Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4135 |
| ensemblid | ENSG00000171533.12 |
| hgncid | 6868 |
| symbol | MAP6 |
| name | microtubule associated protein 6 |
| refseq_nuc | NM_033063.2 |
| refseq_prot | NP_149052.1 |
| ensembl_nuc | ENST00000304771.8 |
| ensembl_prot | ENSP00000307093.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 75586918 |
| end | 75669038 |
| strand | - |
| ver | v1.2 |
| region | chr11:75586918-75669038 |
| region5000 | chr11:75581918-75674038 |
| regionname0 | MAP6_chr11_75586918_75669038 |
| regionname5000 | MAP6_chr11_75581918_75674038 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 813 | 207 | 48 | 31 | 107 | 4 | 17 | 87 | MAP6_chr11_75581918_75674038 | MAP6 | MAWPC others(808): Show |
chr11 | 75581918 | 75674038 |
| a0002 | 1/0 | 813 | 172 | 35 | 25 | 82 | 6 | 23 | 65 | MAP6_chr11_75581918_75674038 | MAP6 | MAWPC others(808): Show |
chr11 | 75581918 | 75674038 |
| a0003 | 0/1 | 813 | 4 | 0 | 0 | 2 | 1 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | MAWPC others(808): Show |
chr11 | 75581918 | 75674038 |
| a0004 | 0/0 | 813 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | MAWPC others(808): Show |
chr11 | 75581918 | 75674038 |
| a0005 | 0/0 | 813 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | MAWPC others(808): Show |
chr11 | 75581918 | 75674038 |
| a0006 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | MAWPC others(808): Show |
chr11 | 75581918 | 75674038 |
| a0007 | 0/0 | 813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | MAWPC others(808): Show |
chr11 | 75581918 | 75674038 |
| a0008 | 0/0 | 813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | MAWPC others(808): Show |
chr11 | 75581918 | 75674038 |
| a0009 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | MAWPC others(808): Show |
chr11 | 75581918 | 75674038 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2439 | 140 | 37 | 8 | 85 | 1 | 9 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0001c0004 | 0/0 | 2439 | 63 | 7 | 23 | 22 | 3 | 8 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0001c0007 | 0/0 | 2439 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0001c0009 | 0/0 | 2439 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0001c0012 | 0/0 | 2439 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0002c0002 | 1/0 | 2439 | 87 | 16 | 12 | 43 | 3 | 12 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0002c0003 | 0/0 | 2439 | 76 | 19 | 12 | 32 | 3 | 10 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0002c0005 | 0/0 | 2439 | 5 | 0 | 0 | 5 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0002c0014 | 0/0 | 2439 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0002c0015 | 0/0 | 2439 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0002c0018 | 0/0 | 2439 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0002c0019 | 0/0 | 2439 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0003c0006 | 0/1 | 2439 | 4 | 0 | 0 | 2 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0004c0008 | 0/0 | 2439 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0005c0016 | 0/0 | 2439 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0006c0010 | 0/0 | 2439 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0007c0013 | 0/0 | 2439 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0008c0017 | 0/0 | 2439 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 | ||
| a0009c0011 | 0/0 | 2439 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | ATGGC others(2434): Show |
chr11 | 75581918 | 75674038 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3252 | 139 | 36 | 8 | 85 | 1 | 9 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0001c0001t0002 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0001c0004t0001 | 0/0 | 3252 | 63 | 7 | 23 | 22 | 3 | 8 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0001c0007t0001 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0001c0009t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0001c0012t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0002c0002t0001 | 1/0 | 3252 | 87 | 16 | 12 | 43 | 3 | 12 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0002c0003t0001 | 0/0 | 3252 | 76 | 19 | 12 | 32 | 3 | 10 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0002c0005t0001 | 0/0 | 3252 | 5 | 0 | 0 | 5 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0002c0014t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0002c0015t0001 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0002c0018t0001 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0002c0019t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0003c0006t0001 | 0/1 | 3252 | 4 | 0 | 0 | 2 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0004c0008t0001 | 0/0 | 3252 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0005c0016t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0006c0010t0001 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0007c0013t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0008c0017t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| a0009c0011t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | AGAGG others(3247): Show |
chr11 | 75581918 | 75674038 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0001 | 0/0 | 13 | 0 | 10 | 1 | 2 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0007t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0007t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0009t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0012t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0005 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0014t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0015t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0018t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0019t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0003c0006t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0003c0006t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0003c0006t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0003c0006t0001g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0004c0008t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0004c0008t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0005c0016t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0006c0010t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0007c0013t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0008c0017t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0009c0011t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | GBR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0001 | EUR | GBR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0246 | EUR | GBR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0138 | EUR | GBR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00280 | hp1 | a0005 | c0016 | t0001 | g0294 | EUR | FIN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | FIN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0309 | EUR | FIN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | FIN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00408 | hp2 | a0006 | c0010 | t0001 | g0031 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0245 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0067 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0277 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00735 | hp1 | a0001 | c0004 | t0001 | g0128 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00735 | hp2 | a0007 | c0013 | t0001 | g0064 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0139 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0048 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0235 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0046 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01074 | hp1 | a0002 | c0019 | t0001 | g0333 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01074 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0049 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0298 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0289 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0098 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0122 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0132 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01192 | hp2 | a0001 | c0004 | t0001 | g0089 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01243 | hp1 | a0008 | c0017 | t0001 | g0308 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0058 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0232 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01258 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01346 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0293 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0229 | EUR | IBS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01515 | hp2 | a0001 | c0004 | t0001 | g0001 | EUR | IBS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0268 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0290 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0047 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0286 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0125 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02027 | hp1 | a0002 | c0015 | t0001 | g0242 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0126 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02055 | hp1 | a0001 | c0012 | t0001 | g0050 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02056 | hp1 | a0003 | c0006 | t0001 | g0188 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02071 | hp2 | a0004 | c0008 | t0001 | g0032 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0313 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02074 | hp2 | a0002 | c0018 | t0001 | g0238 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0310 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02129 | hp1 | a0001 | c0004 | t0001 | g0112 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0295 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02148 | hp1 | a0002 | c0003 | t0001 | g0300 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02148 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | CDX | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0305 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02273 | hp1 | a0002 | c0003 | t0001 | g0271 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02273 | hp2 | a0001 | c0004 | t0001 | g0127 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0027 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0272 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02300 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0166 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0255 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0070 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0315 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02717 | hp1 | a0001 | c0007 | t0001 | g0028 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0322 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0311 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02735 | hp2 | a0001 | c0004 | t0001 | g0130 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0056 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0282 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0205 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0035 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0204 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0281 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0304 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0026 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0026 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0321 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0302 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03225 | hp1 | a0001 | c0007 | t0001 | g0030 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03239 | hp1 | a0002 | c0003 | t0001 | g0291 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0199 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0261 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0256 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0303 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03540 | hp1 | a0001 | c0009 | t0001 | g0029 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0200 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03654 | hp1 | a0002 | c0003 | t0001 | g0292 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03669 | hp2 | a0002 | c0003 | t0001 | g0299 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0137 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0022 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0110 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0109 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0022 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0248 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0024 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03834 | hp1 | a0002 | c0014 | t0001 | g0225 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0214 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0191 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0249 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0288 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0135 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0258 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0318 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04199 | hp2 | a0002 | c0003 | t0001 | g0301 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0024 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0247 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0243 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0155 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0060 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0027 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | CHB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18942 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18949 | hp2 | a0002 | c0003 | t0001 | g0296 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18950 | hp1 | a0002 | c0003 | t0001 | g0239 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0114 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18952 | hp1 | a0001 | c0004 | t0001 | g0145 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18953 | hp1 | a0001 | c0004 | t0001 | g0111 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18954 | hp2 | a0002 | c0003 | t0001 | g0278 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18956 | hp2 | a0002 | c0005 | t0001 | g0332 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0280 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18962 | hp2 | a0002 | c0005 | t0001 | g0329 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0252 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18965 | hp2 | a0002 | c0003 | t0001 | g0284 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0129 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0312 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0124 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18975 | hp2 | a0002 | c0003 | t0001 | g0266 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18977 | hp2 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0253 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18982 | hp2 | a0001 | c0004 | t0001 | g0090 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18984 | hp1 | a0002 | c0003 | t0001 | g0273 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0274 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18985 | hp2 | a0001 | c0004 | t0001 | g0113 