Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55831 |
| ensemblid | ENSG00000125037.13 |
| hgncid | 23999 |
| symbol | EMC3 |
| name | ER membrane protein complex subunit 3 |
| refseq_nuc | NM_001394674.1 |
| refseq_prot | NP_001381603.1 |
| ensembl_nuc | ENST00000245046.7 |
| ensembl_prot | ENSP00000245046.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 9962682 |
| end | 9986841 |
| strand | - |
| ver | v1.2 |
| region | chr3:9962682-9986841 |
| region5000 | chr3:9957682-9991841 |
| regionname0 | EMC3_chr3_9962682_9986841 |
| regionname5000 | EMC3_chr3_9957682_9991841 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 261 | 320 | 92 | 64 | 124 | 6 | 32 | 96 | EMC3_chr3_9957682_9991841 | EMC3 | MAGPE others(256): Show |
chr3 | 9957682 | 9991841 |
| a0002 | 0/0 | 261 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | MAWPE others(256): Show |
chr3 | 9957682 | 9991841 |
| a0003 | 0/0 | 250 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | MAGPE others(245): Show |
chr3 | 9957682 | 9991841 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 783 | 310 | 92 | 62 | 117 | 6 | 31 | EMC3_chr3_9957682_9991841 | EMC3 | ATGGC others(778): Show |
chr3 | 9957682 | 9991841 | ||
| a0001c0002 | 0/0 | 783 | 5 | 0 | 0 | 5 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | ATGGC others(778): Show |
chr3 | 9957682 | 9991841 | ||
| a0001c0003 | 0/0 | 783 | 3 | 0 | 2 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | ATGGC others(778): Show |
chr3 | 9957682 | 9991841 | ||
| a0001c0004 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | ATGGC others(778): Show |
chr3 | 9957682 | 9991841 | ||
| a0001c0005 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | ATGGC others(778): Show |
chr3 | 9957682 | 9991841 | ||
| a0002c0007 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | ATGGC others(778): Show |
chr3 | 9957682 | 9991841 | ||
| a0003c0006 | 0/0 | 750 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | ATGGC others(745): Show |
chr3 | 9957682 | 9991841 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2353 | 97 | 11 | 22 | 50 | 0 | 13 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0002 | 0/0 | 2373 | 53 | 5 | 15 | 24 | 3 | 6 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0003 | 0/0 | 2353 | 30 | 22 | 6 | 1 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0004 | 0/0 | 2373 | 17 | 17 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0005 | 0/0 | 2353 | 13 | 3 | 3 | 6 | 1 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0006 | 0/0 | 2359 | 9 | 9 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2354): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0007 | 0/0 | 2373 | 8 | 3 | 1 | 4 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0008 | 0/0 | 2350 | 6 | 1 | 2 | 2 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2345): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0009 | 0/0 | 2359 | 6 | 4 | 2 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2354): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0010 | 0/0 | 2355 | 6 | 0 | 0 | 4 | 1 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2350): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0011 | 0/0 | 2354 | 5 | 0 | 0 | 4 | 1 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2349): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0012 | 0/0 | 2359 | 2 | 0 | 0 | 2 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2354): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0013 | 0/0 | 2375 | 4 | 0 | 0 | 4 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2370): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0014 | 0/0 | 2350 | 4 | 0 | 0 | 3 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2345): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0015 | 0/0 | 2357 | 3 | 0 | 0 | 3 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2352): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0016 | 0/0 | 2353 | 3 | 0 | 0 | 2 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0017 | 0/0 | 2374 | 3 | 1 | 2 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2369): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0018 | 0/0 | 2371 | 3 | 0 | 3 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2366): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0019 | 0/0 | 2350 | 3 | 0 | 0 | 0 | 0 | 3 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2345): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0020 | 0/0 | 2373 | 3 | 2 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0021 | 0/0 | 2353 | 2 | 1 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0022 | 0/0 | 2372 | 2 | 1 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2367): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0023 | 0/0 | 2353 | 2 | 2 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0024 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0025 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0026 | 0/0 | 2374 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2369): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0027 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0028 | 0/1 | 2359 | 1 | 0 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2354): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0029 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2347): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0030 | 0/0 | 2363 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2358): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0031 | 0/0 | 2341 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2336): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0032 | 0/0 | 2357 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2352): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0033 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0034 | 0/0 | 2354 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2349): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0035 | 0/0 | 2377 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2372): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0036 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0037 | 0/0 | 2371 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2366): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0038 | 0/0 | 2374 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2369): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0039 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0040 | 0/0 | 2359 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2354): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0041 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0042 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0043 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2392): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0044 | 0/0 | 2393 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2388): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0045 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0046 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0047 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0048 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0001t0049 | 0/0 | 2375 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2370): Show |
chr3 | 9957682 | 9991841 |
| a0001c0002t0001 | 0/0 | 2353 | 3 | 0 | 0 | 3 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0002t0012 | 0/0 | 2359 | 2 | 0 | 0 | 2 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2354): Show |
chr3 | 9957682 | 9991841 |
| a0001c0003t0001 | 0/0 | 2353 | 3 | 0 | 2 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0001c0004t0008 | 0/0 | 2350 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2345): Show |
chr3 | 9957682 | 9991841 |
| a0001c0005t0001 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2348): Show |
chr3 | 9957682 | 9991841 |
| a0002c0007t0002 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2368): Show |
chr3 | 9957682 | 9991841 |
| a0003c0006t0001 | 0/0 | 2320 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | AAGTG others(2315): Show |
chr3 | 9957682 | 9991841 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0019 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0007g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0008g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0009g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0010g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0010g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0010g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0011g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0011g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0011g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0012g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0012g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0013g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0013g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0013g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0013g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0014g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0014g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0014g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0015g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0015g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0015g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0016g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0016g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0016g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0017g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0017g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0017g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0018g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0018g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0018g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0019g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0019g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0019g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0020g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0020g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0020g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0021g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0021g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0022g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0022g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0023g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0023g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0024g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0025g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0026g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0027g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0028g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0029g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0030g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0031g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0032g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0033g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0034g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0035g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0036g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0037g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0038g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0039g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0040g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0041g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0042g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0043g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0044g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0045g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0046g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0047g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0048g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0001t0049g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0002t0012g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0002t0012g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0004t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0001c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0002c0007t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| a0003c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0010 | g0160 | EUR | FIN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00280 | hp2 | a0001 | c0001 | t0011 | g0199 | EUR | FIN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00408 | hp1 | a0001 | c0001 | t0013 | g0032 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00408 | hp2 | a0001 | c0001 | t0011 | g0186 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00423 | hp1 | a0001 | c0005 | t0001 | g0218 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00423 | hp2 | a0001 | c0001 | t0011 | g0190 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00438 | hp2 | a0001 | c0001 | t0011 | g0196 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00558 | hp1 | a0001 | c0001 | t0014 | g0014 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00609 | hp1 | a0001 | c0001 | t0007 | g0046 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00621 | hp1 | a0001 | c0001 | t0016 | g0175 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00639 | hp1 | a0001 | c0001 | t0017 | g0031 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0050 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00741 | hp1 | a0001 | c0001 | t0027 | g0173 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG00741 | hp2 | a0001 | c0001 | t0018 | g0038 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01069 | hp2 | a0001 | c0001 | t0020 | g0270 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01081 | hp1 | a0001 | c0001 | t0022 | g0074 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01099 | hp2 | a0001 | c0001 | t0009 | g0006 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01109 | hp1 | a0001 | c0001 | t0031 | g0193 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0006 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0154 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01192 | hp1 | a0001 | c0001 | t0030 | g0220 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0235 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0251 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0146 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0265 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0157 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0080 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0252 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02004 | hp1 | a0001 | c0001 | t0017 | g0051 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0112 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02148 | hp2 | a0001 | c0001 | t0025 | g0029 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02155 | hp1 | a0001 | c0001 | t0041 | g0187 | EAS | CDX | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02155 | hp2 | a0001 | c0001 | t0011 | g0202 | EAS | CDX | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02258 | hp2 | a0001 | c0001 | t0023 | g0260 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02273 | hp1 | a0001 | c0001 | t0018 | g0065 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0100 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02293 | hp2 | a0001 | c0001 | t0018 | g0061 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02451 | hp1 | a0001 | c0001 | t0049 | g0272 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0239 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02602 | hp1 | a0001 | c0001 | t0032 | g0203 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02602 | hp2 | a0001 | c0001 | t0026 | g0066 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0267 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0277 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02683 | hp1 | a0001 | c0001 | t0019 | g0227 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02698 | hp1 | a0001 | c0001 | t0019 | g0228 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02717 | hp1 | a0001 | c0001 | t0038 | g0043 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02723 | hp1 | a0001 | c0001 | t0045 | g0259 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02735 | hp1 | a0001 | c0001 | t0016 | g0166 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02738 | hp1 | a0001 | c0001 | t0014 | g0082 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02818 | hp1 | a0001 | c0001 | t0046 | g0258 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0280 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0060 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0279 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02976 | hp1 | a0001 | c0001 | t0047 | g0266 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02976 | hp2 | a0001 | c0001 | t0037 | g0073 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03041 | hp2 | a0001 | c0001 | t0020 | g0269 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03098 | hp1 | a0001 | c0001 | t0023 | g0268 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0262 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0121 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03209 | hp1 | a0001 | c0001 | t0044 | g0256 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0083 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03453 | hp1 | a0001 | c0001 | t0021 | g0122 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03486 | hp1 | a0001 | c0001 | t0034 | g0087 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0253 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0264 | AFR | ESN | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0278 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03688 | hp2 | a0001 | c0001 | t0019 | g0229 | SAS | STU | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG04115 | hp1 | a0001 | c0001 | t0043 | g0257 | SAS | STU | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG04199 | hp1 | a0001 | c0001 | t0039 | g0244 | SAS | STU | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | STU | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | YRI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0076 | AFR | YRI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | CHB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18747 | hp1 | a0001 | c0001 | t0042 | g0255 | EAS | CHB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18747 | hp2 | a0001 | c0001 | t0014 | g0014 | EAS | CHB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | YRI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | YRI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18942 | hp1 | a0001 | c0002 | t0012 | g0248 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18948 | hp2 | a0001 | c0001 | t0013 | g0036 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18952 | hp1 | a0001 | c0001 | t0040 | g0168 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18957 | hp2 | a0001 | c0001 | t0035 | g0030 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18959 | hp1 | a0001 | c0001 | t0010 | g0205 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18959 | hp2 | a0002 | c0007 | t0002 | g0254 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18962 | hp1 | a0001 | c0001 | t0029 | g0184 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18967 | hp1 | a0001 | c0001 | t0014 | g0081 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18969 | hp1 | a0001 | c0001 | t0015 | g0209 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18971 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18978 | hp1 | a0001 | c0001 | t0010 | g0179 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18980 | hp2 | a0001 | c0001 | t0015 | g0115 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18982 | hp1 | a0001 | c0001 | t0024 | g0028 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18982 | hp2 | a0001 | c0001 | t0012 | g0145 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18986 | hp1 | a0001 | c0001 | t0008 | g0079 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18986 | hp2 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18988 | hp1 | a0001 | c0004 | t0008 | g0078 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18991 | hp1 | a0001 | c0001 | t0010 | g0086 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18991 | hp2 | a0001 | c0001 | t0013 | g0053 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | LWK | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19055 | hp1 | a0001 | c0002 | t0012 | g0247 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19057 | hp2 | a0001 | c0001 | t0010 | g0180 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19065 | hp1 | a0003 | c0006 | t0001 | g0245 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19077 | hp2 | a0001 | c0001 | t0012 | g0195 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19078 | hp1 | a0001 | c0001 | t0015 | g0170 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19078 | hp2 | a0001 | c0001 | t0013 | g0072 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19083 | hp1 | a0001 | c0001 | t0021 | g0084 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19084 | hp2 | a0001 | c0001 | t0016 | g0163 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19091 | hp1 | a0001 | c0001 | t0036 | g0047 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0285 | AFR | YRI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA19240 | hp2 | a0001 | c0001 | t0022 | g0063 | AFR | YRI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20129 | hp1 | a0001 | c0001 | t0048 | g0261 | AFR | ASW | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20129 | hp2 | a0001 | c0001 | t0033 | g0211 | AFR | ASW | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0237 | EUR | TSI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0167 | EUR | TSI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0243 | EUR | TSI | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0207 | SAS | GIH | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | GIH | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0127 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | USA | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | USA | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0077 | AFR | USA | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | USA | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0028 | g0092 | REF | REF | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0019 | REF | REF | EMC3_chr3_9957682_9991841 | EMC3 | chr3 | 9957682 | 9991841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:9986517 | CTTGTTCC others(26): Show |
C | 1 | a0003 | 1 | NA19065.hp1 | conservative_inframe_deletion | MODERATE | c.112_144delCTGCAGAG others(25): Show |
p.Leu38_Gln48del | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 324/2353 | 112/786 | 38/261 | chr3 | 9986517 | |||
| chr3:9986655 | C | A | 1 | a0002 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.7G>T | p.Gly3Trp | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 187/2353 | 7/786 | 3/261 | chr3 | 9986655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:9970607 | G | A | 1 | a0001c0005 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.549C>T | p.Tyr183Tyr | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 6/8 | 729/2353 | 549/786 | 183/261 | chr3 | 9970607 | |||
| chr3:9973681 | A | T | 1 | a0001c0004 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.441T>A | p.Arg147Arg | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/8 | 621/2353 | 441/786 | 147/261 | chr3 | 9973681 | |||
