Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10982 |
| ensemblid | ENSG00000166974.13 |
| hgncid | 6891 |
| symbol | MAPRE2 |
| name | microtubule associated protein RP/EB family member 2 |
| refseq_nuc | NM_014268.4 |
| refseq_prot | NP_055083.1 |
| ensembl_nuc | ENST00000300249.10 |
| ensembl_prot | ENSP00000300249.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 35041413 |
| end | 35143470 |
| strand | + |
| ver | v1.2 |
| region | chr18:35041413-35143470 |
| region5000 | chr18:35036413-35148470 |
| regionname0 | MAPRE2_chr18_35041413_35143470 |
| regionname5000 | MAPRE2_chr18_35036413_35148470 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 327 | 369 | 86 | 64 | 176 | 8 | 33 | 136 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | MPGPT others(322): Show |
chr18 | 35036413 | 35148470 |
| a0002 | 0/0 | 327 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | MPGPT others(322): Show |
chr18 | 35036413 | 35148470 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 981 | 367 | 86 | 63 | 175 | 8 | 33 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | ATGCC others(976): Show |
chr18 | 35036413 | 35148470 | ||
| a0001c0002 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | ATGCC others(976): Show |
chr18 | 35036413 | 35148470 | ||
| a0001c0004 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | ATGCC others(976): Show |
chr18 | 35036413 | 35148470 | ||
| a0002c0003 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | ATGCC others(976): Show |
chr18 | 35036413 | 35148470 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4213 | 90 | 6 | 16 | 55 | 2 | 11 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4208): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0002 | 0/1 | 4211 | 47 | 25 | 3 | 13 | 0 | 5 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4206): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0003 | 1/0 | 4212 | 45 | 2 | 14 | 22 | 2 | 4 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4207): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0004 | 0/0 | 4210 | 41 | 0 | 4 | 34 | 0 | 3 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4205): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0005 | 0/0 | 4208 | 29 | 1 | 8 | 15 | 0 | 5 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4203): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0006 | 0/0 | 4208 | 19 | 0 | 1 | 18 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4203): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0007 | 0/0 | 4212 | 14 | 10 | 0 | 3 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4207): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0008 | 0/0 | 4204 | 9 | 1 | 4 | 0 | 2 | 2 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4199): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0009 | 0/0 | 4204 | 9 | 7 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4199): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0010 | 0/0 | 4212 | 6 | 0 | 0 | 5 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4207): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0011 | 0/0 | 4210 | 5 | 4 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4205): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0012 | 0/0 | 4214 | 5 | 5 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4209): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0013 | 0/0 | 4215 | 4 | 4 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4210): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0014 | 0/0 | 4213 | 3 | 0 | 3 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4208): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0015 | 0/0 | 4212 | 3 | 3 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4207): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0016 | 0/0 | 4211 | 3 | 0 | 2 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4206): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0017 | 0/0 | 4209 | 3 | 3 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4204): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0018 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4208): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0019 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4208): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0020 | 0/0 | 4213 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4208): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0021 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4208): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0022 | 0/0 | 4211 | 2 | 0 | 1 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4206): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0023 | 0/0 | 4207 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4202): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0024 | 0/0 | 4208 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4203): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0025 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4209): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0026 | 0/0 | 4212 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4207): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0027 | 0/0 | 4211 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4206): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0028 | 0/0 | 4211 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4206): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0029 | 0/0 | 4212 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4207): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0030 | 0/0 | 4211 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4206): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0031 | 0/0 | 4210 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4205): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0032 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4207): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0033 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4211): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0034 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4209): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0035 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4209): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0036 | 0/0 | 4205 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4200): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0037 | 0/0 | 4203 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4198): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0038 | 0/0 | 4204 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4199): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0039 | 0/0 | 4204 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4199): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0040 | 0/0 | 4207 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4202): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0041 | 0/0 | 4207 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4202): Show |
chr18 | 35036413 | 35148470 |
| a0001c0001t0042 | 0/0 | 4207 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4202): Show |
chr18 | 35036413 | 35148470 |
| a0001c0002t0002 | 0/0 | 4211 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4206): Show |
chr18 | 35036413 | 35148470 |
| a0001c0004t0004 | 0/0 | 4210 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4205): Show |
chr18 | 35036413 | 35148470 |
| a0002c0003t0001 | 0/0 | 4213 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | GAGAA others(4208): Show |
chr18 | 35036413 | 35148470 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0008g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0008g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0008g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0008g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0008g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0009g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0009g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0010g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0010g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0010g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0010g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0011g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0011g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0012g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0014g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0014g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0014g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0015g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0015g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0015g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0016g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0016g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0016g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0017g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0017g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0017g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0018g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0018g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0019g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0020g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0020g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0021g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0021g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0022g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0022g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0023g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0023g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0024g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0024g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0025g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0026g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0027g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0028g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0029g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0030g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0031g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0032g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0033g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0034g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0035g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0036g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0037g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0038g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0039g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0040g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0041g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0001t0042g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0001c0004t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0029 | g0150 | EUR | FIN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0118 | EUR | FIN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0139 | EUR | FIN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00408 | hp1 | a0001 | c0001 | t0040 | g0185 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0183 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0189 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0182 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG00735 | hp2 | a0001 | c0001 | t0009 | g0249 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01069 | hp2 | a0001 | c0001 | t0016 | g0277 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01070 | hp2 | a0001 | c0001 | t0037 | g0316 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01081 | hp1 | a0001 | c0001 | t0020 | g0307 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01106 | hp1 | a0001 | c0001 | t0020 | g0304 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01167 | hp1 | a0001 | c0001 | t0022 | g0067 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0074 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0011 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0258 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0176 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0044 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0011 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0308 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01346 | hp1 | a0001 | c0004 | t0004 | g0093 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0276 | EUR | IBS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0013 | EUR | IBS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0060 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01928 | hp1 | a0001 | c0001 | t0014 | g0306 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0178 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01934 | hp2 | a0001 | c0001 | t0014 | g0305 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01943 | hp1 | a0001 | c0001 | t0026 | g0323 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0197 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0089 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0127 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0175 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02015 | hp1 | a0001 | c0001 | t0027 | g0035 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02040 | hp1 | a0001 | c0001 | t0030 | g0293 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CDX | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | CDX | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CDX | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | CDX | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02258 | hp1 | a0001 | c0001 | t0042 | g0113 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0223 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0210 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0174 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02300 | hp2 | a0001 | c0001 | t0014 | g0310 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0225 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02523 | hp2 | a0001 | c0001 | t0032 | g0124 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02615 | hp2 | a0001 | c0001 | t0018 | g0247 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0260 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02630 | hp1 | a0001 | c0001 | t0034 | g0219 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0057 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0214 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02717 | hp1 | a0001 | c0001 | t0019 | g0207 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0212 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0201 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02738 | hp2 | a0001 | c0001 | t0008 | g0014 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0230 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0152 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0229 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0242 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0245 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02922 | hp2 | a0001 | c0001 | t0015 | g0261 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02965 | hp2 | a0001 | c0001 | t0021 | g0106 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0243 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03041 | hp1 | a0001 | c0001 | t0039 | g0251 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0181 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0334 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03098 | hp2 | a0001 | c0001 | t0017 | g0203 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03130 | hp1 | a0001 | c0001 | t0035 | g0208 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0231 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0179 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0217 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03209 | hp1 | a0001 | c0001 | t0024 | g0237 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03209 | hp2 | a0001 | c0001 | t0028 | g0259 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03225 | hp1 | a0001 | c0001 | t0033 | g0218 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03239 | hp2 | a0001 | c0001 | t0038 | g0321 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0228 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0248 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0206 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0058 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0226 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0205 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0148 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0038 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0068 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0100 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0168 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0296 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG04204 | hp1 | a0001 | c0001 | t0036 | g0123 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18522 | hp1 | a0001 | c0001 | t0015 | g0240 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | CHB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | CHB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | CHB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | CHB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18906 | hp1 | a0001 | c0001 | t0019 | g0216 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0244 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18957 | hp1 | a0001 | c0001 | t0016 | g0146 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18957 | hp2 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0043 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18960 | hp1 | a0001 | c0001 | t0041 | g0158 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18969 | hp1 | a0001 | c0001 | t0010 | g0286 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18987 | hp2 | a0001 | c0001 | t0010 | g0275 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18988 | hp2 | a0001 | c0001 | t0022 | g0140 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18997 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19002 | hp2 | a0001 | c0001 | t0031 | g0083 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0302 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | LWK | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | LWK | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0246 | AFR | LWK | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0211 | AFR | LWK | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19055 | hp1 | a0001 | c0001 | t0023 | g0006 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19060 | hp2 | a0001 | c0001 | t0010 | g0297 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19064 | hp1 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0162 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19070 | hp2 | a0001 | c0001 | t0023 | g0171 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19078 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0262 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19240 | hp1 | a0001 | c0001 | t0021 | g0063 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA20129 | hp1 | a0001 | c0001 | t0024 | g0238 | AFR | ASW | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | ASW | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | TSI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA20752 | hp2 | a0001 | c0001 | t0008 | g0128 | EUR | TSI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0157 | SAS | GIH | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0199 | SAS | GIH | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG01123 | hp2 | a0001 | c0001 | t0016 | g0131 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02109 | hp1 | a0001 | c0001 | t0025 | g0026 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0125 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0250 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| HG03471 | hp2 | a0001 | c0001 | t0012 | g0209 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0221 | REF | REF | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0133 | REF | REF | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:35132062 | G | A | 1 | a0002 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.781G>A | p.Val261Met | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/7 | 908/4212 | 781/984 | 261/327 | chr18 | 35132062 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:35102038 | T | C | 1 | a0001c0002 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.489T>C | p.Asp163Asp | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/7 | 616/4212 | 489/984 | 163/327 | chr18 | 35102038 | |||
| chr18:35140351 | G | A | 1 | a0001c0004 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.966G>A | p.Pro322Pro | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1093/4212 | 966/984 | 322/327 | chr18 | 35140351 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:35140395 | C | T | 14 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(11): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*26C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 26 | chr18 | 35140395 | ||||||
| chr18:35140412 | G | A | 1 | a0001c0001t0025 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 43 | chr18 | 35140412 | ||||||
| chr18:35140578 | G | A | 4 | a0001c0001t0008 a0001c0001t0036 a0001c0001t0037 others(1): Show |
12 | HG00280.hp2 HG00735.hp1 HG01070.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*209G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 209 | chr18 | 35140578 | ||||||
| chr18:35140889 | G | A | 1 | a0001c0001t0018 | 2 | HG02615.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*520G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 520 | chr18 | 35140889 | ||||||
| chr18:35141114 | C | T | 14 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(11): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*745C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 745 | chr18 | 35141114 | ||||||
| chr18:35141134 | C | G | 6 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0025 others(3): Show |
13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*765C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 765 | chr18 | 35141134 | ||||||
| chr18:35141149 | G | T | 1 | a0001c0001t0032 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*780G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 780 | chr18 | 35141149 | ||||||
| chr18:35141226 | G | A | 6 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0025 others(3): Show |
13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*857G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 857 | chr18 | 35141226 | ||||||
| chr18:35141362 | A | T | 6 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0025 others(3): Show |
13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*993A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 993 | chr18 | 35141362 | ||||||
| chr18:35141438 | G | A | 13 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(10): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1069G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1069 | chr18 | 35141438 | ||||||
| chr18:35141564 | A | C | 1 | a0001c0001t0031 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1195A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1195 | chr18 | 35141564 | ||||||
| chr18:35141627 | T | TTTC | 6 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0025 others(3): Show |
13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1261_*1263dupCTT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1264 | INFO_REALIGN_3_PRIME | chr18 | 35141627 | |||||
| chr18:35141661 | TTTTC | T | 6 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0036 others(3): Show |
22 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1296_*1299delCTTT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1296 | INFO_REALIGN_3_PRIME | chr18 | 35141661 | |||||
| chr18:35141759 | T | G | 1 | a0001c0001t0019 | 2 | HG02717.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1390T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1390 | chr18 | 35141759 | ||||||
| chr18:35141797 | T | C | 2 | a0001c0001t0006 a0001c0001t0023 |
21 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1428T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1428 | chr18 | 35141797 | ||||||
| chr18:35141942 | AAAAT | A | 14 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(11): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1578_*1581delAAAT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1578 | INFO_REALIGN_3_PRIME | chr18 | 35141942 | |||||
| chr18:35141987 | A | T | 4 | a0001c0001t0004 a0001c0001t0022 a0001c0001t0031 others(1): Show |
45 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1618A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1618 | chr18 | 35141987 | ||||||
| chr18:35142069 | C | A | 1 | a0001c0001t0020 | 2 | HG01081.hp1 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1700C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1700 | chr18 | 35142069 | ||||||
| chr18:35142118 | G | A | 2 | a0001c0001t0014 a0001c0001t0026 |
4 | HG01928.hp1 HG01934.hp2 HG01943.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1749 | chr18 | 35142118 | ||||||
| chr18:35142148 | T | C | 1 | a0001c0001t0039 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1779T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1779 | chr18 | 35142148 | ||||||
| chr18:35142190 | C | A | 14 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(11): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1821C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1821 | chr18 | 35142190 | ||||||
| chr18:35142697 | C | T | 1 | a0001c0001t0035 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2328C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2328 | chr18 | 35142697 | ||||||
| chr18:35142849 | G | C | 32 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(29): Show |
211 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*2480G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2480 | chr18 | 35142849 | ||||||
| chr18:35142904 | A | G | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(37): Show |
318 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*2535A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2535 | chr18 | 35142904 | ||||||
| chr18:35142905 | T | G | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(37): Show |
318 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*2536T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2536 | chr18 | 35142905 | ||||||
| chr18:35142953 | A | C | 16 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(13): Show |
84 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2584A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2584 | chr18 | 35142953 | ||||||
| chr18:35142959 | C | G | 1 | a0001c0001t0038 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2590C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2590 | chr18 | 35142959 | ||||||
| chr18:35143071 | G | GA | 10 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0017 others(7): Show |
107 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2720dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2721 | INFO_REALIGN_3_PRIME | chr18 | 35143071 | |||||
| chr18:35143071 | GA | G | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(13): Show |
108 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2720delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2720 | INFO_REALIGN_3_PRIME | chr18 | 35143071 | |||||
| chr18:35143086 | A | G | 2 | a0001c0001t0024 a0001c0001t0042 |
3 | HG02258.hp1 HG03209.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2717A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2717 | chr18 | 35143086 | ||||||
| chr18:35143377 | A | G | 1 | a0001c0001t0029 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3008A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 3008 | chr18 | 35143377 | ||||||
| chr18:35143447 | TA | T | 8 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0012 others(5): Show |
57 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3088delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 3088 | INFO_REALIGN_3_PRIME | chr18 | 35143447 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:35041922 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.122+261G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35041922 | |||||||
| chr18:35042204 | G | C | 41 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(38): Show |
44 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.122+543G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042204 | |||||||
| chr18:35042230 | T | G | 47 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(44): Show |
50 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.122+569T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042230 | |||||||
| chr18:35042400 | G | C | 4 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | NA18945.hp1 NA18977.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+739G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042400 | |||||||