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18987 | hp2 | a0001 | c0004 | t0001 | g0093 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18989 | hp2 | a0004 | c0008 | t0001 | g0033 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18994 | hp2 | a0001 | c0004 | t0001 | g0120 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0131 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19005 | hp1 | a0002 | c0005 | t0001 | g0330 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0283 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0270 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0121 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19011 | hp2 | a0002 | c0005 | t0001 | g0331 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0323 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0327 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19063 | hp1 | a0002 | c0003 | t0001 | g0241 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19063 | hp2 | a0002 | c0005 | t0001 | g0328 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0287 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19072 | hp2 | a0002 | c0003 | t0001 | g0275 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19076 | hp1 | a0001 | c0004 | t0001 | g0096 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19077 | hp2 | a0002 | c0003 | t0001 | g0276 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19078 | hp1 | a0003 | c0006 | t0001 | g0189 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19081 | hp1 | a0001 | c0004 | t0001 | g0115 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19082 | hp1 | a0002 | c0003 | t0001 | g0267 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19084 | hp1 | a0001 | c0004 | t0001 | g0182 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19085 | hp2 | a0002 | c0003 | t0001 | g0262 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0279 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0269 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0123 | AFR | ASW | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0316 | AFR | ASW | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20752 | hp1 | a0003 | c0006 | t0001 | g0117 | EUR | TSI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0317 | EUR | TSI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0134 | SAS | GIH | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02109 | hp2 | a0009 | c0011 | t0001 | g0116 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0314 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0036 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0042 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | USA | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0297 | AFR | USA | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | USA | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | USA | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0211 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0334 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| homoSapiens | chm13v2 | a0003 | c0006 | t0001 | g0190 | REF | REF | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0233 | REF | REF | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75587108 | A | G | 1 | a0008 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.2393T>C | p.Val798Ala | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 3062/3252 | 2393/2442 | 798/813 | chr11 | 75587108 | |||
| chr11:75587282 | C | T | 1 | a0009 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2219G>A | p.Arg740His | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2888/3252 | 2219/2442 | 740/813 | chr11 | 75587282 | |||
| chr11:75587423 | A | C | 2 | a0003 a0005 |
4 | HG00280.hp1 HG02056.hp1 NA19078.hp1 others(1): Show |
missense_variant | MODERATE | c.2078T>G | p.Val693Gly | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2747/3252 | 2078/2442 | 693/813 | chr11 | 75587423 | |||
| chr11:75587872 | C | A | 1 | a0007 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1629G>T | p.Met543Ile | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2298/3252 | 1629/2442 | 543/813 | chr11 | 75587872 | |||
| chr11:75667629 | A | C | 5 | a0001 a0003 a0004 others(2): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(211): Show |
missense_variant | MODERATE | c.741T>G | p.Ile247Met | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1410/3252 | 741/2442 | 247/813 | chr11 | 75667629 | |||
| chr11:75667838 | C | T | 1 | a0004 | 2 | HG02071.hp2 NA18989.hp2 |
missense_variant | MODERATE | c.532G>A | p.Val178Met | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1201/3252 | 532/2442 | 178/813 | chr11 | 75667838 | |||
| chr11:75667973 | G | T | 1 | a0006 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.397C>A | p.Pro133Thr | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1066/3252 | 397/2442 | 133/813 | chr11 | 75667973 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75587161 | C | T | 2 | a0001c0012 a0002c0019 |
2 | HG01074.hp1 HG02055.hp1 |
synonymous_variant | LOW | c.2340G>A | p.Lys780Lys | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 3009/3252 | 2340/2442 | 780/813 | chr11 | 75587161 | |||
| chr11:75587752 | A | G | 6 | a0001c0004 a0001c0009 a0002c0003 others(3): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
synonymous_variant | LOW | c.1749T>C | p.Asp583Asp | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2418/3252 | 1749/2442 | 583/813 | chr11 | 75587752 | |||
| chr11:75587971 | C | T | 1 | a0002c0015 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.1530G>A | p.Thr510Thr | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2199/3252 | 1530/2442 | 510/813 | chr11 | 75587971 | |||
| chr11:75605927 | G | A | 1 | a0002c0018 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.1197C>T | p.Asp399Asp | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/4 | 1866/3252 | 1197/2442 | 399/813 | chr11 | 75605927 | |||
| chr11:75605942 | C | T | 1 | a0002c0014 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1182G>A | p.Thr394Thr | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/4 | 1851/3252 | 1182/2442 | 394/813 | chr11 | 75605942 | |||
| chr11:75667710 | G | C | 1 | a0002c0005 | 5 | NA18956.hp2 NA18962.hp2 NA19005.hp1 others(2): Show |
synonymous_variant | LOW | c.660C>G | p.Gly220Gly | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1329/3252 | 660/2442 | 220/813 | chr11 | 75667710 | |||
| chr11:75667977 | C | T | 2 | a0001c0007 a0001c0009 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.393G>A | p.Gln131Gln | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1062/3252 | 393/2442 | 131/813 | chr11 | 75667977 | |||
| chr11:75668190 | G | A | 1 | a0002c0019 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.180C>T | p.Pro60Pro | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 849/3252 | 180/2442 | 60/813 | chr11 | 75668190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75668740 | G | C | 1 | a0001c0001t0002 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-371C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 371 | chr11 | 75668740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75588216 | A | G | 1 | a0003c0006t0001g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1317-32T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588216 | |||||||
| chr11:75588381 | C | T | 3 | a0002c0003t0001g0199 a0002c0003t0001g0200 a0002c0003t0001g0297 |
3 | HG03453.hp2 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1317-197G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588381 | |||||||
| chr11:75588572 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1317-388C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588572 | |||||||
| chr11:75588902 | C | T | 95 | a0001c0001t0001g0010 a0001c0001t0001g0037 a0001c0001t0001g0039 others(92): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.1317-718G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588902 | |||||||
| chr11:75588963 | G | A | 1 | a0003c0006t0001g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1317-779C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588963 | |||||||
| chr11:75588963 | G | T | 1 | a0002c0003t0001g0295 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1317-779C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588963 | |||||||
| chr11:75588988 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1317-804G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588988 | |||||||
| chr11:75589003 | G | A | 95 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0040 others(92): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.1317-819C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589003 | |||||||
| chr11:75589247 | G | A | 3 | a0002c0003t0001g0293 a0002c0003t0001g0300 a0005c0016t0001g0294 |
3 | HG00280.hp1 HG01346.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1317-1063C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589247 | |||||||
| chr11:75589333 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1317-1149G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589333 | |||||||
| chr11:75589479 | A | C | 1 | a0002c0002t0001g0207 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1317-1295T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589479 | |||||||
| chr11:75589552 | G | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1317-1368C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589552 | |||||||
| chr11:75589622 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(256): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1317-1438A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589622 | |||||||
| chr11:75589710 | T | G | 8 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1317-1526A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589710 | |||||||
| chr11:75589847 | G | T | 1 | a0002c0003t0001g0279 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1317-1663C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589847 | |||||||
| chr11:75590133 | T | A | 1 | a0002c0002t0001g0258 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1317-1949A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590133 | |||||||
| chr11:75590234 | G | A | 1 | a0002c0003t0001g0312 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1317-2050C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590234 | |||||||
| chr11:75590255 | T | C | 6 | a0001c0001t0001g0078 a0002c0002t0001g0219 a0002c0002t0001g0223 others(3): Show |
6 | NA18956.hp1 NA18986.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1317-2071A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590255 | |||||||
| chr11:75590274 | G | C | 1 | a0002c0002t0001g0258 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1317-2090C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590274 | |||||||
| chr11:75590462 | G | A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317-2278C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590462 | |||||||
| chr11:75590570 | C | T | 1 | a0002c0003t0001g0295 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1317-2386G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590570 | |||||||
| chr11:75590613 | T | A | 1 | a0001c0001t0002g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1317-2429A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590613 | |||||||
| chr11:75590707 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0055 |
4 | HG02451.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1317-2523G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590707 | |||||||
| chr11:75590970 | GA | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(101): Show |
127 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.1317-2787delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590970 | |||||||
| chr11:75591022 | G | A | 3 | a0001c0001t0001g0104 a0001c0012t0001g0050 a0002c0019t0001g0333 |
3 | HG01074.hp1 HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1317-2838C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591022 | |||||||
| chr11:75591103 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0061 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1317-2919G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591103 | |||||||
| chr11:75591219 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1317-3035T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591219 | |||||||
| chr11:75591230 | A | G | 26 | a0001c0004t0001g0042 a0002c0003t0001g0021 a0002c0003t0001g0022 others(23): Show |
30 | HG00597.hp1 HG00621.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1317-3046T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591230 | |||||||
| chr11:75591330 | T | G | 1 | a0002c0002t0001g0213 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1317-3146A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591330 | |||||||
| chr11:75591375 | T | C | 5 | a0002c0003t0001g0293 a0002c0003t0001g0299 a0002c0003t0001g0300 others(2): Show |
5 | HG00280.hp1 HG01346.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317-3191A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591375 | |||||||
| chr11:75591380 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1317-3196A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591380 | |||||||
| chr11:75591523 | C | G | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1317-3339G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591523 | |||||||
| chr11:75591657 | A | G | 3 | a0002c0002t0001g0248 a0002c0002t0001g0249 a0002c0014t0001g0225 |
3 | HG03831.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1317-3473T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591657 | |||||||
| chr11:75591681 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0193 others(5): Show |
10 | HG01074.hp1 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1317-3497G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591681 | |||||||
| chr11:75591710 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1317-3526C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591710 | |||||||
| chr11:75591810 | A | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(264): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1317-3626T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591810 | |||||||
| chr11:75592181 | G | C | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317-3997C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592181 | |||||||
| chr11:75592222 | T | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(151): Show |
183 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1317-4038A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592222 | |||||||
| chr11:75592238 | G | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | NA18946.hp2 NA18964.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1317-4054C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592238 | |||||||
| chr11:75592313 | C | T | 2 | a0002c0002t0001g0006 a0002c0002t0001g0224 |
4 | NA18942.hp2 NA18945.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1317-4129G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592313 | |||||||
| chr11:75592394 | A | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(256): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1317-4210T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592394 | |||||||
| chr11:75592500 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1317-4316G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592500 | |||||||
| chr11:75592578 | C | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | NA18957.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1317-4394G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592578 | |||||||
