Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4200 |
| ensemblid | ENSG00000082212.13 |
| hgncid | 6984 |
| symbol | ME2 |
| name | malic enzyme 2 |
| refseq_nuc | NM_002396.5 |
| refseq_prot | NP_002387.1 |
| ensembl_nuc | ENST00000321341.11 |
| ensembl_prot | ENSP00000321070.5 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 50879118 |
| end | 50954257 |
| strand | + |
| ver | v1.2 |
| region | chr18:50879118-50954257 |
| region5000 | chr18:50874118-50959257 |
| regionname0 | ME2_chr18_50879118_50954257 |
| regionname5000 | ME2_chr18_50874118_50959257 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 584 | 262 | 60 | 52 | 118 | 9 | 21 | 96 | ME2_chr18_50874118_50959257 | ME2 | MLSRL others(579): Show |
chr18 | 50874118 | 50959257 |
| a0002 | 0/0 | 584 | 74 | 29 | 9 | 30 | 1 | 5 | 24 | ME2_chr18_50874118_50959257 | ME2 | MLSRL others(579): Show |
chr18 | 50874118 | 50959257 |
| a0003 | 0/0 | 584 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | MLSRL others(579): Show |
chr18 | 50874118 | 50959257 |
| a0004 | 0/0 | 224 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | MLSRL others(219): Show |
chr18 | 50874118 | 50959257 |
| a0005 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | MLSRL others(579): Show |
chr18 | 50874118 | 50959257 |
| a0006 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | MLSRL others(579): Show |
chr18 | 50874118 | 50959257 |
| a0007 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | MLSRL others(579): Show |
chr18 | 50874118 | 50959257 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1752 | 248 | 60 | 51 | 106 | 9 | 20 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0001c0003 | 0/0 | 1752 | 10 | 0 | 1 | 9 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0001c0005 | 0/0 | 1752 | 2 | 0 | 0 | 1 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0001c0006 | 0/0 | 1752 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0002c0002 | 0/0 | 1752 | 71 | 29 | 9 | 27 | 1 | 5 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0002c0004 | 0/0 | 1752 | 3 | 0 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0003c0007 | 0/0 | 1752 | 2 | 0 | 2 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0004c0011 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0005c0009 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0006c0008 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 | ||
| a0007c0010 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | ATGTT others(1747): Show |
chr18 | 50874118 | 50959257 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9027 | 35 | 3 | 8 | 19 | 1 | 4 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0002 | 0/0 | 9031 | 13 | 0 | 1 | 11 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0003 | 0/0 | 9028 | 12 | 1 | 5 | 5 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0004 | 0/0 | 9028 | 9 | 8 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0006 | 0/0 | 9030 | 7 | 0 | 2 | 5 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0007 | 0/0 | 9028 | 7 | 0 | 4 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0008 | 0/0 | 9031 | 6 | 0 | 0 | 6 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0009 | 0/0 | 9032 | 5 | 0 | 0 | 5 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0010 | 0/0 | 9031 | 5 | 2 | 0 | 1 | 1 | 1 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0012 | 0/0 | 9012 | 4 | 4 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9007): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0014 | 0/0 | 9032 | 4 | 0 | 4 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0015 | 0/0 | 9031 | 4 | 0 | 3 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0016 | 0/0 | 9033 | 4 | 1 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0017 | 0/0 | 9026 | 4 | 0 | 1 | 1 | 0 | 2 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0018 | 0/0 | 9029 | 4 | 0 | 2 | 1 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0019 | 0/0 | 9032 | 3 | 0 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0022 | 0/0 | 9030 | 3 | 1 | 0 | 0 | 0 | 2 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0024 | 0/0 | 9029 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0025 | 0/0 | 9043 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9038): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0026 | 0/0 | 9044 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9039): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0027 | 0/0 | 9017 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9012): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0028 | 0/0 | 9030 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0029 | 0/0 | 9017 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9012): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0030 | 0/0 | 9032 | 2 | 1 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0031 | 0/0 | 9033 | 2 | 0 | 1 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0032 | 0/0 | 9030 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0033 | 0/0 | 9026 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0036 | 0/0 | 9034 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9029): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0037 | 0/0 | 9028 | 2 | 0 | 2 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0038 | 0/0 | 9013 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9008): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0040 | 0/0 | 9029 | 2 | 0 | 0 | 1 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0041 | 0/0 | 9029 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0043 | 0/0 | 9026 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0044 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9039): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0045 | 0/0 | 9048 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9043): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0046 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0047 | 0/0 | 9031 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0048 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0049 | 0/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0050 | 0/0 | 9028 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0051 | 0/0 | 9051 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9046): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0052 | 0/0 | 9051 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9046): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0053 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0054 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0056 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0057 | 0/0 | 9032 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0058 | 0/0 | 9032 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0059 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0060 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0061 | 0/0 | 9029 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0062 | 0/0 | 9030 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0063 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0064 | 0/0 | 9033 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0065 | 0/0 | 9022 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9017): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0066 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0067 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0069 | 0/0 | 9030 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0070 | 0/0 | 9018 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9013): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0071 | 0/0 | 9012 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9007): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0072 | 0/0 | 9032 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0073 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0074 | 0/0 | 9019 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9014): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0075 | 0/0 | 9032 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0076 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0077 | 0/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0078 | 0/0 | 9033 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0079 | 0/0 | 9034 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9029): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0080 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0081 | 0/0 | 9033 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0082 | 0/0 | 9032 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0083 | 0/0 | 9026 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0084 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0085 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0090 | 0/0 | 9026 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0091 | 0/0 | 9032 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0092 | 0/0 | 9028 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0106 | 0/0 | 9033 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0107 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9036): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0108 | 0/0 | 9033 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0109 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9036): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0110 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9036): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0111 | 0/0 | 9042 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9037): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0122 | 0/0 | 9050 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9045): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0123 | 0/0 | 9027 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0124 | 0/0 | 9028 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0125 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0126 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0127 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0128 | 0/0 | 9027 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0134 | 0/0 | 9026 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0135 | 0/0 | 9028 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0137 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0138 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0141 | 0/0 | 9018 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9013): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0142 | 0/0 | 9017 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9012): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0144 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0145 | 0/0 | 9060 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9055): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0150 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0152 | 0/0 | 9030 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0153 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0154 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9039): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0155 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0157 | 0/0 | 9030 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0158 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0159 | 0/1 | 9028 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0161 | 0/0 | 9028 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0163 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0164 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0165 | 0/0 | 9030 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0166 | 0/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0167 | 0/0 | 9035 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9030): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0168 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0169 | 0/0 | 9027 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0170 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0171 | 0/0 | 9016 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9011): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0177 | 1/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0178 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0179 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0180 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0001t0183 | 0/0 | 9019 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9014): Show |
chr18 | 50874118 | 50959257 |
| a0001c0003t0013 | 0/0 | 9021 | 5 | 0 | 1 | 4 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9016): Show |
chr18 | 50874118 | 50959257 |
| a0001c0003t0039 | 0/0 | 9022 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9017): Show |
chr18 | 50874118 | 50959257 |
| a0001c0003t0139 | 0/0 | 9023 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9018): Show |
chr18 | 50874118 | 50959257 |
| a0001c0003t0140 | 0/0 | 9020 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9015): Show |
chr18 | 50874118 | 50959257 |
| a0001c0003t0143 | 0/0 | 9024 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9019): Show |
chr18 | 50874118 | 50959257 |
| a0001c0005t0024 | 0/0 | 9029 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0001c0005t0129 | 0/0 | 9027 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0001c0006t0006 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0001c0006t0055 | 0/0 | 9029 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0005 | 0/0 | 9028 | 8 | 0 | 0 | 7 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0011 | 0/0 | 9027 | 4 | 0 | 0 | 3 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0020 | 0/0 | 9024 | 3 | 0 | 2 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9019): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0021 | 0/0 | 9032 | 3 | 2 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0023 | 0/0 | 9028 | 3 | 3 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0034 | 0/0 | 9029 | 2 | 1 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0035 | 0/0 | 9026 | 2 | 1 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0042 | 0/0 | 9027 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0086 | 0/0 | 9069 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9064): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0088 | 0/0 | 9026 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0089 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0093 | 0/0 | 9024 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9019): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0094 | 0/0 | 9033 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0095 | 0/0 | 9028 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0096 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0097 | 0/0 | 9025 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9020): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0098 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9026): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0099 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0100 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0101 | 0/0 | 9025 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9020): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0102 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0103 | 0/0 | 9025 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9020): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0104 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0105 | 0/0 | 9028 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0112 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0113 | 0/0 | 9032 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9027): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0114 | 0/0 | 9025 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9020): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0115 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0116 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0117 | 0/0 | 9029 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0118 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0119 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0120 | 0/0 | 9033 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0121 | 0/0 | 9026 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0130 | 0/0 | 9038 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9033): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0131 | 0/0 | 9037 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9032): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0132 | 0/0 | 9036 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9031): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0133 | 0/0 | 9035 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9030): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0136 | 0/0 | 9038 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9033): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0147 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0148 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0149 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9025): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0151 | 0/0 | 9038 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9033): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0156 | 0/0 | 9025 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9020): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0162 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0172 | 0/0 | 9026 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9021): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0173 | 0/0 | 9025 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9020): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0174 | 0/0 | 9025 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9020): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0175 | 0/0 | 9024 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9019): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0176 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0181 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0002c0002t0182 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9024): Show |
chr18 | 50874118 | 50959257 |
| a0002c0004t0005 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0002c0004t0011 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0002c0004t0146 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| a0003c0007t0012 | 0/0 | 9012 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9007): Show |
chr18 | 50874118 | 50959257 |
| a0003c0007t0160 | 0/0 | 9013 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9008): Show |
chr18 | 50874118 | 50959257 |
| a0004c0011t0003 | 0/0 | 9028 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0005c0009t0068 | 0/0 | 9033 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CACTC others(9028): Show |
chr18 | 50874118 | 50959257 |
| a0006c0008t0004 | 0/0 | 9028 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9023): Show |
chr18 | 50874118 | 50959257 |
| a0007c0010t0087 | 0/0 | 9027 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | CTCTC others(9022): Show |
chr18 | 50874118 | 50959257 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0008g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0010g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0010g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0012g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0014g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0014g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0014g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0014g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0015g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0015g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0015g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0015g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0016g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0016g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0016g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0016g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0017g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0017g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0017g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0017g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0018g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0018g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0018g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0019g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0019g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0022g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0022g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0022g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0024g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0024g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0025g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0025g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0026g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0026g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0027g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0027g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0028g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0028g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0029g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0029g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0030g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0030g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0031g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0031g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0032g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0033g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0033g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0036g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0036g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0037g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0037g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0038g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0038g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0040g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0040g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0041g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0041g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0043g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0043g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0044g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0045g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0046g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0047g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0048g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0049g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0050g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0051g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0052g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0053g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0054g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0056g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0057g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0058g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0059g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0060g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0061g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0062g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0063g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0064g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0065g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0066g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0067g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0069g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0070g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0071g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0072g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0073g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0074g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0075g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0076g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0077g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0078g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0079g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0080g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0081g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0082g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0083g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0084g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0085g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0090g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0091g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0092g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0106g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0107g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0108g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0109g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0110g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0111g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0122g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0123g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0124g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0125g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0126g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0127g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0128g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0134g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0135g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0137g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0138g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0141g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0142g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0144g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0145g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0150g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0152g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0153g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0154g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0155g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0157g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0158g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0159g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0161g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0163g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0164g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0165g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0166g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0167g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0168g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0169g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0170g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0171g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0177g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0178g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0179g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0180g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0001t0183g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0013g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0013g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0013g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0013g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0013g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0039g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0039g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0139g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0140g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0003t0143g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0005t0024g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0005t0129g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0006t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0001c0006t0055g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0011g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0011g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0011g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0011g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0020g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0020g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0020g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0021g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0021g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0023g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0023g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0023g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0034g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0034g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0035g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0035g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0042g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0042g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0086g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0088g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0089g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0093g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0094g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0095g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0096g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0097g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0098g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0099g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0100g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0101g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0102g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0103g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0104g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0105g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0112g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0113g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0114g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0115g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0116g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0117g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0118g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0119g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0120g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0121g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0130g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0131g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0132g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0133g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0136g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0147g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0148g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0149g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0151g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0156g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0162g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0172g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0173g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0174g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0175g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0176g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0181g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0002t0182g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0004t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0004t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0002c0004t0146g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0003c0007t0012g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0003c0007t0160g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0004c0011t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0005c0009t0068g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0006c0008t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| a0007c0010t0087g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0049 | EUR | GBR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00099 | hp2 | a0001 | c0001 | t0145 | g0302 | EUR | GBR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00140 | hp1 | a0001 | c0001 | t0135 | g0296 | EUR | GBR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00140 | hp2 | a0001 | c0001 | t0015 | g0085 | EUR | GBR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00280 | hp1 | a0001 | c0001 | t0040 | g0274 | EUR | FIN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00280 | hp2 | a0001 | c0001 | t0075 | g0088 | EUR | FIN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00323 | hp1 | a0001 | c0001 | t0123 | g0228 | EUR | FIN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | FIN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00408 | hp1 | a0001 | c0001 | t0183 | g0247 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00408 | hp2 | a0001 | c0003 | t0013 | g0213 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00423 | hp2 | a0002 | c0002 | t0005 | g0127 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00544 | hp1 | a0001 | c0001 | t0008 | g0112 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00558 | hp2 | a0001 | c0001 | t0090 | g0270 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00597 | hp1 | a0001 | c0001 | t0084 | g0036 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00609 | hp1 | a0002 | c0002 | t0094 | g0156 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00609 | hp2 | a0001 | c0001 | t0040 | g0269 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00621 | hp2 | a0002 | c0002 | t0120 | g0150 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00639 | hp1 | a0002 | c0002 | t0020 | g0323 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00639 | hp2 | a0001 | c0001 | t0073 | g0098 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00642 | hp1 | a0002 | c0002 | t0103 | g0324 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00642 | hp2 | a0001 | c0001 | t0031 | g0051 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00733 | hp1 | a0001 | c0001 | t0128 | g0001 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0054 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00735 | hp1 | a0001 | c0001 | t0030 | g0068 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0218 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00738 | hp2 | a0001 | c0001 | t0058 | g0031 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00741 | hp1 | a0001 | c0001 | t0053 | g0061 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG00741 | hp2 | a0001 | c0001 | t0157 | g0288 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01069 | hp2 | a0001 | c0001 | t0014 | g0115 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01070 | hp2 | a0001 | c0001 | t0015 | g0071 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01071 | hp1 | a0001 | c0001 | t0018 | g0255 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01071 | hp2 | a0001 | c0001 | t0015 | g0114 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01074 | hp1 | a0003 | c0007 | t0160 | g0311 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01074 | hp2 | a0001 | c0001 | t0017 | g0319 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01081 | hp1 | a0001 | c0001 | t0142 | g0224 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01081 | hp2 | a0002 | c0002 | t0114 | g0164 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01106 | hp1 | a0002 | c0002 | t0105 | g0133 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01106 | hp2 | a0003 | c0007 | t0012 | g0184 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01167 | hp1 | a0001 | c0001 | t0018 | g0320 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0067 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01168 | hp1 | a0001 | c0001 | t0037 | g0298 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01168 | hp2 | a0001 | c0001 | t0015 | g0074 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01169 | hp1 | a0001 | c0001 | t0061 | g0069 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01169 | hp2 | a0001 | c0001 | t0037 | g0297 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01175 | hp1 | a0002 | c0002 | t0174 | g0182 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01175 | hp2 | a0001 | c0001 | t0072 | g0097 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01192 | hp1 | a0001 | c0001 | t0122 | g0326 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01243 | hp1 | a0001 | c0001 | t0108 | g0157 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01261 | hp1 | a0004 | c0011 | t0003 | g0292 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01261 | hp2 | a0001 | c0001 | t0014 | g0090 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01346 | hp2 | a0002 | c0002 | t0035 | g0325 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01358 | hp2 | a0002 | c0002 | t0098 | g0158 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01361 | hp2 | a0001 | c0001 | t0083 | g0099 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01433 | hp1 | a0001 | c0001 | t0082 | g0063 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01433 | hp2 | a0001 | c0001 | t0092 | g0293 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01496 | hp1 | a0001 | c0001 | t0014 | g0032 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0216 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0187 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01884 | hp2 | a0002 | c0002 | t0131 | g0172 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01891 | hp1 | a0001 | c0001 | t0036 | g0191 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01891 | hp2 | a0001 | c0001 | t0026 | g0030 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01928 | hp1 | a0001 | c0001 | t0069 | g0034 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01934 | hp1 | a0001 | c0001 | t0161 | g0264 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01934 | hp2 | a0002 | c0002 | t0020 | g0322 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01943 | hp2 | a0001 | c0001 | t0081 | g0091 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0222 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0220 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01978 | hp1 | a0001 | c0003 | t0013 | g0210 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01993 | hp1 | a0001 | c0001 | t0014 | g0086 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG01993 | hp2 | a0002 | c0002 | t0021 | g0005 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02015 | hp1 | a0001 | c0003 | t0140 | g0214 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02040 | hp1 | a0001 | c0001 | t0029 | g0044 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02040 | hp2 | a0002 | c0002 | t0176 | g0148 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02056 | hp1 | a0001 | c0001 | t0027 | g0047 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02056 | hp2 | a0001 | c0001 | t0016 | g0062 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0266 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02071 | hp2 | a0001 | c0003 | t0143 | g0211 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02129 | hp1 | a0002 | c0002 | t0034 | g0147 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02145 | hp1 | a0002 | c0002 | t0149 | g0179 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02145 | hp2 | a0001 | c0001 | t0022 | g0261 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02155 | hp1 | a0001 | c0001 | t0063 | g0078 | EAS | CDX | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02155 | hp2 | a0001 | c0001 | t0179 | g0259 | EAS | CDX | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0006 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02257 | hp2 | a0002 | c0002 | t0034 | g0159 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02258 | hp1 | a0002 | c0002 | t0104 | g0162 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02258 | hp2 | a0001 | c0001 | t0111 | g0204 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02280 | hp2 | a0002 | c0002 | t0097 | g0163 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02451 | hp1 | a0005 | c0009 | t0068 | g0053 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02572 | hp2 | a0002 | c0002 | t0042 | g0316 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02602 | hp1 | a0001 | c0005 | t0129 | g0312 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02622 | hp1 | a0002 | c0002 | t0162 | g0181 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02622 | hp2 | a0001 | c0001 | t0025 | g0027 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02630 | hp2 | a0001 | c0001 | t0036 | g0201 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02647 | hp1 | a0001 | c0001 | t0025 | g0029 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02647 | hp2 | a0001 | c0001 | t0067 | g0033 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02717 | hp1 | a0001 | c0001 | t0030 | g0060 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02717 | hp2 | a0002 | c0002 | t0119 | g0161 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02723 | hp2 | a0001 | c0001 | t0046 | g0087 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02735 | hp1 | a0001 | c0001 | t0062 | g0040 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02735 | hp2 | a0001 | c0001 | t0017 | g0283 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02809 | hp1 | a0002 | c0002 | t0133 | g0173 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02818 | hp1 | a0002 | c0002 | t0181 | g0015 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02818 | hp2 | a0006 | c0008 | t0004 | g0303 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02895 | hp1 | a0001 | c0001 | t0032 | g0004 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02895 | hp2 | a0002 | c0002 | t0151 | g0169 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02896 | hp2 | a0002 | c0002 | t0173 | g0318 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02897 | hp1 | a0001 | c0001 | t0032 | g0004 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02922 | hp1 | a0001 | c0001 | t0059 | g0017 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02922 | hp2 | a0001 | c0001 | t0041 | g0198 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02965 | hp1 | a0001 | c0001 | t0091 | g0189 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02965 | hp2 | a0001 | c0001 | t0124 | g0196 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02970 | hp1 | a0002 | c0002 | t0148 | g0160 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02970 | hp2 | a0001 | c0001 | t0045 | g0002 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02976 | hp1 | a0001 | c0001 | t0041 | g0200 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02976 | hp2 | a0001 | c0001 | t0109 | g0007 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03041 | hp1 | a0002 | c0002 | t0182 | g0015 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03041 | hp2 | a0002 | c0002 | t0093 | g0177 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03098 | hp1 | a0002 | c0002 | t0023 | g0180 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03098 | hp2 | a0001 | c0001 | t0168 | g0192 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03130 | hp1 | a0002 | c0002 | t0021 | g0126 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03130 | hp2 | a0001 | c0001 | t0012 | g0186 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0188 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03195 | hp1 | a0001 | c0001 | t0107 | g0203 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03195 | hp2 | a0002 | c0002 | t0130 | g0171 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03225 | hp1 | a0001 | c0001 | t0028 | g0057 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03225 | hp2 | a0001 | c0001 | t0106 | g0202 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03453 | hp1 | a0001 | c0001 | t0169 | g0193 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03453 | hp2 | a0001 | c0001 | t0047 | g0055 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03486 | hp1 | a0001 | c0001 | t0110 | g0007 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03516 | hp1 | a0001 | c0001 | t0051 | g0118 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03516 | hp2 | a0001 | c0001 | t0038 | g0006 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03540 | hp1 | a0001 | c0001 | t0158 | g0307 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03540 | hp2 | a0002 | c0002 | t0023 | g0174 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03579 | hp1 | a0002 | c0002 | t0042 | g0315 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03579 | hp2 | a0001 | c0001 | t0026 | g0002 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03654 | hp1 | a0001 | c0001 | t0018 | g0278 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03654 | hp2 | a0001 | c0001 | t0010 | g0052 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03688 | hp1 | a0001 | c0001 | t0152 | g0242 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03688 | hp2 | a0002 | c0002 | t0020 | g0120 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03704 | hp1 | a0002 | c0002 | t0101 | g0122 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03710 | hp2 | a0001 | c0001 | t0077 | g0050 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03831 | hp1 | a0001 | c0001 | t0022 | g0225 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03831 | hp2 | a0001 | c0001 | t0022 | g0237 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03834 | hp1 | a0002 | c0002 | t0005 | g0134 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03834 | hp2 | a0001 | c0001 | t0017 | g0250 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03927 | hp2 | a0001 | c0001 | t0165 | g0223 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG04184 | hp1 | a0001 | c0001 | t0050 | g0105 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG04184 | hp2 | a0001 | c0001 | t0078 | g0037 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG04204 | hp1 | a0002 | c0002 | t0011 | g0165 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG04204 | hp2 | a0001 | c0001 | t0049 | g0016 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG04228 | hp1 | a0001 | c0001 | t0166 | g0263 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG04228 | hp2 | a0002 | c0002 | t0113 | g0125 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18522 | hp1 | a0001 | c0001 | t0180 | g0197 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18522 | hp2 | a0002 | c0002 | t0095 | g0175 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18612 | hp1 | a0002 | c0002 | t0005 | g0149 | EAS | CHB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18906 | hp1 | a0001 | c0001 | t0048 | g0056 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18906 | hp2 | a0002 | c0002 | t0172 | g0317 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18940 | hp1 | a0001 | c0001 | t0127 | g0246 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18940 | hp2 | a0001 | c0001 | t0009 | g0106 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18945 | hp1 | a0002 | c0002 | t0147 | g0141 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18948 | hp2 | a0002 | c0002 | t0005 | g0140 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18949 | hp1 | a0001 | c0001 | t0171 | g0251 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18949 | hp2 | a0001 | c0001 | t0019 | g0003 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18953 | hp2 | a0002 | c0002 | t0096 | g0135 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0083 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18957 | hp1 | a0001 | c0006 | t0006 | g0103 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18957 | hp2 | a0001 | c0001 | t0027 | g0042 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18960 | hp2 | a0001 | c0003 | t0013 | g0206 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18964 | hp1 | a0002 | c0002 | t0102 | g0155 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18964 | hp2 | a0001 | c0001 | t0006 | g0084 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18965 | hp1 | a0001 | c0005 | t0024 | g0313 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18965 | hp2 | a0001 | c0001 | t0019 | g0070 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18966 | hp1 | a0001 | c0003 | t0139 | g0009 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18966 | hp2 | a0001 | c0001 | t0144 | g0012 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18967 | hp1 | a0001 | c0001 | t0079 | g0064 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18967 | hp2 | a0001 | c0001 | t0167 | g0282 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18968 | hp2 | a0002 | c0004 | t0005 | g0138 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18969 | hp1 | a0002 | c0002 | t0088 | g0151 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18969 | hp2 | a0001 | c0001 | t0033 | g0248 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18970 | hp1 | a0002 | c0002 | t0011 | g0139 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18971 | hp1 | a0001 | c0001 | t0170 | g0212 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18971 | hp2 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18974 | hp2 | a0001 | c0001 | t0043 | g0300 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18978 | hp1 | a0001 | c0001 | t0076 | g0093 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18982 | hp1 | a0001 | c0001 | t0033 | g0231 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18982 | hp2 | a0001 | c0001 | t0054 | g0119 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18984 | hp1 | a0001 | c0001 | t0125 | g0275 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18984 | hp2 | a0001 | c0001 | t0009 | g0072 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18985 | hp2 | a0002 | c0002 | t0117 | g0124 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18990 | hp1 | a0001 | c0003 | t0039 | g0208 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18990 | hp2 | a0002 | c0002 | t0011 | g0154 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18992 | hp2 | a0001 | c0001 | t0065 | g0075 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18994 | hp1 | a0001 | c0001 | t0060 | g0024 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18995 | hp1 | a0001 | c0001 | t0178 | g0260 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18998 | hp1 | a0002 | c0002 | t0089 | g0146 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18998 | hp2 | a0001 | c0001 | t0017 | g0280 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18999 | hp1 | a0002 | c0002 | t0118 | g0131 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0262 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19000 | hp1 | a0001 | c0001 | t0074 | g0039 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19000 | hp2 | a0001 | c0001 | t0164 | g0301 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19001 | hp1 | a0001 | c0001 | t0155 | g0267 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19001 | hp2 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19004 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19005 | hp1 | a0002 | c0002 | t0011 | g0132 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19005 | hp2 | a0001 | c0001 | t0008 | g0066 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19006 | hp1 | a0001 | c0001 | t0024 | g0286 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19006 | hp2 | a0001 | c0001 | t0056 | g0082 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19007 | hp1 | a0001 | c0001 | t0071 | g0041 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19007 | hp2 | a0002 | c0002 | t0116 | g0152 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19009 | hp2 | a0002 | c0002 | t0112 | g0145 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19010 | hp1 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19011 | hp2 | a0001 | c0001 | t0126 | g0249 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19030 | hp1 | a0002 | c0002 | t0121 | g0123 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19030 | hp2 | a0001 | c0001 | t0085 | g0116 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19043 | hp1 | a0001 | c0001 | t0028 | g0059 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19043 | hp2 | a0001 | c0001 | t0163 | g0194 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19054 | hp2 | a0001 | c0001 | t0150 | g0013 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19056 | hp1 | a0002 | c0002 | t0005 | g0142 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19056 | hp2 | a0001 | c0006 | t0055 | g0104 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19057 | hp1 | a0002 | c0002 | t0005 | g0137 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19057 | hp2 | a0001 | c0001 | t0080 | g0018 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19058 | hp1 | a0002 | c0004 | t0011 | g0143 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19058 | hp2 | a0001 | c0001 | t0153 | g0268 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19065 | hp1 | a0002 | c0002 | t0099 | g0166 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19065 | hp2 | a0001 | c0001 | t0016 | g0089 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19066 | hp2 | a0002 | c0002 | t0115 | g0128 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19067 | hp1 | a0001 | c0001 | t0031 | g0094 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19067 | hp2 | a0001 | c0001 | t0066 | g0038 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19068 | hp1 | a0002 | c0002 | t0005 | g0129 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19068 | hp2 | a0001 | c0001 | t0016 | g0073 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19070 | hp1 | a0001 | c0001 | t0019 | g0101 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19070 | hp2 | a0001 | c0001 | t0043 | g0299 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19072 | hp1 | a0001 | c0001 | t0134 | g0277 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19072 | hp2 | a0002 | c0004 | t0146 | g0130 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19074 | hp1 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19074 | hp2 | a0001 | c0001 | t0029 | g0046 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19077 | hp1 | a0001 | c0001 | t0138 | g0215 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19077 | hp2 | a0002 | c0002 | t0005 | g0136 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19080 | hp1 | a0001 | c0001 | t0010 | g0043 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19082 | hp1 | a0001 | c0003 | t0013 | g0207 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19082 | hp2 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19084 | hp1 | a0001 | c0001 | t0009 | g0107 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19084 | hp2 | a0001 | c0001 | t0070 | g0045 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19086 | hp2 | a0002 | c0002 | t0100 | g0144 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19088 | hp1 | a0001 | c0003 | t0039 | g0209 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19088 | hp2 | a0001 | c0001 | t0024 | g0271 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19089 | hp1 | a0002 | c0002 | t0086 | g0153 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19091 | hp2 | a0001 | c0001 | t0141 | g0294 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19240 | hp1 | a0002 | c0002 | t0132 | g0168 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA19240 | hp2 | a0002 | c0002 | t0021 | g0005 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ASW | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA20129 | hp2 | a0007 | c0010 | t0087 | g0321 | AFR | ASW | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA20805 | hp1 | a0001 | c0001 | t0064 | g0095 | EUR | TSI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA20805 | hp2 | a0002 | c0002 | t0175 | g0183 | EUR | TSI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | GIH | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | GIH | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02109 | hp1 | a0002 | c0002 | t0023 | g0176 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02109 | hp2 | a0001 | c0001 | t0038 | g0185 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02486 | hp1 | a0001 | c0001 | t0154 | g0190 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02486 | hp2 | a0001 | c0001 | t0052 | g0117 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0048 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG02559 | hp2 | a0002 | c0002 | t0156 | g0178 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03471 | hp1 | a0001 | c0001 | t0137 | g0306 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG03471 | hp2 | a0002 | c0002 | t0136 | g0170 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG06807 | hp1 | a0001 | c0001 | t0057 | g0058 | AFR | USA | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| HG06807 | hp2 | a0002 | c0002 | t0035 | g0314 | AFR | USA | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18955 | hp1 | a0001 | c0003 | t0013 | g0009 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | USA | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA20300 | hp2 | a0001 | c0001 | t0016 | g0096 | AFR | USA | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA21309 | hp1 | a0001 | c0001 | t0044 | g0028 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0100 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0159 | g0221 | REF | REF | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0177 | g0167 | REF | REF | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:50917459 | G | A | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.581G>A | p.Arg194Gln | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/16 | 784/9031 | 581/1755 | 194/584 | chr18 | 50917459 | |||