| chr18:35042485 | A | G | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122+824A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042485 | |||||||
| chr18:35042730 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.122+1069C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042730 | |||||||
| chr18:35042824 | G | A | 1 | a0001c0001t0021g0063 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122+1163G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042824 | |||||||
| chr18:35042879 | C | T | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122+1218C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042879 | |||||||
| chr18:35042924 | CA | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(240): Show |
263 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.122+1276delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35042924 | ||||||
| chr18:35042924 | CAA | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(35): Show |
41 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.122+1275_122+1276d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35042924 | ||||||
| chr18:35043008 | A | G | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.122+1347A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043008 | |||||||
| chr18:35043017 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0002g0105 |
2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.122+1356C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043017 | |||||||
| chr18:35043380 | C | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
259 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.122+1719C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043380 | |||||||
| chr18:35043491 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.122+1830T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043491 | |||||||
| chr18:35043600 | A | G | 1 | a0001c0001t0001g0333 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.122+1939A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043600 | |||||||
| chr18:35043635 | G | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(83): Show |
97 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(94): Show |
intron_variant | MODIFIER | c.122+1974G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043635 | |||||||
| chr18:35044090 | G | T | 1 | a0001c0001t0006g0262 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.122+2429G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044090 | |||||||
| chr18:35044176 | G | C | 2 | a0001c0001t0001g0104 a0001c0001t0002g0105 |
2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.122+2515G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044176 | |||||||
| chr18:35044239 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+2578T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044239 | |||||||
| chr18:35044294 | A | C | 4 | a0001c0001t0009g0258 a0001c0001t0015g0260 a0001c0001t0015g0261 others(1): Show |
4 | HG01243.hp1 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+2633A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044294 | |||||||
| chr18:35044597 | T | C | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.122+2936T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044597 | |||||||
| chr18:35044703 | A | G | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
307 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.122+3042A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044703 | |||||||
| chr18:35044845 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(83): Show |
92 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.122+3184T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044845 | |||||||
| chr18:35044865 | A | C | 27 | a0001c0001t0001g0254 a0001c0001t0002g0018 a0001c0001t0002g0236 others(24): Show |
28 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.122+3204A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044865 | |||||||
| chr18:35044895 | C | G | 4 | a0001c0001t0001g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+3234C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044895 | |||||||
| chr18:35044962 | T | C | 76 | a0001c0001t0001g0173 a0001c0001t0001g0254 a0001c0001t0002g0018 others(73): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.122+3301T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044962 | |||||||
| chr18:35045197 | C | T | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.122+3536C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045197 | |||||||
| chr18:35045433 | T | G | 3 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 |
3 | NA18987.hp1 NA18993.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.122+3772T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045433 | |||||||
| chr18:35045443 | T | TA | 86 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(83): Show |
92 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.122+3782_122+3783i others(3): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045443 | |||||||
| chr18:35045444 | T | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(83): Show |
92 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.122+3783T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045444 | |||||||
| chr18:35045444 | T | TA | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(102): Show |
118 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.122+3794dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35045444 | ||||||
| chr18:35045542 | G | C | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122+3881G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045542 | |||||||
| chr18:35045650 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0013g0024 a0001c0001t0025g0026 |
3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+3989G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045650 | |||||||
| chr18:35045752 | A | G | 1 | a0001c0001t0002g0007 | 3 | HG00642.hp1 HG01099.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.122+4091A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045752 | |||||||
| chr18:35045919 | C | A | 1 | a0001c0001t0006g0162 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.122+4258C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045919 | |||||||
| chr18:35046618 | A | G | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.122+4957A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35046618 | |||||||
| chr18:35046682 | A | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(39): Show |
45 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.122+5021A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35046682 | |||||||
| chr18:35046770 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.122+5109G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35046770 | |||||||
| chr18:35046860 | C | A | 2 | a0001c0001t0001g0222 a0001c0001t0007g0223 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.122+5199C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35046860 | |||||||
| chr18:35047002 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0013g0024 a0001c0001t0025g0026 |
3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+5341G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047002 | |||||||
| chr18:35047013 | T | C | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122+5352T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047013 | |||||||
| chr18:35047030 | T | C | 3 | a0001c0001t0007g0025 a0001c0001t0013g0024 a0001c0001t0025g0026 |
3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+5369T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047030 | |||||||
| chr18:35047050 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
202 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.122+5389G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047050 | |||||||
| chr18:35047126 | A | T | 43 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0002g0105 others(40): Show |
46 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.122+5465A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047126 | |||||||
| chr18:35047415 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(78): Show |
87 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.122+5754T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047415 | |||||||
| chr18:35047524 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(104): Show |
120 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.122+5863A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047524 | |||||||
| chr18:35047621 | A | G | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122+5960A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047621 | |||||||
| chr18:35047716 | T | TA | 107 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(104): Show |
115 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.122+6071dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35047716 | ||||||
| chr18:35047716 | T | TAA | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(81): Show |
95 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(92): Show |
intron_variant | MODIFIER | c.122+6070_122+6071d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35047716 | ||||||
| chr18:35047902 | A | G | 1 | a0001c0001t0003g0156 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.122+6241A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047902 | |||||||
| chr18:35048095 | C | G | 2 | a0001c0001t0033g0218 a0001c0001t0034g0219 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.122+6434C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048095 | |||||||
| chr18:35048147 | C | T | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122+6486C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048147 | |||||||
| chr18:35048148 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0013g0024 a0001c0001t0025g0026 |
3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+6487G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048148 | |||||||
| chr18:35048428 | G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.122+6767G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048428 | |||||||
| chr18:35048514 | A | G | 3 | a0001c0001t0007g0025 a0001c0001t0013g0024 a0001c0001t0025g0026 |
3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+6853A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048514 | |||||||
| chr18:35048555 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0160 others(37): Show |
43 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.122+6894A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048555 | |||||||
| chr18:35048671 | A | C | 1 | a0001c0001t0003g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.122+7010A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048671 | |||||||
| chr18:35048681 | G | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(23): Show |
29 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.122+7020G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048681 | |||||||
| chr18:35048699 | A | G | 43 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0002g0105 others(40): Show |
46 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.122+7038A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048699 | |||||||
| chr18:35049325 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.122+7664G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049325 | |||||||
| chr18:35049628 | C | G | 3 | a0001c0001t0033g0218 a0001c0001t0034g0219 a0001c0001t0035g0208 |
3 | HG02630.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.122+7967C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049628 | |||||||
| chr18:35049633 | C | T | 3 | a0001c0001t0005g0215 a0001c0001t0009g0217 a0001c0001t0019g0216 |
3 | HG03195.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.122+7972C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049633 | |||||||
| chr18:35049809 | G | A | 3 | a0001c0001t0033g0218 a0001c0001t0034g0219 a0001c0001t0035g0208 |
3 | HG02630.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.122+8148G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049809 | |||||||
| chr18:35049858 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(94): Show |
109 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.122+8197C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049858 | |||||||
| chr18:35049865 | A | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0317 a0001c0001t0001g0318 others(2): Show |
6 | HG02080.hp1 NA18944.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+8204A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049865 | |||||||
| chr18:35049939 | C | T | 1 | a0001c0001t0037g0316 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.122+8278C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049939 | |||||||
| chr18:35050121 | G | A | 1 | a0001c0001t0008g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.122+8460G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050121 | |||||||
| chr18:35050380 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+8719A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050380 | |||||||
| chr18:35050429 | C | T | 27 | a0001c0001t0001g0254 a0001c0001t0002g0018 a0001c0001t0002g0236 others(24): Show |
28 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.122+8768C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050429 | |||||||
| chr18:35050500 | T | C | 44 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0002g0105 others(41): Show |
47 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.122+8839T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050500 | |||||||
| chr18:35050663 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.122+9002G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050663 | |||||||
| chr18:35050796 | C | G | 1 | a0001c0001t0002g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.122+9135C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050796 | |||||||
| chr18:35051013 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.122+9352C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051013 | |||||||
| chr18:35051606 | A | C | 1 | a0001c0001t0001g0315 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.122+9945A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051606 | |||||||
| chr18:35051658 | G | A | 10 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 others(7): Show |
10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+9997G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051658 | |||||||
| chr18:35051752 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
238 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.122+10091C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051752 | |||||||
| chr18:35051859 | C | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.122+10198C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051859 | |||||||
| chr18:35051860 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.122+10199G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051860 | |||||||
| chr18:35051891 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
238 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.122+10230A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051891 | |||||||
| chr18:35051909 | G | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
238 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.122+10248G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051909 | |||||||
| chr18:35051916 | G | A | 10 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 others(7): Show |
10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+10255G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051916 | |||||||
| chr18:35052035 | A | G | 6 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(3): Show |
6 | HG02280.hp1 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+10374A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052035 | |||||||
| chr18:35052057 | C | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
245 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.122+10396C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052057 | |||||||
| chr18:35052236 | T | C | 44 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0002g0105 others(41): Show |
47 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.122+10575T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052236 | |||||||
| chr18:35052279 | A | G | 10 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 others(7): Show |
10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+10618A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052279 | |||||||
| chr18:35052296 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.122+10635A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052296 | |||||||
| chr18:35052379 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.122+10718A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052379 | |||||||
| chr18:35052609 | G | A | 77 | a0001c0001t0001g0173 a0001c0001t0001g0254 a0001c0001t0002g0018 others(74): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.122+10948G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052609 | |||||||
| chr18:35052782 | A | G | 84 | a0001c0001t0001g0021 a0001c0001t0001g0173 a0001c0001t0001g0254 others(81): Show |
89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.122+11121A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052782 | |||||||
| chr18:35052826 | C | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
146 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.122+11165C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052826 | |||||||
| chr18:35053008 | C | CCA | 54 | a0001c0001t0001g0021 a0001c0001t0001g0173 a0001c0001t0001g0327 others(51): Show |
58 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.122+11360_122+1136 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35053008 | ||||||
| chr18:35053008 | CCA | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
141 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.122+11360_122+1136 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35053008 | ||||||
| chr18:35053009 | CA | C | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0005g0215 |
3 | HG03831.hp2 NA18975.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.122+11349delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053009 | |||||||
| chr18:35053010 | A | C | 3 | a0001c0001t0002g0239 a0001c0001t0007g0223 a0001c0001t0018g0247 |
3 | HG02258.hp2 HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.122+11349A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053010 | |||||||
| chr18:35053012 | A | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
140 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.122+11351A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053012 | |||||||
| chr18:35053012 | A | G | 1 | a0001c0001t0005g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.122+11351A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053012 | |||||||
| chr18:35053014 | A | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(84): Show |
99 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.122+11353A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053014 | |||||||
| chr18:35053107 | A | G | 1 | a0001c0001t0001g0004 | 3 | NA18952.hp1 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.122+11446A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053107 | |||||||
| chr18:35053588 | A | G | 10 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 others(7): Show |
10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+11927A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053588 | |||||||
| chr18:35053611 | G | GT | 4 | a0001c0001t0002g0028 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | HG02735.hp2 HG03492.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+11951dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35053611 | ||||||
| chr18:35053634 | A | G | 1 | a0001c0001t0012g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.122+11973A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053634 | |||||||
| chr18:35053797 | T | TA | 3 | a0001c0001t0007g0025 a0001c0001t0013g0024 a0001c0001t0025g0026 |
3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+12137dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35053797 | ||||||
| chr18:35053921 | T | C | 1 | a0001c0001t0005g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.122+12260T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053921 | |||||||
| chr18:35054032 | C | T | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0325 |
3 | NA18997.hp1 NA19076.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.122+12371C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054032 | |||||||
| chr18:35054051 | C | A | 1 | a0001c0001t0004g0065 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.122+12390C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054051 | |||||||
| chr18:35054191 | A | T | 1 | a0001c0001t0003g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.122+12530A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054191 | |||||||
| chr18:35054336 | A | G | 1 | a0001c0001t0003g0153 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.122+12675A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054336 | |||||||
| chr18:35054449 | T | G | 3 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 |
3 | HG02886.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.122+12788T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054449 | |||||||
| chr18:35054613 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.122+12952C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054613 | |||||||
| chr18:35054670 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
300 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.122+13009A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054670 | |||||||
| chr18:35054877 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122+13216G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054877 | |||||||
| chr18:35055108 | G | A | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02280.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+13447G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055108 | |||||||
| chr18:35055162 | C | T | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122+13501C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055162 | |||||||
| chr18:35055362 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.122+13701C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055362 | |||||||
| chr18:35055537 | C | CTCTG | 4 | a0001c0001t0002g0107 a0001c0001t0013g0205 a0001c0001t0013g0206 others(1): Show |
4 | HG02280.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+13877_122+1387 others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTCTGTGT others(7): Show |
1 | a0001c0001t0022g0067 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.122+13877_122+1387 others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTG | 4 | a0001c0001t0007g0228 a0001c0001t0008g0014 a0001c0001t0021g0063 others(1): Show |
5 | HG00735.hp1 HG02258.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+13902_122+1390 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTG | 5 | a0001c0001t0002g0015 a0001c0001t0007g0229 a0001c0001t0012g0230 others(2): Show |
6 | HG02559.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+13900_122+1390 others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTGTG | 4 | a0001c0001t0001g0271 a0001c0001t0004g0068 a0001c0001t0004g0069 others(1): Show |
4 | HG01433.hp2 HG03927.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+13898_122+1390 others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTGTGT others(1): Show |
11 | a0001c0001t0001g0020 a0001c0001t0001g0272 a0001c0001t0001g0273 others(8): Show |
12 | HG02080.hp1 HG03139.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+13896_122+1390 others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTGTGT others(3): Show |
100 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0019 others(97): Show |
111 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.122+13894_122+1390 others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTGTGT others(5): Show |
71 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0102 others(68): Show |
75 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.122+13892_122+1390 others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTGTGT others(7): Show |
11 | a0001c0001t0001g0309 a0001c0001t0003g0308 a0001c0001t0004g0101 others(8): Show |
11 | HG01081.hp1 HG01106.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+13890_122+1390 others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTGTGT others(9): Show |
5 | a0001c0001t0003g0311 a0001c0001t0005g0204 a0001c0001t0009g0245 others(2): Show |
5 | HG02300.hp2 HG02897.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+13888_122+1390 others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTGTGT others(11): Show |
5 | a0001c0001t0009g0246 a0001c0001t0009g0249 a0001c0001t0009g0250 others(2): Show |
5 | HG00735.hp2 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+13886_122+1390 others(22): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0039g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.122+13884_122+1390 others(24): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055537 | C | CTGTGTGT others(19): Show |
1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122+13878_122+1390 others(30): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | ||||||
| chr18:35055539 | G | C | 3 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0033g0218 |
3 | HG02280.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.122+13878G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055539 | |||||||
| chr18:35055563 | G | GTGTA | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+13903_122+1390 others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | ||||||
| chr18:35055563 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0002g0029 a0001c0001t0007g0030 |
2 | NA18948.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.122+13903_122+1390 others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | ||||||
| chr18:35055563 | G | GTGTGTGT others(5): Show |
11 | a0001c0001t0001g0002 a0001c0001t0001g0288 a0001c0001t0001g0289 others(8): Show |
15 | HG00423.hp1 HG02040.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.122+13903_122+1390 others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | ||||||
| chr18:35055563 | G | GTGTGTGT others(7): Show |
4 | a0001c0001t0001g0303 a0001c0001t0002g0033 a0001c0001t0007g0025 others(1): Show |
4 | HG02109.hp1 HG03540.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+13903_122+1390 others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | ||||||
| chr18:35055563 | G | GTGTGTGT others(9): Show |
27 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0160 others(24): Show |
30 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.122+13903_122+1390 others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | ||||||
| chr18:35055563 | G | GTGTGTGT others(11): Show |
2 | a0001c0001t0002g0028 a0001c0001t0002g0047 |
2 | HG02056.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.122+13903_122+1390 others(22): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | ||||||
| chr18:35055565 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0034 others(66): Show |
76 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.122+13904A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055565 | |||||||
| chr18:35055690 | C | T | 4 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG02280.hp1 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+14029C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055690 | |||||||
| chr18:35055901 | G | T | 2 | a0001c0001t0004g0073 a0001c0001t0004g0100 |
2 | HG02080.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.122+14240G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055901 | |||||||
| chr18:35055955 | C | CA | 42 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(39): Show |
47 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.123-14224dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055955 | ||||||
| chr18:35056078 | AT | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(81): Show |
90 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.123-14110delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35056078 | ||||||
| chr18:35056213 | A | C | 1 | a0001c0001t0009g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-13982A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056213 | |||||||
| chr18:35056254 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.123-13941A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056254 | |||||||
| chr18:35056444 | A | G | 9 | a0001c0001t0002g0107 a0001c0001t0012g0209 a0001c0001t0012g0210 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-13751A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056444 | |||||||
| chr18:35056528 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(86): Show |
97 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.123-13667C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056528 | |||||||
| chr18:35056621 | ATCTAC | A | 10 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 others(7): Show |
10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-13569_123-1356 others(9): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35056621 | ||||||