| chr3:9986536 | C | T | 1 | a0001c0001 | 2 | HG01358.hp2 NA20752.hp2 |
synonymous_variant | LOW | c.126G>A | p.Lys42Lys | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 306/2353 | 126/786 | 42/261 | chr3 | 9986536 | |||
| chr3:9986605 | G | C | 1 | a0001c0002 | 5 | NA18612.hp2 NA18942.hp1 NA18943.hp1 others(2): Show |
synonymous_variant | LOW | c.57C>G | p.Pro19Pro | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 237/2353 | 57/786 | 19/261 | chr3 | 9986605 | |||
| chr3:9986610 | G | A | 1 | a0001c0003 | 3 | HG01496.hp1 HG01981.hp1 HG03490.hp1 |
synonymous_variant | LOW | c.52C>T | p.Leu18Leu | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 232/2353 | 52/786 | 18/261 | chr3 | 9986610 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:9962862 | G | A | 1 | a0001c0001t0019 | 3 | HG02683.hp1 HG02698.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1207C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 1207 | chr3 | 9962862 | ||||||
| chr3:9962962 | CACT | C | 4 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0019 others(1): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1104_*1106delAGT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 1104 | chr3 | 9962962 | ||||||
| chr3:9963084 | G | A | 22 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(19): Show |
107 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*985C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 985 | chr3 | 9963084 | ||||||
| chr3:9963450 | G | GATAGATA others(11): Show |
3 | a0001c0001t0018 a0001c0001t0022 a0001c0001t0037 |
6 | HG00741.hp2 HG01081.hp1 HG02273.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*618_*619insATCTAT others(12): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 618 | chr3 | 9963450 | ||||||
| chr3:9963450 | G | GATAGATA others(17): Show |
1 | a0001c0001t0035 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*618_*619insATCTAT others(18): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 618 | chr3 | 9963450 | ||||||
| chr3:9963450 | GATAGATA others(5): Show |
G | 1 | a0001c0001t0031 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*607_*618delATATAT others(6): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 607 | chr3 | 9963450 | ||||||
| chr3:9963454 | G | GAT | 1 | a0001c0001t0010 | 6 | HG00280.hp1 NA18959.hp1 NA18978.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*613_*614dupAT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 614 | chr3 | 9963454 | ||||||
| chr3:9963454 | G | GATAGAT | 1 | a0001c0001t0009 | 6 | HG01099.hp2 HG01109.hp2 HG01891.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*614_*615insATCTAT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 614 | chr3 | 9963454 | ||||||
| chr3:9963454 | G | GATAGATA others(13): Show |
10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(7): Show |
87 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*614_*615insATCTAT others(14): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 614 | chr3 | 9963454 | ||||||
| chr3:9963454 | G | GATAGATA others(37): Show |
1 | a0001c0001t0043 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*614_*615insATCTAT others(38): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 614 | chr3 | 9963454 | ||||||
| chr3:9963454 | G | GATAGATA others(3): Show |
1 | a0001c0001t0030 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*614_*615insATATAT others(4): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 614 | chr3 | 9963454 | ||||||
| chr3:9963454 | G | GATAT | 2 | a0001c0001t0015 a0001c0001t0032 |
4 | HG02602.hp1 NA18969.hp1 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*611_*614dupATAT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 614 | chr3 | 9963454 | ||||||
| chr3:9963454 | G | GATATAT | 3 | a0001c0001t0012 a0001c0001t0040 a0001c0002t0012 |
5 | NA18942.hp1 NA18952.hp1 NA18982.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*609_*614dupATATAT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 614 | chr3 | 9963454 | ||||||
| chr3:9963454 | G | T | 2 | a0001c0001t0005 a0001c0001t0021 |
15 | HG01168.hp2 HG01934.hp2 HG02293.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*615C>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 615 | chr3 | 9963454 | ||||||
| chr3:9963456 | T | TAGATAGA others(15): Show |
5 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0026 others(2): Show |
10 | HG00408.hp1 HG00639.hp1 HG02004.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*612_*613insCTATAT others(16): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 612 | chr3 | 9963456 | ||||||
| chr3:9963456 | T | TAGATAGA others(33): Show |
1 | a0001c0001t0044 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612_*613insCTATAT others(34): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 612 | chr3 | 9963456 | ||||||
| chr3:9963458 | T | G | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(13): Show |
132 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*611A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 611 | chr3 | 9963458 | ||||||
| chr3:9963460 | T | G | 3 | a0001c0001t0018 a0001c0001t0022 a0001c0001t0037 |
6 | HG00741.hp2 HG01081.hp1 HG02273.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*609A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 609 | chr3 | 9963460 | ||||||
| chr3:9963462 | T | G | 3 | a0001c0001t0008 a0001c0001t0019 a0001c0004t0008 |
10 | HG01952.hp2 HG01975.hp1 HG02683.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*607A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 607 | chr3 | 9963462 | ||||||
| chr3:9963466 | T | G | 2 | a0001c0001t0019 a0001c0001t0036 |
4 | HG02683.hp1 HG02698.hp1 HG03688.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*603A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 603 | chr3 | 9963466 | ||||||
| chr3:9963470 | T | G | 1 | a0001c0001t0019 | 3 | HG02683.hp1 HG02698.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*599A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 599 | chr3 | 9963470 | ||||||
| chr3:9963471 | A | ATTTTTT | 1 | a0001c0001t0006 | 9 | HG01891.hp2 HG02257.hp1 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*597_*598insAAAAAA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 597 | chr3 | 9963471 | ||||||
| chr3:9963473 | A | T | 2 | a0001c0001t0006 a0001c0001t0047 |
10 | HG01891.hp2 HG02257.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*596T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 596 | chr3 | 9963473 | ||||||
| chr3:9963474 | T | G | 1 | a0001c0001t0019 | 3 | HG02683.hp1 HG02698.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*595A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 595 | chr3 | 9963474 | ||||||
| chr3:9963475 | A | T | 3 | a0001c0001t0006 a0001c0001t0047 a0001c0001t0048 |
11 | HG01891.hp2 HG02257.hp1 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*594T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 594 | chr3 | 9963475 | ||||||
| chr3:9963476 | TA | T | 4 | a0001c0001t0017 a0001c0001t0026 a0001c0001t0029 others(1): Show |
6 | HG00639.hp1 HG02004.hp1 HG02602.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*592delT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 592 | chr3 | 9963476 | ||||||
| chr3:9963477 | A | AGATAGAT others(24): Show |
1 | a0001c0001t0019 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591_*592insAAATAT others(25): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | AGATAGAT others(24): Show |
1 | a0001c0001t0019 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*591_*592insAAATAT others(25): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | AGATAGAT others(20): Show |
1 | a0001c0001t0019 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591_*592insAAAAAT others(21): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*591_*592insAAAATA others(26): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATATAT others(27): Show |
1 | a0001c0001t0008 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*591_*592insAAAAAA others(28): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATATAT others(27): Show |
1 | a0001c0001t0008 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591_*592insAAAAAA others(28): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATATAT others(25): Show |
1 | a0001c0001t0008 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591_*592insAAAAAA others(26): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATATAT others(26): Show |
1 | a0001c0001t0008 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591_*592insAAAAAA others(27): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATATAT others(27): Show |
2 | a0001c0001t0008 a0001c0004t0008 |
3 | NA18971.hp2 NA18986.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*591_*592insAAAAAA others(28): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATATAT others(3): Show |
1 | a0001c0001t0005 | 2 | HG01168.hp2 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*591_*592insAATATA others(4): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATATT | 5 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0024 others(2): Show |
18 | HG00741.hp1 HG01081.hp2 HG01255.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*591_*592insAATATA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATATTT | 3 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0046 |
12 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*591_*592insAAATAT others(1): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATTT | 3 | a0001c0001t0001 a0001c0001t0003 a0001c0003t0001 |
6 | HG01981.hp1 HG02280.hp2 HG02735.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*591_*592insAAATA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | ATATTTT | 3 | a0001c0001t0001 a0001c0001t0003 a0001c0003t0001 |
16 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*591_*592insAAAATA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 591 | chr3 | 9963477 | ||||||
| chr3:9963477 | A | T | 12 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(9): Show |
50 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*592T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 592 | chr3 | 9963477 | ||||||
| chr3:9963478 | T | TA | 3 | a0001c0001t0011 a0001c0001t0022 a0001c0001t0034 |
8 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*590_*591insT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 590 | chr3 | 9963478 | ||||||
| chr3:9963479 | T | A | 7 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0020 others(4): Show |
19 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*590A>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 590 | chr3 | 9963479 | ||||||
| chr3:9963480 | T | A | 2 | a0001c0001t0033 a0001c0001t0034 |
2 | HG03486.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*589A>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 589 | chr3 | 9963480 | ||||||
| chr3:9963659 | G | C | 1 | a0001c0001t0038 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410C>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 410 | chr3 | 9963659 | ||||||
| chr3:9963689 | G | A | 1 | a0001c0001t0039 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 380 | chr3 | 9963689 | ||||||
| chr3:9963708 | T | C | 26 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(23): Show |
121 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*361A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 361 | chr3 | 9963708 | ||||||
| chr3:9963768 | G | A | 1 | a0001c0001t0040 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*301C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 301 | chr3 | 9963768 | ||||||
| chr3:9963785 | T | C | 1 | a0001c0001t0041 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*284A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 284 | chr3 | 9963785 | ||||||
| chr3:9963810 | C | T | 2 | a0001c0001t0043 a0001c0001t0044 |