| chr18:50918152 | C | T | 1 | a0004 | 1 | HG01261.hp1 | stop_gained | HIGH | c.673C>T | p.Arg225* | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/16 | 876/9031 | 673/1755 | 225/584 | chr18 | 50918152 | |||
| chr18:50921092 | A | C | 1 | a0003 | 2 | HG01074.hp1 HG01106.hp2 |
missense_variant | MODERATE | c.961A>C | p.Asn321His | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/16 | 1164/9031 | 961/1755 | 321/584 | chr18 | 50921092 | |||
| chr18:50924113 | A | G | 1 | a0007 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1072A>G | p.Ile358Val | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/16 | 1275/9031 | 1072/1755 | 358/584 | chr18 | 50924113 | |||
| chr18:50924131 | C | G | 2 | a0005 a0007 |
2 | HG02451.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.1090C>G | p.Pro364Ala | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/16 | 1293/9031 | 1090/1755 | 364/584 | chr18 | 50924131 | |||
| chr18:50932292 | G | A | 2 | a0002 a0007 |
75 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(72): Show |
missense_variant | MODERATE | c.1349G>A | p.Gly450Glu | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/16 | 1552/9031 | 1349/1755 | 450/584 | chr18 | 50932292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:50912900 | G | A | 1 | a0001c0005 | 2 | HG02602.hp1 NA18965.hp1 |
synonymous_variant | LOW | c.342G>A | p.Pro114Pro | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/16 | 545/9031 | 342/1755 | 114/584 | chr18 | 50912900 | |||
| chr18:50932347 | T | A | 1 | a0001c0003 | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
synonymous_variant | LOW | c.1404T>A | p.Val468Val | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/16 | 1607/9031 | 1404/1755 | 468/584 | chr18 | 50932347 | |||
| chr18:50947031 | A | G | 1 | a0001c0006 | 2 | NA18957.hp1 NA19056.hp2 |
synonymous_variant | LOW | c.1602A>G | p.Leu534Leu | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1805/9031 | 1602/1755 | 534/584 | chr18 | 50947031 | |||
| chr18:50947127 | G | T | 1 | a0002c0004 | 3 | NA18968.hp2 NA19058.hp1 NA19072.hp2 |
synonymous_variant | LOW | c.1698G>T | p.Leu566Leu | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1901/9031 | 1698/1755 | 566/584 | chr18 | 50947127 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:50879119 | T | A | 60 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(57): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-202T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/16 | 16702 | chr18 | 50879119 | ||||||
| chr18:50879160 | C | A | 4 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0044 others(1): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-161C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/16 | 16661 | chr18 | 50879160 | ||||||
| chr18:50879168 | T | C | 1 | a0001c0001t0046 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-153T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/16 | 16653 | chr18 | 50879168 | ||||||
| chr18:50879294 | G | A | 2 | a0001c0001t0047 a0001c0001t0048 |
2 | HG03453.hp2 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-27G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/16 | 16527 | chr18 | 50879294 | ||||||
| chr18:50947383 | G | A | 121 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(118): Show |
223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*199G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 199 | chr18 | 50947383 | ||||||
| chr18:50947416 | C | T | 2 | a0001c0001t0041 a0001c0001t0169 |
3 | HG02922.hp2 HG02976.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*232C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 232 | chr18 | 50947416 | ||||||
| chr18:50947492 | A | G | 2 | a0001c0001t0032 a0001c0001t0085 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*308A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 308 | chr18 | 50947492 | ||||||
| chr18:50947629 | G | A | 1 | a0002c0002t0086 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*445G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 445 | chr18 | 50947629 | ||||||
| chr18:50947706 | G | C | 1 | a0001c0001t0053 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*522G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 522 | chr18 | 50947706 | ||||||
| chr18:50948167 | T | C | 1 | a0002c0002t0086 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 983 | chr18 | 50948167 | ||||||
| chr18:50948263 | T | A | 2 | a0001c0001t0032 a0001c0001t0085 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1079T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1079 | chr18 | 50948263 | ||||||
| chr18:50948378 | A | G | 4 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0044 others(1): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1194A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1194 | chr18 | 50948378 | ||||||
| chr18:50948449 | G | A | 4 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0044 others(1): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1265G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1265 | chr18 | 50948449 | ||||||
| chr18:50948470 | A | G | 1 | a0001c0001t0168 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1286A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1286 | chr18 | 50948470 | ||||||
| chr18:50948541 | C | CT | 19 | a0001c0001t0040 a0001c0001t0041 a0001c0001t0080 others(16): Show |
21 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1378dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1379 | INFO_REALIGN_3_PRIME | chr18 | 50948541 | |||||
| chr18:50948541 | CT | C | 60 | a0001c0001t0027 a0001c0001t0028 a0001c0001t0033 others(57): Show |
81 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1378delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1378 | INFO_REALIGN_3_PRIME | chr18 | 50948541 | |||||
| chr18:50948581 | G | C | 4 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0044 others(1): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1397G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1397 | chr18 | 50948581 | ||||||
| chr18:50948743 | C | A | 1 | a0002c0002t0086 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1559C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1559 | chr18 | 50948743 | ||||||
| chr18:50948785 | G | A | 1 | a0001c0001t0059 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1601G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1601 | chr18 | 50948785 | ||||||
| chr18:50948814 | T | A | 1 | a0002c0002t0086 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1630T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1630 | chr18 | 50948814 | ||||||
| chr18:50948830 | C | A | 1 | a0007c0010t0087 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1646C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1646 | chr18 | 50948830 | ||||||
| chr18:50948834 | A | G | 135 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(132): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*1650A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1650 | chr18 | 50948834 | ||||||
| chr18:50948838 | A | T | 1 | a0001c0001t0079 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1654A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1654 | chr18 | 50948838 | ||||||
| chr18:50948843 | A | AT | 9 | a0001c0001t0031 a0001c0001t0076 a0001c0001t0077 others(6): Show |
10 | HG00621.hp2 HG00642.hp2 HG02717.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1679dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1680 | INFO_REALIGN_3_PRIME | chr18 | 50948843 | |||||
| chr18:50948843 | AT | A | 76 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(73): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1679delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1679 | INFO_REALIGN_3_PRIME | chr18 | 50948843 | |||||
| chr18:50949032 | G | A | 1 | a0001c0001t0122 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1848G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1848 | chr18 | 50949032 | ||||||
| chr18:50949070 | C | CTTCAGGT others(26): Show |
1 | a0001c0001t0145 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1888_*1920dupTCAG others(29): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1921 | INFO_REALIGN_3_PRIME | chr18 | 50949070 | |||||
| chr18:50949123 | A | G | 1 | a0001c0001t0075 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1939A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1939 | chr18 | 50949123 | ||||||
| chr18:50949286 | T | C | 1 | a0002c0002t0086 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2102T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2102 | chr18 | 50949286 | ||||||
| chr18:50949318 | G | A | 1 | a0001c0001t0037 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2134G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2134 | chr18 | 50949318 | ||||||
| chr18:50949384 | G | C | 1 | a0002c0002t0094 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2200G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2200 | chr18 | 50949384 | ||||||
| chr18:50949387 | C | G | 3 | a0002c0002t0115 a0002c0002t0116 a0002c0002t0117 |
3 | NA18985.hp2 NA19007.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2203C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2203 | chr18 | 50949387 | ||||||
| chr18:50949425 | C | A | 1 | a0001c0001t0123 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2241C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2241 | chr18 | 50949425 | ||||||
| chr18:50949446 | G | A | 1 | a0001c0001t0124 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2262G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2262 | chr18 | 50949446 | ||||||
| chr18:50949544 | G | A | 1 | a0001c0001t0125 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2360 | chr18 | 50949544 | ||||||
| chr18:50949827 | A | G | 1 | a0002c0002t0114 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2643A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2643 | chr18 | 50949827 | ||||||
| chr18:50949870 | A | AT | 3 | a0002c0002t0042 a0002c0002t0172 a0002c0002t0173 |
4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2688dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2689 | INFO_REALIGN_3_PRIME | chr18 | 50949870 | |||||
| chr18:50949962 | T | TAAAACAT others(31): Show |
1 | a0002c0002t0086 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2779_*2816dupAAAA others(34): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2817 | INFO_REALIGN_3_PRIME | chr18 | 50949962 | |||||
| chr18:50950030 | A | G | 2 | a0001c0001t0051 a0001c0001t0052 |
2 | HG02486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2846A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2846 | chr18 | 50950030 | ||||||
| chr18:50950058 | C | T | 1 | a0002c0002t0094 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2874C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2874 | chr18 | 50950058 | ||||||
| chr18:50950080 | G | A | 27 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(24): Show |
65 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2896G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2896 | chr18 | 50950080 | ||||||
| chr18:50950232 | C | G | 1 | a0002c0002t0113 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3048C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3048 | chr18 | 50950232 | ||||||
| chr18:50950305 | C | T | 1 | a0001c0001t0046 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3121C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3121 | chr18 | 50950305 | ||||||
| chr18:50950309 | C | T | 1 | a0001c0001t0161 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3125C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3125 | chr18 | 50950309 | ||||||
| chr18:50950350 | T | A | 2 | a0001c0001t0169 a0002c0002t0181 |
2 | HG02818.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3166T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3166 | chr18 | 50950350 | ||||||
| chr18:50950417 | C | T | 1 | a0001c0001t0144 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3233C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3233 | chr18 | 50950417 | ||||||
| chr18:50950466 | G | GC | 33 | a0002c0002t0005 a0002c0002t0011 a0002c0002t0020 others(30): Show |
51 | HG00423.hp2 HG00639.hp1 HG01175.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3283dupC | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | INFO_REALIGN_3_PRIME | chr18 | 50950466 | |||||
| chr18:50950466 | G | GCTTTTTT others(3): Show |
35 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(32): Show |
85 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*3283_*3292dupCTTT others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950466 | |||||
| chr18:50950467 | C | CCT | 12 | a0002c0002t0035 a0002c0002t0086 a0002c0002t0094 others(9): Show |
13 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3283_*3284insCT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950467 | ||||||
| chr18:50950467 | C | CCTTTTTT others(11): Show |
1 | a0001c0001t0122 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3283_*3284insCTTT others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950467 | ||||||
| chr18:50950467 | C | CCTTTTTT others(12): Show |
1 | a0001c0001t0051 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3283_*3284insCTTT others(15): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950467 | ||||||
| chr18:50950467 | C | CCTTTTTT others(13): Show |
1 | a0001c0001t0052 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3283_*3284insCTTT others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950467 | ||||||
| chr18:50950467 | C | CT | 9 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0016 others(6): Show |
22 | HG00544.hp1 HG00642.hp2 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3311dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3312 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950467 | C | CTTTTTTT others(4): Show |
18 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0022 others(15): Show |
37 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3292_*3293insCTTT others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950467 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0153 a0001c0001t0154 a0001c0001t0167 |
3 | HG02486.hp1 NA18967.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3292_*3293insCTTT others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950467 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0138 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3292_*3293insCTTT others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950467 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0155 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3293_*3294insCTTT others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3294 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950467 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0025 | 2 | HG02622.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3300_*3311dupTTTT others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3312 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950467 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0026 a0001c0001t0044 |
3 | HG01891.hp2 HG03579.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3299_*3311dupTTTT others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3312 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950467 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0045 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3294_*3311dupTTTT others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3312 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950467 | CTT | C | 5 | a0001c0001t0067 a0001c0003t0013 a0001c0003t0039 others(2): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3310_*3311delTT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3310 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950467 | CTTTTTTT | C | 5 | a0001c0001t0012 a0001c0001t0038 a0001c0001t0083 others(2): Show |
9 | HG01074.hp1 HG01106.hp2 HG01361.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3305_*3311delTTTT others(3): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3305 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | |||||
| chr18:50950468 | T | C | 1 | a0002c0004t0146 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3284T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950468 | ||||||
| chr18:50950468 | T | TTTTTTTT others(2): Show |
7 | a0001c0001t0017 a0001c0001t0033 a0001c0001t0043 others(4): Show |
12 | HG01074.hp2 HG02735.hp2 HG03453.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3292_*3293insCTTT others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950468 | |||||
| chr18:50950479 | T | C | 1 | a0001c0001t0106 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3295T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3295 | chr18 | 50950479 | ||||||
| chr18:50950573 | T | C | 139 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(136): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*3389T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3389 | chr18 | 50950573 | ||||||
| chr18:50950597 | G | A | 1 | a0001c0001t0067 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3413G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3413 | chr18 | 50950597 | ||||||
| chr18:50950764 | C | T | 1 | a0002c0002t0102 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3580C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3580 | chr18 | 50950764 | ||||||
| chr18:50951034 | A | C | 5 | a0001c0003t0013 a0001c0003t0039 a0001c0003t0139 others(2): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3850A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3850 | chr18 | 50951034 | ||||||
| chr18:50951064 | G | A | 185 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(182): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*3880G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3880 | chr18 | 50951064 | ||||||
| chr18:50951168 | A | G | 2 | a0002c0002t0181 a0002c0002t0182 |
2 | HG02818.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3984A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3984 | chr18 | 50951168 | ||||||
| chr18:50951443 | G | A | 3 | a0001c0001t0027 a0001c0001t0029 a0001c0001t0084 |
5 | HG00597.hp1 HG02040.hp1 HG02056.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4259G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4259 | chr18 | 50951443 | ||||||
| chr18:50951456 | A | G | 1 | a0001c0001t0078 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4272A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4272 | chr18 | 50951456 | ||||||
| chr18:50951547 | C | CT | 6 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0075 others(3): Show |
12 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4380dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4381 | INFO_REALIGN_3_PRIME | chr18 | 50951547 | |||||
| chr18:50951547 | CT | C | 69 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(66): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*4380delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4380 | INFO_REALIGN_3_PRIME | chr18 | 50951547 | |||||
| chr18:50951565 | A | T | 1 | a0001c0001t0066 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4381A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4381 | chr18 | 50951565 | ||||||
| chr18:50951567 | C | A | 1 | a0001c0001t0066 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4383C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4383 | chr18 | 50951567 | ||||||
| chr18:50951568 | T | C | 1 | a0001c0001t0066 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4384T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4384 | chr18 | 50951568 | ||||||
| chr18:50951634 | T | G | 1 | a0001c0003t0143 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4450T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4450 | chr18 | 50951634 | ||||||
| chr18:50951705 | T | C | 137 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(134): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*4521T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4521 | chr18 | 50951705 | ||||||
| chr18:50951839 | C | T | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(55): Show |
135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*4655C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4655 | chr18 | 50951839 | ||||||
| chr18:50951853 | T | C | 131 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(128): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*4669T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4669 | chr18 | 50951853 | ||||||
| chr18:50951866 | C | CA | 9 | a0001c0001t0016 a0001c0001t0019 a0001c0001t0030 others(6): Show |
15 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4719dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4720 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | C | CAA | 8 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0051 others(5): Show |
10 | HG01192.hp1 HG01891.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4718_*4719dupAA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4720 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CA | C | 16 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0015 others(13): Show |
30 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4719delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4719 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAA | C | 9 | a0001c0003t0039 a0001c0003t0143 a0002c0002t0034 others(6): Show |
11 | HG02071.hp2 HG02129.hp1 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4717_*4719delAAA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4717 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAA | C | 23 | a0001c0003t0013 a0001c0003t0139 a0002c0002t0005 others(20): Show |
37 | HG00408.hp2 HG00423.hp2 HG01884.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4716_*4719delAAAA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4716 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAA | C | 15 | a0001c0003t0140 a0002c0002t0011 a0002c0002t0093 others(12): Show |
18 | HG01106.hp1 HG02015.hp1 HG02040.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4715_*4719delAAAA others(1): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4715 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAAA | C | 5 | a0002c0002t0035 a0002c0002t0097 a0002c0002t0101 others(2): Show |
6 | HG01175.hp1 HG01346.hp2 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4714_*4719delAAAA others(2): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4714 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAAAA | C | 4 | a0002c0002t0020 a0002c0002t0103 a0002c0002t0114 others(1): Show |
6 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4713_*4719delAAAA others(3): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4713 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0036 a0001c0001t0049 a0001c0001t0091 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4712_*4719delAAAA others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4712 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0065 a0001c0001t0157 a0001c0001t0167 |
3 | HG00741.hp2 NA18967.hp2 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4710_*4719delAAAA others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4710 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAAAA others(4): Show |
C | 16 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0022 others(13): Show |
30 | HG00408.hp1 HG00735.hp2 HG01071.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4709_*4719delAAAA others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4709 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAAAA others(5): Show |
C | 39 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(36): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*4708_*4719delAAAA others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4708 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0027 a0001c0001t0070 a0001c0001t0074 |
4 | HG02056.hp1 NA18957.hp2 NA19000.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4707_*4719delAAAA others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4707 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0029 | 2 | HG02040.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4706_*4719delAAAA others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4706 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951866 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0071 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4701_*4719delAAAA others(15): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4701 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | |||||
| chr18:50951977 | T | G | 5 | a0001c0003t0013 a0001c0003t0039 a0001c0003t0139 others(2): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4793T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4793 | chr18 | 50951977 | ||||||
| chr18:50952076 | G | A | 3 | a0001c0001t0051 a0001c0001t0052 a0001c0001t0122 |
3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4892G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4892 | chr18 | 50952076 | ||||||
| chr18:50952163 | G | T | 55 | a0001c0001t0036 a0001c0001t0091 a0001c0001t0106 others(52): Show |
75 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*4979G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4979 | chr18 | 50952163 | ||||||
| chr18:50952456 | G | A | 1 | a0001c0001t0155 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5272G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5272 | chr18 | 50952456 | ||||||
| chr18:50952887 | C | T | 1 | a0001c0001t0135 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5703C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5703 | chr18 | 50952887 | ||||||
| chr18:50952893 | T | C | 3 | a0002c0002t0042 a0002c0002t0172 a0002c0002t0173 |
4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5709T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5709 | chr18 | 50952893 | ||||||
| chr18:50953074 | T | C | 58 | a0001c0001t0036 a0001c0001t0091 a0001c0001t0106 others(55): Show |
78 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5890T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5890 | chr18 | 50953074 | ||||||
| chr18:50953092 | C | CT | 65 | a0001c0001t0012 a0001c0001t0022 a0001c0001t0036 others(62): Show |
91 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*5926dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5927 | INFO_REALIGN_3_PRIME | chr18 | 50953092 | |||||
| chr18:50953092 | CTT | C | 5 | a0001c0001t0134 a0001c0003t0013 a0001c0003t0039 others(2): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5925_*5926delTT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5925 | INFO_REALIGN_3_PRIME | chr18 | 50953092 | |||||
| chr18:50953148 | G | C | 1 | a0001c0001t0128 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5964G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5964 | chr18 | 50953148 | ||||||
| chr18:50953199 | T | C | 2 | a0001c0001t0051 a0001c0001t0052 |
2 | HG02486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6015T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6015 | chr18 | 50953199 | ||||||
| chr18:50953648 | C | G | 1 | a0002c0002t0104 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6464C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6464 | chr18 | 50953648 | ||||||
| chr18:50953702 | T | C | 1 | a0001c0001t0032 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6518T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6518 | chr18 | 50953702 | ||||||
| chr18:50953795 | A | T | 1 | a0001c0001t0051 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6611A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6611 | chr18 | 50953795 | ||||||
| chr18:50953847 | T | A | 4 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0044 others(1): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6663T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6663 | chr18 | 50953847 | ||||||
| chr18:50953867 | T | C | 5 | a0001c0001t0012 a0001c0001t0038 a0003c0007t0012 others(2): Show |
9 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6683T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6683 | chr18 | 50953867 | ||||||