| chr18:35056734 | T | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(84): Show |
95 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.123-13461T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056734 | |||||||
| chr18:35056781 | G | T | 1 | a0001c0001t0009g0249 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.123-13414G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056781 | |||||||
| chr18:35056895 | G | A | 1 | a0001c0001t0012g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-13300G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056895 | |||||||
| chr18:35057063 | G | T | 2 | a0001c0001t0001g0222 a0001c0001t0007g0223 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.123-13132G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057063 | |||||||
| chr18:35057073 | G | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
276 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.123-13122G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057073 | |||||||
| chr18:35057102 | C | T | 10 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 others(7): Show |
10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-13093C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057102 | |||||||
| chr18:35057171 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
286 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.123-13024T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057171 | |||||||
| chr18:35057305 | A | C | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.123-12890A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057305 | |||||||
| chr18:35057334 | G | T | 9 | a0001c0001t0002g0107 a0001c0001t0012g0209 a0001c0001t0012g0210 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-12861G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057334 | |||||||
| chr18:35057507 | C | CGT | 9 | a0001c0001t0001g0274 a0001c0001t0002g0220 a0001c0001t0002g0233 others(6): Show |
9 | HG01109.hp1 HG02615.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-12665_123-1266 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGT | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(52): Show |
64 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.123-12667_123-1266 others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGT | 49 | a0001c0001t0001g0019 a0001c0001t0001g0103 a0001c0001t0001g0108 others(46): Show |
50 | HG00323.hp1 HG01070.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.123-12669_123-1266 others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(1): Show |
30 | a0001c0001t0002g0018 a0001c0001t0002g0107 a0001c0001t0002g0224 others(27): Show |
33 | HG00735.hp2 HG01255.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.123-12671_123-1266 others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(3): Show |
39 | a0001c0001t0001g0034 a0001c0001t0002g0007 a0001c0001t0002g0234 others(36): Show |
42 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.123-12673_123-1266 others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(5): Show |
19 | a0001c0001t0001g0021 a0001c0001t0001g0294 a0001c0001t0001g0327 others(16): Show |
20 | HG01099.hp2 HG01496.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.123-12675_123-1266 others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(7): Show |
27 | a0001c0001t0001g0104 a0001c0001t0001g0160 a0001c0001t0001g0332 others(24): Show |
28 | HG00558.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-12677_123-1266 others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(9): Show |
10 | a0001c0001t0001g0161 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01168.hp2 HG01255.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-12679_123-1266 others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(11): Show |
9 | a0001c0001t0001g0102 a0001c0001t0002g0056 a0001c0001t0002g0062 others(6): Show |
9 | HG00558.hp2 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-12681_123-1266 others(22): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(13): Show |
8 | a0001c0001t0001g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(5): Show |
10 | HG02155.hp2 HG03927.hp2 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.123-12683_123-1266 others(24): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(15): Show |
23 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0065 others(20): Show |
26 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.123-12685_123-1266 others(26): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(17): Show |
1 | a0001c0001t0004g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.123-12687_123-1266 others(28): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | C | CGTGTGTG others(19): Show |
1 | a0001c0001t0004g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.123-12664_123-1266 others(30): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057507 | CGT | C | 4 | a0001c0001t0003g0119 a0001c0001t0003g0153 a0001c0001t0003g0154 others(1): Show |
4 | HG01074.hp2 HG01433.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-12665_123-1266 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | ||||||
| chr18:35057654 | A | G | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.123-12541A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057654 | |||||||
| chr18:35057672 | G | C | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-12523G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057672 | |||||||
| chr18:35057827 | C | T | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02080.hp1 NA18944.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-12368C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057827 | |||||||
| chr18:35057837 | C | T | 10 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 others(7): Show |
10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-12358C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057837 | |||||||
| chr18:35057975 | G | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
276 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.123-12220G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057975 | |||||||
| chr18:35058080 | A | G | 1 | a0001c0001t0006g0198 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.123-12115A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058080 | |||||||
| chr18:35058144 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.123-12051A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058144 | |||||||
| chr18:35058269 | C | A | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-11926C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058269 | |||||||
| chr18:35058373 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.123-11822C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058373 | |||||||
| chr18:35058395 | G | T | 10 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 others(7): Show |
10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-11800G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058395 | |||||||
| chr18:35058397 | G | A | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0325 |
3 | NA18997.hp1 NA19076.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.123-11798G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058397 | |||||||
| chr18:35058555 | G | A | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.123-11640G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058555 | |||||||
| chr18:35058564 | T | C | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
311 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.123-11631T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058564 | |||||||
| chr18:35058797 | CT | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
276 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.123-11395delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35058797 | ||||||
| chr18:35058830 | G | T | 1 | a0001c0001t0001g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.123-11365G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058830 | |||||||
| chr18:35058866 | A | G | 10 | a0001c0001t0002g0224 a0001c0001t0002g0234 a0001c0001t0002g0235 others(7): Show |
10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-11329A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058866 | |||||||
| chr18:35058888 | C | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
276 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.123-11307C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058888 | |||||||
| chr18:35059042 | GATTAA | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(78): Show |
87 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.123-11146_123-1114 others(9): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35059042 | ||||||
| chr18:35059075 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-11120A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059075 | |||||||
| chr18:35059109 | T | C | 9 | a0001c0001t0002g0107 a0001c0001t0012g0209 a0001c0001t0012g0210 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-11086T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059109 | |||||||
| chr18:35059323 | TA | T | 20 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0313 others(17): Show |
20 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(17): Show |
intron_variant | MODIFIER | c.123-10859delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35059323 | ||||||
| chr18:35059396 | A | G | 1 | a0001c0001t0003g0308 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.123-10799A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059396 | |||||||
| chr18:35059407 | G | C | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02080.hp1 NA18944.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-10788G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059407 | |||||||
| chr18:35059541 | A | G | 1 | a0001c0001t0012g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.123-10654A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059541 | |||||||
| chr18:35059687 | T | G | 1 | a0001c0001t0004g0074 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.123-10508T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059687 | |||||||
| chr18:35059689 | A | C | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-10506A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059689 | |||||||
| chr18:35059749 | A | T | 1 | a0001c0001t0039g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.123-10446A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059749 | |||||||
| chr18:35059766 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.123-10429A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059766 | |||||||
| chr18:35059801 | G | A | 1 | a0001c0001t0004g0084 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.123-10394G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059801 | |||||||
| chr18:35059810 | C | T | 1 | a0001c0001t0004g0151 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.123-10385C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059810 | |||||||
| chr18:35059911 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.123-10284A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059911 | |||||||
| chr18:35059943 | A | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(77): Show |
86 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.123-10252A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059943 | |||||||
| chr18:35060023 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-10172G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060023 | |||||||
| chr18:35060049 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
285 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(282): Show |
intron_variant | MODIFIER | c.123-10146G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060049 | |||||||
| chr18:35060219 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.123-9976C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060219 | |||||||
| chr18:35060302 | A | AG | 18 | a0001c0001t0001g0272 a0001c0001t0001g0300 a0001c0001t0001g0317 others(15): Show |
18 | HG00735.hp2 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.123-9888dupG | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35060302 | ||||||
| chr18:35060320 | T | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0102 others(77): Show |
86 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.123-9875T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060320 | |||||||
| chr18:35060841 | G | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(78): Show |
91 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.123-9354G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060841 | |||||||
| chr18:35061001 | A | C | 9 | a0001c0001t0002g0107 a0001c0001t0012g0209 a0001c0001t0012g0210 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-9194A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061001 | |||||||
| chr18:35061095 | TC | T | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
275 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.123-9099delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061095 | |||||||
| chr18:35061302 | T | G | 1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-8893T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061302 | |||||||
| chr18:35061479 | C | T | 1 | a0001c0001t0005g0214 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.123-8716C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061479 | |||||||
| chr18:35061537 | A | G | 6 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(3): Show |
6 | HG02280.hp1 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-8658A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061537 | |||||||
| chr18:35061623 | T | TGGAGACA others(8): Show |
1 | a0001c0001t0009g0245 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.123-8571_123-8570i others(17): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35061623 | ||||||
| chr18:35061714 | C | G | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-8481C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061714 | |||||||
| chr18:35061900 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123-8295G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061900 | |||||||
| chr18:35062272 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0009g0217 a0001c0001t0019g0207 others(1): Show |
6 | HG00642.hp1 HG01099.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-7923A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35062272 | |||||||
| chr18:35062473 | G | A | 1 | a0001c0001t0007g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.123-7722G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35062473 | |||||||
| chr18:35062488 | T | C | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123-7707T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35062488 | |||||||
| chr18:35062868 | A | G | 1 | a0001c0001t0031g0083 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.123-7327A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35062868 | |||||||
| chr18:35063080 | G | A | 3 | a0001c0001t0003g0122 a0001c0001t0021g0063 a0001c0001t0021g0106 |
3 | HG01106.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.123-7115G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063080 | |||||||
| chr18:35063116 | T | C | 3 | a0001c0001t0006g0006 a0001c0001t0006g0169 a0001c0001t0023g0006 |
4 | NA18968.hp2 NA19000.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-7079T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063116 | |||||||
| chr18:35063125 | A | T | 1 | a0001c0001t0001g0326 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.123-7070A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063125 | |||||||
| chr18:35063143 | G | T | 69 | a0001c0001t0002g0018 a0001c0001t0002g0236 a0001c0001t0002g0239 others(66): Show |
73 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.123-7052G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063143 | |||||||
| chr18:35063165 | G | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(160): Show |
175 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.123-7030G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063165 | |||||||
| chr18:35063205 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.123-6990G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063205 | |||||||
| chr18:35063251 | A | C | 77 | a0001c0001t0002g0018 a0001c0001t0002g0236 a0001c0001t0002g0239 others(74): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.123-6944A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063251 | |||||||
| chr18:35063253 | A | G | 77 | a0001c0001t0002g0018 a0001c0001t0002g0236 a0001c0001t0002g0239 others(74): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.123-6942A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063253 | |||||||
| chr18:35063257 | C | T | 1 | a0001c0001t0001g0319 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.123-6938C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063257 | |||||||
| chr18:35063260 | C | T | 2 | a0001c0001t0004g0074 a0001c0004t0004g0093 |
2 | HG01168.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.123-6935C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063260 | |||||||
| chr18:35063261 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.123-6934G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063261 | |||||||
| chr18:35063296 | A | G | 1 | a0001c0001t0005g0214 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.123-6899A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063296 | |||||||
| chr18:35063297 | T | C | 4 | a0001c0001t0005g0214 a0001c0001t0006g0180 a0001c0001t0007g0025 others(1): Show |
4 | HG02647.hp1 HG02683.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-6898T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063297 | |||||||
| chr18:35063309 | G | A | 2 | a0001c0001t0017g0181 a0001c0001t0017g0203 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.123-6886G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063309 | |||||||
| chr18:35063328 | T | C | 28 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0002g0009 others(25): Show |
29 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-6867T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063328 | |||||||
| chr18:35063343 | G | A | 26 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0029 others(23): Show |
27 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.123-6852G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063343 | |||||||
| chr18:35063360 | T | A | 1 | a0001c0001t0002g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-6835T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063360 | |||||||
| chr18:35063360 | T | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(140): Show |
158 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.123-6835T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063360 | |||||||
| chr18:35063386 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-6809C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063386 | |||||||
| chr18:35063396 | T | C | 6 | a0001c0001t0009g0258 a0001c0001t0015g0240 a0001c0001t0015g0260 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-6799T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063396 | |||||||
| chr18:35063402 | C | T | 5 | a0001c0001t0009g0258 a0001c0001t0015g0240 a0001c0001t0015g0260 others(2): Show |
5 | HG01243.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-6793C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063402 | |||||||
| chr18:35063428 | A | G | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-6767A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063428 | |||||||
| chr18:35063478 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.123-6717G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063478 | |||||||
| chr18:35063484 | TA | T | 169 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(166): Show |
181 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.123-6697delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35063484 | ||||||
| chr18:35063513 | C | T | 8 | a0001c0001t0008g0011 a0001c0001t0008g0014 a0001c0001t0008g0118 others(5): Show |
10 | HG00280.hp2 HG00735.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-6682C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063513 | |||||||
| chr18:35063525 | A | C | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-6670A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063525 | |||||||
| chr18:35063616 | A | G | 9 | a0001c0001t0007g0025 a0001c0001t0007g0225 a0001c0001t0007g0226 others(6): Show |
9 | HG02451.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-6579A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063616 | |||||||
| chr18:35063705 | A | C | 4 | a0001c0001t0004g0065 a0001c0001t0004g0072 a0001c0001t0004g0076 others(1): Show |
4 | NA18956.hp1 NA19066.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-6490A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063705 | |||||||
| chr18:35063847 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.123-6348A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063847 | |||||||
| chr18:35063856 | G | C | 2 | a0001c0001t0002g0236 a0001c0001t0002g0253 |
2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.123-6339G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063856 | |||||||
| chr18:35063980 | C | G | 3 | a0001c0001t0009g0217 a0001c0001t0019g0207 a0001c0001t0019g0216 |
3 | HG02717.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.123-6215C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063980 | |||||||
| chr18:35063980 | C | T | 17 | a0001c0001t0002g0009 a0001c0001t0002g0029 a0001c0001t0002g0031 others(14): Show |
18 | HG00558.hp1 HG02027.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.123-6215C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063980 | |||||||
| chr18:35063997 | CT | C | 4 | a0001c0001t0009g0243 a0001c0001t0009g0258 a0001c0001t0017g0181 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-6195delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35063997 | ||||||
| chr18:35063999 | T | TA | 21 | a0001c0001t0005g0017 a0001c0001t0005g0177 a0001c0001t0005g0186 others(18): Show |
23 | HG00408.hp1 HG00544.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.123-6196_123-6195i others(3): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | T | TAA | 27 | a0001c0001t0001g0021 a0001c0001t0001g0294 a0001c0001t0003g0167 others(24): Show |
29 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-6196_123-6195i others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | T | TAAA | 5 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0330 others(2): Show |
5 | HG02647.hp1 HG03540.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-6196_123-6195i others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0002g0255 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123-6196_123-6195i others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | T | TAAAAAAA others(4): Show |
1 | a0001c0001t0002g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.123-6196_123-6195i others(13): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0001g0327 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.123-6196_123-6195i others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | T | TAAAAAAA others(7): Show |
4 | a0001c0001t0002g0018 a0001c0001t0002g0236 a0001c0001t0002g0239 others(1): Show |
5 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-6196_123-6195i others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | T | TAAAAAAA others(8): Show |
2 | a0001c0001t0001g0332 a0001c0001t0002g0253 |
2 | HG02451.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.123-6196_123-6195i others(17): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-6196_123-6195i others(19): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | TTA | T | 14 | a0001c0001t0009g0242 a0001c0001t0009g0244 a0001c0001t0009g0245 others(11): Show |
14 | HG02258.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.123-6195_123-6194d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | TTAAAAAA others(1): Show |
T | 14 | a0001c0001t0002g0031 a0001c0001t0002g0040 a0001c0001t0002g0046 others(11): Show |
14 | HG00621.hp2 HG01168.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.123-6195_123-6188d others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | TTAAAAAA others(2): Show |
T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(60): Show |
69 | HG00408.hp2 HG00558.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.123-6195_123-6187d others(11): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | TTAAAAAA others(3): Show |
T | 2 | a0001c0001t0004g0092 a0001c0001t0004g0098 |
2 | HG00639.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.123-6195_123-6186d others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | TTAAAAAA others(7): Show |
T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-6195_123-6182d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | TTAAAAAA others(10): Show |
T | 5 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0009g0217 others(2): Show |
5 | HG02717.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-6195_123-6179d others(19): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35063999 | TTAAAAAA others(11): Show |
T | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.123-6195_123-6178d others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | |||||||
| chr18:35064000 | T | A | 70 | a0001c0001t0001g0021 a0001c0001t0001g0294 a0001c0001t0001g0327 others(67): Show |
77 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.123-6195T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064000 | |||||||
| chr18:35064000 | T | TA | 26 | a0001c0001t0001g0160 a0001c0001t0001g0222 a0001c0001t0001g0312 others(23): Show |
29 | HG00597.hp1 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-6162dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAA | 13 | a0001c0001t0001g0102 a0001c0001t0001g0213 a0001c0001t0001g0254 others(10): Show |
14 | HG00558.hp2 HG02559.hp2 HG02683.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-6163_123-6162d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAA | 16 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0109 others(13): Show |
16 | HG01123.hp1 HG02074.hp2 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.123-6164_123-6162d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(1): Show |
7 | a0001c0001t0001g0003 a0001c0001t0001g0265 a0001c0001t0001g0299 others(4): Show |
7 | HG01168.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-6169_123-6162d others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(2): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0269 a0001c0001t0001g0270 others(5): Show |
8 | HG01192.hp1 HG01243.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-6170_123-6162d others(11): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(4): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0020 |
2 | HG03669.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.123-6172_123-6162d others(13): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(5): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0022 others(7): Show |
10 | HG01167.hp2 HG01433.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.123-6173_123-6162d others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(6): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(9): Show |
13 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-6174_123-6162d others(15): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(7): Show |
3 | a0001c0001t0001g0019 a0001c0001t0001g0173 a0001c0001t0010g0275 |
4 | HG01109.hp2 HG02683.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-6175_123-6162d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(8): Show |
5 | a0001c0001t0001g0266 a0001c0001t0001g0272 a0001c0001t0001g0282 others(2): Show |
5 | HG01081.hp1 HG01106.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-6176_123-6162d others(17): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(9): Show |
1 | a0001c0001t0001g0287 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.123-6177_123-6162d others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0280 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.123-6178_123-6162d others(19): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(11): Show |
1 | a0001c0001t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.123-6179_123-6162d others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(12): Show |
2 | a0001c0001t0001g0002 a0001c0001t0030g0293 |
2 | HG02040.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.123-6180_123-6162d others(21): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(13): Show |
1 | a0001c0001t0001g0002 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.123-6181_123-6162d others(22): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0001g0273 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.123-6182_123-6162d others(23): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0320 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.123-6184_123-6162d others(25): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | T | TAAAAAAA others(17): Show |
1 | a0001c0001t0001g0002 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.123-6185_123-6162d others(26): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | TA | T | 8 | a0001c0001t0003g0143 a0001c0001t0003g0156 a0001c0001t0007g0225 others(5): Show |