2 | HG03209.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*259G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 259 | chr3 | 9963810 | ||||||
| chr3:9964009 | C | G | 1 | a0001c0001t0027 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60G>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 60 | chr3 | 9964009 | ||||||
| chr3:9964010 | A | T | 1 | a0001c0001t0027 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 59 | chr3 | 9964010 | ||||||
| chr3:9964057 | C | T | 1 | a0001c0001t0026 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 8/8 | 12 | chr3 | 9964057 | ||||||
| chr3:9986691 | A | T | 1 | a0001c0001t0025 | 1 | HG02148.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 30 | chr3 | 9986691 | ||||||
| chr3:9986739 | G | A | 1 | a0001c0001t0042 | 1 | NA18747.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 78 | chr3 | 9986739 | ||||||
| chr3:9986761 | C | T | 1 | a0001c0001t0024 | 1 | NA18982.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 100 | chr3 | 9986761 | ||||||
| chr3:9986768 | C | G | 2 | a0001c0001t0043 a0001c0001t0044 |
2 | HG03209.hp1 HG04115.hp1 |
5_prime_UTR_variant | MODIFIER | c.-107G>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 107 | chr3 | 9986768 | ||||||
| chr3:9986776 | C | A | 7 | a0001c0001t0004 a0001c0001t0020 a0001c0001t0043 others(4): Show |
25 | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-115G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 115 | chr3 | 9986776 | ||||||
| chr3:9986824 | C | A | 4 | a0001c0001t0006 a0001c0001t0023 a0001c0001t0047 others(1): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-163G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 163 | chr3 | 9986824 | ||||||
| chr3:9986830 | G | A | 3 | a0001c0001t0004 a0001c0001t0020 a0001c0001t0049 |
21 | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-169C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/8 | 169 | chr3 | 9986830 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:9964395 | A | C | 130 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0142 others(127): Show |
149 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.658-198T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9964395 | |||||||
| chr3:9964417 | G | A | 4 | a0001c0001t0002g0234 a0001c0001t0002g0237 a0001c0001t0002g0238 others(1): Show |
4 | HG00735.hp2 HG01257.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-220C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9964417 | |||||||
| chr3:9964635 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.658-438C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9964635 | |||||||
| chr3:9964642 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.658-445G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9964642 | |||||||
| chr3:9965003 | T | G | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.658-806A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965003 | |||||||
| chr3:9965009 | T | C | 1 | a0001c0001t0023g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.658-812A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965009 | |||||||
| chr3:9965088 | G | A | 1 | a0001c0001t0018g0038 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.658-891C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965088 | |||||||
| chr3:9965104 | T | TA | 14 | a0001c0001t0002g0068 a0001c0001t0004g0026 a0001c0001t0004g0271 others(11): Show |
15 | HG01884.hp2 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.658-908dupT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965104 | |||||||
| chr3:9965104 | TA | T | 7 | a0001c0001t0002g0033 a0001c0001t0002g0037 a0001c0001t0002g0056 others(4): Show |
7 | HG00639.hp1 HG01257.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.658-908delT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965104 | |||||||
| chr3:9965104 | TAA | T | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.658-909_658-908del others(2): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965104 | |||||||
| chr3:9965141 | T | C | 3 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0021g0122 |
3 | HG02615.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.658-944A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965141 | |||||||
| chr3:9965142 | C | T | 1 | a0001c0001t0017g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.658-945G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965142 | |||||||
| chr3:9965353 | C | T | 1 | a0001c0001t0004g0276 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.658-1156G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965353 | |||||||
| chr3:9965389 | C | G | 1 | a0001c0001t0001g0194 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.658-1192G>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965389 | |||||||
| chr3:9965416 | C | CGATA | 99 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0021 others(96): Show |
112 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.658-1223_658-1220d others(6): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965416 | |||||||
| chr3:9965416 | C | CGATAGAT others(1): Show |
29 | a0001c0001t0001g0095 a0001c0001t0001g0114 a0001c0001t0001g0116 others(26): Show |
32 | HG00621.hp1 HG02257.hp1 HG02293.hp2 others(29): Show |
intron_variant | MODIFIER | c.658-1227_658-1220d others(10): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965416 | |||||||
| chr3:9965416 | C | CGATAGAT others(5): Show |
19 | a0001c0001t0001g0164 a0001c0001t0002g0048 a0001c0001t0002g0057 others(16): Show |
19 | HG00558.hp2 HG00673.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.658-1231_658-1220d others(14): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965416 | |||||||
| chr3:9965416 | CGATA | C | 43 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0091 others(40): Show |
49 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.658-1223_658-1220d others(6): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965416 | |||||||
| chr3:9965416 | CGATAGAT others(1): Show |
C | 9 | a0001c0001t0001g0158 a0001c0001t0001g0208 a0001c0001t0003g0001 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.658-1227_658-1220d others(10): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965416 | |||||||
| chr3:9965840 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.658-1643G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9965840 | |||||||
| chr3:9966094 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.658-1897G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966094 | |||||||
| chr3:9966156 | C | T | 131 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0142 others(128): Show |
151 | HG00558.hp1 HG00609.hp1 HG00639.hp1 others(148): Show |
intron_variant | MODIFIER | c.658-1959G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966156 | |||||||
| chr3:9966161 | C | G | 1 | a0001c0001t0008g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.658-1964G>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966161 | |||||||
| chr3:9966283 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0171 others(1): Show |
4 | HG00438.hp1 HG02080.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-2086G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966283 | |||||||
| chr3:9966372 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.658-2175C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966372 | |||||||
| chr3:9966537 | G | A | 1 | a0001c0001t0014g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.658-2340C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966537 | |||||||
| chr3:9966679 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.658-2482T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966679 | |||||||
| chr3:9966713 | T | TA | 9 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(6): Show |
11 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.658-2517dupT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966713 | |||||||
| chr3:9966715 | C | T | 9 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(6): Show |
11 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.658-2518G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966715 | |||||||
| chr3:9966866 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.658-2669C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966866 | |||||||
| chr3:9966920 | C | G | 10 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0262 others(7): Show |
12 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.658-2723G>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966920 | |||||||
| chr3:9966950 | T | A | 12 | a0001c0001t0004g0026 a0001c0001t0004g0271 a0001c0001t0004g0273 others(9): Show |
13 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.658-2753A>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9966950 | |||||||
| chr3:9967135 | G | A | 142 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0142 others(139): Show |
163 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(160): Show |
intron_variant | MODIFIER | c.657+2584C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967135 | |||||||
| chr3:9967180 | G | A | 1 | a0001c0001t0023g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.657+2539C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967180 | |||||||
| chr3:9967221 | C | A | 107 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(104): Show |
121 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.657+2498G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967221 | |||||||
| chr3:9967329 | AT | A | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.657+2389delA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967329 | |||||||
| chr3:9967346 | G | T | 1 | a0001c0001t0022g0063 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.657+2373C>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967346 | |||||||
| chr3:9967379 | A | ACTTTTGT others(27): Show |
130 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0142 others(127): Show |
149 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.657+2306_657+2339d others(36): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967379 | |||||||
| chr3:9967437 | T | C | 1 | a0001c0001t0014g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.657+2282A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967437 | |||||||
| chr3:9967624 | T | C | 3 | a0001c0001t0003g0093 a0001c0001t0003g0133 a0001c0001t0003g0143 |
3 | HG01069.hp1 HG01071.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.657+2095A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967624 | |||||||
| chr3:9967643 | G | A | 20 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0271 others(17): Show |
22 | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.657+2076C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967643 | |||||||
| chr3:9967660 | A | T | 1 | a0001c0001t0007g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.657+2059T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967660 | |||||||
| chr3:9967986 | A | T | 2 | a0001c0001t0017g0031 a0001c0001t0038g0043 |
2 | HG00639.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.657+1733T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9967986 | |||||||
| chr3:9968124 | G | A | 12 | a0001c0001t0001g0165 a0001c0001t0006g0024 a0001c0001t0006g0025 others(9): Show |
14 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.657+1595C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968124 | |||||||
| chr3:9968153 | G | A | 1 | a0001c0001t0016g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.657+1566C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968153 | |||||||
| chr3:9968199 | C | T | 2 | a0001c0001t0006g0263 a0001c0001t0023g0268 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.657+1520G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968199 | |||||||