| chr18:50953868 | T | G | 116 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(113): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*6684T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6684 | chr18 | 50953868 | ||||||
| chr18:50954124 | G | A | 4 | a0001c0001t0012 a0001c0001t0038 a0003c0007t0012 others(1): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6940G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6940 | chr18 | 50954124 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:50879366 | C | T | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+58C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879366 | |||||||
| chr18:50879476 | T | C | 109 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-13+168T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879476 | |||||||
| chr18:50879529 | C | G | 4 | a0002c0002t0020g0322 a0002c0002t0020g0323 a0002c0002t0035g0325 others(1): Show |
4 | HG00639.hp1 HG00642.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+221C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879529 | |||||||
| chr18:50879653 | C | T | 2 | a0002c0002t0181g0015 a0002c0002t0182g0015 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-13+345C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879653 | |||||||
| chr18:50879693 | AC | A | 3 | a0002c0002t0181g0015 a0002c0002t0182g0015 a0007c0010t0087g0321 |
3 | HG02818.hp1 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13+388delC | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50879693 | ||||||
| chr18:50879926 | T | A | 1 | a0001c0001t0049g0016 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-13+618T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879926 | |||||||
| chr18:50879996 | A | T | 2 | a0001c0001t0017g0319 a0001c0001t0018g0320 |
2 | HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-13+688A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879996 | |||||||
| chr18:50880138 | A | G | 1 | a0001c0001t0054g0119 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-13+830A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880138 | |||||||
| chr18:50880141 | G | A | 1 | a0002c0002t0020g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-13+833G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880141 | |||||||
| chr18:50880168 | G | A | 1 | a0001c0001t0004g0121 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-13+860G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880168 | |||||||
| chr18:50880179 | G | A | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+871G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880179 | |||||||
| chr18:50880378 | A | G | 2 | a0001c0001t0051g0118 a0001c0001t0052g0117 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-13+1070A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880378 | |||||||
| chr18:50880527 | A | C | 4 | a0002c0002t0042g0315 a0002c0002t0042g0316 a0002c0002t0172g0317 others(1): Show |
4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+1219A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880527 | |||||||
| chr18:50880539 | C | T | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-13+1231C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880539 | |||||||
| chr18:50880645 | T | A | 1 | a0002c0002t0101g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-13+1337T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880645 | |||||||
| chr18:50880703 | C | G | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-13+1395C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880703 | |||||||
| chr18:50880728 | C | T | 2 | a0001c0001t0014g0115 a0001c0001t0015g0114 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-13+1420C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880728 | |||||||
| chr18:50880956 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-13+1648C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880956 | |||||||
| chr18:50881026 | A | G | 2 | a0002c0002t0174g0182 a0002c0002t0175g0183 |
2 | HG01175.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-13+1718A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881026 | |||||||
| chr18:50881084 | A | C | 2 | a0001c0005t0024g0313 a0001c0005t0129g0312 |
2 | HG02602.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-13+1776A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881084 | |||||||
| chr18:50881182 | C | T | 1 | a0003c0007t0160g0311 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-13+1874C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881182 | |||||||
| chr18:50881252 | G | A | 1 | a0001c0001t0059g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-13+1944G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881252 | |||||||
| chr18:50881282 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(108): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-13+1974C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881282 | |||||||
| chr18:50881303 | C | G | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13+1995C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881303 | |||||||
| chr18:50881332 | C | T | 10 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0111 others(7): Show |
10 | HG00544.hp1 NA18940.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+2024C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881332 | |||||||
| chr18:50881423 | A | G | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+2115A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881423 | |||||||
| chr18:50881470 | A | G | 4 | a0002c0002t0042g0315 a0002c0002t0042g0316 a0002c0002t0172g0317 others(1): Show |
4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+2162A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881470 | |||||||
| chr18:50881793 | A | C | 1 | a0001c0001t0001g0310 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-13+2485A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881793 | |||||||
| chr18:50881915 | T | A | 107 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-13+2607T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881915 | |||||||
| chr18:50881946 | G | A | 10 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0006g0025 others(7): Show |
10 | HG00423.hp1 NA18971.hp2 NA18982.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+2638G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881946 | |||||||
| chr18:50881990 | A | G | 1 | a0002c0002t0133g0173 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13+2682A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881990 | |||||||
| chr18:50882026 | G | A | 1 | a0001c0001t0138g0215 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-13+2718G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882026 | |||||||
| chr18:50882029 | C | A | 105 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13+2721C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882029 | |||||||
| chr18:50882049 | A | G | 1 | a0001c0001t0004g0205 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-13+2741A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882049 | |||||||
| chr18:50882201 | G | A | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+2893G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882201 | |||||||
| chr18:50882239 | C | T | 1 | a0002c0002t0162g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+2931C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882239 | |||||||
| chr18:50882241 | C | T | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+2933C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882241 | |||||||
| chr18:50882451 | T | C | 1 | a0001c0001t0007g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-13+3143T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882451 | |||||||
| chr18:50882746 | C | G | 2 | a0001c0006t0006g0103 a0001c0006t0055g0104 |
2 | NA18957.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-13+3438C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882746 | |||||||
| chr18:50882778 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0219 a0001c0001t0007g0218 |
3 | HG00735.hp2 HG01361.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-13+3470G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882778 | |||||||
| chr18:50882810 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-13+3502A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882810 | |||||||
| chr18:50882813 | G | A | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3505G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882813 | |||||||
| chr18:50882864 | G | A | 1 | a0002c0002t0023g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-13+3556G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882864 | |||||||
| chr18:50883005 | A | T | 7 | a0001c0001t0001g0308 a0001c0001t0004g0304 a0001c0001t0004g0305 others(4): Show |
7 | HG01109.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+3697A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883005 | |||||||
| chr18:50883233 | G | C | 1 | a0001c0001t0007g0220 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-13+3925G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883233 | |||||||
| chr18:50883245 | A | G | 4 | a0001c0001t0036g0201 a0001c0001t0106g0202 a0001c0001t0107g0203 others(1): Show |
4 | HG02258.hp2 HG02630.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+3937A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883245 | |||||||
| chr18:50883325 | C | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(138): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-13+4017C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883325 | |||||||
| chr18:50883373 | T | C | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13+4065T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883373 | |||||||
| chr18:50883587 | G | A | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+4279G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883587 | |||||||
| chr18:50883637 | C | T | 105 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13+4329C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883637 | |||||||
| chr18:50883650 | A | T | 3 | a0001c0001t0001g0199 a0001c0001t0041g0198 a0001c0001t0041g0200 |
3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13+4342A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883650 | |||||||
| chr18:50883755 | T | G | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13+4447T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883755 | |||||||
| chr18:50883984 | T | A | 2 | a0002c0002t0181g0015 a0002c0002t0182g0015 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-13+4676T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883984 | |||||||
| chr18:50884047 | A | T | 1 | a0001c0001t0019g0101 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-13+4739A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884047 | |||||||
| chr18:50884381 | A | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(268): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-13+5073A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884381 | |||||||
| chr18:50884494 | C | T | 1 | a0002c0002t0131g0172 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-13+5186C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884494 | |||||||
| chr18:50884697 | A | G | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-13+5389A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884697 | |||||||
| chr18:50884704 | G | A | 1 | a0001c0001t0007g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-13+5396G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884704 | |||||||
| chr18:50884842 | TTG | T | 74 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(71): Show |
75 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.-13+5560_-13+5561d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50884842 | ||||||
| chr18:50884842 | TTGTG | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.-13+5558_-13+5561d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50884842 | ||||||
| chr18:50884858 | G | A | 1 | a0001c0001t0058g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-13+5550G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884858 | |||||||
| chr18:50884876 | C | T | 2 | a0002c0002t0181g0015 a0002c0002t0182g0015 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-13+5568C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884876 | |||||||
| chr18:50884884 | C | T | 1 | a0001c0001t0004g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13+5576C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884884 | |||||||
| chr18:50884958 | A | G | 107 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-13+5650A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884958 | |||||||
| chr18:50885117 | A | T | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+5809A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885117 | |||||||
| chr18:50885184 | A | G | 5 | a0001c0001t0010g0100 a0001c0001t0059g0017 a0001c0001t0072g0097 others(2): Show |
5 | HG00639.hp2 HG01175.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+5876A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885184 | |||||||
| chr18:50885259 | T | C | 2 | a0001c0001t0051g0118 a0001c0001t0052g0117 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-13+5951T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885259 | |||||||
| chr18:50885345 | C | T | 1 | a0001c0001t0016g0096 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-13+6037C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885345 | |||||||
| chr18:50885373 | C | T | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+6065C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885373 | |||||||
| chr18:50885528 | A | T | 7 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(4): Show |
7 | HG00099.hp2 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+6220A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885528 | |||||||
| chr18:50885552 | A | G | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13+6244A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885552 | |||||||
| chr18:50885821 | G | C | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+6513G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885821 | |||||||
| chr18:50885945 | G | A | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-13+6637G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885945 | |||||||
| chr18:50886031 | T | C | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+6723T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886031 | |||||||
| chr18:50886108 | CTA | C | 105 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13+6808_-13+6809d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50886108 | ||||||
| chr18:50886166 | T | TAAA | 9 | a0001c0001t0036g0191 a0001c0001t0036g0201 a0001c0001t0091g0189 others(6): Show |
9 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+6858_-13+6859i others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886166 | |||||||
| chr18:50886167 | T | A | 9 | a0001c0001t0036g0191 a0001c0001t0036g0201 a0001c0001t0091g0189 others(6): Show |
9 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+6859T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886167 | |||||||
| chr18:50886167 | T | TAAA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(131): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-13+6866_-13+6868d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50886167 | ||||||
| chr18:50886246 | A | AT | 115 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(112): Show |
116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-13+6953dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50886246 | ||||||
| chr18:50886263 | A | G | 1 | a0001c0001t0043g0299 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-13+6955A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886263 | |||||||
| chr18:50886444 | A | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+7136A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886444 | |||||||
| chr18:50886445 | T | C | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+7137T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886445 | |||||||
| chr18:50886524 | G | A | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+7216G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886524 | |||||||
| chr18:50886750 | C | T | 1 | a0002c0002t0023g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-13+7442C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886750 | |||||||
| chr18:50886782 | A | G | 4 | a0002c0002t0042g0315 a0002c0002t0042g0316 a0002c0002t0172g0317 others(1): Show |
4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+7474A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886782 | |||||||
| chr18:50886949 | T | C | 105 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13+7641T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886949 | |||||||
| chr18:50887204 | T | C | 2 | a0001c0003t0013g0009 a0001c0003t0139g0009 |
2 | NA18955.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-13+7896T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50887204 | |||||||
| chr18:50887546 | C | T | 1 | a0002c0002t0011g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-13+8238C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50887546 | |||||||
| chr18:50887865 | A | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(139): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-12-7944A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50887865 | |||||||
| chr18:50887961 | A | G | 105 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-12-7848A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50887961 | |||||||
| chr18:50888034 | G | A | 97 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(94): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-12-7775G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888034 | |||||||
| chr18:50888244 | C | T | 2 | a0001c0001t0037g0297 a0001c0001t0037g0298 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-12-7565C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888244 | |||||||
| chr18:50888310 | A | C | 2 | a0001c0001t0049g0016 a0001c0001t0050g0105 |
2 | HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-12-7499A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888310 | |||||||
| chr18:50888344 | CA | C | 11 | a0001c0001t0080g0018 a0001c0001t0165g0223 a0001c0001t0168g0192 others(8): Show |
12 | HG01358.hp2 HG01993.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12-7448delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50888344 | ||||||
| chr18:50888344 | CAA | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-12-7449_-12-7448d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50888344 | ||||||
| chr18:50888344 | CAAA | C | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-7450_-12-7448d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50888344 | ||||||
| chr18:50888452 | C | G | 2 | a0001c0001t0051g0118 a0001c0001t0052g0117 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-12-7357C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888452 | |||||||
| chr18:50888520 | G | A | 327 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(324): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-12-7289G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888520 | |||||||
| chr18:50888556 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(268): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-12-7253T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888556 | |||||||
| chr18:50888567 | A | AT | 8 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(5): Show |
9 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-7233dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50888567 | ||||||
| chr18:50888876 | A | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(151): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-12-6933A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888876 | |||||||
| chr18:50888885 | A | T | 97 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(94): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-12-6924A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888885 | |||||||
| chr18:50889024 | GTTC | G | 6 | a0002c0002t0023g0176 a0002c0002t0023g0180 a0002c0002t0093g0177 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-6780_-12-6778d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50889024 | ||||||
| chr18:50889067 | T | C | 1 | a0001c0001t0142g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-12-6742T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889067 | |||||||
| chr18:50889075 | A | G | 2 | a0002c0002t0181g0015 a0002c0002t0182g0015 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-6734A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889075 | |||||||
| chr18:50889283 | G | C | 2 | a0001c0001t0051g0118 a0001c0001t0052g0117 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-12-6526G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889283 | |||||||
| chr18:50889381 | T | C | 1 | a0001c0001t0067g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-12-6428T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889381 | |||||||
| chr18:50889764 | G | A | 3 | a0001c0001t0069g0034 a0001c0006t0006g0103 a0001c0006t0055g0104 |
3 | HG01928.hp1 NA18957.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-12-6045G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889764 | |||||||
| chr18:50889914 | T | G | 1 | a0001c0001t0022g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12-5895T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889914 | |||||||
| chr18:50890273 | ATT | A | 4 | a0002c0002t0042g0315 a0002c0002t0042g0316 a0002c0002t0172g0317 others(1): Show |
4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-5533_-12-5532d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50890273 | ||||||
| chr18:50890411 | G | A | 1 | a0001c0001t0006g0035 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-12-5398G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890411 | |||||||
| chr18:50890502 | C | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-12-5307C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890502 | |||||||
| chr18:50890547 | C | T | 1 | a0002c0002t0023g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-12-5262C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890547 | |||||||
| chr18:50890578 | A | C | 105 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-12-5231A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890578 | |||||||
| chr18:50890583 | T | C | 1 | a0001c0001t0003g0226 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12-5226T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890583 | |||||||
| chr18:50890842 | G | A | 17 | a0001c0001t0010g0043 a0001c0001t0010g0048 a0001c0001t0010g0049 others(14): Show |
17 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-4967G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890842 | |||||||
| chr18:50890914 | G | C | 1 | a0001c0001t0003g0227 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-12-4895G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890914 | |||||||
| chr18:50891016 | A | G | 1 | a0002c0002t0162g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-12-4793A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891016 | |||||||
| chr18:50891194 | A | G | 6 | a0002c0002t0023g0176 a0002c0002t0023g0180 a0002c0002t0093g0177 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-4615A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891194 | |||||||
| chr18:50891294 | C | T | 1 | a0001c0001t0135g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-12-4515C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891294 | |||||||
| chr18:50891326 | A | G | 1 | a0001c0001t0003g0226 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12-4483A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891326 | |||||||
| chr18:50891600 | A | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(259): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-12-4209A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891600 | |||||||
| chr18:50891715 | A | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-4094A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891715 | |||||||
| chr18:50891791 | G | A | 1 | a0005c0009t0068g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-4018G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891791 | |||||||
| chr18:50891812 | T | C | 1 | a0001c0001t0123g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-12-3997T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891812 | |||||||
| chr18:50891903 | C | T | 8 | a0001c0001t0001g0308 a0001c0001t0004g0121 a0001c0001t0004g0304 others(5): Show |
8 | HG01109.hp1 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-3906C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891903 | |||||||
| chr18:50891988 | G | GT | 90 | a0001c0001t0001g0295 a0001c0001t0025g0027 a0001c0001t0025g0029 others(87): Show |
91 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.-12-3809dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50891988 | ||||||
| chr18:50892041 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-12-3768G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892041 | |||||||
| chr18:50892169 | T | C | 1 | a0001c0001t0006g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-12-3640T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892169 | |||||||
| chr18:50892207 | G | A | 70 | a0001c0001t0108g0157 a0002c0002t0005g0127 a0002c0002t0005g0129 others(67): Show |
71 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.-12-3602G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892207 | |||||||
| chr18:50892221 | C | A | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-3588C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892221 | |||||||
| chr18:50892398 | G | C | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3411G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892398 | |||||||
| chr18:50892528 | T | C | 2 | a0001c0001t0047g0055 a0001c0001t0048g0056 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-12-3281T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892528 | |||||||
| chr18:50892727 | T | C | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3082T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892727 | |||||||
| chr18:50893026 | G | A | 4 | a0001c0001t0028g0057 a0001c0001t0028g0059 a0001c0001t0057g0058 others(1): Show |
4 | HG00738.hp2 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-2783G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893026 | |||||||
| chr18:50893124 | C | CA | 40 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(37): Show |
40 | HG00423.hp1 HG00423.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12-2657dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893124 | C | CAA | 5 | a0001c0001t0030g0060 a0001c0001t0084g0036 a0002c0002t0021g0005 others(2): Show |
6 | HG00597.hp1 HG01358.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-2658_-12-2657d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893124 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0180g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-12-2667_-12-2657d others(13): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893124 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0032g0004 a0001c0001t0169g0193 |
3 | HG02895.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-12-2674_-12-2657d others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893124 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0038g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-12-2683_-12-2657d others(29): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893124 | C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-12-2657_-12-2656i others(31): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893124 | C | CAAAAAAA others(26): Show |
1 | a0001c0001t0041g0198 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-12-2657_-12-2656i others(35): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893124 | CA | C | 17 | a0001c0001t0002g0092 a0001c0001t0010g0100 a0001c0001t0014g0090 others(14): Show |
17 | HG00609.hp1 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-2657delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893124 | CAAAAAAA others(2): Show |
C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-12-2665_-12-2657d others(11): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893124 | CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0308 a0001c0001t0004g0304 a0001c0001t0004g0305 others(6): Show |
9 | HG01109.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12-2666_-12-2657d others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | ||||||
| chr18:50893148 | A | C | 2 | a0001c0001t0067g0033 a0005c0009t0068g0053 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-12-2661A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893148 | |||||||
| chr18:50893151 | A | AAAAAAAA others(10): Show |