| chr11:75592579 | C | T | 2 | a0001c0004t0001g0035 a0001c0004t0001g0036 |
2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1317-4395G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592579 | |||||||
| chr11:75592629 | G | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(255): Show |
300 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1317-4445C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592629 | |||||||
| chr11:75592680 | A | C | 1 | a0002c0002t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1317-4496T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592680 | |||||||
| chr11:75592897 | G | A | 2 | a0001c0001t0001g0079 a0002c0002t0001g0272 |
2 | HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1317-4713C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592897 | |||||||
| chr11:75592949 | G | A | 1 | a0002c0002t0001g0203 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1317-4765C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592949 | |||||||
| chr11:75593047 | C | G | 1 | a0001c0001t0001g0017 | 2 | NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1317-4863G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593047 | |||||||
| chr11:75593048 | A | G | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317-4864T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593048 | |||||||
| chr11:75593306 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0069 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1317-5122A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593306 | |||||||
| chr11:75593497 | A | G | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317-5313T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593497 | |||||||
| chr11:75593601 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1317-5417A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593601 | |||||||
| chr11:75593655 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1317-5471C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593655 | |||||||
| chr11:75593786 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0083 others(1): Show |
4 | HG01975.hp1 NA18957.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-5602G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593786 | |||||||
| chr11:75593787 | G | A | 1 | a0002c0003t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1317-5603C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593787 | |||||||
| chr11:75593864 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0193 others(6): Show |
11 | HG01074.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1317-5680T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593864 | |||||||
| chr11:75593954 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(263): Show |
310 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1317-5770G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593954 | |||||||
| chr11:75593970 | A | T | 21 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 others(18): Show |
22 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.1317-5786T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593970 | |||||||
| chr11:75593986 | GA | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(124): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1317-5803delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593986 | |||||||
| chr11:75594062 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
29 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1317-5878G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594062 | |||||||
| chr11:75594342 | T | C | 2 | a0002c0002t0001g0019 a0002c0002t0001g0261 |
3 | HG01123.hp1 HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1317-6158A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594342 | |||||||
| chr11:75594363 | C | T | 1 | a0002c0003t0001g0281 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1317-6179G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594363 | |||||||
| chr11:75594486 | C | T | 47 | a0001c0004t0001g0056 a0001c0007t0001g0028 a0001c0007t0001g0030 others(44): Show |
54 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1317-6302G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594486 | |||||||
| chr11:75594512 | G | A | 78 | a0001c0004t0001g0042 a0001c0004t0001g0056 a0001c0004t0001g0060 others(75): Show |
89 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1317-6328C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594512 | |||||||
| chr11:75594820 | G | A | 47 | a0001c0004t0001g0056 a0001c0007t0001g0028 a0001c0007t0001g0030 others(44): Show |
54 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1317-6636C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594820 | |||||||
| chr11:75594931 | G | A | 1 | a0001c0004t0001g0047 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1317-6747C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594931 | |||||||
| chr11:75595172 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(254): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1317-6988G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595172 | |||||||
| chr11:75595184 | C | T | 1 | a0002c0003t0001g0315 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1317-7000G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595184 | |||||||
| chr11:75595245 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1317-7061G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595245 | |||||||
| chr11:75595437 | C | A | 2 | a0002c0002t0001g0306 a0002c0002t0001g0307 |
2 | NA18941.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1317-7253G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595437 | |||||||
| chr11:75595640 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1317-7456G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595640 | |||||||
| chr11:75595702 | T | C | 19 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(16): Show |
19 | HG02056.hp1 HG02109.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1317-7518A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595702 | |||||||
| chr11:75595934 | G | T | 128 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(125): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1317-7750C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595934 | |||||||
| chr11:75596253 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(265): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1317-8069G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596253 | |||||||
| chr11:75596318 | T | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(260): Show |
307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1317-8134A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596318 | |||||||
| chr11:75596354 | T | G | 22 | a0002c0003t0001g0021 a0002c0003t0001g0022 a0002c0003t0001g0023 others(19): Show |
25 | HG00597.hp1 HG00621.hp1 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.1317-8170A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596354 | |||||||
| chr11:75596375 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(28): Show |
43 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1317-8191G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596375 | |||||||
| chr11:75596481 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1317-8297T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596481 | |||||||
| chr11:75596559 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(168): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1317-8375C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596559 | |||||||
| chr11:75596775 | C | T | 128 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(125): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1317-8591G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596775 | |||||||
| chr11:75596814 | T | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(256): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1317-8630A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596814 | |||||||
| chr11:75596831 | G | C | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1317-8647C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596831 | |||||||
| chr11:75596872 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1317-8688C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596872 | |||||||
| chr11:75596886 | G | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(125): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1317-8702C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596886 | |||||||
| chr11:75596953 | T | A | 29 | a0001c0004t0001g0042 a0002c0003t0001g0021 a0002c0003t0001g0022 others(26): Show |
33 | HG00597.hp1 HG00621.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1317-8769A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596953 | |||||||
| chr11:75597072 | C | T | 1 | a0002c0003t0001g0241 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1316+8736G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597072 | |||||||
| chr11:75597128 | C | T | 128 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(125): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1316+8680G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597128 | |||||||
| chr11:75597138 | A | T | 51 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0040 others(48): Show |
65 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1316+8670T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597138 | |||||||
| chr11:75597272 | T | G | 2 | a0002c0003t0001g0241 a0002c0003t0001g0262 |
2 | NA19063.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1316+8536A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597272 | |||||||
| chr11:75597402 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(253): Show |
298 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1316+8406C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597402 | |||||||
| chr11:75597602 | C | T | 6 | a0002c0003t0001g0003 a0002c0003t0001g0274 a0002c0003t0001g0278 others(3): Show |
10 | HG00738.hp2 HG01081.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1316+8206G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597602 | |||||||
| chr11:75597646 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0061 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1316+8162A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597646 | |||||||
| chr11:75597717 | A | G | 2 | a0002c0003t0001g0026 a0002c0003t0001g0314 |
3 | HG02559.hp1 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1316+8091T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597717 | |||||||
| chr11:75598100 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(255): Show |
300 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1316+7708T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598100 | |||||||
| chr11:75598179 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0180 |
2 | NA18970.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1316+7629G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598179 | |||||||
| chr11:75598241 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1316+7567G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598241 | |||||||
| chr11:75598291 | G | C | 1 | a0001c0004t0001g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1316+7517C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598291 | |||||||
| chr11:75598526 | T | G | 257 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(254): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1316+7282A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598526 | |||||||
| chr11:75598675 | A | T | 1 | a0003c0006t0001g0189 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1316+7133T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598675 | |||||||
| chr11:75599092 | C | T | 1 | a0001c0004t0001g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1316+6716G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599092 | |||||||
| chr11:75599250 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1316+6558A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599250 | |||||||
| chr11:75599703 | T | C | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1316+6105A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599703 | |||||||
| chr11:75599710 | G | A | 1 | a0002c0003t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1316+6098C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599710 | |||||||
| chr11:75599782 | G | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(28): Show |
43 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1316+6026C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599782 | |||||||
| chr11:75599878 | C | T | 1 | a0002c0003t0001g0304 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1316+5930G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599878 | |||||||
| chr11:75600034 | T | C | 4 | a0002c0002t0001g0205 a0002c0002t0001g0210 a0002c0002t0001g0212 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316+5774A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600034 | |||||||
| chr11:75600056 | T | A | 1 | a0001c0004t0001g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1316+5752A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600056 | |||||||
| chr11:75600155 | G | A | 10 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(7): Show |
10 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1316+5653C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600155 | |||||||
| chr11:75600398 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18957.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1316+5410T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600398 | |||||||
| chr11:75600635 | A | G | 10 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(7): Show |
10 | HG02622.hp1 HG02622.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1316+5173T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600635 | |||||||
| chr11:75600650 | G | A | 2 | a0002c0002t0001g0248 a0002c0002t0001g0249 |
2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1316+5158C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600650 | |||||||
| chr11:75600659 | T | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(180): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1316+5149A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600659 | |||||||
| chr11:75601114 | A | G | 1 | a0002c0003t0001g0288 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1316+4694T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601114 | |||||||
| chr11:75601381 | T | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+4427A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601381 | |||||||
| chr11:75601502 | C | T | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1316+4306G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601502 | |||||||
| chr11:75601619 | C | T | 1 | a0002c0002t0001g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1316+4189G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601619 | |||||||
| chr11:75601741 | G | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+4067C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601741 | |||||||
| chr11:75601858 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0069 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1316+3950A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601858 | |||||||
| chr11:75601965 | G | A | 2 | a0002c0002t0001g0020 a0002c0002t0001g0265 |
3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1316+3843C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601965 | |||||||
| chr11:75601986 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1316+3822G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601986 | |||||||