| chr3:9968216 | G | A | 1 | a0001c0001t0048g0261 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.657+1503C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968216 | |||||||
| chr3:9968235 | G | A | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(87): Show |
102 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.657+1484C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968235 | |||||||
| chr3:9968292 | T | C | 1 | a0001c0001t0005g0167 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.657+1427A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968292 | |||||||
| chr3:9968513 | A | C | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.657+1206T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968513 | |||||||
| chr3:9968624 | T | C | 95 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(92): Show |
107 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.657+1095A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968624 | |||||||
| chr3:9968668 | G | A | 21 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0142 others(18): Show |
25 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.657+1051C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968668 | |||||||
| chr3:9968708 | G | A | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.657+1011C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968708 | |||||||
| chr3:9968721 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.657+998A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968721 | |||||||
| chr3:9968819 | AT | A | 116 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(113): Show |
132 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.657+899delA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968819 | |||||||
| chr3:9968852 | CTT | C | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.657+865_657+866del others(2): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968852 | |||||||
| chr3:9968997 | G | A | 156 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0136 others(153): Show |
179 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.657+722C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9968997 | |||||||
| chr3:9969026 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(90): Show |
105 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.657+693A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9969026 | |||||||
| chr3:9969104 | C | A | 1 | a0001c0001t0002g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.657+615G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9969104 | |||||||
| chr3:9969115 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.657+604C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9969115 | |||||||
| chr3:9969205 | C | T | 1 | a0001c0001t0007g0058 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.657+514G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9969205 | |||||||
| chr3:9969259 | C | A | 1 | a0001c0001t0008g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.657+460G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9969259 | |||||||
| chr3:9969509 | T | C | 1 | a0001c0001t0039g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.657+210A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 7/7 | chr3 | 9969509 | |||||||
| chr3:9969932 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0010g0179 a0001c0001t0010g0205 |
3 | NA18959.hp1 NA18978.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.575-131C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 6/7 | chr3 | 9969932 | |||||||
| chr3:9969935 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.575-134T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 6/7 | chr3 | 9969935 | |||||||
| chr3:9969998 | G | C | 1 | a0001c0001t0002g0041 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.575-197C>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 6/7 | chr3 | 9969998 | |||||||
| chr3:9970107 | TC | T | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.575-307delG | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 6/7 | chr3 | 9970107 | |||||||
| chr3:9970111 | C | T | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.575-310G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 6/7 | chr3 | 9970111 | |||||||
| chr3:9970242 | G | A | 5 | a0001c0001t0001g0114 a0001c0001t0010g0086 a0001c0001t0010g0207 others(2): Show |
5 | NA18980.hp2 NA18991.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.574+340C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 6/7 | chr3 | 9970242 | |||||||
| chr3:9970319 | C | T | 1 | a0001c0001t0009g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.574+263G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 6/7 | chr3 | 9970319 | |||||||
| chr3:9970756 | T | C | 1 | a0001c0001t0046g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.495-95A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9970756 | |||||||
| chr3:9970867 | G | A | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.495-206C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9970867 | |||||||
| chr3:9970927 | C | CT | 104 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(101): Show |
118 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.495-267dupA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9970927 | |||||||
| chr3:9970991 | T | C | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.495-330A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9970991 | |||||||
| chr3:9970992 | G | A | 1 | a0001c0001t0046g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.495-331C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9970992 | |||||||
| chr3:9971037 | C | T | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.495-376G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971037 | |||||||
| chr3:9971044 | TC | T | 8 | a0001c0001t0003g0001 a0001c0001t0003g0093 a0001c0001t0003g0132 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.495-384delG | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971044 | |||||||
| chr3:9971073 | C | A | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(87): Show |
102 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.495-412G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971073 | |||||||
| chr3:9971104 | T | G | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.495-443A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971104 | |||||||
| chr3:9971265 | A | T | 2 | a0001c0001t0001g0153 a0001c0001t0024g0028 |
2 | NA18982.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.495-604T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971265 | |||||||
| chr3:9971270 | C | G | 1 | a0001c0001t0002g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.495-609G>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971270 | |||||||
| chr3:9971426 | T | C | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.495-765A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971426 | |||||||
| chr3:9971550 | T | C | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.495-889A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971550 | |||||||
| chr3:9971589 | A | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(90): Show |
105 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.495-928T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971589 | |||||||
| chr3:9971698 | G | T | 1 | a0001c0001t0007g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.495-1037C>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971698 | |||||||
| chr3:9971703 | G | C | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 |
4 | HG02647.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-1042C>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971703 | |||||||
| chr3:9971886 | T | C | 2 | a0001c0002t0012g0247 a0001c0002t0012g0248 |
2 | NA18942.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.495-1225A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9971886 | |||||||
| chr3:9972014 | C | A | 34 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0142 others(31): Show |
41 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.495-1353G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972014 | |||||||
| chr3:9972230 | GA | G | 109 | a0001c0001t0001g0114 a0001c0001t0002g0003 a0001c0001t0002g0004 others(106): Show |
123 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.494+1397delT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972230 | |||||||
| chr3:9972317 | G | T | 3 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0021g0122 |
3 | HG02615.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.494+1311C>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972317 | |||||||
| chr3:9972462 | G | GA | 21 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0142 others(18): Show |
22 | HG00673.hp2 HG01891.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.494+1165dupT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972462 | |||||||
| chr3:9972462 | GAAA | G | 102 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(99): Show |
116 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.494+1163_494+1165d others(5): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972462 | |||||||
| chr3:9972462 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0001g0198 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.494+1156_494+1165d others(12): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972462 | |||||||
| chr3:9972478 | A | C | 1 | a0001c0001t0002g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.494+1150T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972478 | |||||||
| chr3:9972481 | A | C | 103 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(100): Show |
117 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.494+1147T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972481 | |||||||
| chr3:9972487 | C | T | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.494+1141G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972487 | |||||||
| chr3:9972507 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.494+1121T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972507 | |||||||
| chr3:9972513 | G | A | 1 | a0001c0001t0042g0255 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.494+1115C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972513 | |||||||
| chr3:9972607 | T | C | 11 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0262 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.494+1021A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972607 | |||||||
| chr3:9972615 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.494+1013T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972615 | |||||||
| chr3:9972720 | G | A | 3 | a0001c0001t0019g0227 a0001c0001t0019g0228 a0001c0001t0019g0229 |
3 | HG02683.hp1 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.494+908C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972720 | |||||||
| chr3:9972753 | A | G | 1 | a0001c0001t0023g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.494+875T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972753 | |||||||
| chr3:9972766 | A | G | 3 | a0001c0001t0003g0126 a0001c0001t0003g0130 a0001c0001t0003g0131 |
3 | HG01884.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.494+862T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972766 | |||||||
| chr3:9972777 | C | G | 1 | a0001c0001t0002g0049 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.494+851G>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972777 | |||||||
| chr3:9972801 | C | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(90): Show |
105 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.494+827G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972801 | |||||||
| chr3:9972832 | CT | C | 104 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(101): Show |
118 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+795delA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972832 | |||||||