1 | a0003c0007t0012g0184 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12-2657_-12-2656i others(19): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893151 | ||||||
| chr18:50893153 | C | A | 4 | a0001c0001t0028g0057 a0001c0001t0028g0059 a0001c0001t0057g0058 others(1): Show |
4 | HG00738.hp2 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-2656C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893153 | |||||||
| chr18:50893264 | A | T | 6 | a0002c0002t0023g0176 a0002c0002t0023g0180 a0002c0002t0093g0177 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2545A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893264 | |||||||
| chr18:50893710 | A | T | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-2099A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893710 | |||||||
| chr18:50893858 | A | G | 1 | a0001c0001t0163g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-12-1951A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893858 | |||||||
| chr18:50893898 | C | T | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG01069.hp1 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-1911C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893898 | |||||||
| chr18:50894002 | A | C | 3 | a0001c0001t0001g0199 a0001c0001t0041g0198 a0001c0001t0041g0200 |
3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-12-1807A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894002 | |||||||
| chr18:50894057 | C | T | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-12-1752C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894057 | |||||||
| chr18:50894137 | C | T | 1 | a0001c0001t0007g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-12-1672C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894137 | |||||||
| chr18:50894166 | A | G | 1 | a0001c0001t0010g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-12-1643A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894166 | |||||||
| chr18:50894289 | C | T | 11 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0006g0025 others(8): Show |
11 | HG00423.hp1 NA18965.hp2 NA18971.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-1520C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894289 | |||||||
| chr18:50894291 | C | T | 1 | a0001c0003t0143g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-12-1518C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894291 | |||||||
| chr18:50894366 | C | T | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-12-1443C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894366 | |||||||
| chr18:50894517 | G | A | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1292G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894517 | |||||||
| chr18:50894528 | G | A | 2 | a0002c0002t0181g0015 a0002c0002t0182g0015 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-1281G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894528 | |||||||
| chr18:50894567 | CA | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(236): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-12-1231delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50894567 | ||||||
| chr18:50894653 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(233): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-12-1156A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894653 | |||||||
| chr18:50894746 | G | A | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG01069.hp1 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-1063G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894746 | |||||||
| chr18:50894750 | G | T | 1 | a0005c0009t0068g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-1059G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894750 | |||||||
| chr18:50894856 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-12-953A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894856 | |||||||
| chr18:50894860 | G | C | 1 | a0001c0001t0078g0037 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-12-949G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894860 | |||||||
| chr18:50894876 | CA | C | 15 | a0001c0001t0001g0287 a0001c0001t0014g0115 a0001c0001t0061g0069 others(12): Show |
15 | HG00408.hp2 HG01069.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-12-917delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50894876 | ||||||
| chr18:50894892 | A | T | 14 | a0001c0001t0122g0326 a0001c0001t0157g0288 a0001c0001t0170g0212 others(11): Show |
14 | HG00408.hp2 HG00741.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-917A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894892 | |||||||
| chr18:50894955 | CA | C | 13 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(10): Show |
13 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-840delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50894955 | ||||||
| chr18:50894966 | A | C | 1 | a0001c0001t0010g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-12-843A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894966 | |||||||
| chr18:50895002 | A | G | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-807A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895002 | |||||||
| chr18:50895115 | T | C | 1 | a0002c0002t0042g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-12-694T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895115 | |||||||
| chr18:50895185 | T | C | 1 | a0001c0001t0032g0004 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-12-624T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895185 | |||||||
| chr18:50895252 | ATTAC | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-12-554_-12-551del others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50895252 | ||||||
| chr18:50895308 | T | G | 2 | a0002c0002t0181g0015 a0002c0002t0182g0015 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-501T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895308 | |||||||
| chr18:50895334 | G | A | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-12-475G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895334 | |||||||
| chr18:50895357 | G | A | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-12-452G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895357 | |||||||
| chr18:50895501 | C | T | 1 | a0005c0009t0068g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-308C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895501 | |||||||
| chr18:50895582 | C | T | 1 | a0001c0001t0075g0088 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-12-227C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895582 | |||||||
| chr18:50895983 | T | C | 10 | a0001c0001t0010g0043 a0001c0001t0027g0042 a0001c0001t0027g0047 others(7): Show |
10 | HG00597.hp1 HG02040.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+55T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50895983 | |||||||
| chr18:50895991 | A | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+63A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50895991 | |||||||
| chr18:50896067 | G | A | 1 | a0001c0001t0015g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.108+139G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896067 | |||||||
| chr18:50896347 | C | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+419C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896347 | |||||||
| chr18:50896366 | T | C | 2 | a0001c0001t0051g0118 a0001c0001t0052g0117 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.108+438T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896366 | |||||||
| chr18:50896529 | T | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.108+601T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896529 | |||||||
| chr18:50896615 | A | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.108+687A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896615 | |||||||
| chr18:50897092 | T | A | 1 | a0002c0002t0097g0163 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.108+1164T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897092 | |||||||
| chr18:50897238 | C | T | 2 | a0002c0002t0011g0154 a0002c0002t0086g0153 |
2 | NA18990.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.108+1310C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897238 | |||||||
| chr18:50897571 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.108+1643C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897571 | |||||||
| chr18:50897582 | C | T | 1 | a0002c0002t0119g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.108+1654C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897582 | |||||||
| chr18:50897831 | C | A | 3 | a0001c0001t0001g0199 a0001c0001t0041g0198 a0001c0001t0041g0200 |
3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.108+1903C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897831 | |||||||
| chr18:50897861 | A | G | 1 | a0001c0001t0046g0087 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.108+1933A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897861 | |||||||
| chr18:50897865 | AAAAAAG | A | 81 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(78): Show |
82 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.108+1955_108+1960d others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50897865 | ||||||
| chr18:50898084 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(237): Show |
245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.108+2156A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898084 | |||||||
| chr18:50898621 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(236): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.108+2693T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898621 | |||||||
| chr18:50898668 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(236): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.108+2740G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898668 | |||||||
| chr18:50898671 | G | A | 1 | a0001c0001t0004g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.108+2743G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898671 | |||||||
| chr18:50898823 | C | T | 1 | a0001c0001t0024g0286 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.108+2895C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898823 | |||||||
| chr18:50898865 | T | G | 1 | a0001c0001t0049g0016 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.108+2937T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898865 | |||||||
| chr18:50898869 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(236): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.108+2941C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898869 | |||||||
| chr18:50898881 | A | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.108+2953A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898881 | |||||||
| chr18:50898955 | T | G | 1 | a0001c0001t0007g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.108+3027T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898955 | |||||||
| chr18:50899092 | G | A | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108+3164G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899092 | |||||||
| chr18:50899160 | T | C | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108+3232T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899160 | |||||||
| chr18:50899376 | G | A | 5 | a0001c0001t0001g0230 a0001c0001t0001g0232 a0001c0001t0003g0010 others(2): Show |
5 | HG01358.hp1 NA18955.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.108+3448G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899376 | |||||||
| chr18:50899451 | C | T | 2 | a0001c0001t0004g0008 a0001c0001t0168g0192 |
3 | HG02896.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.108+3523C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899451 | |||||||
| chr18:50899567 | G | A | 1 | a0001c0001t0009g0072 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.108+3639G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899567 | |||||||
| chr18:50899718 | G | A | 1 | a0001c0001t0015g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.108+3790G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899718 | |||||||
| chr18:50899796 | T | C | 1 | a0002c0002t0121g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108+3868T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899796 | |||||||
| chr18:50899947 | A | G | 60 | a0001c0001t0001g0014 a0001c0001t0001g0217 a0001c0001t0001g0219 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.108+4019A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899947 | |||||||
| chr18:50900216 | G | GT | 8 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0003g0257 others(5): Show |
8 | HG02647.hp2 HG03704.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+4299dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50900216 | ||||||
| chr18:50900270 | T | TTTTA | 16 | a0001c0001t0002g0113 a0001c0001t0006g0067 a0001c0001t0010g0100 others(13): Show |
17 | HG00408.hp2 HG00735.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.108+4381_108+4384d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50900270 | ||||||
| chr18:50900270 | TTTTA | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(199): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.108+4381_108+4384d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50900270 | ||||||
| chr18:50900340 | G | T | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108+4412G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900340 | |||||||
| chr18:50900363 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108+4435C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900363 | |||||||
| chr18:50900443 | T | C | 4 | a0002c0002t0042g0315 a0002c0002t0042g0316 a0002c0002t0172g0317 others(1): Show |
4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+4515T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900443 | |||||||
| chr18:50900463 | T | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+4535T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900463 | |||||||
| chr18:50900727 | GT | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+4802delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50900727 | ||||||
| chr18:50900782 | T | C | 1 | a0001c0001t0016g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.108+4854T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900782 | |||||||
| chr18:50900922 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0041g0198 a0001c0001t0041g0200 others(3): Show |
6 | HG02451.hp2 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+4994A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900922 | |||||||
| chr18:50900975 | CAAT | C | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+5048_108+5050d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900975 | |||||||
| chr18:50901071 | T | C | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.108+5143T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901071 | |||||||
| chr18:50901110 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.108+5182C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901110 | |||||||
| chr18:50901309 | C | T | 1 | a0001c0001t0123g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.108+5381C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901309 | |||||||
| chr18:50901622 | T | C | 1 | a0001c0001t0010g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.108+5694T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901622 | |||||||
| chr18:50901763 | C | G | 3 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0122g0326 |
3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.108+5835C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901763 | |||||||
| chr18:50901824 | A | C | 1 | a0002c0002t0156g0178 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.108+5896A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901824 | |||||||
| chr18:50901940 | C | T | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+6012C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901940 | |||||||
| chr18:50902043 | A | T | 1 | a0001c0001t0008g0026 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.109-6020A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902043 | |||||||
| chr18:50902219 | T | C | 1 | a0001c0001t0004g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.109-5844T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902219 | |||||||
| chr18:50902455 | A | G | 4 | a0002c0002t0021g0005 a0002c0002t0098g0158 a0002c0002t0119g0161 others(1): Show |
5 | HG01358.hp2 HG01993.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-5608A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902455 | |||||||
| chr18:50902485 | G | C | 1 | a0001c0001t0180g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.109-5578G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902485 | |||||||
| chr18:50902543 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.109-5520A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902543 | |||||||
| chr18:50902585 | C | T | 64 | a0001c0001t0108g0157 a0002c0002t0005g0127 a0002c0002t0005g0129 others(61): Show |
65 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.109-5478C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902585 | |||||||
| chr18:50902597 | G | A | 3 | a0001c0001t0001g0199 a0001c0001t0041g0198 a0001c0001t0041g0200 |
3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.109-5466G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902597 | |||||||
| chr18:50902630 | C | T | 1 | a0001c0001t0169g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.109-5433C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902630 | |||||||
| chr18:50902778 | A | G | 49 | a0001c0001t0108g0157 a0002c0002t0005g0127 a0002c0002t0005g0129 others(46): Show |
50 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.109-5285A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902778 | |||||||
| chr18:50902809 | A | G | 2 | a0001c0001t0051g0118 a0001c0001t0052g0117 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109-5254A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902809 | |||||||
| chr18:50903067 | A | G | 1 | a0002c0002t0120g0150 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.109-4996A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903067 | |||||||
| chr18:50903102 | G | C | 8 | a0001c0001t0036g0191 a0001c0001t0036g0201 a0001c0001t0106g0202 others(5): Show |
8 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-4961G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903102 | |||||||
| chr18:50903113 | G | C | 1 | a0001c0001t0003g0233 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.109-4950G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903113 | |||||||
| chr18:50903126 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(237): Show |
245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.109-4937A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903126 | |||||||
| chr18:50903234 | T | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(219): Show |
227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.109-4829T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903234 | |||||||
| chr18:50903335 | T | C | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-4728T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903335 | |||||||
| chr18:50903455 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(236): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.109-4608G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903455 | |||||||
| chr18:50903535 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.109-4528C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903535 | |||||||
| chr18:50903695 | C | T | 1 | a0001c0001t0014g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.109-4368C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903695 | |||||||
| chr18:50903697 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.109-4366T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903697 | |||||||
| chr18:50903787 | A | G | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.109-4276A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903787 | |||||||
| chr18:50903791 | G | T | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-4272G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903791 | |||||||
| chr18:50903937 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0009g0023 |
2 | NA18985.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.109-4126G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903937 | |||||||
| chr18:50904007 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.109-4056G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904007 | |||||||
| chr18:50904194 | G | A | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-3869G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904194 | |||||||
| chr18:50904279 | G | GT | 10 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0083g0099 others(7): Show |
10 | HG01361.hp2 HG01884.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-3769dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50904279 | ||||||
| chr18:50904280 | T | C | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.109-3783T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904280 | |||||||
| chr18:50904360 | C | T | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.109-3703C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904360 | |||||||
| chr18:50904410 | C | A | 74 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(71): Show |
75 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.109-3653C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904410 | |||||||
| chr18:50904532 | C | T | 1 | a0001c0001t0015g0085 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.109-3531C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904532 | |||||||
| chr18:50904717 | C | T | 1 | a0002c0002t0149g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109-3346C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904717 | |||||||
| chr18:50904819 | A | C | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-3244A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904819 | |||||||
| chr18:50905073 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0041g0198 a0001c0001t0041g0200 others(3): Show |
6 | HG02451.hp2 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-2990G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50905073 | |||||||
| chr18:50905159 | G | A | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.109-2904G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50905159 | |||||||
| chr18:50905410 | T | C | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-2653T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50905410 | |||||||
| chr18:50906432 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0245 a0001c0001t0001g0287 others(11): Show |
14 | HG00408.hp1 HG00544.hp2 HG03834.hp2 others(11): Show |
intron_variant | MODIFIER | c.109-1631C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50906432 | |||||||
| chr18:50906489 | T | G | 9 | a0001c0001t0006g0067 a0001c0001t0014g0090 a0001c0001t0014g0115 others(6): Show |
9 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-1574T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50906489 | |||||||
| chr18:50906714 | G | A | 1 | a0001c0001t0003g0234 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.109-1349G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50906714 | |||||||
| chr18:50906770 | G | A | 2 | a0001c0003t0013g0207 a0001c0003t0039g0208 |
2 | NA18990.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.109-1293G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50906770 | |||||||
| chr18:50907124 | C | T | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.109-939C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907124 | |||||||
| chr18:50907213 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(229): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.109-850A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907213 | |||||||
| chr18:50907386 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.109-677G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907386 | |||||||
| chr18:50907509 | C | T | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-554C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907509 | |||||||
| chr18:50907635 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.109-428A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907635 | |||||||
| chr18:50907655 | G | A | 1 | a0001c0001t0091g0189 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.109-408G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907655 | |||||||
| chr18:50907697 | C | G | 2 | a0002c0002t0181g0015 a0002c0002t0182g0015 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.109-366C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907697 | |||||||
| chr18:50907740 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(236): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.109-323G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907740 | |||||||
| chr18:50907850 | A | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-213A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907850 | |||||||
| chr18:50907853 | C | G | 1 | a0001c0001t0085g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.109-210C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907853 | |||||||
| chr18:50907862 | A | G | 1 | a0001c0001t0008g0026 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.109-201A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907862 | |||||||
| chr18:50907909 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(134): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.109-154A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907909 | |||||||
| chr18:50908247 | C | T | 1 | a0001c0001t0008g0112 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.242+51C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908247 | |||||||
| chr18:50908350 | C | T | 1 | a0001c0001t0030g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.242+154C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908350 | |||||||
| chr18:50908419 | C | A | 57 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(54): Show |
58 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.242+223C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908419 | |||||||
| chr18:50908520 | T | C | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.242+324T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908520 | |||||||
| chr18:50908712 | C | T | 3 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0122g0326 |
3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.242+516C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908712 | |||||||
| chr18:50908786 | G | A | 1 | a0001c0001t0015g0074 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.242+590G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908786 | |||||||
| chr18:50908786 | G | T | 57 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(54): Show |
58 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.242+590G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908786 | |||||||
| chr18:50908887 | C | T | 1 | a0001c0001t0006g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.242+691C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908887 | |||||||
| chr18:50908956 | C | CT | 7 | a0001c0001t0010g0052 a0001c0001t0025g0027 a0001c0001t0025g0029 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.242+775dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50908956 | ||||||
| chr18:50908956 | CT | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(222): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.242+775delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50908956 | ||||||
| chr18:50908961 | T | C | 2 | a0001c0001t0015g0071 a0001c0001t0075g0088 |
2 | HG00280.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.242+765T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908961 | |||||||
| chr18:50909166 | A | G | 1 | a0001c0001t0081g0091 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.242+970A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909166 | |||||||
| chr18:50909210 | C | T | 1 | a0002c0002t0023g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.242+1014C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909210 | |||||||
| chr18:50909371 | C | T | 1 | a0001c0003t0039g0209 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.242+1175C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909371 | |||||||
| chr18:50909389 | G | A | 1 | a0001c0001t0007g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.242+1193G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909389 | |||||||
| chr18:50909429 | A | G | 2 | a0001c0001t0001g0279 a0001c0001t0017g0280 |
2 | NA18998.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.242+1233A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909429 | |||||||