| chr11:75602045 | T | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+3763A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75602045 | |||||||
| chr11:75602328 | G | T | 1 | a0002c0003t0001g0267 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1316+3480C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75602328 | |||||||
| chr11:75602346 | T | C | 5 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 others(2): Show |
6 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316+3462A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75602346 | |||||||
| chr11:75602972 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1316+2836A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75602972 | |||||||
| chr11:75603077 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(25): Show |
40 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1316+2731C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603077 | |||||||
| chr11:75603211 | C | T | 5 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 others(2): Show |
6 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316+2597G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603211 | |||||||
| chr11:75603251 | G | A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1316+2557C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603251 | |||||||
| chr11:75603549 | C | T | 2 | a0001c0004t0001g0060 a0001c0004t0001g0070 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1316+2259G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603549 | |||||||
| chr11:75603741 | C | T | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+2067G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603741 | |||||||
| chr11:75603742 | G | T | 170 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(167): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1316+2066C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603742 | |||||||
| chr11:75603743 | C | T | 170 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(167): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1316+2065G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603743 | |||||||
| chr11:75603924 | C | T | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+1884G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603924 | |||||||
| chr11:75604017 | A | G | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+1791T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604017 | |||||||
| chr11:75604071 | C | A | 1 | a0001c0007t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1316+1737G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604071 | |||||||
| chr11:75604126 | T | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+1682A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604126 | |||||||
| chr11:75604458 | G | A | 1 | a0002c0002t0001g0235 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1316+1350C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604458 | |||||||
| chr11:75604501 | G | GT | 31 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(28): Show |
43 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1316+1306_1316+130 others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604501 | |||||||
| chr11:75604507 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0069 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1316+1301C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604507 | |||||||
| chr11:75604597 | GT | G | 9 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0075 others(6): Show |
9 | HG00558.hp1 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+1210delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604597 | |||||||
| chr11:75604598 | T | A | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1316+1210A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604598 | |||||||
| chr11:75604687 | C | CCA | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1316+1119_1316+112 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604687 | |||||||
| chr11:75604744 | C | T | 1 | a0007c0013t0001g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1316+1064G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604744 | |||||||
| chr11:75604830 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1316+978G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604830 | |||||||
| chr11:75604985 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1316+823A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604985 | |||||||
| chr11:75604997 | C | T | 1 | a0002c0003t0001g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1316+811G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604997 | |||||||
| chr11:75605004 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1316+804G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605004 | |||||||
| chr11:75605133 | C | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(26): Show |
41 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1316+675G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605133 | |||||||
| chr11:75605154 | G | A | 2 | a0001c0001t0001g0079 a0002c0002t0001g0272 |
2 | HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1316+654C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605154 | |||||||
| chr11:75605155 | T | C | 1 | a0002c0003t0001g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1316+653A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605155 | |||||||
| chr11:75605486 | C | T | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316+322G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605486 | |||||||
| chr11:75605487 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(26): Show |
41 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1316+321C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605487 | |||||||
| chr11:75605501 | G | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+307C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605501 | |||||||
| chr11:75605549 | A | G | 7 | a0001c0001t0001g0063 a0001c0001t0001g0156 a0001c0001t0001g0157 others(4): Show |
7 | HG02622.hp2 HG02809.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+259T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605549 | |||||||
| chr11:75605554 | A | G | 7 | a0001c0001t0001g0063 a0001c0001t0001g0156 a0001c0001t0001g0157 others(4): Show |
7 | HG02622.hp2 HG02809.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+254T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605554 | |||||||
| chr11:75606128 | G | A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0059 others(8): Show |
11 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1120-124C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606128 | |||||||
| chr11:75606227 | T | G | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120-223A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606227 | |||||||
| chr11:75606332 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1120-328C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606332 | |||||||
| chr11:75606418 | T | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(177): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1120-414A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606418 | |||||||
| chr11:75606557 | C | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120-553G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606557 | |||||||
| chr11:75606717 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(181): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1120-713T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606717 | |||||||
| chr11:75606777 | A | T | 267 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(264): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1120-773T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606777 | |||||||
| chr11:75606997 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1120-993C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606997 | |||||||
| chr11:75607252 | G | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
52 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1119+857C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607252 | |||||||
| chr11:75607392 | T | C | 1 | a0002c0003t0001g0309 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1119+717A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607392 | |||||||
| chr11:75607574 | T | C | 5 | a0002c0002t0001g0311 a0002c0002t0001g0319 a0002c0002t0001g0320 others(2): Show |
5 | HG02451.hp2 HG02723.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119+535A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607574 | |||||||
| chr11:75607619 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(26): Show |
41 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1119+490C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607619 | |||||||
| chr11:75607619 | GAGA | G | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1119+487_1119+489d others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607619 | |||||||
| chr11:75607733 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(26): Show |
41 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1119+376C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607733 | |||||||
| chr11:75608344 | T | C | 1 | a0002c0018t0001g0238 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.906-22A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75608344 | |||||||
| chr11:75608737 | T | C | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-415A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75608737 | |||||||
| chr11:75608923 | G | A | 1 | a0004c0008t0001g0032 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.906-601C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75608923 | |||||||
| chr11:75609032 | G | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(5): Show |
8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.906-710C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609032 | |||||||
| chr11:75609060 | C | T | 5 | a0002c0003t0001g0293 a0002c0003t0001g0299 a0002c0003t0001g0300 others(2): Show |
5 | HG00280.hp1 HG01346.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-738G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609060 | |||||||
| chr11:75609161 | T | A | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.906-839A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609161 | |||||||
| chr11:75609330 | C | A | 1 | a0002c0002t0001g0220 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.906-1008G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609330 | |||||||
| chr11:75609366 | G | C | 2 | a0001c0004t0001g0060 a0001c0004t0001g0070 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.906-1044C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609366 | |||||||
| chr11:75609434 | G | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(247): Show |
292 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.906-1112C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609434 | |||||||
| chr11:75609452 | C | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(242): Show |
287 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.906-1130G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609452 | |||||||
| chr11:75609552 | C | T | 7 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(4): Show |
7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-1230G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609552 | |||||||
| chr11:75609623 | C | T | 73 | a0001c0004t0001g0042 a0002c0002t0001g0285 a0002c0002t0001g0303 others(70): Show |
84 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.906-1301G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609623 | |||||||
| chr11:75609806 | G | T | 1 | a0001c0001t0001g0017 | 2 | NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.906-1484C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609806 | |||||||
| chr11:75609846 | G | T | 1 | a0002c0002t0001g0302 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.906-1524C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609846 | |||||||
| chr11:75610339 | A | T | 1 | a0002c0002t0001g0324 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.906-2017T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610339 | |||||||
| chr11:75610765 | G | C | 1 | a0007c0013t0001g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.906-2443C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610765 | |||||||
| chr11:75610832 | C | T | 2 | a0002c0003t0001g0289 a0002c0003t0001g0298 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.906-2510G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610832 | |||||||
| chr11:75610843 | T | C | 1 | a0002c0014t0001g0225 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.906-2521A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610843 | |||||||
| chr11:75610917 | T | C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(20): Show |
25 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.906-2595A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610917 | |||||||
| chr11:75611162 | G | A | 7 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(4): Show |
7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-2840C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611162 | |||||||
| chr11:75611187 | C | G | 2 | a0002c0002t0001g0020 a0002c0002t0001g0265 |
3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.906-2865G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611187 | |||||||
| chr11:75611546 | C | T | 7 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(4): Show |
7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-3224G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611546 | |||||||
| chr11:75611574 | A | T | 7 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(4): Show |
7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-3252T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611574 | |||||||
| chr11:75611628 | A | C | 1 | a0001c0004t0001g0182 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.906-3306T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611628 | |||||||
| chr11:75611787 | C | T | 1 | a0002c0003t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.906-3465G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611787 | |||||||
| chr11:75611793 | T | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(4): Show |
7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-3471A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611793 | |||||||
| chr11:75611923 | A | G | 1 | a0002c0003t0001g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.906-3601T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611923 | |||||||
| chr11:75611958 | C | T | 2 | a0002c0002t0001g0020 a0002c0002t0001g0265 |
3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.906-3636G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611958 | |||||||
| chr11:75611995 | G | A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-3673C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611995 | |||||||
| chr11:75612204 | C | G | 1 | a0002c0003t0001g0281 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.906-3882G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75612204 | |||||||
| chr11:75612338 | G | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0105 others(1): Show |
4 | HG02976.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-4016C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75612338 | |||||||
| chr11:75612596 | C | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(4): Show |
7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-4274G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75612596 | |||||||