| chr3:9972868 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.494+760C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9972868 | |||||||
| chr3:9973072 | G | A | 1 | a0001c0001t0023g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.494+556C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973072 | |||||||
| chr3:9973089 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18956.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.494+539A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973089 | |||||||
| chr3:9973179 | G | T | 1 | a0001c0004t0008g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.494+449C>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973179 | |||||||
| chr3:9973180 | T | G | 1 | a0001c0004t0008g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.494+448A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973180 | |||||||
| chr3:9973185 | G | GT | 13 | a0001c0001t0002g0041 a0001c0001t0002g0045 a0001c0001t0002g0048 others(10): Show |
13 | HG00408.hp1 HG01081.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.494+442dupA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973185 | |||||||
| chr3:9973192 | G | T | 107 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(104): Show |
121 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.494+436C>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973192 | |||||||
| chr3:9973295 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.494+333A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973295 | |||||||
| chr3:9973298 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.494+330T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973298 | |||||||
| chr3:9973315 | C | T | 35 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0142 others(32): Show |
42 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.494+313G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973315 | |||||||
| chr3:9973426 | T | C | 152 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0136 others(149): Show |
175 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(172): Show |
intron_variant | MODIFIER | c.494+202A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 5/7 | chr3 | 9973426 | |||||||
| chr3:9973753 | T | C | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.413-44A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 4/7 | chr3 | 9973753 | |||||||
| chr3:9974000 | A | G | 1 | a0001c0001t0007g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.413-291T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 4/7 | chr3 | 9974000 | |||||||
| chr3:9974056 | C | T | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.412+328G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 4/7 | chr3 | 9974056 | |||||||
| chr3:9974111 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.412+273G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 4/7 | chr3 | 9974111 | |||||||
| chr3:9974185 | C | T | 2 | a0001c0001t0017g0031 a0001c0001t0038g0043 |
2 | HG00639.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.412+199G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 4/7 | chr3 | 9974185 | |||||||
| chr3:9974582 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.308-94C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9974582 | |||||||
| chr3:9974621 | C | T | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.308-133G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9974621 | |||||||
| chr3:9974693 | G | T | 1 | a0001c0004t0008g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.308-205C>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9974693 | |||||||
| chr3:9974750 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.308-262C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9974750 | |||||||
| chr3:9974857 | G | GT | 119 | a0001c0001t0001g0021 a0001c0001t0001g0099 a0001c0001t0001g0103 others(116): Show |
133 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.308-370dupA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9974857 | |||||||
| chr3:9974857 | G | GTT | 31 | a0001c0001t0002g0011 a0001c0001t0002g0039 a0001c0001t0002g0040 others(28): Show |
32 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.308-371_308-370dup others(2): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9974857 | |||||||
| chr3:9975012 | T | C | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.308-524A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975012 | |||||||
| chr3:9975049 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.308-561G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975049 | |||||||
| chr3:9975092 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.308-604A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975092 | |||||||
| chr3:9975227 | A | C | 31 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(28): Show |
35 | HG00609.hp1 HG00673.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.308-739T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975227 | |||||||
| chr3:9975285 | T | A | 1 | a0001c0001t0010g0180 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.308-797A>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975285 | |||||||
| chr3:9975321 | G | C | 1 | a0001c0001t0004g0274 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.308-833C>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975321 | |||||||
| chr3:9975348 | T | A | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.308-860A>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975348 | |||||||
| chr3:9975506 | TA | T | 14 | a0001c0001t0001g0169 a0001c0001t0004g0275 a0001c0001t0006g0024 others(11): Show |
16 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.308-1019delT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975506 | |||||||
| chr3:9975555 | G | C | 1 | a0001c0001t0010g0160 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.308-1067C>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975555 | |||||||
| chr3:9975587 | C | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(90): Show |
105 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.308-1099G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975587 | |||||||
| chr3:9975669 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.308-1181C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975669 | |||||||
| chr3:9975761 | G | A | 1 | a0001c0001t0040g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.307+1196C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975761 | |||||||
| chr3:9975815 | G | GA | 14 | a0001c0001t0001g0108 a0001c0001t0001g0198 a0001c0001t0001g0221 others(11): Show |
16 | HG01891.hp2 HG01978.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+1141dupT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975815 | |||||||
| chr3:9975815 | GA | G | 44 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0124 others(41): Show |
52 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.307+1141delT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975815 | |||||||
| chr3:9975815 | GAA | G | 6 | a0001c0001t0013g0072 a0001c0001t0019g0227 a0001c0001t0019g0228 others(3): Show |
6 | HG02683.hp1 HG02698.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.307+1140_307+1141d others(4): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975815 | |||||||
| chr3:9975815 | GAAA | G | 87 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(84): Show |
99 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.307+1139_307+1141d others(5): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975815 | |||||||
| chr3:9975845 | G | A | 14 | a0001c0001t0002g0003 a0001c0001t0002g0232 a0001c0001t0002g0233 others(11): Show |
17 | HG00735.hp1 HG00735.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.307+1112C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975845 | |||||||
| chr3:9975862 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.307+1095T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9975862 | |||||||
| chr3:9976005 | T | A | 12 | a0001c0001t0004g0026 a0001c0001t0004g0271 a0001c0001t0004g0273 others(9): Show |
13 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.307+952A>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9976005 | |||||||
| chr3:9976076 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.307+881G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9976076 | |||||||
| chr3:9976176 | A | G | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.307+781T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9976176 | |||||||
| chr3:9976232 | G | A | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.307+725C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9976232 | |||||||
| chr3:9976422 | A | G | 5 | a0001c0002t0001g0246 a0001c0002t0001g0249 a0001c0002t0001g0250 others(2): Show |
5 | NA18612.hp2 NA18942.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+535T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9976422 | |||||||
| chr3:9976620 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.307+337T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9976620 | |||||||
| chr3:9976639 | A | G | 13 | a0001c0001t0002g0003 a0001c0001t0002g0232 a0001c0001t0002g0234 others(10): Show |
16 | HG00735.hp1 HG00735.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.307+318T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 3/7 | chr3 | 9976639 | |||||||
| chr3:9977283 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213+106A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 2/7 | chr3 | 9977283 | |||||||
| chr3:9977577 | C | T | 19 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0271 others(16): Show |
21 | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.156-131G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9977577 | |||||||
| chr3:9977581 | A | T | 1 | a0001c0001t0002g0042 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.156-135T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9977581 | |||||||
| chr3:9977729 | T | C | 1 | a0001c0001t0009g0146 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.156-283A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9977729 | |||||||
| chr3:9978089 | T | C | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.156-643A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978089 | |||||||
| chr3:9978145 | T | TAAAA | 19 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0089 others(16): Show |
22 | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.156-703_156-700dup others(4): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | T | TAAAAA | 19 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0090 others(16): Show |
21 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.156-704_156-700dup others(5): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | T | TAAAAAA | 12 | a0001c0001t0001g0094 a0001c0001t0001g0106 a0001c0001t0001g0107 others(9): Show |
12 | HG00280.hp2 HG01346.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.156-705_156-700dup others(6): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | T | TAAAAAAA others(3): Show |
4 | a0001c0001t0001g0023 a0001c0001t0001g0206 a0001c0001t0002g0096 others(1): Show |
5 | HG02135.hp2 HG03239.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.156-709_156-700dup others(10): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | T | TAAAAAAA others(4): Show |
2 | a0001c0001t0001g0097 a0001c0001t0001g0208 |
2 | HG01433.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.156-710_156-700dup others(11): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0015g0209 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.156-711_156-700dup others(12): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0210 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.156-712_156-700dup others(13): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | T | TAAAAAAA others(7): Show |