| chr18:50909531 | A | G | 13 | a0002c0002t0005g0127 a0002c0002t0005g0149 a0002c0002t0034g0147 others(10): Show |
13 | HG00423.hp2 HG00621.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.242+1335A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909531 | |||||||
| chr18:50909538 | G | A | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.242+1342G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909538 | |||||||
| chr18:50909553 | C | T | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.242+1357C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909553 | |||||||
| chr18:50909575 | T | C | 1 | a0001c0001t0044g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.242+1379T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909575 | |||||||
| chr18:50909606 | G | A | 2 | a0001c0001t0067g0033 a0005c0009t0068g0053 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.242+1410G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909606 | |||||||
| chr18:50909625 | A | G | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.242+1429A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909625 | |||||||
| chr18:50909954 | A | G | 9 | a0001c0001t0036g0191 a0001c0001t0036g0201 a0001c0001t0091g0189 others(6): Show |
9 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.242+1758A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909954 | |||||||
| chr18:50910045 | G | T | 3 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0122g0326 |
3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.242+1849G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910045 | |||||||
| chr18:50910192 | G | A | 1 | a0002c0002t0088g0151 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.242+1996G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910192 | |||||||
| chr18:50910268 | C | CA | 117 | a0001c0001t0001g0230 a0001c0001t0001g0244 a0001c0001t0001g0245 others(114): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.242+2096dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50910268 | ||||||
| chr18:50910268 | C | CAA | 62 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0012g0006 others(59): Show |
62 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.242+2095_242+2096d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50910268 | ||||||
| chr18:50910268 | C | CAAA | 17 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0020g0120 others(14): Show |
18 | HG00423.hp2 HG01175.hp1 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.242+2094_242+2096d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50910268 | ||||||
| chr18:50910355 | C | A | 1 | a0001c0001t0022g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.242+2159C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910355 | |||||||
| chr18:50910440 | G | GA | 15 | a0001c0001t0003g0236 a0001c0001t0004g0121 a0001c0001t0004g0253 others(12): Show |
15 | HG00621.hp2 HG00735.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.242+2261dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50910440 | ||||||
| chr18:50910454 | A | AG | 9 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(6): Show |
9 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.242+2258_242+2259i others(3): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910454 | |||||||
| chr18:50910454 | A | G | 4 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0122g0326 others(1): Show |
4 | HG01192.hp1 HG02071.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+2258A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910454 | |||||||
| chr18:50910458 | G | A | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.242+2262G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910458 | |||||||
| chr18:50910459 | A | G | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.242+2263A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910459 | |||||||
| chr18:50910460 | A | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.242+2264A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910460 | |||||||
| chr18:50910720 | C | T | 1 | a0001c0001t0029g0046 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.243-2081C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910720 | |||||||
| chr18:50910987 | G | A | 2 | a0001c0005t0024g0313 a0001c0005t0129g0312 |
2 | HG02602.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.243-1814G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910987 | |||||||
| chr18:50911103 | G | C | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.243-1698G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911103 | |||||||
| chr18:50911196 | C | T | 1 | a0005c0009t0068g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.243-1605C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911196 | |||||||
| chr18:50911347 | G | A | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.243-1454G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911347 | |||||||
| chr18:50911453 | A | G | 2 | a0001c0001t0004g0253 a0001c0001t0004g0309 |
2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.243-1348A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911453 | |||||||
| chr18:50911814 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.243-987C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911814 | |||||||
| chr18:50912165 | A | G | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.243-636A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50912165 | |||||||
| chr18:50912296 | T | C | 9 | a0002c0002t0020g0120 a0002c0002t0020g0322 a0002c0002t0020g0323 others(6): Show |
9 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.243-505T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50912296 | |||||||
| chr18:50912304 | G | T | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.243-497G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50912304 | |||||||
| chr18:50912420 | A | T | 1 | a0002c0004t0146g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.243-381A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50912420 | |||||||
| chr18:50913074 | C | T | 4 | a0001c0001t0003g0256 a0001c0001t0018g0255 a0001c0001t0018g0278 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.392+124C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913074 | |||||||
| chr18:50913170 | T | C | 1 | a0001c0001t0179g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.392+220T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913170 | |||||||
| chr18:50913265 | C | A | 57 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(54): Show |
58 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.392+315C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913265 | |||||||
| chr18:50913746 | G | A | 1 | a0001c0001t0166g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.392+796G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913746 | |||||||
| chr18:50913811 | A | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.392+861A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913811 | |||||||
| chr18:50913860 | T | TACACAC | 18 | a0001c0001t0002g0077 a0001c0001t0170g0212 a0001c0003t0013g0009 others(15): Show |
18 | HG00408.hp2 HG00738.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.392+936_392+941dup others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TACACACA others(1): Show |
37 | a0001c0001t0028g0057 a0001c0001t0051g0118 a0001c0001t0057g0058 others(34): Show |
38 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.392+934_392+941dup others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TACACACA others(3): Show |
15 | a0001c0001t0028g0059 a0001c0001t0107g0203 a0002c0002t0011g0165 others(12): Show |
15 | HG01934.hp2 HG02145.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.392+932_392+941dup others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TACACACA others(5): Show |
11 | a0001c0001t0052g0117 a0002c0002t0020g0323 a0002c0002t0023g0176 others(8): Show |
11 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.392+930_392+941dup others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TACACACA others(7): Show |
12 | a0001c0001t0001g0295 a0001c0001t0004g0121 a0001c0001t0036g0191 others(9): Show |
12 | HG01175.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.392+928_392+941dup others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TACACACA others(9): Show |
1 | a0002c0002t0020g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.392+926_392+941dup others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TACACACA others(13): Show |
3 | a0001c0001t0169g0193 a0002c0002t0181g0015 a0002c0002t0182g0015 |
3 | HG02818.hp1 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.392+922_392+941dup others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TATAC | 4 | a0001c0001t0001g0232 a0001c0001t0003g0256 a0001c0001t0007g0220 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TATACACA others(1): Show |
3 | a0001c0001t0004g0195 a0001c0001t0122g0326 a0001c0001t0124g0196 |
3 | HG01192.hp1 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.392+911_392+912ins others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TATACACA others(3): Show |
10 | a0001c0001t0001g0199 a0001c0001t0025g0027 a0001c0001t0026g0002 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TATACACA others(5): Show |
6 | a0001c0001t0003g0236 a0001c0001t0004g0008 a0001c0001t0004g0205 others(3): Show |
7 | HG01243.hp2 HG01433.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TATACACA others(7): Show |
25 | a0001c0001t0001g0014 a0001c0001t0001g0273 a0001c0001t0001g0276 others(22): Show |
26 | HG00280.hp1 HG00621.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TATACACA others(9): Show |
72 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
74 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TATACACA others(11): Show |
21 | a0001c0001t0001g0245 a0001c0001t0003g0010 a0001c0001t0004g0305 others(18): Show |
21 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(18): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TATACACA others(13): Show |
3 | a0001c0001t0001g0279 a0001c0001t0003g0235 a0001c0001t0180g0197 |
3 | HG02280.hp1 NA18522.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.392+911_392+912ins others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913860 | T | TATACACA others(17): Show |
2 | a0003c0007t0012g0184 a0003c0007t0160g0311 |
2 | HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.392+911_392+912ins others(24): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | ||||||
| chr18:50913862 | C | T | 1 | a0001c0001t0017g0283 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.392+912C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913862 | |||||||
| chr18:50913892 | T | C | 14 | a0001c0001t0001g0199 a0001c0001t0001g0273 a0001c0001t0041g0198 others(11): Show |
14 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+942T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913892 | |||||||
| chr18:50913997 | G | A | 1 | a0001c0001t0008g0020 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.392+1047G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913997 | |||||||
| chr18:50914329 | A | G | 6 | a0002c0002t0020g0120 a0002c0002t0020g0322 a0002c0002t0020g0323 others(3): Show |
6 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.392+1379A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914329 | |||||||
| chr18:50914454 | A | T | 1 | a0001c0001t0059g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.392+1504A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914454 | |||||||
| chr18:50914471 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.392+1521A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914471 | |||||||
| chr18:50914474 | G | T | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.392+1524G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914474 | |||||||
| chr18:50914608 | T | G | 1 | a0001c0001t0141g0294 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.393-1560T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914608 | |||||||
| chr18:50914867 | C | T | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.393-1301C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914867 | |||||||
| chr18:50914972 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(146): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.393-1196T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914972 | |||||||
| chr18:50915089 | C | CCCT | 5 | a0001c0001t0001g0240 a0001c0001t0001g0279 a0001c0001t0017g0280 others(2): Show |
5 | HG02809.hp1 NA18940.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.393-1053_393-1051d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50915089 | ||||||
| chr18:50915089 | CCCT | C | 72 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(69): Show |
73 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.393-1053_393-1051d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50915089 | ||||||
| chr18:50915271 | G | A | 1 | a0002c0004t0146g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.393-897G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915271 | |||||||
| chr18:50915272 | A | G | 1 | a0002c0004t0146g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.393-896A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915272 | |||||||
| chr18:50915292 | C | T | 3 | a0001c0001t0043g0299 a0001c0001t0043g0300 a0001c0001t0171g0251 |
3 | NA18949.hp1 NA18974.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.393-876C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915292 | |||||||
| chr18:50915315 | C | T | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.393-853C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915315 | |||||||
| chr18:50915324 | A | G | 6 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.393-844A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915324 | |||||||
| chr18:50915346 | C | T | 10 | a0001c0001t0010g0043 a0001c0001t0027g0042 a0001c0001t0027g0047 others(7): Show |
10 | HG00597.hp1 HG02040.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.393-822C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915346 | |||||||
| chr18:50915363 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.393-805C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915363 | |||||||
| chr18:50915621 | A | G | 4 | a0001c0001t0036g0201 a0001c0001t0106g0202 a0001c0001t0107g0203 others(1): Show |
4 | HG02258.hp2 HG02630.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-547A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915621 | |||||||
| chr18:50915685 | T | A | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.393-483T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915685 | |||||||
| chr18:50916269 | C | T | 1 | a0001c0001t0059g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+26C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50916269 | |||||||
| chr18:50916539 | A | T | 1 | a0002c0002t0011g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.468+296A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50916539 | |||||||
| chr18:50916580 | T | C | 2 | a0002c0002t0023g0174 a0002c0002t0149g0179 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.468+337T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50916580 | |||||||
| chr18:50916772 | A | G | 12 | a0001c0001t0002g0065 a0001c0001t0002g0076 a0001c0001t0006g0083 others(9): Show |
12 | NA18954.hp1 NA18964.hp2 NA18967.hp1 others(9): Show |
intron_variant | MODIFIER | c.468+529A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50916772 | |||||||
| chr18:50916925 | CCTTTTT | C | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-414_469-409del others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr18 | 50916925 | ||||||
| chr18:50917010 | C | A | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-337C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50917010 | |||||||
| chr18:50917617 | A | AT | 10 | a0002c0002t0020g0120 a0002c0002t0020g0322 a0002c0002t0020g0323 others(7): Show |
10 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.630+118dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr18 | 50917617 | ||||||
| chr18:50917691 | T | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.630+183T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/15 | chr18 | 50917691 | |||||||
| chr18:50917709 | T | G | 1 | a0002c0002t0101g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.630+201T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/15 | chr18 | 50917709 | |||||||
| chr18:50917919 | C | T | 1 | a0005c0009t0068g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.631-191C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/15 | chr18 | 50917919 | |||||||
| chr18:50918407 | C | CT | 67 | a0001c0001t0017g0283 a0001c0001t0059g0017 a0001c0001t0108g0157 others(64): Show |
68 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.734+195dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr18 | 50918407 | ||||||
| chr18:50918433 | C | G | 50 | a0001c0001t0108g0157 a0002c0002t0005g0127 a0002c0002t0005g0129 others(47): Show |
51 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.734+220C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918433 | |||||||
| chr18:50918517 | C | G | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.734+304C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918517 | |||||||
| chr18:50918702 | C | CT | 147 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(144): Show |
150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.734+504dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr18 | 50918702 | ||||||
| chr18:50918704 | T | C | 63 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0065 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.734+491T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918704 | |||||||
| chr18:50918705 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.734+492T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918705 | |||||||
| chr18:50918879 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(217): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.734+666A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918879 | |||||||
| chr18:50918898 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(227): Show |
234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.734+685G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918898 | |||||||
| chr18:50919006 | G | A | 1 | a0001c0001t0015g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.734+793G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919006 | |||||||
| chr18:50919062 | C | CTCCCG | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.734+849_734+850ins others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919062 | |||||||
| chr18:50919063 | A | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.734+850A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919063 | |||||||
| chr18:50919065 | A | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.734+852A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919065 | |||||||
| chr18:50919066 | T | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.734+853T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919066 | |||||||
| chr18:50919067 | T | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.734+854T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919067 | |||||||
| chr18:50919128 | G | A | 76 | a0001c0001t0032g0004 a0001c0001t0085g0116 a0002c0002t0005g0127 others(73): Show |
78 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.734+915G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919128 | |||||||
| chr18:50919249 | T | A | 332 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(329): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.734+1036T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919249 | |||||||
| chr18:50919413 | A | G | 9 | a0002c0002t0020g0120 a0002c0002t0020g0322 a0002c0002t0020g0323 others(6): Show |
9 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.735-1043A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919413 | |||||||
| chr18:50919433 | T | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.735-1023T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919433 | |||||||
| chr18:50919807 | T | C | 6 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-649T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919807 | |||||||
| chr18:50920020 | T | G | 1 | a0001c0001t0044g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735-436T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50920020 | |||||||
| chr18:50920225 | G | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(237): Show |
245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.735-231G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50920225 | |||||||
| chr18:50920338 | G | T | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-118G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50920338 | |||||||
| chr18:50920340 | C | G | 1 | a0001c0001t0062g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.735-116C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50920340 | |||||||
| chr18:50920573 | A | C | 4 | a0002c0002t0042g0315 a0002c0002t0042g0316 a0002c0002t0172g0317 others(1): Show |
4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.844+8A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 8/15 | chr18 | 50920573 | |||||||
| chr18:50920583 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.844+18C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 8/15 | chr18 | 50920583 | |||||||
| chr18:50920794 | C | T | 1 | a0001c0001t0008g0026 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.942+36C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 9/15 | chr18 | 50920794 | |||||||
| chr18:50921035 | T | G | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.943-39T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 9/15 | chr18 | 50921035 | |||||||
| chr18:50921194 | T | C | 1 | a0001c0001t0123g0228 | 1 | HG00323.hp1 | splice_region_variant&intron_variant | LOW | c.1056+7T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921194 | |||||||
| chr18:50921384 | A | G | 5 | a0002c0002t0005g0149 a0002c0002t0100g0144 a0002c0002t0115g0128 others(2): Show |
5 | NA18612.hp1 NA18985.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056+197A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921384 | |||||||
| chr18:50921406 | T | TA | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1056+220dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr18 | 50921406 | ||||||
| chr18:50921500 | T | C | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1056+313T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921500 | |||||||
| chr18:50921641 | A | G | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1056+454A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921641 | |||||||
| chr18:50921701 | C | A | 1 | a0001c0001t0166g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1056+514C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921701 | |||||||
| chr18:50921702 | G | T | 1 | a0001c0001t0166g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1056+515G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921702 | |||||||
| chr18:50921711 | G | C | 1 | a0001c0001t0007g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1056+524G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921711 | |||||||
| chr18:50921940 | G | C | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1056+753G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921940 | |||||||
| chr18:50922100 | C | T | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1056+913C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922100 | |||||||
| chr18:50922333 | G | A | 10 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1056+1146G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922333 | |||||||
| chr18:50922398 | C | T | 4 | a0001c0001t0001g0272 a0001c0001t0007g0262 a0001c0001t0134g0277 others(1): Show |
4 | NA18978.hp2 NA18999.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1056+1211C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922398 | |||||||
| chr18:50922425 | T | C | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1056+1238T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922425 | |||||||
| chr18:50922669 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1057-1429C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922669 | |||||||
| chr18:50922816 | T | C | 7 | a0001c0001t0108g0157 a0002c0002t0130g0171 a0002c0002t0131g0172 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1057-1282T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922816 | |||||||
| chr18:50922870 | T | C | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-1228T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922870 | |||||||
| chr18:50922971 | C | A | 4 | a0002c0002t0020g0322 a0002c0002t0020g0323 a0002c0002t0035g0325 others(1): Show |
4 | HG00639.hp1 HG00642.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1127C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922971 | |||||||
| chr18:50923052 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1057-1046T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923052 | |||||||
| chr18:50923055 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1057-1043C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923055 | |||||||
| chr18:50923056 | T | A | 1 | a0001c0001t0001g0273 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1057-1042T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923056 | |||||||
| chr18:50923095 | T | C | 2 | a0001c0001t0056g0082 a0001c0001t0076g0093 |
2 | NA18978.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1057-1003T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923095 | |||||||
| chr18:50923320 | CAA | C | 7 | a0001c0001t0014g0090 a0001c0001t0014g0115 a0001c0001t0015g0074 others(4): Show |
7 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-776_1057-775d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr18 | 50923320 | ||||||
| chr18:50923435 | C | T | 2 | a0001c0001t0030g0060 a0001c0001t0030g0068 |
2 | HG00735.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1057-663C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923435 | |||||||
| chr18:50923457 | A | G | 1 | a0001c0001t0022g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1057-641A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923457 | |||||||
| chr18:50923676 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(16): Show |
20 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1057-422C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923676 | |||||||
| chr18:50923800 | A | G | 1 | a0002c0002t0121g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1057-298A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923800 | |||||||
| chr18:50923852 | G | A | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1057-246G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923852 | |||||||
| chr18:50924443 | T | A | 1 | a0002c0002t0121g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1171+231T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924443 | |||||||
| chr18:50924452 | C | CTGTTGGA others(73): Show |
2 | a0001c0001t0051g0118 a0001c0001t0052g0117 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1171+243_1171+322d others(82): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50924452 | ||||||
| chr18:50924536 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(139): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1171+324G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924536 | |||||||
| chr18:50924637 | A | G | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171+425A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924637 | |||||||
| chr18:50924665 | G | A | 1 | a0001c0001t0033g0248 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1171+453G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924665 | |||||||
| chr18:50924703 | G | GT | 18 | a0001c0001t0001g0232 a0001c0001t0006g0025 a0001c0001t0008g0110 others(15): Show |
18 | HG00597.hp1 HG01358.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1171+502dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50924703 | ||||||
| chr18:50924704 | T | TTTTTTG | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171+497_1171+498i others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50924704 | ||||||
| chr18:50924830 | C | T | 1 | a0001c0001t0051g0118 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1171+618C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924830 | |||||||
| chr18:50924831 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(139): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1171+619G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924831 | |||||||
| chr18:50924896 | G | A | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171+684G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924896 | |||||||
| chr18:50925245 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1172-511G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50925245 | |||||||