8 | HG01993.hp2 HG02451.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-6162delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | TAAAA | T | 8 | a0001c0001t0002g0107 a0001c0001t0003g0276 a0001c0001t0012g0209 others(5): Show |
8 | HG01517.hp1 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-6165_123-6162d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064000 | TAAAAAAA others(7): Show |
T | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.123-6175_123-6162d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | ||||||
| chr18:35064033 | A | T | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123-6162A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064033 | |||||||
| chr18:35064150 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-6045C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064150 | |||||||
| chr18:35064197 | CA | C | 182 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0034 others(179): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.123-5985delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064197 | ||||||
| chr18:35064217 | T | C | 1 | a0001c0001t0003g0012 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.123-5978T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064217 | |||||||
| chr18:35064292 | C | T | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
307 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.123-5903C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064292 | |||||||
| chr18:35064361 | G | C | 12 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(9): Show |
15 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.123-5834G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064361 | |||||||
| chr18:35064372 | G | GA | 175 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0034 others(172): Show |
188 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.123-5821dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064372 | ||||||
| chr18:35064430 | G | A | 3 | a0001c0001t0004g0066 a0001c0001t0004g0081 a0001c0001t0004g0096 |
3 | NA18983.hp2 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.123-5765G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064430 | |||||||
| chr18:35064496 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.123-5699A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064496 | |||||||
| chr18:35064527 | A | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0034 others(172): Show |
188 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.123-5668A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064527 | |||||||
| chr18:35064562 | A | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0034 others(172): Show |
188 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.123-5633A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064562 | |||||||
| chr18:35064624 | C | T | 330 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(327): Show |
363 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(360): Show |
intron_variant | MODIFIER | c.123-5571C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064624 | |||||||
| chr18:35065222 | A | G | 1 | a0001c0001t0029g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.123-4973A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065222 | |||||||
| chr18:35065276 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0041g0158 |
2 | HG02922.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.123-4919C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065276 | |||||||
| chr18:35065350 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-4845T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065350 | |||||||
| chr18:35065768 | G | A | 11 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(8): Show |
14 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-4427G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065768 | |||||||
| chr18:35065774 | G | A | 1 | a0001c0001t0005g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.123-4421G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065774 | |||||||
| chr18:35065890 | T | C | 174 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0034 others(171): Show |
187 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.123-4305T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065890 | |||||||
| chr18:35065946 | G | T | 1 | a0001c0001t0030g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.123-4249G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065946 | |||||||
| chr18:35065948 | A | C | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.123-4247A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065948 | |||||||
| chr18:35065981 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.123-4214G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065981 | |||||||
| chr18:35066213 | G | A | 66 | a0001c0001t0003g0167 a0001c0001t0003g0322 a0001c0001t0005g0016 others(63): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.123-3982G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066213 | |||||||
| chr18:35066313 | G | A | 10 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(7): Show |
13 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-3882G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066313 | |||||||
| chr18:35066365 | T | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0160 others(79): Show |
88 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.123-3830T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066365 | |||||||
| chr18:35066379 | C | T | 1 | a0001c0001t0009g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-3816C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066379 | |||||||
| chr18:35066468 | C | T | 27 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0002g0009 others(24): Show |
28 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.123-3727C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066468 | |||||||
| chr18:35066768 | T | C | 3 | a0001c0001t0011g0058 a0001c0001t0011g0059 a0001c0001t0011g0060 |
3 | HG01884.hp2 HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.123-3427T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066768 | |||||||
| chr18:35066816 | T | G | 186 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0160 others(183): Show |
198 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.123-3379T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066816 | |||||||
| chr18:35067003 | T | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-3192T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067003 | |||||||
| chr18:35067114 | A | G | 1 | a0001c0001t0006g0197 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.123-3081A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067114 | |||||||
| chr18:35067137 | T | G | 7 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-3058T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067137 | |||||||
| chr18:35067171 | G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-3024G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067171 | |||||||
| chr18:35067399 | C | T | 183 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0160 others(180): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.123-2796C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067399 | |||||||
| chr18:35067515 | G | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-2680G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067515 | |||||||
| chr18:35067601 | T | A | 3 | a0001c0001t0002g0255 a0001c0001t0002g0256 a0001c0001t0002g0257 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.123-2594T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067601 | |||||||
| chr18:35067621 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.123-2574A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067621 | |||||||
| chr18:35067635 | T | G | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-2560T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067635 | |||||||
| chr18:35067685 | G | A | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-2510G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067685 | |||||||
| chr18:35067974 | C | T | 1 | a0001c0001t0005g0193 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.123-2221C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067974 | |||||||
| chr18:35067984 | T | A | 183 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0160 others(180): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.123-2211T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067984 | |||||||
| chr18:35068091 | C | T | 1 | a0001c0001t0012g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123-2104C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068091 | |||||||
| chr18:35068220 | A | G | 166 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0160 others(163): Show |
178 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.123-1975A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068220 | |||||||
| chr18:35068326 | G | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0160 others(80): Show |
89 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.123-1869G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068326 | |||||||
| chr18:35068462 | G | T | 5 | a0001c0001t0009g0258 a0001c0001t0015g0240 a0001c0001t0015g0260 others(2): Show |
5 | HG01243.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-1733G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068462 | |||||||
| chr18:35068506 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0160 others(164): Show |
179 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.123-1689A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068506 | |||||||
| chr18:35068581 | C | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-1614C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068581 | |||||||
| chr18:35068840 | C | T | 1 | a0001c0001t0003g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.123-1355C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068840 | |||||||
| chr18:35068887 | C | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-1308C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068887 | |||||||
| chr18:35068929 | C | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-1266C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068929 | |||||||
| chr18:35069226 | A | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0004g0005 others(39): Show |
47 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.123-969A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069226 | |||||||
| chr18:35069273 | T | C | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.123-922T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069273 | |||||||
| chr18:35069381 | G | GT | 10 | a0001c0001t0002g0107 a0001c0001t0012g0209 a0001c0001t0012g0210 others(7): Show |
10 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-806dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35069381 | ||||||
| chr18:35069388 | T | TA | 136 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(133): Show |
145 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.123-807_123-806ins others(1): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069388 | |||||||
| chr18:35069389 | T | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0288 others(137): Show |
149 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.123-806T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069389 | |||||||
| chr18:35069389 | T | TA | 35 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(32): Show |
38 | HG00642.hp1 HG00735.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-801dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35069389 | ||||||
| chr18:35069425 | T | C | 11 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0236 others(8): Show |
14 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-770T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069425 | |||||||
| chr18:35069469 | G | A | 3 | a0001c0001t0004g0005 a0001c0001t0004g0071 a0001c0001t0004g0082 |
5 | HG00408.hp2 NA18964.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-726G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069469 | |||||||
| chr18:35069531 | A | T | 164 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(161): Show |
176 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.123-664A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069531 | |||||||
| chr18:35069542 | T | C | 1 | a0001c0001t0008g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.123-653T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069542 | |||||||
| chr18:35069662 | A | T | 171 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(168): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.123-533A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069662 | |||||||
| chr18:35069754 | C | A | 1 | a0001c0001t0001g0283 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.123-441C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069754 | |||||||
| chr18:35069802 | C | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-393C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069802 | |||||||
| chr18:35069870 | G | GCTA | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-323_123-321dup others(3): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35069870 | ||||||
| chr18:35069901 | C | T | 2 | a0001c0001t0005g0191 a0001c0001t0005g0192 |
2 | NA18981.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.123-294C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069901 | |||||||
| chr18:35070092 | T | C | 1 | a0001c0001t0004g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.123-103T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35070092 | |||||||
| chr18:35070128 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0333 |
2 | NA18612.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.123-67G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35070128 | |||||||
| chr18:35070181 | T | C | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-14T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35070181 | |||||||
| chr18:35070330 | A | T | 7 | a0001c0001t0004g0075 a0001c0001t0004g0091 a0001c0001t0004g0095 others(4): Show |
7 | NA18939.hp2 NA18975.hp2 NA19001.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.250+8A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070330 | |||||||
| chr18:35070332 | AT | A | 7 | a0001c0001t0004g0075 a0001c0001t0004g0091 a0001c0001t0004g0095 others(4): Show |
7 | NA18939.hp2 NA18975.hp2 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+12delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35070332 | ||||||
| chr18:35070363 | G | C | 2 | a0001c0001t0013g0205 a0001c0001t0013g0206 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.250+41G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070363 | |||||||
| chr18:35070377 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(88): Show |
102 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.250+55A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070377 | |||||||
| chr18:35070585 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250+263C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070585 | |||||||
| chr18:35070685 | C | T | 3 | a0001c0001t0001g0264 a0001c0001t0033g0218 a0001c0001t0034g0219 |
3 | HG02630.hp1 HG03225.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.250+363C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070685 | |||||||
| chr18:35070842 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250+520C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070842 | |||||||
| chr18:35071003 | A | G | 164 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(161): Show |
176 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.250+681A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071003 | |||||||
| chr18:35071095 | T | C | 4 | a0001c0001t0001g0103 a0001c0001t0001g0213 a0001c0001t0001g0274 others(1): Show |
4 | HG01123.hp1 HG03239.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+773T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071095 | |||||||
| chr18:35071124 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02074.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.250+802G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071124 | |||||||
| chr18:35071299 | TG | T | 164 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(161): Show |
176 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.250+978delG | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071299 | |||||||
| chr18:35071607 | G | A | 10 | a0001c0001t0002g0107 a0001c0001t0012g0209 a0001c0001t0012g0210 others(7): Show |
10 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.250+1285G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071607 | |||||||
| chr18:35071756 | C | G | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250+1434C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071756 | |||||||
| chr18:35071832 | C | G | 172 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0034 others(169): Show |
185 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.250+1510C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071832 | |||||||
| chr18:35071834 | C | A | 1 | a0001c0001t0001g0315 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250+1512C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071834 | |||||||
| chr18:35071993 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250+1671G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071993 | |||||||
| chr18:35072021 | A | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+1699A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072021 | |||||||
| chr18:35072087 | C | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+1765C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072087 | |||||||
| chr18:35072102 | A | G | 1 | a0001c0001t0003g0149 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.250+1780A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072102 | |||||||
| chr18:35072346 | G | A | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250+2024G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072346 | |||||||
| chr18:35072415 | T | G | 83 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(80): Show |
89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.250+2093T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072415 | |||||||
| chr18:35072697 | A | T | 1 | a0001c0001t0002g0031 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.250+2375A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072697 | |||||||
| chr18:35072761 | G | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+2439G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072761 | |||||||
| chr18:35072816 | A | G | 1 | a0001c0001t0004g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.250+2494A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072816 | |||||||
| chr18:35072925 | A | G | 1 | a0001c0001t0002g0031 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.250+2603A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072925 | |||||||
| chr18:35072934 | G | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+2612G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072934 | |||||||
| chr18:35072959 | CTCCATAG others(3): Show |
C | 1 | a0001c0001t0002g0031 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.250+2638_250+2647d others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072959 | |||||||
| chr18:35073029 | T | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0034 others(176): Show |
192 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.250+2707T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073029 | |||||||
| chr18:35073057 | A | G | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+2735A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073057 | |||||||
| chr18:35073083 | G | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(161): Show |
176 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.250+2761G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073083 | |||||||
| chr18:35073153 | T | G | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.250+2831T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073153 | |||||||
| chr18:35073184 | A | T | 1 | a0001c0001t0003g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.250+2862A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073184 | |||||||
| chr18:35073243 | C | G | 1 | a0001c0001t0010g0297 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.250+2921C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073243 | |||||||
| chr18:35073244 | T | C | 2 | a0001c0001t0013g0205 a0001c0001t0013g0206 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.250+2922T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073244 | |||||||
| chr18:35073285 | T | A | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250+2963T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073285 | |||||||
| chr18:35073320 | C | A | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250+2998C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073320 | |||||||
| chr18:35073445 | G | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+3123G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073445 | |||||||
| chr18:35073526 | A | C | 1 | a0001c0001t0023g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.250+3204A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073526 | |||||||
| chr18:35073565 | T | G | 25 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0029 others(22): Show |
26 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.250+3243T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073565 | |||||||
| chr18:35073954 | A | G | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.250+3632A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073954 | |||||||
| chr18:35074273 | A | G | 1 | a0001c0001t0017g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.250+3951A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074273 | |||||||
| chr18:35074279 | G | T | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.250+3957G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074279 | |||||||
| chr18:35074289 | A | AT | 8 | a0001c0001t0001g0325 a0001c0001t0007g0225 a0001c0001t0007g0226 others(5): Show |
8 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+3976dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35074289 | ||||||
| chr18:35074472 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.250+4150G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074472 | |||||||
| chr18:35074576 | G | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+4254G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074576 | |||||||
| chr18:35074590 | A | G | 1 | a0001c0001t0006g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.250+4268A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074590 | |||||||
| chr18:35074783 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.250+4461G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074783 | |||||||
| chr18:35074865 | ACTGTCAC others(3): Show |
A | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.250+4553_250+4562d others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35074865 | ||||||
| chr18:35075003 | A | G | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.250+4681A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075003 | |||||||
| chr18:35075218 | A | T | 1 | a0001c0001t0008g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.250+4896A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075218 | |||||||
| chr18:35075249 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(150): Show |
162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.250+4927G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075249 | |||||||
| chr18:35075602 | A | G | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+5280A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075602 | |||||||
| chr18:35075620 | T | G | 1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.250+5298T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075620 | |||||||
| chr18:35075727 | A | G | 2 | a0001c0001t0004g0077 a0001c0001t0004g0079 |
2 | NA18989.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.250+5405A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075727 | |||||||
| chr18:35075914 | TC | T | 66 | a0001c0001t0003g0167 a0001c0001t0003g0322 a0001c0001t0005g0016 others(63): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.250+5595delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35075914 | ||||||
| chr18:35075921 | A | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(152): Show |
164 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.250+5599A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075921 | |||||||
| chr18:35075966 | G | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+5644G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075966 | |||||||
| chr18:35076026 | T | C | 2 | a0001c0001t0009g0245 a0001c0001t0009g0246 |
2 | HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.250+5704T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076026 | |||||||
| chr18:35076111 | A | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(152): Show |
164 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.250+5789A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076111 | |||||||
| chr18:35076140 | C | T | 154 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(151): Show |
163 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.250+5818C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076140 | |||||||
| chr18:35076226 | C | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+5904C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076226 | |||||||
| chr18:35076539 | G | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6217G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076539 | |||||||
| chr18:35076561 | C | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6239C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076561 | |||||||
| chr18:35076768 | C | T | 10 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(7): Show |
13 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.250+6446C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076768 | |||||||
| chr18:35076793 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.250+6471T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076793 | |||||||
| chr18:35076825 | C | T | 10 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(7): Show |
13 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.250+6503C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076825 | |||||||
| chr18:35076971 | T | C | 180 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(177): Show |
192 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.250+6649T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076971 | |||||||
| chr18:35077024 | C | T | 38 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0029 others(35): Show |
39 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.250+6702C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077024 | |||||||
| chr18:35077238 | CGT | C | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6918_250+6919d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077238 | ||||||
| chr18:35077239 | G | A | 1 | a0001c0001t0013g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.250+6917G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077239 | |||||||
| chr18:35077240 | TGC | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(49): Show |
62 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.250+6927_250+6928d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077240 | ||||||
| chr18:35077243 | G | A | 4 | a0001c0001t0004g0065 a0001c0001t0004g0072 a0001c0001t0004g0076 others(1): Show |
4 | NA18956.hp1 NA19066.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+6921G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077243 | |||||||
| chr18:35077244 | C | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6922C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077244 | |||||||
| chr18:35077245 | GCGCGCAC others(5): Show |
G | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.250+6925_250+6936d others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077245 | ||||||
| chr18:35077247 | GCGCA | G | 22 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(19): Show |
23 | HG01884.hp1 HG01891.hp1 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.250+6927_250+6930d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | ||||||
| chr18:35077247 | GCGCACA | G | 22 | a0001c0001t0002g0007 a0001c0001t0002g0224 a0001c0001t0002g0233 others(19): Show |
24 | HG00642.hp1 HG01099.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.250+6927_250+6932d others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | ||||||
| chr18:35077247 | GCGCACAC others(7): Show |
G | 1 | a0001c0001t0005g0187 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.250+6927_250+6940d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | ||||||
| chr18:35077247 | GCGCACAC others(9): Show |
G | 72 | a0001c0001t0001g0021 a0001c0001t0001g0294 a0001c0001t0001g0327 others(69): Show |
75 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.250+6927_250+6942d others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | ||||||