| chr11:75612755 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-4433G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75612755 | |||||||
| chr11:75613067 | T | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0156 others(4): Show |
7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-4745A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613067 | |||||||
| chr11:75613135 | C | T | 73 | a0002c0002t0001g0285 a0002c0002t0001g0302 a0002c0002t0001g0303 others(70): Show |
84 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.906-4813G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613135 | |||||||
| chr11:75613353 | C | T | 2 | a0001c0004t0001g0060 a0001c0004t0001g0070 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.906-5031G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613353 | |||||||
| chr11:75613442 | G | A | 1 | a0002c0002t0001g0235 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.906-5120C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613442 | |||||||
| chr11:75613499 | C | T | 69 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0051 others(66): Show |
74 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.906-5177G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613499 | |||||||
| chr11:75613554 | G | A | 40 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0059 others(37): Show |
43 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.906-5232C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613554 | |||||||
| chr11:75613564 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.906-5242C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613564 | |||||||
| chr11:75613703 | T | A | 2 | a0001c0001t0001g0043 a0001c0004t0001g0042 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.906-5381A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613703 | |||||||
| chr11:75613704 | C | G | 2 | a0001c0001t0001g0043 a0001c0004t0001g0042 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.906-5382G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613704 | |||||||
| chr11:75613733 | A | G | 259 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(256): Show |
297 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.906-5411T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613733 | |||||||
| chr11:75613837 | C | T | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-5515G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613837 | |||||||
| chr11:75614057 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
5 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-5735G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614057 | |||||||
| chr11:75614139 | T | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(201): Show |
240 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.906-5817A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614139 | |||||||
| chr11:75614241 | C | T | 12 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0051 others(9): Show |
12 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.906-5919G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614241 | |||||||
| chr11:75614354 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.906-6032G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614354 | |||||||
| chr11:75614524 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.906-6202G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614524 | |||||||
| chr11:75614545 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.906-6223G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614545 | |||||||
| chr11:75615120 | G | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.906-6798C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615120 | |||||||
| chr11:75615223 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.906-6901A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615223 | |||||||
| chr11:75615312 | T | C | 1 | a0002c0002t0001g0303 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.906-6990A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615312 | |||||||
| chr11:75615328 | G | A | 2 | a0001c0001t0001g0106 a0002c0003t0001g0283 |
2 | HG02129.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.906-7006C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615328 | |||||||
| chr11:75615418 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-7096C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615418 | |||||||
| chr11:75615541 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.906-7219G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615541 | |||||||
| chr11:75615578 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0193 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-7256G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615578 | |||||||
| chr11:75615626 | G | C | 19 | a0002c0002t0001g0311 a0002c0002t0001g0319 a0002c0002t0001g0320 others(16): Show |
20 | HG00323.hp1 HG00639.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.906-7304C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615626 | |||||||
| chr11:75615686 | C | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.906-7364G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615686 | |||||||
| chr11:75615691 | G | C | 72 | a0001c0001t0001g0153 a0002c0002t0001g0285 a0002c0002t0001g0302 others(69): Show |
83 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.906-7369C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615691 | |||||||
| chr11:75615967 | C | T | 1 | a0002c0002t0001g0251 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.906-7645G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615967 | |||||||
| chr11:75616029 | T | C | 1 | a0002c0003t0001g0280 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.906-7707A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616029 | |||||||
| chr11:75616307 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-7985G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616307 | |||||||
| chr11:75616404 | T | C | 3 | a0002c0003t0001g0281 a0002c0003t0001g0282 a0002c0003t0001g0305 |
3 | HG02257.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.906-8082A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616404 | |||||||
| chr11:75616425 | A | G | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-8103T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616425 | |||||||
| chr11:75616667 | G | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0045 others(33): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.906-8345C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616667 | |||||||
| chr11:75616829 | A | G | 1 | a0001c0004t0001g0122 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.906-8507T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616829 | |||||||
| chr11:75616845 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0082 others(1): Show |
4 | NA18981.hp1 NA19003.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-8523C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616845 | |||||||
| chr11:75616975 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0181 |
3 | NA18964.hp2 NA18993.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.906-8653T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616975 | |||||||
| chr11:75617342 | C | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
5 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-9020G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617342 | |||||||
| chr11:75617514 | C | CA | 114 | a0001c0001t0001g0034 a0001c0001t0001g0040 a0001c0001t0001g0041 others(111): Show |
130 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.906-9193dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | |||||||
| chr11:75617514 | C | CAA | 20 | a0001c0001t0001g0039 a0001c0004t0001g0036 a0002c0002t0001g0243 others(17): Show |
20 | HG01167.hp2 HG01346.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.906-9194_906-9193d others(4): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | |||||||
| chr11:75617514 | CA | C | 10 | a0001c0001t0001g0193 a0001c0004t0001g0049 a0001c0007t0001g0028 others(7): Show |
10 | HG01099.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.906-9193delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | |||||||
| chr11:75617514 | CAA | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0038 others(8): Show |
13 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.906-9194_906-9193d others(4): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | |||||||
| chr11:75617514 | CAAA | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(22): Show |
36 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.906-9195_906-9193d others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | |||||||
| chr11:75617519 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-9197T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617519 | |||||||
| chr11:75617802 | G | A | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-9480C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617802 | |||||||
| chr11:75618107 | CT | C | 265 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(262): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.906-9786delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618107 | |||||||
| chr11:75618107 | CTT | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(43): Show |
58 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.906-9787_906-9786d others(4): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618107 | |||||||
| chr11:75618245 | C | A | 1 | a0002c0002t0001g0249 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.906-9923G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618245 | |||||||
| chr11:75618376 | G | A | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-10054C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618376 | |||||||
| chr11:75618396 | C | T | 9 | a0002c0003t0001g0309 a0002c0003t0001g0310 a0002c0003t0001g0312 others(6): Show |
9 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-10074G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618396 | |||||||
| chr11:75618489 | C | A | 1 | a0002c0002t0001g0302 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.906-10167G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618489 | |||||||
| chr11:75618599 | TA | T | 11 | a0001c0001t0001g0143 a0001c0001t0001g0153 a0001c0001t0001g0185 others(8): Show |
12 | HG01099.hp2 HG02056.hp1 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.906-10278delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618599 | |||||||
| chr11:75618692 | G | A | 2 | a0001c0004t0001g0114 a0001c0004t0001g0124 |
2 | NA18950.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.906-10370C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618692 | |||||||
| chr11:75618744 | T | C | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-10422A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618744 | |||||||
| chr11:75618771 | A | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.906-10449T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618771 | |||||||
| chr11:75618800 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.906-10478C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618800 | |||||||
| chr11:75618803 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-10481C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618803 | |||||||
| chr11:75618890 | C | G | 2 | a0002c0002t0001g0222 a0002c0002t0001g0229 |
2 | HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.906-10568G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618890 | |||||||
| chr11:75618923 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-10601C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618923 | |||||||
| chr11:75618976 | G | T | 3 | a0002c0003t0001g0021 a0002c0003t0001g0266 a0002c0003t0001g0273 |
4 | NA18942.hp1 NA18975.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-10654C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618976 | |||||||
| chr11:75618998 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0194 a0001c0001t0001g0196 |
4 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-10676C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618998 | |||||||
| chr11:75619098 | T | G | 1 | a0002c0005t0001g0332 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.906-10776A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619098 | |||||||
| chr11:75619152 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(32): Show |
48 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.906-10830C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619152 | |||||||
| chr11:75619307 | C | T | 5 | a0002c0002t0001g0306 a0002c0002t0001g0307 a0002c0003t0001g0003 others(2): Show |
9 | HG00738.hp2 HG01081.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.906-10985G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619307 | |||||||
| chr11:75619308 | A | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-10986T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619308 | |||||||
| chr11:75619380 | TTTTTAAC | T | 8 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(5): Show |
8 | HG02056.hp1 HG02717.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.906-11065_906-1105 others(11): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619380 | |||||||
| chr11:75619453 | C | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0193 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-11131G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619453 | |||||||
| chr11:75619507 | C | T | 4 | a0002c0002t0001g0302 a0002c0003t0001g0297 a0002c0003t0001g0316 others(1): Show |
4 | HG02970.hp2 HG06807.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-11185G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619507 | |||||||
| chr11:75619662 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-11340G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619662 | |||||||
| chr11:75619757 | T | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0097 |
3 | NA18972.hp2 NA18991.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.906-11435A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619757 | |||||||
| chr11:75620176 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-11854A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620176 | |||||||
| chr11:75620235 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(32): Show |
47 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.906-11913G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620235 | |||||||
| chr11:75620278 | C | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0069 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.906-11956G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620278 | |||||||
| chr11:75620326 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-12004G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620326 | |||||||
| chr11:75620483 | G | GA | 40 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
53 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.906-12162dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620483 | |||||||
| chr11:75620483 | GA | G | 11 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0038 others(8): Show |
12 | HG01515.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.906-12162delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620483 | |||||||
| chr11:75620514 | G | T | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-12192C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620514 | |||||||
| chr11:75620522 | A | C | 5 | a0001c0004t0001g0046 a0001c0004t0001g0047 a0001c0004t0001g0048 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-12200T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620522 | |||||||
