66978286 | ||||||
| chr1:66978305 | G | C | 2 | a0001c0001t0002g0171 a0001c0001t0019g0175 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1229+1583G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978305 | |||||||
| chr1:66978360 | G | A | 27 | a0001c0001t0002g0016 a0001c0001t0002g0177 a0001c0001t0002g0179 others(24): Show |
28 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1229+1638G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978360 | |||||||
| chr1:66978402 | A | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0151 a0001c0001t0001g0155 |
3 | NA18971.hp2 NA19003.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1229+1680A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978402 | |||||||
| chr1:66978442 | AT | A | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 |
3 | HG01243.hp2 HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1229+1722delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66978442 | ||||||
| chr1:66978681 | C | CATTATTC others(9): Show |
1 | a0001c0001t0005g0048 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1229+1959_1229+196 others(20): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978681 | |||||||
| chr1:66978807 | G | T | 11 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(8): Show |
11 | HG01106.hp2 HG02027.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.1229+2085G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66978807 | |||||||
| chr1:66979081 | G | T | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1229+2359G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979081 | |||||||
| chr1:66979097 | G | GT | 3 | a0001c0001t0005g0006 a0001c0001t0008g0007 a0001c0001t0008g0042 |
5 | HG02451.hp2 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1229+2385dupT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66979097 | ||||||
| chr1:66979100 | T | C | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1229+2378T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979100 | |||||||
| chr1:66979113 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1229+2391G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979113 | |||||||
| chr1:66979156 | C | T | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1229+2434C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979156 | |||||||
| chr1:66979280 | G | T | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(44): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.1230-2499G>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979280 | |||||||
| chr1:66979340 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1230-2439C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979340 | |||||||
| chr1:66979638 | T | C | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1230-2141T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979638 | |||||||
| chr1:66979784 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1230-1995C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979784 | |||||||
| chr1:66979880 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1230-1899G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66979880 | |||||||
| chr1:66980294 | T | C | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1230-1485T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980294 | |||||||
| chr1:66980371 | C | T | 6 | a0001c0001t0004g0010 a0001c0001t0004g0071 a0001c0001t0004g0072 others(3): Show |
7 | HG02615.hp1 HG03195.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230-1408C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980371 | |||||||
| chr1:66980439 | T | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0152 a0001c0001t0001g0159 |
3 | HG01934.hp2 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1230-1340T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980439 | |||||||
| chr1:66980684 | T | A | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1230-1095T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980684 | |||||||
| chr1:66980812 | A | T | 1 | a0001c0001t0001g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1230-967A>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66980812 | |||||||
| chr1:66981003 | C | A | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1230-776C>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981003 | |||||||
| chr1:66981009 | T | A | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-770T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981009 | |||||||
| chr1:66981010 | T | A | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-769T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981010 | |||||||
| chr1:66981011 | T | A | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-768T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981011 | |||||||
| chr1:66981013 | T | G | 6 | a0001c0001t0007g0168 a0001c0001t0007g0169 a0001c0001t0007g0170 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230-766T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981013 | |||||||
| chr1:66981087 | T | TTAGA | 138 | a0001c0001t0001g0137 a0001c0001t0001g0156 a0001c0001t0001g0163 others(135): Show |
147 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.1230-691_1230-688d others(6): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66981087 | ||||||
| chr1:66981253 | A | AC | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1230-524dupC | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 66981253 | ||||||
| chr1:66981306 | G | A | 1 | a0001c0001t0007g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1230-473G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981306 | |||||||
| chr1:66981367 | C | G | 5 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(2): Show |
5 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230-412C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981367 | |||||||
| chr1:66981519 | A | G | 1 | a0002c0003t0001g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1230-260A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981519 | |||||||
| chr1:66981540 | T | C | 1 | a0001c0001t0008g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1230-239T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981540 | |||||||
| chr1:66981767 | A | G | 57 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(54): Show |