| chr18:35077247 | GCGCACAC others(11): Show |
G | 6 | a0001c0001t0006g0006 a0001c0001t0006g0190 a0001c0001t0007g0025 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+6927_250+6944d others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | ||||||
| chr18:35077247 | GCGCACAC others(15): Show |
G | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.250+6927_250+6948d others(24): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | ||||||
| chr18:35077249 | G | A | 67 | a0001c0001t0001g0013 a0001c0001t0001g0102 a0001c0001t0001g0103 others(64): Show |
77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.250+6927G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077249 | |||||||
| chr18:35077251 | A | G | 3 | a0001c0001t0002g0107 a0001c0001t0011g0060 a0001c0001t0035g0208 |
3 | HG01884.hp2 HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.250+6929A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077251 | |||||||
| chr18:35077258 | CACACACA others(7): Show |
C | 2 | a0001c0001t0002g0107 a0001c0001t0035g0208 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.250+6950_250+6963d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077258 | ||||||
| chr18:35077260 | CACACACA others(5): Show |
C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250+6950_250+6961d others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077260 | ||||||
| chr18:35077262 | CACACACA others(3): Show |
C | 7 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6950_250+6959d others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077262 | ||||||
| chr18:35077264 | CACACACA others(1): Show |
C | 3 | a0001c0001t0002g0220 a0001c0001t0004g0010 a0001c0001t0004g0097 |
3 | HG01109.hp1 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.250+6950_250+6957d others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077264 | ||||||
| chr18:35077266 | CACACAT | C | 40 | a0001c0001t0001g0034 a0001c0001t0002g0009 a0001c0001t0002g0029 others(37): Show |
41 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.250+6950_250+6955d others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077266 | ||||||
| chr18:35077268 | CACAT | C | 26 | a0001c0001t0002g0028 a0001c0001t0002g0047 a0001c0001t0002g0049 others(23): Show |
28 | HG01167.hp1 HG01168.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.250+6950_250+6953d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077268 | ||||||
| chr18:35077270 | CAT | C | 3 | a0001c0001t0001g0004 a0001c0001t0004g0071 a0001c0001t0031g0083 |
5 | HG00408.hp2 NA18952.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+6950_250+6951d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077270 | ||||||
| chr18:35077272 | T | C | 81 | a0001c0001t0001g0021 a0001c0001t0001g0294 a0001c0001t0001g0327 others(78): Show |
85 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.250+6950T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077272 | |||||||
| chr18:35077272 | TAC | T | 8 | a0001c0001t0002g0224 a0001c0001t0007g0225 a0001c0001t0007g0226 others(5): Show |
8 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+6968_250+6969d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077272 | ||||||
| chr18:35077275 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0004g0070 a0001c0001t0004g0080 |
3 | HG02155.hp2 NA18945.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.250+6953A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077275 | |||||||
| chr18:35077292 | A | G | 2 | a0001c0001t0007g0228 a0001c0001t0007g0231 |
2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.250+6970A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077292 | |||||||
| chr18:35077303 | G | A | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.250+6981G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077303 | |||||||
| chr18:35077315 | G | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6993G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077315 | |||||||
| chr18:35077578 | T | C | 4 | a0001c0001t0003g0122 a0001c0001t0003g0136 a0001c0001t0003g0137 others(1): Show |
4 | HG01106.hp2 HG01346.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+7256T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077578 | |||||||
| chr18:35077622 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.250+7300A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077622 | |||||||
| chr18:35077652 | A | G | 8 | a0001c0001t0001g0222 a0001c0001t0002g0232 a0001c0001t0002g0233 others(5): Show |
8 | HG02257.hp2 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+7330A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077652 | |||||||
| chr18:35077676 | G | A | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.250+7354G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077676 | |||||||
| chr18:35078052 | G | A | 1 | a0001c0001t0003g0167 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.250+7730G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078052 | |||||||
| chr18:35078064 | A | C | 1 | a0001c0001t0001g0319 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.250+7742A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078064 | |||||||
| chr18:35078286 | T | G | 1 | a0001c0001t0006g0194 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.250+7964T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078286 | |||||||
| chr18:35078629 | G | T | 1 | a0001c0001t0002g0037 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250+8307G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078629 | |||||||
| chr18:35078630 | G | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(80): Show |
89 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.250+8308G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078630 | |||||||
| chr18:35078640 | A | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(152): Show |
164 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.250+8318A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078640 | |||||||
| chr18:35078671 | A | T | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250+8349A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078671 | |||||||
| chr18:35078729 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.250+8407C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078729 | |||||||
| chr18:35078751 | C | CT | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+8432dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35078751 | ||||||
| chr18:35078760 | C | T | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.250+8438C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078760 | |||||||
| chr18:35078819 | G | C | 2 | a0001c0001t0005g0157 a0001c0001t0005g0214 |
2 | HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.250+8497G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078819 | |||||||
| chr18:35078920 | T | G | 1 | a0001c0001t0027g0035 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.250+8598T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078920 | |||||||
| chr18:35078952 | T | A | 4 | a0001c0001t0002g0233 a0001c0001t0005g0157 a0001c0001t0005g0214 others(1): Show |
4 | HG02615.hp1 HG02683.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+8630T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078952 | |||||||
| chr18:35078965 | TC | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+8645delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35078965 | ||||||
| chr18:35079254 | A | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(80): Show |
89 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.250+8932A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079254 | |||||||
| chr18:35079305 | C | T | 1 | a0001c0001t0002g0007 | 3 | HG00642.hp1 HG01099.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.250+8983C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079305 | |||||||
| chr18:35079385 | T | C | 1 | a0001c0001t0036g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.250+9063T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079385 | |||||||
| chr18:35079456 | C | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+9134C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079456 | |||||||
| chr18:35079496 | C | T | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+9174C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079496 | |||||||
| chr18:35079736 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0007g0223 a0001c0001t0013g0152 |
3 | HG02257.hp2 HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.250+9414C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079736 | |||||||
| chr18:35079747 | A | G | 2 | a0001c0001t0037g0316 a0001c0001t0038g0321 |
2 | HG01070.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.250+9425A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079747 | |||||||
| chr18:35079851 | A | C | 9 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0236 others(6): Show |
12 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+9529A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079851 | |||||||
| chr18:35079902 | T | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+9580T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079902 | |||||||
| chr18:35079976 | A | G | 1 | a0001c0001t0005g0170 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.250+9654A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079976 | |||||||
| chr18:35080000 | C | A | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.250+9678C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080000 | |||||||
| chr18:35080025 | C | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+9703C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080025 | |||||||
| chr18:35080065 | CCAAA | C | 3 | a0001c0001t0024g0237 a0001c0001t0024g0238 a0001c0001t0028g0259 |
3 | HG03209.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.250+9746_250+9749d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35080065 | ||||||
| chr18:35080212 | A | G | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250+9890A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080212 | |||||||
| chr18:35080228 | A | G | 180 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(177): Show |
192 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.250+9906A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080228 | |||||||
| chr18:35080785 | C | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+10463C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080785 | |||||||
| chr18:35080812 | GC | G | 157 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(154): Show |
166 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.250+10491delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080812 | |||||||
| chr18:35080813 | C | G | 3 | a0001c0001t0005g0168 a0001c0001t0005g0199 a0001c0001t0005g0201 |
3 | HG02735.hp1 HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.250+10491C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080813 | |||||||
| chr18:35080815 | T | G | 157 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(154): Show |
166 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.250+10493T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080815 | |||||||
| chr18:35080880 | C | G | 1 | a0001c0001t0002g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.250+10558C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080880 | |||||||
| chr18:35080980 | T | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+10658T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080980 | |||||||
| chr18:35081042 | T | C | 1 | a0001c0001t0018g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.250+10720T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081042 | |||||||
| chr18:35081055 | A | T | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+10733A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081055 | |||||||
| chr18:35081213 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0007g0223 a0001c0001t0013g0152 |
3 | HG02257.hp2 HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.250+10891T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081213 | |||||||
| chr18:35081291 | A | T | 191 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0222 others(188): Show |
203 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.250+10969A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081291 | |||||||
| chr18:35081453 | T | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0009 others(150): Show |
162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.250+11131T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081453 | |||||||
| chr18:35081507 | C | T | 4 | a0001c0001t0005g0183 a0001c0001t0005g0184 a0001c0001t0005g0186 others(1): Show |
4 | HG00423.hp2 HG02071.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+11185C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081507 | |||||||
| chr18:35081517 | G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+11195G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081517 | |||||||
| chr18:35081537 | C | T | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250+11215C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081537 | |||||||
| chr18:35081654 | C | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0287 |
3 | HG01167.hp2 HG01361.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.250+11332C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081654 | |||||||
| chr18:35081737 | C | T | 1 | a0001c0001t0013g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.250+11415C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081737 | |||||||
| chr18:35081858 | A | G | 2 | a0001c0001t0033g0218 a0001c0001t0034g0219 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.250+11536A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081858 | |||||||
| chr18:35081990 | TAAAAATA others(310): Show |
T | 183 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(180): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.250+11687_250+1200 others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35081990 | ||||||
| chr18:35082146 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250+11824C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082146 | |||||||
| chr18:35082182 | T | C | 1 | a0001c0001t0003g0001 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.250+11860T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082182 | |||||||
| chr18:35082183 | G | C | 1 | a0001c0001t0003g0001 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.250+11861G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082183 | |||||||
| chr18:35082215 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250+11893G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082215 | |||||||
| chr18:35082246 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.250+11924C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082246 | |||||||
| chr18:35082289 | C | CA | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0108 others(15): Show |
18 | HG00423.hp1 HG01109.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.250+11990dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35082289 | ||||||
| chr18:35082289 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0002g0232 a0001c0001t0007g0252 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.250+11978_250+1199 others(17): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35082289 | ||||||
| chr18:35082289 | CA | C | 6 | a0001c0001t0001g0267 a0001c0001t0001g0325 a0001c0001t0003g0001 others(3): Show |
6 | HG01070.hp2 HG02015.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+11990delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35082289 | ||||||
| chr18:35082320 | G | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+11998G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082320 | |||||||
| chr18:35082382 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.250+12060T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082382 | |||||||
| chr18:35082385 | G | A | 2 | a0001c0001t0002g0236 a0001c0001t0002g0253 |
2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.250+12063G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082385 | |||||||
| chr18:35082399 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.250+12077T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082399 | |||||||
| chr18:35082587 | A | G | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+12265A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082587 | |||||||
| chr18:35082632 | T | G | 1 | a0001c0001t0007g0229 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.250+12310T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082632 | |||||||
| chr18:35082789 | TG | T | 4 | a0001c0001t0002g0009 a0001c0001t0002g0040 a0001c0001t0007g0027 others(1): Show |
5 | NA18939.hp1 NA18951.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+12468delG | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082789 | |||||||
| chr18:35082851 | T | G | 1 | a0001c0001t0011g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.250+12529T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082851 | |||||||
| chr18:35082859 | T | C | 10 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(7): Show |
13 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.250+12537T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082859 | |||||||
| chr18:35082901 | T | C | 1 | a0001c0001t0006g0194 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.250+12579T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082901 | |||||||
| chr18:35083007 | T | G | 1 | a0001c0001t0002g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.250+12685T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083007 | |||||||
| chr18:35083254 | G | A | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+12932G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083254 | |||||||
| chr18:35083563 | G | A | 1 | a0001c0001t0002g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.250+13241G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083563 | |||||||
| chr18:35083564 | C | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(150): Show |
162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.250+13242C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083564 | |||||||
| chr18:35083601 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.250+13279A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083601 | |||||||
| chr18:35083724 | A | G | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+13402A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083724 | |||||||
| chr18:35083764 | C | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(150): Show |
162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.250+13442C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083764 | |||||||
| chr18:35083765 | G | A | 10 | a0001c0001t0001g0021 a0001c0001t0001g0283 a0001c0001t0001g0294 others(7): Show |
11 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+13443G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083765 | |||||||
| chr18:35083775 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250+13453C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083775 | |||||||
| chr18:35083957 | TG | T | 20 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0107 others(17): Show |
23 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.251-13488delG | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083957 | |||||||
| chr18:35084302 | A | G | 1 | a0001c0001t0003g0135 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.251-13144A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084302 | |||||||
| chr18:35084341 | G | C | 1 | a0001c0001t0004g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.251-13105G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084341 | |||||||
| chr18:35084374 | C | T | 2 | a0001c0001t0004g0068 a0001c0001t0004g0069 |
2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.251-13072C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084374 | |||||||
| chr18:35084804 | A | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-12642A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084804 | |||||||
| chr18:35084890 | G | T | 160 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(157): Show |
169 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.251-12556G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084890 | |||||||
| chr18:35085060 | A | G | 10 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(7): Show |
13 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-12386A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085060 | |||||||
| chr18:35085075 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.251-12371A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085075 | |||||||
| chr18:35085205 | T | C | 2 | a0001c0001t0002g0236 a0001c0001t0002g0253 |
2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.251-12241T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085205 | |||||||
| chr18:35085347 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(150): Show |
162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.251-12099G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085347 | |||||||
| chr18:35085386 | C | T | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.251-12060C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085386 | |||||||
| chr18:35085457 | T | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(78): Show |
87 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.251-11989T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085457 | |||||||
| chr18:35085797 | C | G | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
307 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.251-11649C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085797 | |||||||
| chr18:35086215 | A | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(150): Show |
162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.251-11231A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086215 | |||||||
| chr18:35086549 | T | C | 7 | a0001c0001t0001g0222 a0001c0001t0002g0233 a0001c0001t0005g0157 others(4): Show |
7 | HG02257.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-10897T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086549 | |||||||
| chr18:35086581 | T | A | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251-10865T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086581 | |||||||
| chr18:35086847 | A | G | 1 | a0001c0001t0012g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.251-10599A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086847 | |||||||
| chr18:35086896 | T | C | 189 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(186): Show |
201 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(198): Show |
intron_variant | MODIFIER | c.251-10550T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086896 | |||||||
| chr18:35087254 | GT | G | 9 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(6): Show |
9 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-10186delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35087254 | ||||||
| chr18:35087285 | T | G | 3 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0050 |
3 | HG02735.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.251-10161T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35087285 | |||||||
| chr18:35087388 | A | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-10058A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35087388 | |||||||
| chr18:35087634 | T | G | 2 | a0001c0001t0024g0237 a0001c0001t0024g0238 |
2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.251-9812T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35087634 | |||||||
| chr18:35087816 | T | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-9630T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35087816 | |||||||
| chr18:35088184 | A | C | 156 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(153): Show |
165 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.251-9262A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088184 | |||||||
| chr18:35088209 | T | C | 183 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(180): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.251-9237T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088209 | |||||||
| chr18:35088242 | G | A | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251-9204G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088242 | |||||||
| chr18:35088357 | T | C | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-9089T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088357 | |||||||
| chr18:35088431 | G | T | 1 | a0001c0001t0005g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.251-9015G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088431 | |||||||
| chr18:35088500 | G | A | 3 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 |
3 | HG02896.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.251-8946G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088500 | |||||||
| chr18:35089161 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0007g0223 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.251-8285A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089161 | |||||||
| chr18:35089248 | G | A | 98 | a0001c0001t0001g0104 a0001c0001t0002g0009 a0001c0001t0002g0028 others(95): Show |
101 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.251-8198G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089248 | |||||||
| chr18:35089298 | T | C | 1 | a0001c0001t0021g0063 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.251-8148T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089298 | |||||||
| chr18:35089349 | C | A | 1 | a0001c0001t0017g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.251-8097C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089349 | |||||||
| chr18:35089476 | T | A | 91 | a0001c0001t0001g0104 a0001c0001t0002g0009 a0001c0001t0002g0028 others(88): Show |
94 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.251-7970T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089476 | |||||||
| chr18:35089533 | GC | G | 91 | a0001c0001t0001g0104 a0001c0001t0002g0009 a0001c0001t0002g0028 others(88): Show |
94 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.251-7911delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35089533 | ||||||
| chr18:35089648 | A | G | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-7798A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089648 | |||||||
| chr18:35089674 | C | A | 3 | a0001c0001t0003g0130 a0001c0001t0003g0132 a0001c0001t0016g0131 |
3 | HG00642.hp2 HG01123.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.251-7772C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089674 | |||||||
| chr18:35089676 | C | T | 1 | a0001c0001t0004g0101 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.251-7770C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089676 | |||||||
| chr18:35089804 | T | C | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251-7642T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089804 | |||||||
| chr18:35089847 | G | T | 7 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-7599G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089847 | |||||||
| chr18:35089917 | G | A | 49 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0003g0167 others(46): Show |
51 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.251-7529G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089917 | |||||||
| chr18:35089977 | A | G | 1 | a0002c0003t0001g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.251-7469A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089977 | |||||||
| chr18:35090050 | A | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-7396A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090050 | |||||||
| chr18:35090057 | T | C | 293 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
319 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.251-7389T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090057 | |||||||
| chr18:35090173 | G | GT | 6 | a0001c0001t0003g0116 a0001c0001t0003g0132 a0001c0001t0003g0134 others(3): Show |
6 | HG00642.hp2 HG03098.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-7264dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35090173 | ||||||
| chr18:35090324 | A | G | 2 | a0001c0001t0033g0218 a0001c0001t0034g0219 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.251-7122A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090324 | |||||||
| chr18:35090533 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0004g0070 a0001c0001t0004g0080 |
3 | HG02155.hp2 NA18945.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.251-6913A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090533 | |||||||
| chr18:35090570 | A | C | 52 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(49): Show |
60 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.251-6876A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090570 | |||||||
| chr18:35090577 | C | T | 39 | a0001c0001t0001g0104 a0001c0001t0002g0009 a0001c0001t0002g0028 others(36): Show |
40 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.251-6869C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090577 | |||||||
| chr18:35090591 | T | G | 182 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(179): Show |