| chr11:75620543 | A | G | 1 | a0001c0001t0002g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.906-12221T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620543 | |||||||
| chr11:75620709 | C | T | 4 | a0002c0002t0001g0302 a0002c0003t0001g0297 a0002c0003t0001g0316 others(1): Show |
4 | HG02970.hp2 HG06807.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-12387G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620709 | |||||||
| chr11:75620902 | G | A | 1 | a0002c0014t0001g0225 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.906-12580C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620902 | |||||||
| chr11:75620987 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.906-12665G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620987 | |||||||
| chr11:75620992 | G | A | 1 | a0002c0003t0001g0304 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.906-12670C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620992 | |||||||
| chr11:75620997 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-12675C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620997 | |||||||
| chr11:75621060 | G | A | 1 | a0001c0004t0001g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.906-12738C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621060 | |||||||
| chr11:75621304 | T | A | 2 | a0002c0003t0001g0304 a0008c0017t0001g0308 |
2 | HG01243.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.906-12982A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621304 | |||||||
| chr11:75621315 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-12993T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621315 | |||||||
| chr11:75621515 | C | T | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-13193G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621515 | |||||||
| chr11:75621595 | T | C | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-13273A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621595 | |||||||
| chr11:75621720 | A | C | 1 | a0001c0004t0001g0111 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.906-13398T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621720 | |||||||
| chr11:75622060 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
5 | NA18955.hp1 NA18968.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-13738T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622060 | |||||||
| chr11:75622108 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0193 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-13786C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622108 | |||||||
| chr11:75622236 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-13914C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622236 | |||||||
| chr11:75622320 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.906-13998A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622320 | |||||||
| chr11:75622394 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-14072C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622394 | |||||||
| chr11:75622431 | AGTGCAAT others(4): Show |
A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-14120_906-1411 others(15): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622431 | |||||||
| chr11:75622529 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-14207C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622529 | |||||||
| chr11:75622549 | A | G | 5 | a0002c0002t0001g0306 a0002c0002t0001g0307 a0002c0003t0001g0003 others(2): Show |
9 | HG00738.hp2 HG01081.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.906-14227T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622549 | |||||||
| chr11:75622740 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-14418G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622740 | |||||||
| chr11:75622977 | T | C | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-14655A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622977 | |||||||
| chr11:75623023 | A | G | 1 | a0002c0002t0001g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.906-14701T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623023 | |||||||
| chr11:75623096 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-14774A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623096 | |||||||
| chr11:75623119 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.906-14797A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623119 | |||||||
| chr11:75623331 | G | A | 3 | a0002c0003t0001g0026 a0002c0003t0001g0314 a0002c0003t0001g0315 |
4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-15009C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623331 | |||||||
| chr11:75623364 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-15042G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623364 | |||||||
| chr11:75623697 | C | T | 1 | a0002c0002t0001g0232 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.906-15375G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623697 | |||||||
| chr11:75623735 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0193 others(3): Show |
7 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-15413T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623735 | |||||||
| chr11:75623740 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.906-15418G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623740 | |||||||
| chr11:75623771 | G | A | 15 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(12): Show |
15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.906-15449C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623771 | |||||||
| chr11:75623802 | C | T | 2 | a0002c0002t0001g0311 a0002c0002t0001g0319 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.906-15480G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623802 | |||||||
| chr11:75623936 | C | T | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-15614G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623936 | |||||||
| chr11:75624455 | C | T | 1 | a0001c0004t0001g0132 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.906-16133G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75624455 | |||||||
| chr11:75624754 | C | T | 69 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0040 others(66): Show |
83 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.906-16432G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75624754 | |||||||
| chr11:75624760 | G | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-16438C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75624760 | |||||||
| chr11:75624776 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0193 others(3): Show |
7 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-16454T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75624776 | |||||||
| chr11:75625009 | C | A | 1 | a0002c0003t0001g0300 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.906-16687G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625009 | |||||||
| chr11:75625211 | G | A | 1 | a0002c0002t0001g0250 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.906-16889C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625211 | |||||||
| chr11:75625226 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-16904A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625226 | |||||||
| chr11:75625364 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.906-17042T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625364 | |||||||
| chr11:75625443 | A | G | 1 | a0007c0013t0001g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.906-17121T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625443 | |||||||
| chr11:75625559 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.906-17237T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625559 | |||||||
| chr11:75625578 | A | C | 1 | a0003c0006t0001g0189 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906-17256T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625578 | |||||||
| chr11:75625667 | C | A | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-17345G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625667 | |||||||
| chr11:75625708 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-17386T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625708 | |||||||
| chr11:75625885 | C | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0073 others(7): Show |
11 | HG00597.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.906-17563G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625885 | |||||||
| chr11:75626158 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-17836G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626158 | |||||||
| chr11:75626190 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.906-17868G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626190 | |||||||
| chr11:75626481 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-18159T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626481 | |||||||
| chr11:75626499 | G | A | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-18177C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626499 | |||||||
| chr11:75626507 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.906-18185C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626507 | |||||||
| chr11:75626689 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-18367G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626689 | |||||||
| chr11:75626863 | G | A | 1 | a0002c0002t0001g0272 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.906-18541C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626863 | |||||||
| chr11:75626872 | A | G | 8 | a0001c0001t0001g0161 a0001c0004t0001g0013 a0001c0004t0001g0112 others(5): Show |
9 | HG02027.hp2 HG02083.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-18550T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626872 | |||||||
| chr11:75626904 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-18582A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626904 | |||||||
| chr11:75626962 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-18640T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626962 | |||||||
| chr11:75627046 | T | C | 1 | a0002c0003t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.906-18724A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627046 | |||||||
| chr11:75627159 | G | C | 1 | a0003c0006t0001g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.906-18837C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627159 | |||||||
| chr11:75627214 | G | T | 1 | a0001c0004t0001g0111 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.906-18892C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627214 | |||||||
| chr11:75627423 | C | T | 1 | a0002c0002t0001g0231 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.906-19101G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627423 | |||||||
| chr11:75627424 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-19102C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627424 | |||||||
| chr11:75627697 | T | G | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-19375A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627697 | |||||||
| chr11:75627730 | G | A | 1 | a0002c0003t0001g0310 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.906-19408C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627730 | |||||||
| chr11:75627852 | T | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0038 others(6): Show |
10 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.906-19530A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627852 | |||||||
| chr11:75627953 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-19631A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627953 | |||||||
| chr11:75627972 | C | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.906-19650G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627972 | |||||||
| chr11:75628029 | C | T | 2 | a0002c0003t0001g0027 a0002c0003t0001g0327 |
3 | HG02280.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.906-19707G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628029 | |||||||
| chr11:75628148 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-19826G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628148 | |||||||
| chr11:75628210 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-19888T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628210 | |||||||
| chr11:75628449 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-20127A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628449 | |||||||
| chr11:75628583 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-20261G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628583 | |||||||
| chr11:75628600 | T | A | 1 | a0002c0003t0001g0301 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.906-20278A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628600 | |||||||
| chr11:75628761 | A | C | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG03516.hp1 HG06807.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-20439T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628761 | |||||||
| chr11:75628793 | T | C | 19 | a0002c0002t0001g0285 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
22 | HG00621.hp1 HG01928.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.906-20471A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628793 | |||||||
| chr11:75629067 | C | T | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-20745G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629067 | |||||||
| chr11:75629101 | T | C | 134 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(131): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.906-20779A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629101 | |||||||
| chr11:75629142 | C | T | 2 | a0002c0003t0001g0289 a0002c0003t0001g0298 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.906-20820G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629142 | |||||||
| chr11:75629235 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.906-20913C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629235 | |||||||
| chr11:75629365 | G | GC | 3 | a0001c0001t0001g0141 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG01261.hp2 HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.906-21044_906-2104 others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629365 | |||||||
| chr11:75629725 | G | C | 1 | a0001c0004t0001g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.906-21403C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629725 | |||||||
| chr11:75629769 | G | T | 1 | a0002c0003t0001g0275 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-21447C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629769 | |||||||
| chr11:75629770 | T | A | 1 | a0002c0003t0001g0275 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-21448A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629770 | |||||||
| chr11:75629771 | A | T | 1 | a0002c0003t0001g0275 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-21449T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629771 | |||||||
| chr11:75630017 | A | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.906-21695T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630017 | |||||||
| chr11:75630141 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.906-21819G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630141 | |||||||
| chr11:75630142 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-21820C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630142 | |||||||
| chr11:75630180 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-21858C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630180 | |||||||