2 | a0001c0001t0002g0098 a0001c0001t0033g0211 |
2 | NA19077.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.156-713_156-700dup others(14): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0001g0212 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.156-714_156-700dup others(15): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | T | TAAAAAAA others(15): Show |
1 | a0001c0001t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.156-721_156-700dup others(22): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TA | T | 16 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0164 others(13): Show |
19 | HG00558.hp2 HG01255.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.156-700delT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAA | T | 15 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(12): Show |
15 | HG00280.hp1 HG01081.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.156-701_156-700del others(2): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAA | T | 5 | a0001c0001t0002g0010 a0001c0001t0002g0037 a0001c0001t0002g0041 others(2): Show |
6 | HG00741.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-705_156-700del others(6): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA | T | 12 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0232 others(9): Show |
15 | HG00735.hp1 HG01081.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.156-706_156-700del others(7): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(1): Show |
T | 39 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0002g0003 others(36): Show |
44 | HG00408.hp1 HG00735.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.156-707_156-700del others(8): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(2): Show |
T | 47 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0002g0011 others(44): Show |
54 | HG00609.hp1 HG00639.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.156-708_156-700del others(9): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(3): Show |
T | 27 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0226 others(24): Show |
30 | HG01069.hp1 HG01175.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.156-709_156-700del others(10): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(4): Show |
T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0003g0110 others(3): Show |
7 | HG00558.hp1 HG01175.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.156-710_156-700del others(11): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(5): Show |
T | 9 | a0001c0001t0001g0123 a0001c0001t0005g0120 a0001c0001t0005g0121 others(6): Show |
10 | HG01074.hp1 HG01952.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.156-711_156-700del others(12): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(6): Show |
T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0010g0086 others(1): Show |
4 | NA18988.hp1 NA18991.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-712_156-700del others(13): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(7): Show |
T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0006g0267 others(1): Show |
4 | HG02615.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-713_156-700del others(14): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(8): Show |
T | 6 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0262 others(3): Show |
8 | HG01891.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.156-714_156-700del others(15): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(10): Show |
T | 2 | a0001c0001t0001g0114 a0001c0001t0015g0115 |
2 | NA18980.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.156-716_156-700del others(17): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(12): Show |
T | 2 | a0001c0001t0001g0099 a0001c0001t0021g0084 |
2 | HG01433.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.156-718_156-700del others(19): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978145 | TAAAAAAA others(13): Show |
T | 2 | a0001c0001t0001g0113 a0001c0001t0009g0112 |
2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.156-719_156-700del others(20): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978145 | |||||||
| chr3:9978206 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.156-760C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978206 | |||||||
| chr3:9978292 | G | A | 5 | a0001c0001t0003g0110 a0001c0001t0003g0111 a0001c0001t0003g0214 others(2): Show |
5 | HG02280.hp1 HG02559.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.156-846C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978292 | |||||||
| chr3:9978403 | G | A | 10 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0102 others(7): Show |
10 | HG00639.hp2 HG01358.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.156-957C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978403 | |||||||
| chr3:9978447 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.156-1001T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978447 | |||||||
| chr3:9978448 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.156-1002C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978448 | |||||||
| chr3:9978590 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.156-1144C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978590 | |||||||
| chr3:9978597 | C | G | 2 | a0001c0001t0003g0110 a0001c0001t0003g0111 |
2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.156-1151G>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978597 | |||||||
| chr3:9978716 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.156-1270C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978716 | |||||||
| chr3:9978786 | A | T | 2 | a0001c0001t0006g0263 a0001c0001t0023g0268 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.156-1340T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978786 | |||||||
| chr3:9978814 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.156-1368T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978814 | |||||||
| chr3:9978821 | C | T | 10 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0102 others(7): Show |
10 | HG00639.hp2 HG01358.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.156-1375G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978821 | |||||||
| chr3:9978843 | A | AAAAC | 95 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(92): Show |
107 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.156-1401_156-1398d others(6): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978843 | |||||||
| chr3:9978843 | A | C | 1 | a0001c0001t0002g0041 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.156-1397T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978843 | |||||||
| chr3:9978865 | A | T | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.156-1419T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978865 | |||||||
| chr3:9978868 | T | G | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.156-1422A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978868 | |||||||
| chr3:9978938 | C | T | 116 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(113): Show |
132 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.156-1492G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9978938 | |||||||
| chr3:9979045 | T | A | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0243 |
3 | HG01255.hp2 NA18961.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.156-1599A>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979045 | |||||||
| chr3:9979052 | G | A | 7 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0262 others(4): Show |
9 | HG01891.hp2 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.156-1606C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979052 | |||||||
| chr3:9979119 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.156-1673G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979119 | |||||||
| chr3:9979358 | C | A | 3 | a0001c0001t0019g0227 a0001c0001t0019g0228 a0001c0001t0019g0229 |
3 | HG02683.hp1 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.156-1912G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979358 | |||||||
| chr3:9979393 | A | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0002g0096 others(1): Show |
4 | HG02135.hp2 NA18971.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-1947T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979393 | |||||||
| chr3:9979454 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.156-2008T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979454 | |||||||
| chr3:9979470 | T | G | 1 | a0001c0001t0002g0243 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.156-2024A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979470 | |||||||
| chr3:9979659 | T | C | 2 | a0001c0001t0022g0074 a0001c0001t0037g0073 |
2 | HG01081.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.156-2213A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979659 | |||||||
| chr3:9979701 | A | G | 2 | a0001c0001t0043g0257 a0001c0001t0044g0256 |
2 | HG03209.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.156-2255T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979701 | |||||||
| chr3:9979827 | G | A | 22 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0271 others(19): Show |
24 | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.156-2381C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979827 | |||||||
| chr3:9979917 | C | T | 116 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(113): Show |
132 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.156-2471G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9979917 | |||||||
| chr3:9980014 | A | AT | 82 | a0001c0001t0001g0094 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
94 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.156-2569dupA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980014 | |||||||
| chr3:9980014 | A | ATT | 24 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0271 others(21): Show |
26 | HG00639.hp1 HG01069.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.156-2570_156-2569d others(4): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980014 | |||||||
| chr3:9980067 | G | A | 1 | a0001c0005t0001g0218 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.156-2621C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980067 | |||||||
| chr3:9980117 | A | G | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.156-2671T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980117 | |||||||
| chr3:9980228 | GGTCTCGA others(1929): Show |
G | 1 | a0001c0001t0004g0285 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.155+4343_156-2783d others(2): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980228 | |||||||
| chr3:9980230 | T | G | 1 | a0001c0001t0034g0087 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.156-2784A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980230 | |||||||
| chr3:9980368 | A | AT | 100 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(97): Show |
114 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.156-2923dupA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980368 | |||||||
| chr3:9980459 | G | A | 1 | a0001c0001t0023g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.156-3013C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980459 | |||||||
| chr3:9980554 | G | GT | 93 | a0001c0001t0001g0104 a0001c0001t0001g0150 a0001c0001t0001g0169 others(90): Show |
104 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.156-3109dupA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980554 | |||||||
| chr3:9980554 | G | GTT | 9 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0039 others(6): Show |
9 | HG01346.hp2 HG01981.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.156-3110_156-3109d others(4): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980554 | |||||||