194 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.251-6855T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090591 | |||||||
| chr18:35090731 | CA | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
341 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.251-6700delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35090731 | ||||||
| chr18:35090731 | CAA | C | 14 | a0001c0001t0001g0222 a0001c0001t0001g0271 a0001c0001t0001g0317 others(11): Show |
14 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.251-6701_251-6700d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35090731 | ||||||
| chr18:35090733 | AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0033g0218 a0001c0001t0034g0219 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.251-6707_251-6694d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35090733 | ||||||
| chr18:35090839 | A | G | 1 | a0001c0001t0003g0153 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.251-6607A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090839 | |||||||
| chr18:35090886 | G | A | 1 | a0001c0001t0004g0075 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.251-6560G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090886 | |||||||
| chr18:35091152 | C | A | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.251-6294C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091152 | |||||||
| chr18:35091363 | T | C | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-6083T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091363 | |||||||
| chr18:35091497 | C | CTA | 39 | a0001c0001t0001g0104 a0001c0001t0002g0009 a0001c0001t0002g0028 others(36): Show |
40 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.251-5946_251-5945d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35091497 | ||||||
| chr18:35091624 | A | G | 1 | a0001c0001t0010g0302 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.251-5822A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091624 | |||||||
| chr18:35091641 | G | T | 2 | a0001c0001t0004g0087 a0001c0001t0004g0089 |
2 | HG01975.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.251-5805G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091641 | |||||||
| chr18:35091691 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.251-5755A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091691 | |||||||
| chr18:35091716 | C | T | 8 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-5730C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091716 | |||||||
| chr18:35091867 | G | T | 39 | a0001c0001t0001g0104 a0001c0001t0002g0009 a0001c0001t0002g0028 others(36): Show |
40 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.251-5579G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091867 | |||||||
| chr18:35091903 | G | T | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251-5543G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091903 | |||||||
| chr18:35091984 | A | G | 1 | a0001c0001t0005g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.251-5462A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091984 | |||||||
| chr18:35092030 | A | G | 192 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0104 others(189): Show |
204 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.251-5416A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092030 | |||||||
| chr18:35092058 | C | T | 1 | a0001c0001t0039g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.251-5388C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092058 | |||||||
| chr18:35092205 | G | T | 4 | a0001c0001t0009g0249 a0001c0001t0018g0247 a0001c0001t0018g0248 others(1): Show |
4 | HG00735.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-5241G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092205 | |||||||
| chr18:35092572 | A | T | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.251-4874A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092572 | |||||||
| chr18:35092590 | A | G | 5 | a0001c0001t0009g0258 a0001c0001t0015g0240 a0001c0001t0015g0260 others(2): Show |
5 | HG01243.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-4856A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092590 | |||||||
| chr18:35092810 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.251-4636C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092810 | |||||||
| chr18:35092872 | G | A | 293 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
319 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.251-4574G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092872 | |||||||
| chr18:35092904 | G | C | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.251-4542G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092904 | |||||||
| chr18:35092938 | G | A | 38 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0029 others(35): Show |
39 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.251-4508G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092938 | |||||||
| chr18:35093005 | A | G | 1 | a0001c0001t0012g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.251-4441A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093005 | |||||||
| chr18:35093211 | CA | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
186 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.251-4208delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35093211 | ||||||
| chr18:35093211 | CAA | C | 106 | a0001c0001t0001g0284 a0001c0001t0002g0028 a0001c0001t0002g0029 others(103): Show |
109 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.251-4209_251-4208d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35093211 | ||||||
| chr18:35093238 | A | G | 9 | a0001c0001t0001g0021 a0001c0001t0001g0294 a0001c0001t0001g0301 others(6): Show |
10 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.251-4208A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093238 | |||||||
| chr18:35093334 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.251-4112C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093334 | |||||||
| chr18:35093379 | A | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-4067A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093379 | |||||||
| chr18:35093464 | C | G | 2 | a0001c0001t0003g0126 a0001c0001t0003g0129 |
2 | HG04115.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.251-3982C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093464 | |||||||
| chr18:35093537 | T | C | 1 | a0001c0001t0004g0078 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.251-3909T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093537 | |||||||
| chr18:35093647 | C | T | 38 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0029 others(35): Show |
39 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.251-3799C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093647 | |||||||
| chr18:35093770 | A | G | 1 | a0001c0001t0018g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.251-3676A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093770 | |||||||
| chr18:35094101 | C | T | 2 | a0001c0001t0002g0236 a0001c0001t0002g0253 |
2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.251-3345C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094101 | |||||||
| chr18:35094102 | G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-3344G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094102 | |||||||
| chr18:35094201 | A | G | 4 | a0001c0001t0002g0009 a0001c0001t0002g0040 a0001c0001t0007g0027 others(1): Show |
5 | NA18939.hp1 NA18951.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-3245A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094201 | |||||||
| chr18:35094386 | A | G | 1 | a0001c0001t0003g0308 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.251-3060A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094386 | |||||||
| chr18:35094444 | A | G | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251-3002A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094444 | |||||||
| chr18:35094469 | A | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(176): Show |
191 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.251-2977A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094469 | |||||||
| chr18:35094956 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.251-2490C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094956 | |||||||
| chr18:35094965 | G | C | 1 | a0001c0001t0002g0042 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.251-2481G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094965 | |||||||
| chr18:35095278 | T | G | 1 | a0001c0001t0003g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.251-2168T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095278 | |||||||
| chr18:35095363 | T | TAC | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(53): Show |
70 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.251-2046_251-2045d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | ||||||
| chr18:35095363 | T | TACAC | 44 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(41): Show |
49 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.251-2048_251-2045d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | ||||||
| chr18:35095363 | T | TACACAC | 12 | a0001c0001t0001g0274 a0001c0001t0001g0309 a0001c0001t0001g0317 others(9): Show |
12 | HG00323.hp2 HG01099.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-2050_251-2045d others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | ||||||
| chr18:35095363 | T | TATAC | 8 | a0001c0001t0002g0224 a0001c0001t0002g0236 a0001c0001t0002g0253 others(5): Show |
8 | HG02080.hp2 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.251-2082_251-2081i others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | ||||||
| chr18:35095363 | T | TATACAC | 36 | a0001c0001t0001g0004 a0001c0001t0002g0007 a0001c0001t0002g0018 others(33): Show |
44 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.251-2082_251-2081i others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | ||||||
| chr18:35095363 | TAC | T | 4 | a0001c0001t0001g0287 a0001c0001t0003g0145 a0001c0001t0003g0147 others(1): Show |
4 | HG01081.hp2 HG02083.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-2046_251-2045d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | ||||||
| chr18:35095365 | C | T | 8 | a0001c0001t0001g0034 a0001c0001t0004g0070 a0001c0001t0004g0071 others(5): Show |
8 | HG00408.hp2 HG01346.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.251-2081C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095365 | |||||||
| chr18:35095386 | A | G | 1 | a0001c0001t0004g0074 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.251-2060A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095386 | |||||||
| chr18:35095390 | A | G | 1 | a0001c0001t0033g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.251-2056A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095390 | |||||||
| chr18:35095392 | A | ACACACG | 13 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(10): Show |
13 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-2049_251-2048i others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095392 | ||||||
| chr18:35095392 | A | G | 63 | a0001c0001t0001g0324 a0001c0001t0005g0016 a0001c0001t0005g0017 others(60): Show |
66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.251-2054A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095392 | |||||||
| chr18:35095394 | A | G | 54 | a0001c0001t0001g0004 a0001c0001t0002g0007 a0001c0001t0002g0018 others(51): Show |
62 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.251-2052A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095394 | |||||||
| chr18:35095396 | A | ACG | 7 | a0001c0001t0001g0222 a0001c0001t0002g0028 a0001c0001t0002g0105 others(4): Show |
7 | HG01109.hp1 HG02132.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-2049_251-2048i others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095396 | ||||||
| chr18:35095396 | A | G | 39 | a0001c0001t0002g0009 a0001c0001t0002g0029 a0001c0001t0002g0031 others(36): Show |
40 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.251-2050A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095396 | |||||||
| chr18:35095396 | ACACACG | A | 62 | a0001c0001t0001g0324 a0001c0001t0005g0016 a0001c0001t0005g0017 others(59): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.251-2044_251-2039d others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095396 | ||||||
| chr18:35095398 | A | G | 2 | a0001c0001t0007g0025 a0001c0001t0013g0024 |
2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251-2048A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095398 | |||||||
| chr18:35095398 | ACACG | A | 8 | a0001c0001t0003g0167 a0001c0001t0003g0322 a0001c0001t0005g0163 others(5): Show |
8 | HG02818.hp1 HG03041.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-2044_251-2041d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095398 | ||||||
| chr18:35095400 | ACG | A | 9 | a0001c0001t0002g0046 a0001c0001t0002g0107 a0001c0001t0002g0232 others(6): Show |
9 | HG02280.hp2 HG02886.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-2044_251-2043d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095400 | ||||||
| chr18:35095402 | G | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0222 a0001c0001t0002g0007 others(101): Show |
113 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.251-2044G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095402 | |||||||
| chr18:35095402 | G | GCACACAC others(1): Show |
9 | a0001c0001t0001g0034 a0001c0001t0004g0070 a0001c0001t0004g0071 others(6): Show |
9 | HG00408.hp2 HG01346.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-2040_251-2033d others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095402 | ||||||
| chr18:35095456 | C | T | 1 | a0001c0001t0005g0187 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.251-1990C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095456 | |||||||
| chr18:35095457 | G | A | 1 | a0001c0001t0008g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.251-1989G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095457 | |||||||
| chr18:35095483 | G | C | 2 | a0001c0001t0002g0236 a0001c0001t0002g0253 |
2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.251-1963G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095483 | |||||||
| chr18:35095523 | G | GT | 69 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0324 others(66): Show |
79 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.251-1909dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095523 | ||||||
| chr18:35095523 | G | GTT | 109 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0029 others(106): Show |
112 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.251-1910_251-1909d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095523 | ||||||
| chr18:35095523 | G | GTTT | 12 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0005g0168 others(9): Show |
13 | HG01884.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-1911_251-1909d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095523 | ||||||
| chr18:35095590 | G | C | 1 | a0001c0001t0004g0071 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.251-1856G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095590 | |||||||
| chr18:35095627 | A | G | 1 | a0001c0001t0007g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.251-1819A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095627 | |||||||
| chr18:35095682 | G | A | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.251-1764G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095682 | |||||||
| chr18:35095858 | G | A | 66 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(63): Show |
74 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.251-1588G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095858 | |||||||
| chr18:35096046 | T | G | 2 | a0001c0001t0006g0182 a0001c0001t0040g0185 |
2 | HG00408.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.251-1400T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096046 | |||||||
| chr18:35096109 | G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-1337G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096109 | |||||||
| chr18:35096181 | G | A | 1 | a0001c0001t0024g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.251-1265G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096181 | |||||||
| chr18:35096526 | A | G | 1 | a0001c0001t0005g0165 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.251-920A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096526 | |||||||
| chr18:35096589 | G | GACTC | 84 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0005g0016 others(81): Show |
89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.251-856_251-853dup others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35096589 | ||||||
| chr18:35096789 | TATAAGTA others(14): Show |
T | 82 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0005g0016 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.251-639_251-619del others(21): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35096789 | ||||||
| chr18:35096813 | A | AAGTAATA others(17): Show |
1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.251-618_251-595dup others(24): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35096813 | ||||||
| chr18:35096863 | A | G | 1 | a0001c0001t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.251-583A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096863 | |||||||
| chr18:35096941 | A | G | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251-505A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096941 | |||||||
| chr18:35097017 | G | A | 82 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0005g0016 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.251-429G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097017 | |||||||
| chr18:35097056 | T | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0233 |
4 | HG00642.hp1 HG01099.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-390T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097056 | |||||||
| chr18:35097190 | A | G | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.251-256A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097190 | |||||||
| chr18:35097211 | A | ATGCATAT others(4): Show |
1 | a0001c0001t0005g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.251-235_251-234ins others(11): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097211 | |||||||
| chr18:35097214 | A | G | 1 | a0001c0001t0005g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.251-232A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097214 | |||||||
| chr18:35097669 | G | A | 44 | a0001c0001t0001g0034 a0001c0001t0002g0224 a0001c0001t0004g0005 others(41): Show |
47 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.396+78G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35097669 | |||||||
| chr18:35097737 | C | A | 1 | a0001c0001t0004g0081 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.396+146C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35097737 | |||||||
| chr18:35098250 | T | C | 1 | a0001c0001t0007g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.396+659T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098250 | |||||||
| chr18:35098393 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.396+802A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098393 | |||||||
| chr18:35098445 | G | A | 1 | a0001c0001t0008g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.396+854G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098445 | |||||||
| chr18:35098693 | C | A | 1 | a0001c0001t0001g0270 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.396+1102C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098693 | |||||||
| chr18:35098734 | A | G | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.396+1143A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098734 | |||||||
| chr18:35098812 | C | T | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.396+1221C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098812 | |||||||
| chr18:35099155 | A | G | 1 | a0001c0001t0007g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.396+1564A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099155 | |||||||
| chr18:35099177 | C | T | 1 | a0001c0001t0012g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396+1586C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099177 | |||||||
| chr18:35099259 | A | G | 2 | a0001c0001t0003g0115 a0001c0001t0010g0275 |
2 | NA18987.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.396+1668A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099259 | |||||||
| chr18:35099600 | G | A | 1 | a0001c0001t0014g0306 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.396+2009G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099600 | |||||||
| chr18:35099686 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.396+2095A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099686 | |||||||
| chr18:35099822 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.397-2124T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099822 | |||||||
| chr18:35100069 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.397-1877G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100069 | |||||||
| chr18:35100091 | A | G | 1 | a0001c0001t0027g0035 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.397-1855A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100091 | |||||||
| chr18:35100117 | A | T | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.397-1829A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100117 | |||||||
| chr18:35100162 | C | T | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.397-1784C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100162 | |||||||
| chr18:35100407 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.397-1539C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100407 | |||||||
| chr18:35100576 | A | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0160 others(12): Show |
20 | HG00423.hp1 HG02040.hp1 NA18943.hp1 others(17): Show |
intron_variant | MODIFIER | c.397-1370A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100576 | |||||||
| chr18:35100611 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.397-1335C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100611 | |||||||
| chr18:35100741 | A | G | 3 | a0001c0001t0004g0066 a0001c0001t0004g0081 a0001c0001t0004g0096 |
3 | NA18983.hp2 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.397-1205A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100741 | |||||||
| chr18:35100796 | T | A | 1 | a0001c0001t0002g0028 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.397-1150T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100796 | |||||||
| chr18:35100869 | G | A | 2 | a0001c0001t0013g0152 a0001c0001t0033g0218 |
2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.397-1077G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100869 | |||||||
| chr18:35100906 | G | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0029 others(37): Show |
41 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.397-1040G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100906 | |||||||
| chr18:35100930 | T | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0002g0007 others(65): Show |
76 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.397-1016T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100930 | |||||||
| chr18:35101017 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.397-929C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101017 | |||||||
| chr18:35101022 | A | G | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.397-924A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101022 | |||||||
| chr18:35101024 | A | G | 1 | a0001c0001t0004g0078 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.397-922A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101024 | |||||||
| chr18:35101317 | T | C | 1 | a0001c0001t0011g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.397-629T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101317 | |||||||
| chr18:35101783 | A | G | 1 | a0001c0001t0005g0170 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.397-163A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101783 | |||||||
| chr18:35102185 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.610+26G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102185 | |||||||
| chr18:35102373 | C | T | 13 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(10): Show |
13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.610+214C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102373 | |||||||
| chr18:35102405 | C | T | 334 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(331): Show |
367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.610+246C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102405 | |||||||
| chr18:35102569 | T | C | 13 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(10): Show |
13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.610+410T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102569 | |||||||
| chr18:35102753 | C | A | 4 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0230 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.610+594C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102753 | |||||||
| chr18:35102889 | T | C | 1 | a0001c0001t0007g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.610+730T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102889 | |||||||
| chr18:35103019 | G | GTGGTAAG others(9): Show |
2 | a0001c0001t0033g0218 a0001c0001t0034g0219 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.610+860_610+861ins others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103019 | |||||||
| chr18:35103021 | C | T | 2 | a0001c0001t0033g0218 a0001c0001t0034g0219 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.610+862C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103021 | |||||||
| chr18:35103264 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.610+1105A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103264 | |||||||
| chr18:35103437 | A | G | 76 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0163 others(73): Show |
81 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.610+1278A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103437 | |||||||
| chr18:35103583 | T | C | 2 | a0001c0001t0033g0218 a0001c0001t0034g0219 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.610+1424T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103583 | |||||||
| chr18:35103597 | A | G | 1 | a0001c0001t0004g0070 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.610+1438A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103597 | |||||||
| chr18:35103725 | A | G | 1 | a0001c0001t0013g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.610+1566A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103725 | |||||||
| chr18:35103834 | A | G | 1 | a0001c0001t0013g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.610+1675A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103834 | |||||||
| chr18:35103869 | G | A | 1 | a0001c0001t0003g0311 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.610+1710G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103869 | |||||||
| chr18:35103972 | A | G | 2 | a0001c0001t0002g0107 a0001c0001t0002g0232 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.610+1813A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103972 | |||||||
| chr18:35104051 | A | G | 90 | a0001c0001t0001g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(87): Show |
99 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.610+1892A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104051 | |||||||
| chr18:35104161 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+2002C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104161 | |||||||
| chr18:35104220 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+2061T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104220 | |||||||
| chr18:35104238 | T | A | 88 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0005g0016 others(85): Show |
93 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.610+2079T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104238 | |||||||
| chr18:35104288 | A | G | 2 | a0001c0001t0019g0207 a0001c0001t0019g0216 |
2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.610+2129A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104288 | |||||||
| chr18:35104363 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0004g0005 a0001c0001t0004g0010 others(40): Show |
48 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.610+2204T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104363 | |||||||
| chr18:35104369 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.610+2210C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104369 | |||||||
| chr18:35104559 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0002g0052 |
2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.610+2400C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104559 | |||||||
| chr18:35104736 | G | A | 8 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0212 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.610+2577G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104736 | |||||||
| chr18:35104769 | G | A | 4 | a0001c0001t0015g0240 a0001c0001t0015g0260 a0001c0001t0015g0261 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.610+2610G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104769 | |||||||