| chr18:50925265 | G | A | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1172-491G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50925265 | |||||||
| chr18:50925296 | T | C | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1172-460T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50925296 | |||||||
| chr18:50925337 | G | C | 1 | a0005c0009t0068g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1172-419G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50925337 | |||||||
| chr18:50925469 | ACT | A | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1172-284_1172-283d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50925469 | ||||||
| chr18:50925575 | TTTTTC | T | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1172-175_1172-171d others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50925575 | ||||||
| chr18:50925937 | C | T | 5 | a0001c0001t0014g0090 a0001c0001t0014g0115 a0001c0001t0015g0085 others(2): Show |
5 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+39C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50925937 | |||||||
| chr18:50926106 | C | T | 2 | a0001c0001t0006g0067 a0001c0001t0061g0069 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1314+208C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926106 | |||||||
| chr18:50926301 | CT | C | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+405delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50926301 | ||||||
| chr18:50926341 | A | G | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1314+443A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926341 | |||||||
| chr18:50926353 | C | A | 2 | a0002c0002t0181g0015 a0002c0002t0182g0015 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1314+455C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926353 | |||||||
| chr18:50926354 | G | A | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1314+456G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926354 | |||||||
| chr18:50926433 | A | G | 1 | a0001c0001t0002g0081 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1314+535A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926433 | |||||||
| chr18:50926475 | A | G | 4 | a0001c0001t0036g0191 a0001c0001t0109g0007 a0001c0001t0110g0007 others(1): Show |
4 | HG01891.hp1 HG02486.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+577A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926475 | |||||||
| chr18:50926478 | C | T | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+580C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926478 | |||||||
| chr18:50926641 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0252 |
3 | HG00597.hp2 NA18960.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1314+743G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926641 | |||||||
| chr18:50926690 | A | G | 3 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0122g0326 |
3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1314+792A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926690 | |||||||
| chr18:50926732 | G | T | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1314+834G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926732 | |||||||
| chr18:50926897 | A | G | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+999A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926897 | |||||||
| chr18:50927223 | C | T | 2 | a0002c0002t0093g0177 a0002c0002t0156g0178 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1314+1325C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927223 | |||||||
| chr18:50927429 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1314+1531G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927429 | |||||||
| chr18:50927443 | G | C | 1 | a0002c0002t0151g0169 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1314+1545G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927443 | |||||||
| chr18:50927470 | G | A | 2 | a0002c0002t0119g0161 a0002c0002t0148g0160 |
2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1314+1572G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927470 | |||||||
| chr18:50927482 | C | T | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1314+1584C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927482 | |||||||
| chr18:50927633 | C | T | 15 | a0002c0002t0020g0120 a0002c0002t0020g0322 a0002c0002t0020g0323 others(12): Show |
15 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1314+1735C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927633 | |||||||
| chr18:50927710 | C | A | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+1812C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927710 | |||||||
| chr18:50927721 | C | CAT | 19 | a0001c0001t0002g0022 a0001c0001t0008g0110 a0001c0001t0010g0043 others(16): Show |
19 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1314+1853_1314+185 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATAT | 6 | a0001c0001t0003g0256 a0001c0001t0018g0255 a0001c0001t0064g0095 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314+1851_1314+185 others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATAT | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(54): Show |
59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1314+1849_1314+185 others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATATA others(1): Show |
35 | a0001c0001t0001g0001 a0001c0001t0001g0199 a0001c0001t0001g0217 others(32): Show |
36 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1314+1847_1314+185 others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATATA others(3): Show |
20 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0289 others(17): Show |
20 | HG01069.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1314+1845_1314+185 others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATATA others(5): Show |
13 | a0001c0001t0001g0279 a0001c0001t0001g0281 a0001c0001t0003g0235 others(10): Show |
13 | HG01106.hp2 HG01261.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1314+1843_1314+185 others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATATA others(7): Show |
7 | a0001c0001t0001g0273 a0001c0001t0003g0233 a0001c0001t0032g0004 others(4): Show |
8 | HG00621.hp1 HG00741.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+1841_1314+185 others(18): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATATA others(9): Show |
4 | a0001c0001t0001g0272 a0001c0001t0007g0229 a0001c0001t0040g0269 others(1): Show |
4 | HG00609.hp2 NA18978.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+1839_1314+185 others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATATA others(11): Show |
5 | a0001c0001t0004g0121 a0001c0001t0038g0185 a0001c0001t0090g0270 others(2): Show |
5 | HG00558.hp2 HG01074.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+1837_1314+185 others(22): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATATA others(13): Show |
1 | a0001c0001t0012g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1314+1835_1314+185 others(24): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATATA others(17): Show |
1 | a0001c0001t0178g0260 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1314+1831_1314+185 others(28): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATATATA others(19): Show |
1 | a0001c0001t0024g0271 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1314+1829_1314+185 others(30): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | C | CATGTATA others(11): Show |
1 | a0001c0001t0125g0275 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1314+1825_1314+182 others(22): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | CAT | C | 40 | a0001c0001t0002g0065 a0001c0001t0002g0076 a0001c0001t0002g0079 others(37): Show |
40 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1314+1853_1314+185 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | CATATATA others(7): Show |
C | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314+1841_1314+185 others(18): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927721 | CATATATA others(9): Show |
C | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+1839_1314+185 others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | ||||||
| chr18:50927738 | A | C | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+1840A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927738 | |||||||
| chr18:50927751 | T | C | 4 | a0001c0001t0002g0102 a0001c0001t0051g0118 a0001c0001t0052g0117 others(1): Show |
4 | HG02486.hp2 HG03516.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+1853T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927751 | |||||||
| chr18:50927751 | T | TATAC | 9 | a0002c0002t0005g0149 a0002c0002t0023g0180 a0002c0002t0095g0175 others(6): Show |
9 | HG02258.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | ||||||
| chr18:50927751 | T | TATATAC | 26 | a0001c0001t0163g0194 a0002c0002t0005g0134 a0002c0002t0020g0120 others(23): Show |
27 | HG00639.hp1 HG00642.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | ||||||
| chr18:50927751 | T | TATATATA others(1): Show |
18 | a0002c0002t0005g0136 a0002c0002t0005g0137 a0002c0002t0005g0140 others(15): Show |
18 | HG00609.hp1 HG02040.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | ||||||
| chr18:50927751 | T | TATATATA others(3): Show |
4 | a0002c0002t0005g0129 a0002c0002t0011g0139 a0002c0002t0099g0166 others(1): Show |
4 | HG03704.hp1 NA18970.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | ||||||
| chr18:50927751 | T | TATATATA others(5): Show |
2 | a0002c0002t0005g0142 a0007c0010t0087g0321 |
2 | NA19056.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | ||||||
| chr18:50927751 | T | TATATATA others(7): Show |
3 | a0002c0002t0005g0127 a0002c0002t0181g0015 a0002c0002t0182g0015 |
3 | HG00423.hp2 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(18): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | ||||||
| chr18:50927751 | T | TATATATA others(11): Show |
3 | a0002c0004t0005g0138 a0002c0004t0011g0143 a0002c0004t0146g0130 |
3 | NA18968.hp2 NA19058.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(22): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | ||||||
| chr18:50927751 | T | TATATATA others(21): Show |
1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1314+1854_1314+185 others(32): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | ||||||
| chr18:50927810 | A | AT | 6 | a0001c0001t0002g0019 a0001c0001t0030g0068 a0001c0001t0053g0061 others(3): Show |
6 | HG00735.hp1 HG00741.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+1934dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927810 | ||||||
| chr18:50927810 | AT | A | 23 | a0001c0001t0002g0108 a0001c0001t0004g0304 a0001c0001t0025g0027 others(20): Show |
23 | HG00408.hp2 HG00741.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1314+1934delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927810 | ||||||
| chr18:50927810 | ATT | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(210): Show |
217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1314+1933_1314+193 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927810 | ||||||
| chr18:50927974 | C | T | 1 | a0001c0001t0059g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1314+2076C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927974 | |||||||
| chr18:50928054 | A | G | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+2156A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928054 | |||||||
| chr18:50928081 | G | A | 1 | a0001c0001t0007g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1314+2183G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928081 | |||||||
| chr18:50928175 | C | T | 1 | a0005c0009t0068g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1314+2277C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928175 | |||||||
| chr18:50928241 | C | CT | 11 | a0001c0001t0170g0212 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+2353dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50928241 | ||||||
| chr18:50928256 | T | A | 6 | a0001c0001t0006g0083 a0001c0001t0016g0073 a0001c0001t0056g0082 others(3): Show |
6 | NA18954.hp1 NA18967.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314+2358T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928256 | |||||||
| chr18:50928382 | T | C | 12 | a0001c0001t0067g0033 a0001c0001t0170g0212 a0001c0003t0013g0009 others(9): Show |
12 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1314+2484T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928382 | |||||||
| chr18:50928426 | T | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1314+2528T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928426 | |||||||
| chr18:50928445 | A | G | 1 | a0001c0001t0031g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1314+2547A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928445 | |||||||
| chr18:50928515 | G | A | 1 | a0002c0002t0005g0149 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1314+2617G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928515 | |||||||
| chr18:50928543 | T | C | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1314+2645T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928543 | |||||||
| chr18:50928750 | A | G | 53 | a0001c0001t0048g0056 a0002c0002t0005g0129 a0002c0002t0005g0134 others(50): Show |
54 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1314+2852A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928750 | |||||||
| chr18:50928971 | A | G | 69 | a0001c0001t0163g0194 a0002c0002t0005g0127 a0002c0002t0005g0129 others(66): Show |
70 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1314+3073A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928971 | |||||||
| chr18:50928978 | A | G | 1 | a0001c0001t0153g0268 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1314+3080A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928978 | |||||||
| chr18:50929030 | G | A | 2 | a0001c0001t0018g0278 a0001c0001t0165g0223 |
2 | HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1314+3132G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929030 | |||||||
| chr18:50929161 | C | CT | 17 | a0001c0001t0018g0278 a0001c0001t0025g0027 a0001c0001t0031g0051 others(14): Show |
17 | HG00408.hp2 HG00642.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1315-3083dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929161 | ||||||
| chr18:50929161 | CT | C | 42 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(39): Show |
43 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1315-3083delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929161 | ||||||
| chr18:50929175 | T | C | 2 | a0001c0001t0001g0284 a0002c0002t0118g0131 |
2 | NA18954.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1315-3083T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929175 | |||||||
| chr18:50929246 | A | T | 1 | a0001c0001t0014g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1315-3012A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929246 | |||||||
| chr18:50929485 | C | CA | 146 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(143): Show |
148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1315-2757dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929485 | ||||||
| chr18:50929485 | C | CAA | 11 | a0001c0001t0001g0217 a0001c0001t0001g0219 a0001c0001t0001g0272 others(8): Show |
12 | HG00735.hp2 HG01361.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1315-2758_1315-275 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929485 | ||||||
| chr18:50929485 | CA | C | 11 | a0001c0001t0122g0326 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01192.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1315-2757delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929485 | ||||||
| chr18:50929575 | A | G | 332 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(329): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1315-2683A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929575 | |||||||
| chr18:50929656 | A | G | 1 | a0001c0001t0006g0080 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1315-2602A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929656 | |||||||
| chr18:50930026 | T | G | 1 | a0001c0001t0063g0078 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1315-2232T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930026 | |||||||
| chr18:50930027 | A | C | 2 | a0001c0001t0056g0082 a0001c0001t0076g0093 |
2 | NA18978.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1315-2231A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930027 | |||||||
| chr18:50930027 | A | T | 1 | a0002c0002t0020g0322 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1315-2231A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930027 | |||||||
| chr18:50930080 | C | T | 68 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(65): Show |
69 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1315-2178C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930080 | |||||||
| chr18:50930254 | C | T | 2 | a0001c0001t0003g0010 a0001c0001t0018g0010 |
2 | NA18955.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1315-2004C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930254 | |||||||
| chr18:50930397 | A | T | 2 | a0002c0002t0023g0180 a0002c0002t0095g0175 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1315-1861A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930397 | |||||||
| chr18:50930533 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(234): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1315-1725T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930533 | |||||||
| chr18:50930607 | G | A | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1315-1651G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930607 | |||||||
| chr18:50930709 | A | G | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1315-1549A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930709 | |||||||
| chr18:50930883 | C | A | 1 | a0001c0001t0169g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1315-1375C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930883 | |||||||
| chr18:50930934 | T | C | 3 | a0001c0001t0010g0043 a0001c0001t0031g0094 a0001c0001t0071g0041 |
3 | NA19007.hp1 NA19067.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1315-1324T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930934 | |||||||
| chr18:50930943 | C | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(236): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1315-1315C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930943 | |||||||
| chr18:50930988 | A | G | 1 | a0001c0001t0135g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1315-1270A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930988 | |||||||
| chr18:50931138 | C | T | 4 | a0001c0001t0036g0201 a0001c0001t0106g0202 a0001c0001t0107g0203 others(1): Show |
4 | HG02258.hp2 HG02630.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315-1120C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931138 | |||||||
| chr18:50931515 | TA | T | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1315-740delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50931515 | ||||||
| chr18:50931603 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(234): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1315-655A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931603 | |||||||
| chr18:50931682 | C | CTTT | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1315-568_1315-566d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50931682 | ||||||
| chr18:50931770 | G | A | 1 | a0001c0001t0180g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1315-488G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931770 | |||||||
| chr18:50931819 | C | T | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1315-439C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931819 | |||||||
| chr18:50931840 | AATTTTTT others(2): Show |
A | 4 | a0001c0001t0028g0057 a0001c0001t0028g0059 a0001c0001t0057g0058 others(1): Show |
4 | HG00738.hp2 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315-398_1315-390d others(11): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50931840 | ||||||
| chr18:50931847 | TG | T | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1315-410delG | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931847 | |||||||
| chr18:50932110 | C | T | 1 | a0001c0001t0016g0062 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1315-148C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50932110 | |||||||
| chr18:50932111 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1315-147G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50932111 | |||||||
| chr18:50932188 | G | A | 3 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0122g0326 |
3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1315-70G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50932188 | |||||||
| chr18:50932614 | G | T | 1 | a0001c0005t0129g0312 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1417+254G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50932614 | |||||||
| chr18:50932616 | A | T | 1 | a0001c0005t0129g0312 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1417+256A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50932616 | |||||||
| chr18:50932645 | C | G | 1 | a0001c0001t0018g0278 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1417+285C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50932645 | |||||||
| chr18:50932659 | C | A | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1417+299C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50932659 | |||||||
| chr18:50933102 | G | A | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1417+742G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933102 | |||||||
| chr18:50933136 | T | C | 3 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0122g0326 |
3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1417+776T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933136 | |||||||
| chr18:50933154 | A | G | 2 | a0001c0001t0051g0118 a0001c0001t0052g0117 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1417+794A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933154 | |||||||
| chr18:50933186 | T | C | 1 | a0001c0001t0067g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1417+826T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933186 | |||||||
| chr18:50933509 | T | A | 1 | a0001c0001t0178g0260 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1417+1149T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933509 | |||||||
| chr18:50933705 | G | A | 2 | a0001c0001t0056g0082 a0001c0001t0076g0093 |
2 | NA18978.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1417+1345G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933705 | |||||||
| chr18:50933714 | G | T | 1 | a0001c0001t0007g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1417+1354G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933714 | |||||||
| chr18:50933744 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1417+1384A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933744 | |||||||
| chr18:50933765 | C | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(137): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1417+1405C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933765 | |||||||
| chr18:50933812 | T | C | 1 | a0001c0001t0134g0277 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1417+1452T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933812 | |||||||
| chr18:50933813 | C | T | 1 | a0001c0001t0134g0277 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1417+1453C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933813 | |||||||
| chr18:50933816 | G | A | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1417+1456G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933816 | |||||||
| chr18:50933853 | C | G | 1 | a0001c0001t0002g0076 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1417+1493C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933853 | |||||||
| chr18:50933907 | A | G | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1417+1547A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933907 | |||||||
| chr18:50933922 | T | G | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417+1562T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933922 | |||||||
| chr18:50934215 | G | A | 1 | a0001c0001t0003g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1417+1855G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50934215 | |||||||
| chr18:50934363 | C | G | 42 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(39): Show |
43 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1417+2003C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50934363 | |||||||
| chr18:50934680 | C | T | 2 | a0001c0001t0004g0008 a0001c0001t0168g0192 |
3 | HG02896.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1417+2320C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50934680 | |||||||
| chr18:50934787 | C | T | 1 | a0001c0001t0032g0004 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1417+2427C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50934787 | |||||||
| chr18:50935009 | T | C | 1 | a0002c0002t0113g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1417+2649T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935009 | |||||||
| chr18:50935108 | G | T | 1 | a0001c0001t0124g0196 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1417+2748G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935108 | |||||||
| chr18:50935145 | G | A | 1 | a0002c0002t0095g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1417+2785G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935145 | |||||||
| chr18:50935146 | C | T | 1 | a0001c0001t0036g0201 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1417+2786C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935146 | |||||||
| chr18:50935277 | C | T | 2 | a0001c0001t0016g0096 a0001c0001t0053g0061 |
2 | HG00741.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1417+2917C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935277 | |||||||
| chr18:50935394 | A | G | 330 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(327): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1417+3034A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935394 | |||||||
| chr18:50935493 | A | G | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1417+3133A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935493 | |||||||
| chr18:50935584 | A | T | 1 | a0001c0001t0076g0093 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1417+3224A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935584 | |||||||
| chr18:50935586 | T | A | 2 | a0001c0001t0076g0093 a0004c0011t0003g0292 |
2 | HG01261.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1417+3226T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935586 | |||||||
| chr18:50935586 | T | TA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(131): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1417+3242dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935586 | ||||||
| chr18:50935586 | TA | T | 17 | a0001c0001t0009g0072 a0001c0001t0010g0049 a0001c0001t0047g0055 others(14): Show |
17 | HG00099.hp1 HG00280.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1417+3242delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935586 | ||||||
| chr18:50935586 | TAA | T | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417+3241_1417+324 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935586 | ||||||
| chr18:50935624 | T | G | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1417+3264T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935624 | |||||||
| chr18:50935703 | G | A | 2 | a0001c0001t0003g0236 a0001c0001t0022g0225 |
2 | HG01243.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1417+3343G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935703 | |||||||
| chr18:50935751 | C | CA | 48 | a0001c0001t0001g0219 a0001c0001t0002g0108 a0001c0001t0002g0109 others(45): Show |
48 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1417+3412dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935751 | ||||||
| chr18:50935751 | C | CAA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1417+3411_1417+341 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935751 | ||||||
| chr18:50935751 | C | CAAA | 14 | a0001c0001t0001g0245 a0001c0001t0001g0272 a0001c0001t0001g0290 others(11): Show |
15 | HG00323.hp2 HG00621.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1417+3410_1417+341 others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935751 | ||||||
| chr18:50935751 | C | CAAAA | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417+3409_1417+341 others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935751 | ||||||
| chr18:50935770 | A | AG | 48 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(45): Show |