| chr11:75630272 | T | C | 1 | a0001c0009t0001g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.906-21950A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630272 | |||||||
| chr11:75630376 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0170 a0002c0003t0001g0275 others(1): Show |
4 | HG03209.hp1 NA19072.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-22054G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630376 | |||||||
| chr11:75630377 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(257): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.906-22055T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630377 | |||||||
| chr11:75630619 | C | T | 2 | a0002c0003t0001g0281 a0002c0003t0001g0282 |
2 | HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.906-22297G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630619 | |||||||
| chr11:75630716 | T | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(36): Show |
51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.906-22394A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630716 | |||||||
| chr11:75630795 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.906-22473G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630795 | |||||||
| chr11:75630808 | T | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-22486A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630808 | |||||||
| chr11:75630901 | C | T | 9 | a0002c0003t0001g0309 a0002c0003t0001g0310 a0002c0003t0001g0312 others(6): Show |
9 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-22579G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630901 | |||||||
| chr11:75631069 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-22747C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631069 | |||||||
| chr11:75631283 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.906-22961A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631283 | |||||||
| chr11:75631482 | T | C | 1 | a0002c0003t0001g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.906-23160A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631482 | |||||||
| chr11:75631807 | C | G | 136 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.906-23485G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631807 | |||||||
| chr11:75631820 | CACTGGGT others(8): Show |
C | 1 | a0002c0003t0001g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.906-23513_906-2349 others(19): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631820 | |||||||
| chr11:75632106 | A | G | 1 | a0002c0002t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.906-23784T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632106 | |||||||
| chr11:75632126 | C | T | 1 | a0002c0003t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.906-23804G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632126 | |||||||
| chr11:75632413 | C | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0193 others(5): Show |
9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.906-24091G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632413 | |||||||
| chr11:75632484 | G | A | 71 | a0002c0002t0001g0285 a0002c0002t0001g0302 a0002c0002t0001g0303 others(68): Show |
82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.906-24162C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632484 | |||||||
| chr11:75632492 | A | T | 1 | a0002c0003t0001g0275 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-24170T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632492 | |||||||
| chr11:75632737 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.906-24415C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632737 | |||||||
| chr11:75633010 | CT | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.906-24689delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633010 | |||||||
| chr11:75633031 | GAAGAGAC others(5): Show |
G | 1 | a0002c0003t0001g0275 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-24721_906-2471 others(16): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633031 | |||||||
| chr11:75633117 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.906-24795T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633117 | |||||||
| chr11:75633409 | T | C | 4 | a0001c0004t0001g0046 a0001c0004t0001g0047 a0001c0004t0001g0048 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-25087A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633409 | |||||||
| chr11:75633596 | A | T | 1 | a0002c0002t0001g0302 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.906-25274T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633596 | |||||||
| chr11:75633819 | G | A | 9 | a0002c0003t0001g0309 a0002c0003t0001g0310 a0002c0003t0001g0312 others(6): Show |
9 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-25497C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633819 | |||||||
| chr11:75633861 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(122): Show |
149 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.906-25539T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633861 | |||||||
| chr11:75633903 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.906-25581G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633903 | |||||||
| chr11:75634363 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.906-26041C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75634363 | |||||||
| chr11:75634395 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.906-26073C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75634395 | |||||||
| chr11:75634750 | C | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.906-26428G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75634750 | |||||||
| chr11:75635027 | T | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.906-26705A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635027 | |||||||
| chr11:75635061 | C | T | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-26739G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635061 | |||||||
| chr11:75635062 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.906-26740C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635062 | |||||||
| chr11:75635270 | T | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
67 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.906-26948A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635270 | |||||||
| chr11:75635303 | T | C | 3 | a0002c0003t0001g0023 a0002c0003t0001g0286 a0002c0003t0001g0287 |
4 | HG00621.hp1 HG02015.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-26981A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635303 | |||||||
| chr11:75635304 | TA | T | 3 | a0002c0003t0001g0023 a0002c0003t0001g0286 a0002c0003t0001g0287 |
4 | HG00621.hp1 HG02015.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-26983delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635304 | |||||||
| chr11:75635335 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.906-27013T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635335 | |||||||
| chr11:75635477 | CA | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-27156delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635477 | |||||||
| chr11:75635515 | T | C | 1 | a0002c0002t0001g0247 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.906-27193A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635515 | |||||||
| chr11:75635652 | C | T | 7 | a0002c0002t0001g0019 a0002c0002t0001g0222 a0002c0002t0001g0229 others(4): Show |
8 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.906-27330G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635652 | |||||||
| chr11:75635722 | T | C | 2 | a0001c0001t0001g0144 a0001c0004t0001g0145 |
2 | HG02523.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.906-27400A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635722 | |||||||
| chr11:75636065 | C | A | 1 | a0002c0003t0001g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.906-27743G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636065 | |||||||
| chr11:75636210 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-27888T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636210 | |||||||
| chr11:75636357 | CT | C | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-28036delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636357 | |||||||
| chr11:75636386 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.906-28064A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636386 | |||||||
| chr11:75636408 | A | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.906-28086T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636408 | |||||||
| chr11:75636797 | A | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.906-28475T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636797 | |||||||
| chr11:75636909 | T | C | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-28587A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636909 | |||||||
| chr11:75637118 | T | G | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-28796A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637118 | |||||||
| chr11:75637165 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.906-28843A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637165 | |||||||
| chr11:75637293 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.906-28971G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637293 | |||||||
| chr11:75637405 | T | G | 3 | a0002c0003t0001g0025 a0002c0003t0001g0304 a0008c0017t0001g0308 |
4 | HG01243.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-29083A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637405 | |||||||
| chr11:75637504 | T | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.906-29182A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637504 | |||||||
| chr11:75637580 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.906-29258T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637580 | |||||||
| chr11:75637866 | GGGAAGGA others(1): Show |
G | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-29552_906-2954 others(12): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637866 | |||||||
| chr11:75638011 | T | C | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+29454A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638011 | |||||||
| chr11:75638157 | T | TGCTCTGC others(3): Show |
8 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0193 others(5): Show |
9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+29307_905+2930 others(14): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638157 | |||||||
| chr11:75638205 | C | G | 22 | a0002c0002t0001g0285 a0002c0003t0001g0021 a0002c0003t0001g0022 others(19): Show |
26 | HG00621.hp1 HG01243.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.905+29260G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638205 | |||||||
| chr11:75638243 | A | G | 1 | a0002c0003t0001g0025 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.905+29222T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638243 | |||||||
| chr11:75638438 | C | T | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+29027G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638438 | |||||||
| chr11:75638458 | A | C | 1 | a0002c0002t0001g0228 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.905+29007T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638458 | |||||||
| chr11:75638781 | C | A | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+28684G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638781 | |||||||
| chr11:75638968 | C | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(259): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.905+28497G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638968 | |||||||
| chr11:75638984 | C | A | 39 | a0001c0001t0001g0119 a0001c0001t0001g0133 a0001c0001t0001g0136 others(36): Show |
52 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.905+28481G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638984 | |||||||
| chr11:75638986 | T | C | 2 | a0002c0003t0001g0275 a0002c0003t0001g0276 |
2 | NA19072.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.905+28479A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638986 | |||||||
| chr11:75639094 | A | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0004t0001g0145 |
3 | HG02523.hp2 NA18952.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.905+28371T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639094 | |||||||
| chr11:75639122 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+28343T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639122 | |||||||
| chr11:75639358 | G | A | 1 | a0002c0002t0001g0227 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.905+28107C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639358 | |||||||
| chr11:75639359 | G | A | 1 | a0002c0002t0001g0227 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.905+28106C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639359 | |||||||
| chr11:75639360 | A | C | 1 | a0002c0002t0001g0227 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.905+28105T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639360 | |||||||
| chr11:75639361 | A | T | 1 | a0002c0002t0001g0227 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.905+28104T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639361 | |||||||
| chr11:75639805 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.905+27660C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639805 | |||||||
| chr11:75639826 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.905+27639A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639826 | |||||||
| chr11:75640018 | C | T | 1 | a0001c0004t0001g0111 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.905+27447G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640018 | |||||||
| chr11:75640189 | A | AC | 42 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(39): Show |
54 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.905+27275dupG | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640189 | |||||||
| chr11:75640195 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.905+27270G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640195 | |||||||
| chr11:75640195 | C | CA | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+27269_905+2727 others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640195 | |||||||
| chr11:75640197 | A | C | 1 | a0001c0004t0001g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.905+27268T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640197 | |||||||
| chr11:75640213 | AC | A | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+27251delG | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640213 | |||||||
| chr11:75640469 | T | A | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+26996A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640469 | |||||||
| chr11:75640611 | T | C | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+26854A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640611 | |||||||
| chr11:75640654 | A | C | 1 | a0002c0002t0001g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.905+26811T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640654 | |||||||
| chr11:75640687 | G | A | 1 | a0001c0004t0001g0139 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.905+26778C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640687 | |||||||
| chr11:75640744 | C | T | 1 | a0001c0004t0001g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.905+26721G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640744 | |||||||
| chr11:75640851 | T | G | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+26614A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640851 | |||||||