| chr18:35105436 | A | T | 3 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0308 |
3 | HG01257.hp2 NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.610+3277A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35105436 | |||||||
| chr18:35105526 | A | G | 76 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0163 others(73): Show |
81 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.610+3367A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35105526 | |||||||
| chr18:35105669 | A | G | 3 | a0001c0001t0008g0296 a0001c0001t0037g0316 a0001c0001t0038g0321 |
3 | HG01070.hp2 HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.610+3510A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35105669 | |||||||
| chr18:35105729 | A | G | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.610+3570A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35105729 | |||||||
| chr18:35106308 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+4149G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106308 | |||||||
| chr18:35106357 | T | TGC | 195 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0222 others(192): Show |
209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.610+4198_610+4199i others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106357 | |||||||
| chr18:35106528 | A | G | 9 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(6): Show |
9 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.610+4369A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106528 | |||||||
| chr18:35106591 | G | A | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.610+4432G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106591 | |||||||
| chr18:35106598 | G | C | 82 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0005g0016 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.610+4439G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106598 | |||||||
| chr18:35106856 | TAC | T | 49 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0163 others(46): Show |
52 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.610+4701_610+4702d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35106856 | ||||||
| chr18:35107038 | G | T | 1 | a0001c0001t0033g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.610+4879G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107038 | |||||||
| chr18:35107089 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0295 |
2 | NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.610+4930C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107089 | |||||||
| chr18:35107296 | A | G | 2 | a0001c0001t0005g0157 a0001c0001t0005g0214 |
2 | HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.610+5137A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107296 | |||||||
| chr18:35107308 | G | A | 86 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0005g0016 others(83): Show |
91 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.610+5149G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107308 | |||||||
| chr18:35107487 | CCTT | C | 44 | a0001c0001t0001g0004 a0001c0001t0002g0224 a0001c0001t0004g0005 others(41): Show |
49 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.610+5332_610+5334d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35107487 | ||||||
| chr18:35107585 | G | T | 1 | a0001c0001t0013g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.610+5426G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107585 | |||||||
| chr18:35107644 | C | T | 1 | a0001c0001t0004g0082 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.610+5485C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107644 | |||||||
| chr18:35107655 | C | T | 6 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0174 others(3): Show |
8 | HG01255.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.610+5496C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107655 | |||||||
| chr18:35107820 | G | C | 1 | a0001c0001t0003g0145 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.610+5661G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107820 | |||||||
| chr18:35108026 | G | A | 3 | a0001c0001t0002g0255 a0001c0001t0002g0256 a0001c0001t0002g0257 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.610+5867G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108026 | |||||||
| chr18:35108074 | A | G | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.610+5915A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108074 | |||||||
| chr18:35108122 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0294 a0001c0001t0001g0327 others(4): Show |
8 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.610+5963C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108122 | |||||||
| chr18:35108288 | A | G | 2 | a0001c0001t0006g0039 a0001c0001t0006g0041 |
2 | NA18944.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.610+6129A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108288 | |||||||
| chr18:35108363 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0232 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.610+6204G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108363 | |||||||
| chr18:35108607 | A | G | 1 | a0001c0001t0010g0297 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.610+6448A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108607 | |||||||
| chr18:35108635 | T | C | 1 | a0001c0001t0003g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.610+6476T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108635 | |||||||
| chr18:35108876 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+6717C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108876 | |||||||
| chr18:35108995 | A | G | 54 | a0001c0001t0001g0004 a0001c0001t0002g0007 a0001c0001t0002g0018 others(51): Show |
62 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.610+6836A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108995 | |||||||
| chr18:35109316 | A | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+7157A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35109316 | |||||||
| chr18:35109824 | T | A | 90 | a0001c0001t0001g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(87): Show |
99 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.610+7665T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35109824 | |||||||
| chr18:35110204 | C | T | 1 | a0001c0001t0004g0088 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.610+8045C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110204 | |||||||
| chr18:35110350 | T | C | 9 | a0001c0001t0005g0165 a0001c0001t0005g0183 a0001c0001t0005g0184 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.610+8191T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110350 | |||||||
| chr18:35110377 | C | T | 1 | a0001c0001t0005g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.610+8218C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110377 | |||||||
| chr18:35110411 | T | C | 3 | a0001c0001t0009g0245 a0001c0001t0009g0246 a0001c0001t0009g0258 |
3 | HG01243.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.610+8252T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110411 | |||||||
| chr18:35110427 | A | G | 1 | a0001c0001t0005g0175 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.610+8268A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110427 | |||||||
| chr18:35110562 | A | T | 1 | a0001c0001t0007g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.610+8403A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110562 | |||||||
| chr18:35110779 | G | A | 1 | a0001c0001t0029g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.610+8620G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110779 | |||||||
| chr18:35110792 | A | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
106 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.610+8633A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110792 | |||||||
| chr18:35110818 | A | G | 6 | a0001c0001t0004g0065 a0001c0001t0004g0072 a0001c0001t0004g0076 others(3): Show |
6 | NA18956.hp1 NA18988.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.610+8659A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110818 | |||||||
| chr18:35110903 | C | T | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.610+8744C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110903 | |||||||
| chr18:35110908 | A | G | 1 | a0001c0001t0003g0135 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.610+8749A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110908 | |||||||
| chr18:35111543 | T | C | 1 | a0001c0001t0004g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.610+9384T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35111543 | |||||||
| chr18:35111952 | A | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | NA18977.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.610+9793A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35111952 | |||||||
| chr18:35112166 | T | A | 3 | a0001c0001t0013g0024 a0001c0001t0013g0205 a0001c0001t0013g0206 |
3 | HG02647.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.610+10007T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112166 | |||||||
| chr18:35112184 | C | CT | 16 | a0001c0001t0003g0311 a0001c0001t0007g0229 a0001c0001t0012g0209 others(13): Show |
16 | HG01123.hp2 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.610+10040dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35112184 | ||||||
| chr18:35112450 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.610+10291C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112450 | |||||||
| chr18:35112510 | C | T | 3 | a0001c0001t0005g0215 a0001c0001t0024g0237 a0001c0001t0024g0238 |
3 | HG03209.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.610+10351C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112510 | |||||||
| chr18:35112512 | T | C | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+10353T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112512 | |||||||
| chr18:35112626 | C | A | 1 | a0001c0001t0033g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.610+10467C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112626 | |||||||
| chr18:35112806 | A | C | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.610+10647A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112806 | |||||||
| chr18:35112846 | C | T | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+10687C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112846 | |||||||
| chr18:35112877 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0283 a0001c0001t0001g0294 others(6): Show |
10 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.610+10718G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112877 | |||||||
| chr18:35113054 | C | T | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+10895C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113054 | |||||||
| chr18:35113339 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
307 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.610+11180A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113339 | |||||||
| chr18:35113393 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.610+11234C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113393 | |||||||
| chr18:35113460 | T | G | 1 | a0001c0001t0002g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.610+11301T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113460 | |||||||
| chr18:35113467 | TA | T | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+11317delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35113467 | ||||||
| chr18:35113468 | A | T | 10 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0233 others(7): Show |
13 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.610+11309A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113468 | |||||||
| chr18:35113670 | A | T | 4 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0329 others(1): Show |
4 | NA18988.hp1 NA18998.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.610+11511A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113670 | |||||||
| chr18:35113763 | C | T | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.610+11604C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113763 | |||||||
| chr18:35113961 | A | G | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+11802A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113961 | |||||||
| chr18:35113988 | A | G | 5 | a0001c0001t0002g0107 a0001c0001t0002g0232 a0001c0001t0005g0157 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.610+11829A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113988 | |||||||
| chr18:35114166 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.610+12007C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114166 | |||||||
| chr18:35114221 | A | G | 1 | a0001c0001t0006g0190 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.610+12062A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114221 | |||||||
| chr18:35114259 | A | C | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+12100A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114259 | |||||||
| chr18:35114467 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+12308G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114467 | |||||||
| chr18:35114528 | G | A | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.610+12369G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114528 | |||||||
| chr18:35115209 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.611-11739A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115209 | |||||||
| chr18:35115330 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0004g0005 a0001c0001t0004g0010 others(40): Show |
48 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.611-11618T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115330 | |||||||
| chr18:35115370 | T | A | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.611-11578T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115370 | |||||||
| chr18:35115429 | G | A | 10 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(7): Show |
10 | HG01891.hp2 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.611-11519G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115429 | |||||||
| chr18:35115517 | G | A | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.611-11431G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115517 | |||||||
| chr18:35115520 | C | G | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.611-11428C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115520 | |||||||
| chr18:35115560 | T | C | 1 | a0001c0001t0006g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.611-11388T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115560 | |||||||
| chr18:35115716 | G | A | 1 | a0001c0001t0039g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.611-11232G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115716 | |||||||
| chr18:35115719 | G | T | 9 | a0001c0001t0005g0165 a0001c0001t0005g0183 a0001c0001t0005g0184 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-11229G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115719 | |||||||
| chr18:35115731 | G | A | 195 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0015 others(192): Show |
208 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.611-11217G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115731 | |||||||
| chr18:35115824 | A | G | 44 | a0001c0001t0001g0004 a0001c0001t0002g0224 a0001c0001t0004g0005 others(41): Show |
49 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.611-11124A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115824 | |||||||
| chr18:35116089 | G | T | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.611-10859G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116089 | |||||||
| chr18:35116219 | G | A | 1 | a0001c0001t0016g0131 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.611-10729G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116219 | |||||||
| chr18:35116301 | T | C | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.611-10647T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116301 | |||||||
| chr18:35116572 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.611-10376C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116572 | |||||||
| chr18:35116782 | T | C | 1 | a0001c0001t0005g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.611-10166T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116782 | |||||||
| chr18:35116812 | C | T | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.611-10136C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116812 | |||||||
| chr18:35116848 | C | A | 1 | a0001c0001t0003g0119 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.611-10100C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116848 | |||||||
| chr18:35117243 | A | C | 7 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(4): Show |
7 | HG02451.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.611-9705A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117243 | |||||||
| chr18:35117259 | C | T | 6 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.611-9689C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117259 | |||||||
| chr18:35117301 | C | T | 1 | a0001c0001t0004g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.611-9647C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117301 | |||||||
| chr18:35117714 | C | G | 78 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0157 others(75): Show |
83 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.611-9234C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117714 | |||||||
| chr18:35117800 | A | G | 1 | a0001c0001t0005g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.611-9148A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117800 | |||||||
| chr18:35117879 | C | A | 43 | a0001c0001t0002g0224 a0001c0001t0004g0005 a0001c0001t0004g0010 others(40): Show |
46 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.611-9069C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117879 | |||||||
| chr18:35117928 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.611-9020G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117928 | |||||||
| chr18:35118162 | C | A | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.611-8786C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35118162 | |||||||
| chr18:35118291 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.611-8657A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35118291 | |||||||
| chr18:35118380 | A | G | 1 | a0001c0001t0013g0206 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.611-8568A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35118380 | |||||||
| chr18:35118390 | C | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0266 a0001c0001t0001g0295 |
3 | HG02040.hp2 NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.611-8558C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35118390 | |||||||
| chr18:35119031 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.611-7917A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119031 | |||||||
| chr18:35119110 | C | T | 89 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0018 others(86): Show |
96 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.611-7838C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119110 | |||||||
| chr18:35119138 | C | T | 10 | a0001c0001t0009g0217 a0001c0001t0009g0242 a0001c0001t0009g0243 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.611-7810C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119138 | |||||||
| chr18:35119404 | T | C | 1 | a0001c0001t0003g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.611-7544T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119404 | |||||||
| chr18:35119546 | A | G | 1 | a0001c0001t0010g0302 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.611-7402A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119546 | |||||||
| chr18:35119650 | T | A | 2 | a0001c0001t0005g0163 a0001c0001t0005g0177 |
2 | NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.611-7298T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119650 | |||||||
| chr18:35119661 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.611-7287G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119661 | |||||||
| chr18:35119741 | C | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0107 a0001c0001t0002g0232 |
4 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-7207C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119741 | |||||||
| chr18:35119786 | G | T | 46 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0163 others(43): Show |
49 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.611-7162G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119786 | |||||||
| chr18:35119838 | C | A | 11 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(8): Show |
11 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.611-7110C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119838 | |||||||
| chr18:35119960 | G | A | 1 | a0001c0001t0007g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.611-6988G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119960 | |||||||
| chr18:35120283 | C | T | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.611-6665C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120283 | |||||||
| chr18:35120490 | G | A | 1 | a0001c0001t0010g0286 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.611-6458G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120490 | |||||||
| chr18:35120514 | G | A | 74 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0157 others(71): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.611-6434G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120514 | |||||||
| chr18:35120721 | C | G | 1 | a0001c0001t0016g0146 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.611-6227C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120721 | |||||||
| chr18:35120863 | G | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0295 |
2 | NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.611-6085G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120863 | |||||||
| chr18:35120874 | T | C | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-6074T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120874 | |||||||
| chr18:35120880 | A | G | 4 | a0001c0001t0015g0240 a0001c0001t0015g0260 a0001c0001t0015g0261 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.611-6068A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120880 | |||||||
| chr18:35120976 | G | A | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.611-5972G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120976 | |||||||
| chr18:35121576 | C | T | 89 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0018 others(86): Show |
96 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.611-5372C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35121576 | |||||||
| chr18:35121708 | A | G | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.611-5240A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35121708 | |||||||
| chr18:35121878 | G | C | 1 | a0001c0001t0006g0202 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.611-5070G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35121878 | |||||||
| chr18:35121890 | C | CAT | 4 | a0001c0001t0002g0018 a0001c0001t0002g0239 a0001c0001t0002g0241 others(1): Show |
5 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-5056_611-5055d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35121890 | ||||||
| chr18:35121961 | C | CTAG | 1 | a0001c0001t0001g0004 | 3 | NA18952.hp1 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.611-4985_611-4983d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35121961 | ||||||
| chr18:35122034 | G | A | 1 | a0001c0001t0012g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.611-4914G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122034 | |||||||
| chr18:35122162 | G | A | 1 | a0001c0001t0004g0101 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.611-4786G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122162 | |||||||
| chr18:35122207 | A | G | 1 | a0001c0001t0003g0147 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.611-4741A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122207 | |||||||
| chr18:35122305 | CTG | C | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-4641_611-4640d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35122305 | ||||||
| chr18:35122543 | T | G | 1 | a0001c0001t0006g0039 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.611-4405T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122543 | |||||||
| chr18:35122951 | A | C | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.611-3997A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122951 | |||||||
| chr18:35122963 | C | T | 1 | a0001c0001t0003g0167 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.611-3985C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122963 | |||||||
| chr18:35123035 | G | A | 84 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0005g0016 others(81): Show |
89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.611-3913G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123035 | |||||||
| chr18:35123202 | T | G | 1 | a0001c0001t0002g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.611-3746T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123202 | |||||||
| chr18:35123380 | C | T | 1 | a0001c0001t0004g0070 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.611-3568C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123380 | |||||||
| chr18:35123432 | G | A | 195 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0015 others(192): Show |
208 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.611-3516G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123432 | |||||||
| chr18:35123584 | A | G | 89 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0005g0016 others(86): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.611-3364A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123584 | |||||||
| chr18:35123627 | C | T | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-3321C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123627 | |||||||
| chr18:35123962 | C | A | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.611-2986C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123962 | |||||||
| chr18:35124331 | G | A | 1 | a0001c0001t0039g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.611-2617G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124331 | |||||||
| chr18:35124367 | G | A | 1 | a0001c0001t0013g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.611-2581G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124367 | |||||||
| chr18:35124381 | A | G | 2 | a0001c0001t0020g0304 a0001c0001t0020g0307 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.611-2567A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124381 | |||||||
| chr18:35124401 | A | G | 5 | a0001c0001t0002g0015 a0001c0001t0002g0107 a0001c0001t0002g0232 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.611-2547A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124401 | |||||||
| chr18:35124533 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.611-2415C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124533 | |||||||
| chr18:35124604 | C | A | 1 | a0001c0001t0004g0090 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.611-2344C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124604 | |||||||
| chr18:35124605 | A | T | 1 | a0001c0001t0004g0090 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.611-2343A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124605 | |||||||
| chr18:35124606 | T | G | 1 | a0001c0001t0004g0090 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.611-2342T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124606 | |||||||
| chr18:35124913 | A | G | 1 | a0001c0001t0007g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.611-2035A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124913 | |||||||
| chr18:35125084 | A | C | 1 | a0001c0001t0008g0014 | 2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.611-1864A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125084 | |||||||
| chr18:35125320 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.611-1628C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125320 | |||||||
| chr18:35125477 | G | A | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.611-1471G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125477 | |||||||
| chr18:35125491 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.611-1457A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125491 | |||||||
| chr18:35125750 | C | T | 3 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0050 |
3 | HG02735.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.611-1198C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125750 | |||||||
| chr18:35125751 | G | A | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.611-1197G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125751 | |||||||
| chr18:35125818 | A | G | 1 | a0001c0001t0013g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.611-1130A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125818 | |||||||
| chr18:35125833 | T | C | 2 | a0001c0001t0018g0247 a0001c0001t0018g0248 |