49 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1417+3410_1417+341 others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935770 | |||||||
| chr18:50935782 | A | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(139): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1417+3422A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935782 | |||||||
| chr18:50935840 | G | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(232): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1417+3480G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935840 | |||||||
| chr18:50935873 | G | GA | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417+3522dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935873 | ||||||
| chr18:50935955 | C | A | 1 | a0002c0002t0172g0317 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1417+3595C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935955 | |||||||
| chr18:50936019 | A | G | 2 | a0001c0001t0070g0045 a0001c0001t0074g0039 |
2 | NA19000.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1418-3551A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936019 | |||||||
| chr18:50936380 | C | G | 3 | a0001c0001t0001g0199 a0001c0001t0041g0198 a0001c0001t0041g0200 |
3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1418-3190C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936380 | |||||||
| chr18:50936453 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1418-3117T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936453 | |||||||
| chr18:50936480 | G | A | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-3090G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936480 | |||||||
| chr18:50936531 | A | G | 1 | a0001c0001t0007g0266 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1418-3039A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936531 | |||||||
| chr18:50936536 | T | G | 8 | a0001c0001t0015g0071 a0001c0001t0016g0096 a0001c0001t0053g0061 others(5): Show |
8 | HG00741.hp1 HG01070.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1418-3034T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936536 | |||||||
| chr18:50936575 | A | T | 1 | a0001c0001t0155g0267 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1418-2995A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936575 | |||||||
| chr18:50936831 | C | T | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1418-2739C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936831 | |||||||
| chr18:50936883 | G | C | 2 | a0001c0003t0013g0213 a0001c0003t0140g0214 |
2 | HG00408.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1418-2687G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936883 | |||||||
| chr18:50936952 | C | T | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-2618C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936952 | |||||||
| chr18:50937163 | G | A | 65 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(62): Show |
66 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1418-2407G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937163 | |||||||
| chr18:50937369 | C | T | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1418-2201C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937369 | |||||||
| chr18:50937667 | A | T | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1418-1903A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937667 | |||||||
| chr18:50937834 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(137): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1418-1736T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937834 | |||||||
| chr18:50937893 | A | G | 1 | a0002c0002t0011g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1418-1677A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937893 | |||||||
| chr18:50938002 | A | T | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1418-1568A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938002 | |||||||
| chr18:50938138 | G | A | 10 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0111 others(7): Show |
10 | HG00544.hp1 NA18940.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.1418-1432G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938138 | |||||||
| chr18:50938187 | G | A | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-1383G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938187 | |||||||
| chr18:50938191 | G | A | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1418-1379G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938191 | |||||||
| chr18:50938243 | G | A | 9 | a0001c0001t0036g0191 a0001c0001t0036g0201 a0001c0001t0091g0189 others(6): Show |
9 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1418-1327G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938243 | |||||||
| chr18:50938255 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1418-1315G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938255 | |||||||
| chr18:50938332 | T | A | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1418-1238T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938332 | |||||||
| chr18:50938436 | A | C | 2 | a0002c0002t0023g0180 a0002c0002t0095g0175 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1418-1134A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938436 | |||||||
| chr18:50938658 | T | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(234): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1418-912T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938658 | |||||||
| chr18:50938728 | A | G | 1 | a0001c0001t0024g0271 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1418-842A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938728 | |||||||
| chr18:50938747 | G | A | 3 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0139g0009 |
3 | NA18955.hp1 NA18960.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1418-823G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938747 | |||||||
| chr18:50938803 | C | T | 12 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0006g0025 others(9): Show |
12 | HG00423.hp1 NA18965.hp2 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.1418-767C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938803 | |||||||
| chr18:50938809 | T | C | 1 | a0002c0002t0020g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1418-761T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938809 | |||||||
| chr18:50938961 | A | G | 42 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(39): Show |
43 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1418-609A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938961 | |||||||
| chr18:50939071 | GGAAA | G | 3 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0122g0326 |
3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1418-496_1418-493d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50939071 | ||||||
| chr18:50939128 | CA | C | 87 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(84): Show |
89 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.1418-431delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50939128 | ||||||
| chr18:50939139 | A | G | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-431A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939139 | |||||||
| chr18:50939140 | G | A | 12 | a0001c0001t0018g0278 a0001c0001t0036g0201 a0001c0003t0013g0009 others(9): Show |
12 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1418-430G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939140 | |||||||
| chr18:50939140 | G | GA | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1418-419dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50939140 | ||||||
| chr18:50939166 | A | G | 10 | a0001c0001t0001g0272 a0001c0003t0013g0009 a0001c0003t0013g0206 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-404A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939166 | |||||||
| chr18:50939194 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1418-376T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939194 | |||||||
| chr18:50939219 | A | G | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-351A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939219 | |||||||
| chr18:50939266 | T | G | 6 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1418-304T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939266 | |||||||
| chr18:50939407 | G | A | 3 | a0001c0001t0008g0020 a0001c0001t0060g0024 a0001c0001t0165g0223 |
3 | HG03927.hp2 NA18994.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1418-163G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939407 | |||||||
| chr18:50939457 | G | A | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1418-113G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939457 | |||||||
| chr18:50939654 | ATGT | A | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488+19_1488+21del others(3): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr18 | 50939654 | ||||||
| chr18:50939784 | A | G | 1 | a0001c0001t0155g0267 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1488+144A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50939784 | |||||||
| chr18:50939899 | C | A | 8 | a0002c0002t0023g0174 a0002c0002t0023g0176 a0002c0002t0023g0180 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1488+259C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50939899 | |||||||
| chr18:50939903 | A | G | 1 | a0001c0001t0016g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1488+263A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50939903 | |||||||
| chr18:50939909 | A | G | 1 | a0001c0001t0123g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1488+269A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50939909 | |||||||
| chr18:50940280 | C | T | 3 | a0001c0001t0051g0118 a0001c0001t0052g0117 a0001c0001t0122g0326 |
3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
splice_region_variant&intron_variant | LOW | c.1489-8C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50940280 | |||||||
| chr18:50940716 | T | A | 2 | a0001c0001t0003g0256 a0001c0001t0018g0255 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1587+330T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50940716 | |||||||
| chr18:50940832 | A | G | 48 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(45): Show |
49 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1587+446A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50940832 | |||||||
| chr18:50941197 | G | T | 2 | a0001c0001t0169g0193 a0001c0001t0180g0197 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1587+811G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941197 | |||||||
| chr18:50941261 | C | CA | 10 | a0001c0001t0008g0020 a0001c0001t0010g0049 a0001c0001t0010g0052 others(7): Show |
11 | HG00099.hp1 HG00642.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1587+894dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941261 | ||||||
| chr18:50941261 | CAA | C | 96 | a0001c0001t0001g0272 a0001c0001t0001g0287 a0001c0001t0022g0225 others(93): Show |
97 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1587+893_1587+894d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941261 | ||||||
| chr18:50941261 | CAAA | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(131): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1587+892_1587+894d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941261 | ||||||
| chr18:50941300 | G | A | 7 | a0001c0001t0004g0253 a0001c0001t0004g0304 a0001c0001t0004g0305 others(4): Show |
7 | HG01109.hp2 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+914G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941300 | |||||||
| chr18:50941353 | C | CT | 47 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0076 others(44): Show |
47 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1587+998dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTT | 13 | a0001c0001t0001g0199 a0001c0001t0002g0111 a0001c0001t0010g0100 others(10): Show |
13 | HG00735.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1587+997_1587+998d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTT | 13 | a0001c0001t0091g0189 a0002c0002t0005g0136 a0002c0002t0005g0140 others(10): Show |
13 | HG00609.hp1 HG01884.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1587+995_1587+998d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTT | 14 | a0002c0002t0005g0137 a0002c0002t0011g0165 a0002c0002t0021g0005 others(11): Show |
15 | HG01993.hp2 HG02040.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1587+994_1587+998d others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTT | 14 | a0001c0001t0111g0204 a0002c0002t0005g0129 a0002c0002t0005g0134 others(11): Show |
14 | HG01106.hp1 HG01358.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1587+993_1587+998d others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTTT | 7 | a0001c0001t0036g0201 a0001c0001t0107g0203 a0002c0002t0099g0166 others(4): Show |
7 | HG00621.hp2 HG02630.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1587+992_1587+998d others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTTT others(1): Show |
11 | a0001c0001t0109g0007 a0001c0001t0110g0007 a0002c0002t0020g0323 others(8): Show |
11 | HG00639.hp1 HG02129.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1587+991_1587+998d others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0036g0191 a0001c0001t0154g0190 a0002c0002t0020g0120 others(4): Show |
7 | HG01081.hp2 HG01891.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+990_1587+998d others(11): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTTT others(3): Show |
3 | a0002c0002t0005g0127 a0002c0002t0103g0324 a0002c0002t0174g0182 |
3 | HG00423.hp2 HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1587+989_1587+998d others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTTT others(4): Show |
1 | a0002c0002t0035g0325 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1587+988_1587+998d others(13): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0085g0116 a0001c0001t0106g0202 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1587+986_1587+998d others(15): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0180g0197 a0002c0002t0042g0316 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1587+984_1587+998d others(17): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0044g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1587+977_1587+998d others(24): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0169g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1587+972_1587+998d others(29): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | CT | C | 10 | a0001c0001t0002g0065 a0001c0001t0006g0084 a0001c0001t0025g0029 others(7): Show |
10 | HG00408.hp2 HG01891.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+998delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | CTTTTTTT others(3): Show |
C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1587+989_1587+998d others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | CTTTTTTT others(4): Show |
C | 46 | a0001c0001t0001g0014 a0001c0001t0001g0217 a0001c0001t0001g0219 others(43): Show |
47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1587+988_1587+998d others(13): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0065g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1587+987_1587+998d others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941353 | CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1587+984_1587+998d others(17): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | ||||||
| chr18:50941406 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(234): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1587+1020A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941406 | |||||||
| chr18:50941420 | G | A | 1 | a0001c0001t0157g0288 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1587+1034G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941420 | |||||||
| chr18:50941536 | G | A | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+1150G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941536 | |||||||
| chr18:50941621 | G | A | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+1235G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941621 | |||||||
| chr18:50941671 | G | A | 2 | a0001c0001t0032g0004 a0001c0001t0085g0116 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1587+1285G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941671 | |||||||
| chr18:50941682 | G | GT | 215 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(212): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1587+1310dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941682 | ||||||
| chr18:50941682 | G | GTT | 24 | a0001c0001t0001g0232 a0001c0001t0024g0271 a0001c0001t0040g0269 others(21): Show |
24 | HG00408.hp2 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1587+1309_1587+131 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941682 | ||||||
| chr18:50941839 | C | T | 2 | a0002c0002t0181g0015 a0002c0002t0182g0015 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1587+1453C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941839 | |||||||
| chr18:50941864 | C | A | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1587+1478C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941864 | |||||||
| chr18:50941881 | T | C | 1 | a0001c0001t0060g0024 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1587+1495T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941881 | |||||||
| chr18:50941984 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1587+1598A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941984 | |||||||
| chr18:50941985 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(236): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1587+1599C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941985 | |||||||
| chr18:50942092 | TA | T | 8 | a0001c0001t0036g0191 a0001c0001t0036g0201 a0001c0001t0106g0202 others(5): Show |
8 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1587+1708delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50942092 | ||||||
| chr18:50942179 | T | C | 1 | a0001c0001t0053g0061 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1587+1793T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942179 | |||||||
| chr18:50942259 | G | A | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+1873G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942259 | |||||||
| chr18:50942352 | A | G | 1 | a0001c0001t0009g0023 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1587+1966A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942352 | |||||||
| chr18:50942411 | T | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1587+2025T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942411 | |||||||
| chr18:50942635 | T | A | 12 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0006g0025 others(9): Show |
12 | HG00423.hp1 NA18965.hp2 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.1587+2249T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942635 | |||||||
| chr18:50942782 | TTGA | T | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+2400_1587+240 others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50942782 | ||||||
| chr18:50942909 | A | G | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1587+2523A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942909 | |||||||
| chr18:50942978 | T | A | 1 | a0001c0001t0019g0070 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1587+2592T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942978 | |||||||
| chr18:50943232 | G | A | 1 | a0001c0001t0033g0248 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1587+2846G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943232 | |||||||
| chr18:50943281 | A | G | 2 | a0001c0001t0001g0279 a0001c0001t0017g0280 |
2 | NA18998.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1587+2895A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943281 | |||||||
| chr18:50943288 | A | AATTT | 11 | a0001c0001t0155g0267 a0001c0003t0013g0009 a0001c0003t0013g0206 others(8): Show |
11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1587+2927_1587+293 others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50943288 | ||||||
| chr18:50943326 | G | A | 2 | a0001c0001t0040g0274 a0001c0001t0161g0264 |
2 | HG00280.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1587+2940G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943326 | |||||||
| chr18:50943344 | G | A | 1 | a0002c0002t0105g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1587+2958G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943344 | |||||||
| chr18:50943527 | C | T | 1 | a0001c0001t0052g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1587+3141C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943527 | |||||||
| chr18:50943546 | T | G | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1587+3160T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943546 | |||||||
| chr18:50943712 | A | C | 12 | a0001c0001t0002g0065 a0001c0001t0002g0076 a0001c0001t0006g0083 others(9): Show |
12 | NA18954.hp1 NA18964.hp2 NA18967.hp1 others(9): Show |
intron_variant | MODIFIER | c.1588-3305A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943712 | |||||||
| chr18:50943812 | G | A | 8 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1588-3205G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943812 | |||||||
| chr18:50943956 | C | T | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1588-3061C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943956 | |||||||
| chr18:50943960 | A | G | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1588-3057A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943960 | |||||||
| chr18:50944006 | G | T | 1 | a0001c0001t0017g0280 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1588-3011G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944006 | |||||||
| chr18:50944337 | G | T | 68 | a0002c0002t0005g0127 a0002c0002t0005g0129 a0002c0002t0005g0134 others(65): Show |
69 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1588-2680G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944337 | |||||||
| chr18:50944367 | C | T | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588-2650C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944367 | |||||||
| chr18:50944583 | C | T | 6 | a0001c0001t0025g0027 a0001c0001t0025g0029 a0001c0001t0026g0002 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588-2434C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944583 | |||||||
| chr18:50944606 | A | G | 1 | a0001c0001t0010g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1588-2411A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944606 | |||||||
| chr18:50944680 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1588-2337A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944680 | |||||||
| chr18:50944726 | C | G | 1 | a0001c0001t0002g0113 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1588-2291C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944726 | |||||||
| chr18:50944892 | A | T | 1 | a0001c0001t0016g0062 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1588-2125A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944892 | |||||||
| chr18:50944947 | G | A | 1 | a0001c0001t0004g0121 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1588-2070G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944947 | |||||||
| chr18:50945015 | A | G | 1 | a0002c0002t0005g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1588-2002A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945015 | |||||||
| chr18:50945036 | T | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(17): Show |
21 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.1588-1981T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945036 | |||||||
| chr18:50945319 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(138): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1588-1698T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945319 | |||||||
| chr18:50945328 | GCCTGGTC others(26): Show |
G | 1 | a0001c0001t0145g0302 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1588-1687_1588-165 others(37): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50945328 | ||||||
| chr18:50945411 | C | T | 1 | a0001c0001t0122g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1588-1606C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945411 | |||||||
| chr18:50945434 | T | C | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1588-1583T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945434 | |||||||
| chr18:50945488 | C | T | 1 | a0001c0001t0010g0043 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1588-1529C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945488 | |||||||
| chr18:50945497 | C | G | 1 | a0001c0001t0009g0072 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1588-1520C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945497 | |||||||
| chr18:50945712 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(138): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1588-1305A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945712 | |||||||
| chr18:50945807 | C | T | 1 | a0001c0001t0065g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1588-1210C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945807 | |||||||
| chr18:50945881 | A | C | 11 | a0001c0001t0012g0006 a0001c0001t0012g0186 a0001c0001t0012g0187 others(8): Show |
11 | HG01074.hp1 HG01106.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1588-1136A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945881 | |||||||
| chr18:50945884 | T | A | 22 | a0002c0002t0005g0129 a0002c0002t0005g0134 a0002c0002t0005g0136 others(19): Show |
22 | HG00609.hp1 HG01106.hp1 HG03704.hp1 others(19): Show |
intron_variant | MODIFIER | c.1588-1133T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945884 | |||||||
| chr18:50946110 | T | TTAAA | 52 | a0001c0001t0001g0199 a0001c0001t0006g0067 a0001c0001t0025g0027 others(49): Show |
53 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1588-878_1588-875d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50946110 | ||||||
| chr18:50946110 | T | TTAAATAA others(1): Show |
121 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(118): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1588-882_1588-875d others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50946110 | ||||||
| chr18:50946110 | T | TTAAATAA others(5): Show |
24 | a0001c0001t0001g0001 a0001c0001t0001g0238 a0001c0001t0001g0244 others(21): Show |
24 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1588-886_1588-875d others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50946110 | ||||||
| chr18:50946161 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1588-856T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946161 | |||||||
| chr18:50946176 | G | A | 1 | a0007c0010t0087g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1588-841G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946176 | |||||||
| chr18:50946196 | A | T | 10 | a0001c0003t0013g0009 a0001c0003t0013g0206 a0001c0003t0013g0207 others(7): Show |
10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1588-821A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946196 | |||||||
| chr18:50946314 | G | A | 10 | a0001c0001t0004g0195 a0001c0001t0036g0191 a0001c0001t0036g0201 others(7): Show |
10 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1588-703G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946314 | |||||||
| chr18:50946400 | C | T | 2 | a0001c0001t0030g0060 a0001c0001t0030g0068 |
2 | HG00735.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1588-617C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946400 | |||||||
| chr18:50946408 | T | G | 5 | a0002c0002t0005g0149 a0002c0002t0100g0144 a0002c0002t0115g0128 others(2): Show |
5 | NA18612.hp1 NA18985.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1588-609T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946408 | |||||||
| chr18:50946475 | T | C | 9 | a0002c0002t0020g0120 a0002c0002t0020g0322 a0002c0002t0020g0323 others(6): Show |
9 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1588-542T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946475 | |||||||
| chr18:50946539 | G | A | 1 | a0001c0001t0065g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1588-478G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946539 | |||||||
| chr18:50946907 | A | G | 1 | a0002c0002t0121g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1588-110A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946907 | |||||||
| chr18:50946957 | C | T | 1 | a0005c0009t0068g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1588-60C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946957 | |||||||
| chr18:50947014 | C | T | 1 | a0001c0001t0090g0270 | 1 | HG00558.hp2 | splice_region_variant&intron_variant | LOW | c.1588-3C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50947014 |