| chr3:9980554 | G | T | 2 | a0001c0001t0005g0167 a0001c0001t0046g0258 |
2 | HG02818.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.156-3108C>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980554 | |||||||
| chr3:9980974 | T | C | 116 | a0001c0001t0001g0206 a0001c0001t0002g0003 a0001c0001t0002g0004 others(113): Show |
132 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.156-3528A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980974 | |||||||
| chr3:9980978 | TGAGCCCT others(1): Show |
T | 3 | a0001c0002t0001g0250 a0001c0002t0012g0247 a0001c0002t0012g0248 |
3 | NA18612.hp2 NA18942.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.156-3540_156-3533d others(10): Show |
EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9980978 | |||||||
| chr3:9981005 | A | C | 1 | a0001c0001t0046g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.156-3559T>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981005 | |||||||
| chr3:9981009 | C | T | 1 | a0001c0001t0011g0202 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.156-3563G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981009 | |||||||
| chr3:9981056 | T | C | 1 | a0001c0001t0004g0276 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.156-3610A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981056 | |||||||
| chr3:9981073 | C | T | 18 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0271 others(15): Show |
20 | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.156-3627G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981073 | |||||||
| chr3:9981194 | A | G | 110 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(107): Show |
124 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.156-3748T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981194 | |||||||
| chr3:9981236 | C | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(276): Show |
315 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.156-3790G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981236 | |||||||
| chr3:9981251 | G | A | 104 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(101): Show |
118 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.156-3805C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981251 | |||||||
| chr3:9981949 | A | T | 2 | a0001c0001t0011g0186 a0001c0001t0011g0190 |
2 | HG00408.hp2 HG00423.hp2 |
intron_variant | MODIFIER | c.156-4503T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981949 | |||||||
| chr3:9981949 | AT | A | 105 | a0001c0001t0001g0156 a0001c0001t0002g0003 a0001c0001t0002g0004 others(102): Show |
118 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.156-4504delA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981949 | |||||||
| chr3:9981950 | T | A | 2 | a0001c0001t0001g0165 a0001c0001t0003g0162 |
2 | NA19012.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.156-4504A>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9981950 | |||||||
| chr3:9982020 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0015g0115 |
2 | NA18980.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.155+4487C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982020 | |||||||
| chr3:9982073 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.155+4434C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982073 | |||||||
| chr3:9982280 | A | G | 9 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0262 others(6): Show |
11 | HG01891.hp2 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.155+4227T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982280 | |||||||
| chr3:9982324 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.155+4183C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982324 | |||||||
| chr3:9982364 | C | T | 1 | a0001c0001t0007g0046 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.155+4143G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982364 | |||||||
| chr3:9982703 | C | A | 1 | a0001c0001t0039g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.155+3804G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982703 | |||||||
| chr3:9982704 | G | C | 9 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(6): Show |
11 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.155+3803C>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982704 | |||||||
| chr3:9982712 | C | A | 23 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0271 others(20): Show |
25 | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.155+3795G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982712 | |||||||
| chr3:9982760 | G | A | 1 | a0001c0001t0030g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.155+3747C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982760 | |||||||
| chr3:9982802 | CT | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | NA18950.hp1 NA18979.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.155+3704delA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9982802 | |||||||
| chr3:9983015 | T | G | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.155+3492A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983015 | |||||||
| chr3:9983082 | T | G | 1 | a0001c0001t0002g0075 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.155+3425A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983082 | |||||||
| chr3:9983149 | AT | A | 67 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(64): Show |
77 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.155+3357delA | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983149 | |||||||
| chr3:9983173 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.155+3334T>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983173 | |||||||
| chr3:9983188 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02040.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.155+3319G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983188 | |||||||
| chr3:9983200 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | NA18992.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.155+3307A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983200 | |||||||
| chr3:9983238 | C | A | 1 | a0001c0001t0023g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.155+3269G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983238 | |||||||
| chr3:9983275 | G | A | 1 | a0001c0001t0038g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.155+3232C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983275 | |||||||
| chr3:9983465 | G | C | 1 | a0001c0001t0004g0285 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.155+3042C>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983465 | |||||||
| chr3:9983470 | C | T | 3 | a0001c0001t0005g0005 a0001c0001t0005g0015 a0001c0001t0005g0088 |
6 | NA18942.hp2 NA18961.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.155+3037G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983470 | |||||||
| chr3:9983671 | CA | C | 70 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(67): Show |
80 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.155+2835delT | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983671 | |||||||
| chr3:9983709 | T | C | 37 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(34): Show |
41 | HG00609.hp1 HG00673.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.155+2798A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983709 | |||||||
| chr3:9983732 | A | G | 1 | a0001c0001t0023g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.155+2775T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983732 | |||||||
| chr3:9983755 | T | G | 1 | a0001c0001t0008g0083 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.155+2752A>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983755 | |||||||
| chr3:9983779 | G | A | 70 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(67): Show |
80 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.155+2728C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9983779 | |||||||
| chr3:9984059 | C | T | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.155+2448G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9984059 | |||||||
| chr3:9984150 | C | T | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.155+2357G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9984150 | |||||||
| chr3:9984211 | A | G | 1 | a0001c0001t0034g0087 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.155+2296T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9984211 | |||||||
| chr3:9984270 | T | C | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.155+2237A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9984270 | |||||||
| chr3:9984272 | G | T | 1 | a0001c0001t0010g0086 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.155+2235C>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9984272 | |||||||
| chr3:9984274 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155+2233C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9984274 | |||||||
| chr3:9984395 | T | C | 105 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(102): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.155+2112A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9984395 | |||||||
| chr3:9984931 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0021g0084 |
2 | NA18983.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.155+1576T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9984931 | |||||||
| chr3:9985353 | T | C | 9 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0262 others(6): Show |
11 | HG01891.hp2 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.155+1154A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9985353 | |||||||
| chr3:9985550 | T | C | 1 | a0001c0001t0017g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.155+957A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9985550 | |||||||
| chr3:9985574 | T | C | 106 | a0001c0001t0001g0231 a0001c0001t0002g0003 a0001c0001t0002g0004 others(103): Show |
120 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.155+933A>G | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9985574 | |||||||
| chr3:9985668 | G | A | 12 | a0001c0001t0008g0013 a0001c0001t0008g0077 a0001c0001t0008g0079 others(9): Show |
14 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.155+839C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9985668 | |||||||
| chr3:9985957 | C | T | 83 | a0001c0001t0001g0231 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
95 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.155+550G>A | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9985957 | |||||||
| chr3:9986002 | A | G | 106 | a0001c0001t0001g0231 a0001c0001t0002g0003 a0001c0001t0002g0004 others(103): Show |
120 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.155+505T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9986002 | |||||||
| chr3:9986014 | C | A | 3 | a0001c0001t0019g0227 a0001c0001t0019g0228 a0001c0001t0019g0229 |
3 | HG02683.hp1 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.155+493G>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9986014 | |||||||
| chr3:9986032 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.155+475C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9986032 | |||||||
| chr3:9986040 | G | A | 15 | a0001c0001t0001g0231 a0001c0001t0002g0003 a0001c0001t0002g0232 others(12): Show |
18 | HG00735.hp1 HG00735.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.155+467C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9986040 | |||||||
| chr3:9986495 | G | A | 1 | a0002c0007t0002g0254 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.155+12C>T | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9986495 | |||||||
| chr3:9986496 | A | G | 1 | a0002c0007t0002g0254 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.155+11T>C | EMC3 | ENSG00000125037.13 | transcript | ENST00000245046.7 | protein_coding | 1/7 | chr3 | 9986496 |