2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.611-1115T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125833 | |||||||
| chr18:35125982 | G | A | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-966G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125982 | |||||||
| chr18:35126138 | T | C | 1 | a0001c0001t0008g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.611-810T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126138 | |||||||
| chr18:35126228 | A | G | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.611-720A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126228 | |||||||
| chr18:35126555 | T | C | 1 | a0001c0001t0003g0141 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.611-393T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126555 | |||||||
| chr18:35126717 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.611-231T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126717 | |||||||
| chr18:35126852 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0069 |
2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.611-96G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126852 | |||||||
| chr18:35127246 | A | T | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+159A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127246 | |||||||
| chr18:35127335 | C | T | 1 | a0001c0001t0011g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.750+248C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127335 | |||||||
| chr18:35127368 | C | T | 195 | a0001c0001t0001g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(192): Show |
210 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.750+281C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127368 | |||||||
| chr18:35127678 | A | G | 6 | a0001c0001t0004g0065 a0001c0001t0004g0072 a0001c0001t0004g0076 others(3): Show |
6 | NA18956.hp1 NA18988.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+591A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127678 | |||||||
| chr18:35127807 | T | C | 3 | a0001c0001t0003g0122 a0001c0001t0003g0136 a0001c0001t0003g0137 |
3 | HG01106.hp2 HG01981.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.750+720T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127807 | |||||||
| chr18:35127829 | C | G | 6 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.750+742C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127829 | |||||||
| chr18:35127836 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.750+749C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127836 | |||||||
| chr18:35127943 | G | C | 1 | a0001c0001t0007g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.750+856G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127943 | |||||||
| chr18:35128020 | G | A | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.750+933G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128020 | |||||||
| chr18:35128036 | G | A | 4 | a0001c0001t0007g0025 a0001c0001t0007g0252 a0001c0001t0021g0063 others(1): Show |
4 | HG02486.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+949G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128036 | |||||||
| chr18:35128203 | C | A | 1 | a0001c0001t0002g0029 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.750+1116C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128203 | |||||||
| chr18:35128682 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0205 a0001c0001t0013g0206 |
3 | HG02647.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.750+1595A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128682 | |||||||
| chr18:35128686 | G | A | 2 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
2 | HG01361.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.750+1599G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128686 | |||||||
| chr18:35128765 | T | C | 8 | a0001c0001t0002g0018 a0001c0001t0002g0236 a0001c0001t0002g0239 others(5): Show |
9 | HG01884.hp1 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+1678T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128765 | |||||||
| chr18:35128831 | C | T | 90 | a0001c0001t0001g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(87): Show |
99 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.750+1744C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128831 | |||||||
| chr18:35128833 | A | G | 1 | a0001c0001t0021g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.750+1746A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128833 | |||||||
| chr18:35128845 | C | T | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.750+1758C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128845 | |||||||
| chr18:35128874 | A | G | 3 | a0001c0001t0011g0058 a0001c0001t0011g0059 a0001c0001t0011g0060 |
3 | HG01884.hp2 HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.750+1787A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128874 | |||||||
| chr18:35128905 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.750+1818C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128905 | |||||||
| chr18:35128907 | T | C | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.750+1820T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128907 | |||||||
| chr18:35129002 | T | C | 10 | a0001c0001t0008g0011 a0001c0001t0008g0014 a0001c0001t0008g0118 others(7): Show |
12 | HG00280.hp2 HG00735.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.750+1915T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129002 | |||||||
| chr18:35129039 | GAAGA | G | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+1953_750+1956d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129039 | |||||||
| chr18:35129076 | T | C | 1 | a0001c0001t0007g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.750+1989T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129076 | |||||||
| chr18:35129257 | T | G | 1 | a0001c0001t0004g0076 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.750+2170T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129257 | |||||||
| chr18:35129261 | C | T | 1 | a0001c0001t0005g0201 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.750+2174C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129261 | |||||||
| chr18:35129353 | C | T | 1 | a0001c0001t0005g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.750+2266C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129353 | |||||||
| chr18:35129400 | T | C | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.750+2313T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129400 | |||||||
| chr18:35129463 | A | T | 1 | a0001c0001t0005g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.750+2376A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129463 | |||||||
| chr18:35129529 | G | C | 2 | a0001c0001t0005g0186 a0001c0001t0005g0187 |
2 | HG02523.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.750+2442G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129529 | |||||||
| chr18:35129748 | G | A | 1 | a0001c0001t0004g0074 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.751-2284G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129748 | |||||||
| chr18:35129755 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.751-2277A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129755 | |||||||
| chr18:35129792 | G | A | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.751-2240G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129792 | |||||||
| chr18:35130056 | C | T | 4 | a0001c0001t0007g0025 a0001c0001t0007g0252 a0001c0001t0021g0063 others(1): Show |
4 | HG02486.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.751-1976C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130056 | |||||||
| chr18:35130115 | G | A | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-1917G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130115 | |||||||
| chr18:35130153 | G | T | 1 | a0001c0001t0007g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.751-1879G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130153 | |||||||
| chr18:35130326 | T | C | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-1706T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130326 | |||||||
| chr18:35130332 | A | G | 1 | a0001c0001t0003g0143 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.751-1700A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130332 | |||||||
| chr18:35130393 | A | G | 1 | a0001c0001t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.751-1639A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130393 | |||||||
| chr18:35130544 | A | G | 1 | a0001c0001t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.751-1488A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130544 | |||||||
| chr18:35130587 | T | G | 3 | a0001c0001t0017g0179 a0001c0001t0017g0181 a0001c0001t0017g0203 |
3 | HG03041.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.751-1445T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130587 | |||||||
| chr18:35130720 | C | T | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.751-1312C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130720 | |||||||
| chr18:35130876 | G | A | 1 | a0001c0001t0040g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.751-1156G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130876 | |||||||
| chr18:35130979 | G | A | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-1053G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130979 | |||||||
| chr18:35131039 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.751-993T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131039 | |||||||
| chr18:35131053 | C | T | 1 | a0001c0001t0003g0126 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.751-979C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131053 | |||||||
| chr18:35131129 | T | C | 3 | a0001c0001t0001g0309 a0001c0001t0021g0063 a0001c0001t0021g0106 |
3 | HG02965.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.751-903T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131129 | |||||||
| chr18:35131161 | G | A | 75 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0157 others(72): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.751-871G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131161 | |||||||
| chr18:35131400 | A | G | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-632A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131400 | |||||||
| chr18:35131433 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.751-599A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131433 | |||||||
| chr18:35131441 | G | C | 79 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0157 others(76): Show |
84 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.751-591G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131441 | |||||||
| chr18:35131485 | T | C | 18 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(15): Show |
18 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.751-547T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131485 | |||||||
| chr18:35131494 | G | A | 1 | a0001c0001t0003g0308 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.751-538G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131494 | |||||||
| chr18:35131727 | T | A | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-305T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131727 | |||||||
| chr18:35131810 | C | T | 75 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0157 others(72): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.751-222C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131810 | |||||||
| chr18:35131929 | T | TTC | 3 | a0001c0001t0007g0025 a0001c0001t0021g0063 a0001c0001t0021g0106 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.751-87_751-86dupCT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr18 | 35131929 | ||||||
| chr18:35131989 | A | G | 1 | a0001c0001t0001g0004 | 3 | NA18952.hp1 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.751-43A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131989 | |||||||
| chr18:35132001 | G | GT | 95 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0002g0007 others(92): Show |
104 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.751-23dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr18 | 35132001 | ||||||
| chr18:35132334 | A | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0264 a0001c0001t0001g0267 others(5): Show |
9 | NA18956.hp2 NA18957.hp2 NA18975.hp1 others(6): Show |
intron_variant | MODIFIER | c.909+144A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35132334 | |||||||
| chr18:35132618 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.909+428C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35132618 | |||||||
| chr18:35132865 | C | A | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.909+675C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35132865 | |||||||
| chr18:35132875 | AC | A | 9 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.909+686delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35132875 | |||||||
| chr18:35133027 | G | A | 74 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0157 others(71): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.909+837G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133027 | |||||||
| chr18:35133380 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.909+1190G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133380 | |||||||
| chr18:35133483 | C | G | 6 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+1293C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133483 | |||||||
| chr18:35133508 | G | A | 2 | a0001c0001t0006g0164 a0001c0001t0006g0202 |
2 | NA18967.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.909+1318G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133508 | |||||||
| chr18:35133561 | G | T | 89 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0018 others(86): Show |
96 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.909+1371G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133561 | |||||||
| chr18:35133768 | G | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0295 |
2 | NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.909+1578G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133768 | |||||||
| chr18:35133889 | T | C | 3 | a0001c0001t0004g0005 a0001c0001t0004g0071 a0001c0001t0004g0082 |
5 | HG00408.hp2 NA18964.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+1699T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133889 | |||||||
| chr18:35134129 | T | G | 1 | a0001c0001t0030g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.909+1939T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134129 | |||||||
| chr18:35134430 | G | A | 1 | a0001c0001t0027g0035 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.909+2240G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134430 | |||||||
| chr18:35134482 | G | A | 75 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0157 others(72): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.909+2292G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134482 | |||||||
| chr18:35134616 | G | A | 2 | a0001c0001t0005g0157 a0001c0001t0005g0214 |
2 | HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.909+2426G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134616 | |||||||
| chr18:35134775 | C | T | 1 | a0001c0001t0011g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.909+2585C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134775 | |||||||
| chr18:35134889 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.909+2699G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134889 | |||||||
| chr18:35134907 | C | A | 22 | a0001c0001t0007g0025 a0001c0001t0007g0225 a0001c0001t0007g0226 others(19): Show |
22 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.909+2717C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134907 | |||||||
| chr18:35135193 | T | G | 6 | a0001c0001t0002g0015 a0001c0001t0002g0107 a0001c0001t0002g0232 others(3): Show |
7 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+3003T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135193 | |||||||
| chr18:35135247 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.909+3057C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135247 | |||||||
| chr18:35135290 | G | A | 1 | a0001c0001t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.909+3100G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135290 | |||||||
| chr18:35135338 | A | T | 5 | a0001c0001t0002g0015 a0001c0001t0002g0107 a0001c0001t0002g0232 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+3148A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135338 | |||||||
| chr18:35135426 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0205 a0001c0001t0013g0206 |
3 | HG02647.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.909+3236A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135426 | |||||||
| chr18:35135449 | A | G | 1 | a0001c0001t0004g0076 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.909+3259A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135449 | |||||||
| chr18:35135451 | G | A | 12 | a0001c0001t0012g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+3261G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135451 | |||||||
| chr18:35135473 | A | G | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.909+3283A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135473 | |||||||
| chr18:35135475 | A | T | 3 | a0001c0001t0007g0025 a0001c0001t0021g0063 a0001c0001t0021g0106 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.909+3285A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135475 | |||||||
| chr18:35135717 | C | T | 75 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0157 others(72): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.909+3527C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135717 | |||||||
| chr18:35135827 | G | A | 1 | a0001c0001t0005g0183 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.909+3637G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135827 | |||||||
| chr18:35136151 | A | G | 3 | a0001c0001t0013g0024 a0001c0001t0013g0205 a0001c0001t0013g0206 |
3 | HG02647.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.909+3961A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136151 | |||||||
| chr18:35136173 | A | G | 1 | a0001c0001t0025g0026 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.909+3983A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136173 | |||||||
| chr18:35136203 | G | A | 1 | a0001c0001t0007g0223 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.909+4013G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136203 | |||||||
| chr18:35136290 | C | T | 1 | a0001c0001t0004g0078 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.910-4005C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136290 | |||||||
| chr18:35136415 | G | A | 1 | a0001c0001t0007g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.910-3880G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136415 | |||||||
| chr18:35136478 | G | A | 196 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0015 others(193): Show |
209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.910-3817G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136478 | |||||||
| chr18:35136529 | C | T | 36 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0029 others(33): Show |
37 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.910-3766C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136529 | |||||||
| chr18:35136583 | G | A | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.910-3712G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136583 | |||||||
| chr18:35136854 | A | G | 5 | a0001c0001t0002g0015 a0001c0001t0002g0107 a0001c0001t0002g0232 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-3441A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136854 | |||||||
| chr18:35136869 | T | C | 1 | a0001c0001t0042g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.910-3426T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136869 | |||||||
| chr18:35136885 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.910-3410G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136885 | |||||||
| chr18:35136908 | C | A | 4 | a0001c0001t0007g0025 a0001c0001t0007g0252 a0001c0001t0021g0063 others(1): Show |
4 | HG02486.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-3387C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136908 | |||||||
| chr18:35137133 | T | C | 4 | a0001c0001t0007g0025 a0001c0001t0007g0252 a0001c0001t0021g0063 others(1): Show |
4 | HG02486.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-3162T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137133 | |||||||
| chr18:35137274 | T | C | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.910-3021T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137274 | |||||||
| chr18:35137545 | ATCT | A | 3 | a0001c0001t0001g0254 a0001c0001t0021g0063 a0001c0001t0021g0106 |
3 | HG02922.hp1 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.910-2745_910-2743d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr18 | 35137545 | ||||||
| chr18:35137632 | A | G | 1 | a0001c0001t0004g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.910-2663A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137632 | |||||||
| chr18:35137666 | A | G | 1 | a0001c0001t0006g0189 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.910-2629A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137666 | |||||||
| chr18:35137710 | C | T | 1 | a0001c0001t0003g0147 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.910-2585C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137710 | |||||||
| chr18:35137838 | A | C | 6 | a0001c0001t0007g0225 a0001c0001t0007g0226 a0001c0001t0007g0227 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-2457A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137838 | |||||||
| chr18:35137858 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.910-2437G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137858 | |||||||
| chr18:35138057 | G | A | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.910-2238G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138057 | |||||||
| chr18:35138182 | C | T | 36 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0029 others(33): Show |
37 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.910-2113C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138182 | |||||||
| chr18:35138188 | G | C | 57 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0224 others(54): Show |
63 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.910-2107G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138188 | |||||||
| chr18:35138279 | T | C | 118 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0002g0007 others(115): Show |
127 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.910-2016T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138279 | |||||||
| chr18:35138386 | C | G | 1 | a0001c0001t0007g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.910-1909C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138386 | |||||||
| chr18:35138447 | T | C | 1 | a0001c0001t0003g0126 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.910-1848T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138447 | |||||||
| chr18:35138522 | A | T | 1 | a0001c0001t0005g0195 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.910-1773A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138522 | |||||||
| chr18:35138633 | T | A | 195 | a0001c0001t0001g0104 a0001c0001t0002g0007 a0001c0001t0002g0009 others(192): Show |
208 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.910-1662T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138633 | |||||||
| chr18:35138701 | G | A | 2 | a0001c0001t0021g0063 a0001c0001t0021g0106 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.910-1594G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138701 | |||||||
| chr18:35138747 | G | T | 1 | a0001c0001t0002g0015 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.910-1548G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138747 | |||||||
| chr18:35138800 | C | A | 20 | a0001c0001t0008g0011 a0001c0001t0008g0014 a0001c0001t0008g0118 others(17): Show |
22 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.910-1495C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138800 | |||||||
| chr18:35138836 | A | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0294 a0001c0001t0001g0301 others(5): Show |
9 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-1459A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138836 | |||||||
| chr18:35138914 | T | G | 1 | a0001c0001t0003g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.910-1381T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138914 | |||||||
| chr18:35138917 | G | T | 4 | a0001c0001t0015g0240 a0001c0001t0015g0260 a0001c0001t0015g0261 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-1378G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138917 | |||||||
| chr18:35138923 | C | T | 90 | a0001c0001t0001g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(87): Show |
99 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.910-1372C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138923 | |||||||
| chr18:35138960 | G | A | 195 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0015 others(192): Show |
208 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.910-1335G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138960 | |||||||
| chr18:35139006 | G | T | 191 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0002g0007 others(188): Show |
206 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.910-1289G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139006 | |||||||
| chr18:35139043 | G | C | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.910-1252G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139043 | |||||||
| chr18:35139221 | G | A | 1 | a0001c0001t0039g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.910-1074G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139221 | |||||||
| chr18:35139230 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.910-1065G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139230 | |||||||
| chr18:35139235 | C | T | 1 | a0001c0001t0003g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.910-1060C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139235 | |||||||
| chr18:35139270 | A | C | 1 | a0001c0001t0002g0007 | 3 | HG00642.hp1 HG01099.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.910-1025A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139270 | |||||||
| chr18:35139285 | A | G | 46 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0163 others(43): Show |
49 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.910-1010A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139285 | |||||||
| chr18:35139392 | T | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0002g0007 others(96): Show |
109 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.910-903T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139392 | |||||||
| chr18:35139492 | A | T | 1 | a0001c0001t0007g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.910-803A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139492 | |||||||
| chr18:35139572 | G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.910-723G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139572 | |||||||
| chr18:35139618 | C | T | 74 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0157 others(71): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.910-677C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139618 | |||||||
| chr18:35139758 | T | C | 1 | a0001c0001t0004g0084 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.910-537T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139758 | |||||||
| chr18:35139795 | G | A | 2 | a0001c0001t0008g0011 a0001c0001t0008g0127 |
3 | HG01192.hp2 HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.910-500G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139795 | |||||||
| chr18:35139853 | T | C | 1 | a0001c0001t0015g0260 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.910-442T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139853 | |||||||
| chr18:35139911 | C | T | 1 | a0001c0001t0003g0137 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.910-384C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139911 | |||||||
| chr18:35140031 | A | G | 1 | a0001c0001t0007g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.910-264A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140031 | |||||||
| chr18:35140040 | A | G | 1 | a0001c0001t0012g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.910-255A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140040 | |||||||
| chr18:35140111 | G | T | 1 | a0002c0003t0001g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.910-184G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140111 | |||||||
| chr18:35140112 | G | GTGATCAT others(6): Show |
1 | a0002c0003t0001g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.910-183_910-182ins others(13): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140112 | |||||||
| chr18:35140225 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
108 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.910-70A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140225 |