59 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1230-12A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 12/13 | chr1 | 66981767 | |||||||
| chr1:66982005 | T | G | 1 | a0001c0001t0014g0222 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1369+87T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982005 | |||||||
| chr1:66982118 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1369+200A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982118 | |||||||
| chr1:66982126 | C | G | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1369+208C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982126 | |||||||
| chr1:66982146 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1369+228T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982146 | |||||||
| chr1:66982309 | AGTGCACT others(4): Show |
A | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1369+392_1369+402d others(13): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982309 | |||||||
| chr1:66982335 | C | T | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1369+417C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982335 | |||||||
| chr1:66982362 | A | G | 1 | a0001c0001t0009g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1369+444A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982362 | |||||||
| chr1:66982388 | A | G | 2 | a0001c0002t0010g0008 a0001c0002t0010g0050 |
3 | HG02818.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1369+470A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982388 | |||||||
| chr1:66982410 | G | C | 1 | a0001c0001t0001g0140 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1369+492G>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982410 | |||||||
| chr1:66982740 | CAT | C | 3 | a0001c0001t0002g0213 a0001c0001t0002g0224 a0001c0001t0002g0225 |
3 | NA18967.hp1 NA18975.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1369+823_1369+824d others(4): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982740 | |||||||
| chr1:66982745 | G | A | 1 | a0001c0001t0004g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1369+827G>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982745 | |||||||
| chr1:66982767 | T | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1369+849T>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982767 | |||||||
| chr1:66982801 | T | A | 47 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0017 others(44): Show |
52 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.1369+883T>A | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982801 | |||||||
| chr1:66982853 | C | T | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1369+935C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982853 | |||||||
| chr1:66982951 | T | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02486.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1369+1033T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66982951 | |||||||
| chr1:66983050 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1369+1132A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983050 | |||||||
| chr1:66983162 | AAAGG | A | 15 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0018 others(12): Show |
16 | HG01192.hp1 HG01934.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1369+1255_1369+125 others(8): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 66983162 | ||||||
| chr1:66983209 | A | G | 1 | a0001c0001t0005g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1369+1291A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983209 | |||||||
| chr1:66983313 | A | G | 27 | a0001c0001t0002g0016 a0001c0001t0002g0177 a0001c0001t0002g0179 others(24): Show |
28 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1370-1259A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983313 | |||||||
| chr1:66983337 | T | G | 27 | a0001c0001t0002g0016 a0001c0001t0002g0177 a0001c0001t0002g0179 others(24): Show |
28 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1370-1235T>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983337 | |||||||
| chr1:66983395 | A | G | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | NA18980.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1370-1177A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983395 | |||||||
| chr1:66983479 | ACTT | A | 24 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(21): Show |
25 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1370-1089_1370-108 others(7): Show |
MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 66983479 | ||||||
| chr1:66983523 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1370-1049A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983523 | |||||||
| chr1:66983632 | AT | A | 22 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(19): Show |
23 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1370-937delT | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 66983632 | ||||||
| chr1:66983770 | C | G | 1 | a0001c0001t0005g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1370-802C>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983770 | |||||||
| chr1:66983779 | A | G | 135 | a0001c0001t0001g0110 a0001c0001t0001g0157 a0001c0001t0001g0158 others(132): Show |
144 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1370-793A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983779 | |||||||
| chr1:66983990 | C | T | 21 | a0001c0001t0004g0010 a0001c0001t0004g0051 a0001c0001t0004g0052 others(18): Show |
22 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1370-582C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66983990 | |||||||
| chr1:66984126 | A | C | 1 | a0001c0001t0002g0214 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1370-446A>C | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66984126 | |||||||
| chr1:66984258 | A | G | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0171 others(56): Show |
61 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1370-314A>G | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66984258 | |||||||
| chr1:66984307 | C | T | 2 | a0001c0001t0014g0222 a0001c0001t0014g0223 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1370-265C>T | MIER1 | ENSG00000198160.15 | transcript | ENST00000401041.6 | protein_coding | 13/13 | chr1 | 66984307 |