| chr11:75640867 | C | T | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+26598G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640867 | |||||||
| chr11:75640868 | A | G | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+26597T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640868 | |||||||
| chr11:75641035 | G | A | 1 | a0002c0002t0001g0258 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.905+26430C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641035 | |||||||
| chr11:75641147 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.905+26318A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641147 | |||||||
| chr11:75641339 | T | TG | 13 | a0001c0001t0001g0071 a0001c0001t0001g0095 a0001c0001t0001g0107 others(10): Show |
13 | HG00609.hp1 HG01169.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.905+26125dupC | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641339 | |||||||
| chr11:75641376 | T | C | 1 | a0001c0004t0001g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.905+26089A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641376 | |||||||
| chr11:75641433 | T | C | 2 | a0002c0003t0001g0199 a0002c0003t0001g0200 |
2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.905+26032A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641433 | |||||||
| chr11:75641483 | T | TA | 68 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0040 others(65): Show |
82 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+25981dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641483 | |||||||
| chr11:75641484 | A | T | 1 | a0002c0002t0001g0226 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.905+25981T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641484 | |||||||
| chr11:75641540 | T | G | 2 | a0002c0003t0001g0279 a0002c0003t0001g0280 |
2 | NA18959.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.905+25925A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641540 | |||||||
| chr11:75641588 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+25877C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641588 | |||||||
| chr11:75642069 | C | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0193 others(5): Show |
9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+25396G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642069 | |||||||
| chr11:75642095 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+25370G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642095 | |||||||
| chr11:75642245 | T | C | 1 | a0001c0004t0001g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.905+25220A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642245 | |||||||
| chr11:75642424 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.905+25041G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642424 | |||||||
| chr11:75642623 | A | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+24842T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642623 | |||||||
| chr11:75642644 | A | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+24821T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642644 | |||||||
| chr11:75642721 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+24744G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642721 | |||||||
| chr11:75642817 | C | T | 1 | a0002c0019t0001g0333 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.905+24648G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642817 | |||||||
| chr11:75642846 | C | A | 15 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(12): Show |
15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+24619G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642846 | |||||||
| chr11:75642899 | C | T | 1 | a0001c0007t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905+24566G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642899 | |||||||
| chr11:75643068 | C | A | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+24397G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643068 | |||||||
| chr11:75643213 | G | C | 1 | a0002c0003t0001g0271 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.905+24252C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643213 | |||||||
| chr11:75643218 | T | TTA | 4 | a0002c0002t0001g0256 a0002c0003t0001g0274 a0002c0003t0001g0278 others(1): Show |
4 | HG02132.hp1 HG03491.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+24245_905+2424 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643218 | |||||||
| chr11:75643220 | A | T | 6 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 others(3): Show |
7 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.905+24245T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643220 | |||||||
| chr11:75643241 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.905+24224A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643241 | |||||||
| chr11:75643410 | C | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+24055G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643410 | |||||||
| chr11:75643531 | T | C | 3 | a0002c0003t0001g0023 a0002c0003t0001g0286 a0002c0003t0001g0287 |
4 | HG00621.hp1 HG02015.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+23934A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643531 | |||||||
| chr11:75643638 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.905+23827C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643638 | |||||||
| chr11:75643773 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.905+23692G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643773 | |||||||
| chr11:75644045 | T | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0193 others(5): Show |
9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+23420A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644045 | |||||||
| chr11:75644168 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+23297G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644168 | |||||||
| chr11:75644307 | A | T | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+23158T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644307 | |||||||
| chr11:75644491 | A | C | 3 | a0002c0002t0001g0248 a0002c0002t0001g0249 a0002c0014t0001g0225 |
3 | HG03831.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.905+22974T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644491 | |||||||
| chr11:75644590 | T | C | 1 | a0002c0003t0001g0314 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.905+22875A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644590 | |||||||
| chr11:75644750 | T | G | 1 | a0002c0003t0001g0301 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.905+22715A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644750 | |||||||
| chr11:75644769 | T | C | 1 | a0002c0003t0001g0245 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.905+22696A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644769 | |||||||
| chr11:75644829 | C | A | 2 | a0001c0004t0001g0138 a0001c0004t0001g0139 |
2 | HG00140.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.905+22636G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644829 | |||||||
| chr11:75644835 | G | A | 1 | a0002c0003t0001g0304 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.905+22630C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644835 | |||||||
| chr11:75644934 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(41): Show |
57 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.905+22531A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644934 | |||||||
| chr11:75644962 | G | A | 3 | a0002c0003t0001g0274 a0002c0003t0001g0278 a0002c0003t0001g0295 |
3 | HG02132.hp1 NA18954.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.905+22503C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644962 | |||||||
| chr11:75645061 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+22404C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645061 | |||||||
| chr11:75645107 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.905+22358C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645107 | |||||||
| chr11:75645132 | G | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | NA19072.hp1 NA19081.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.905+22333C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645132 | |||||||
| chr11:75645283 | G | A | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+22182C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645283 | |||||||
| chr11:75645290 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+22175A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645290 | |||||||
| chr11:75645669 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+21796G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645669 | |||||||
| chr11:75645875 | G | C | 6 | a0002c0002t0001g0302 a0002c0003t0001g0027 a0002c0003t0001g0297 others(3): Show |
7 | HG02280.hp1 HG02970.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+21590C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645875 | |||||||
| chr11:75646214 | C | T | 4 | a0001c0004t0001g0109 a0001c0004t0001g0110 a0001c0004t0001g0125 others(1): Show |
4 | HG02015.hp2 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+21251G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646214 | |||||||
| chr11:75646239 | A | C | 1 | a0002c0002t0001g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.905+21226T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646239 | |||||||
| chr11:75646305 | G | C | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+21160C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646305 | |||||||
| chr11:75646412 | AGCACTTT others(2): Show |
A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+21044_905+2105 others(13): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646412 | |||||||
| chr11:75646460 | A | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+21005T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646460 | |||||||
| chr11:75646486 | A | C | 71 | a0002c0002t0001g0285 a0002c0002t0001g0302 a0002c0002t0001g0303 others(68): Show |
82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+20979T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646486 | |||||||
| chr11:75646499 | T | TA | 27 | a0001c0001t0001g0037 a0001c0001t0001g0061 a0001c0001t0001g0071 others(24): Show |
28 | HG00140.hp1 HG00423.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.905+20965dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646499 | |||||||
| chr11:75646499 | T | TAA | 34 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0016 others(31): Show |
45 | HG00558.hp2 HG02056.hp1 HG02145.hp1 others(42): Show |
intron_variant | MODIFIER | c.905+20964_905+2096 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646499 | |||||||
| chr11:75646499 | T | TAAA | 6 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(3): Show |
7 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+20963_905+2096 others(7): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646499 | |||||||
| chr11:75646499 | TA | T | 18 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0069 others(15): Show |
19 | HG01168.hp1 HG02895.hp2 HG02965.hp2 others(16): Show |
intron_variant | MODIFIER | c.905+20965delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646499 | |||||||
| chr11:75646525 | G | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
67 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.905+20940C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646525 | |||||||
| chr11:75646559 | C | T | 71 | a0002c0002t0001g0285 a0002c0002t0001g0302 a0002c0002t0001g0303 others(68): Show |
82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+20906G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646559 | |||||||
| chr11:75646603 | G | A | 3 | a0002c0003t0001g0297 a0002c0003t0001g0316 a0002c0003t0001g0317 |
3 | HG06807.hp2 NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.905+20862C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646603 | |||||||
| chr11:75646708 | G | C | 3 | a0002c0003t0001g0281 a0002c0003t0001g0282 a0002c0003t0001g0305 |
3 | HG02257.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.905+20757C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646708 | |||||||
| chr11:75646776 | C | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.905+20689G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646776 | |||||||
| chr11:75646840 | T | G | 1 | a0002c0002t0001g0247 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.905+20625A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646840 | |||||||
| chr11:75646948 | T | G | 2 | a0002c0002t0001g0248 a0002c0002t0001g0249 |
2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.905+20517A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646948 | |||||||
| chr11:75646955 | T | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.905+20510A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646955 | |||||||
| chr11:75646985 | C | CT | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(230): Show |
272 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.905+20479dupA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646985 | |||||||
| chr11:75646985 | C | CTT | 26 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 others(23): Show |
31 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.905+20478_905+2047 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646985 | |||||||
| chr11:75647083 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+20382A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647083 | |||||||
| chr11:75647171 | A | AT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+20293dupA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647171 | |||||||
| chr11:75647272 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+20193A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647272 | |||||||
| chr11:75647298 | A | G | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | NA18946.hp2 NA18964.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.905+20167T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647298 | |||||||
| chr11:75647326 | T | TA | 7 | a0001c0001t0001g0154 a0002c0002t0001g0302 a0002c0003t0001g0287 others(4): Show |
7 | HG01496.hp2 HG02970.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+20138dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647326 | |||||||
| chr11:75647347 | C | CA | 79 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
85 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.905+20117dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | |||||||
| chr11:75647347 | C | CAA | 12 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0069 others(9): Show |
12 | HG02055.hp1 HG02257.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.905+20116_905+2011 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | |||||||
| chr11:75647347 | CA | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(73): Show |
95 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.905+20117delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | |||||||
| chr11:75647347 | CAA | C | 23 | a0001c0001t0001g0038 a0002c0002t0001g0285 a0002c0003t0001g0021 others(20): Show |
27 | HG00621.hp1 HG01243.hp1 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.905+20116_905+2011 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | |||||||
| chr11:75647347 | CAAA | C | 9 | a0001c0001t0001g0198 a0002c0002t0001g0201 a0002c0002t0001g0202 others(6): Show |
9 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+20115_905+2011 others(7): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | |||||||
| chr11:75647402 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+20063C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647402 | |||||||
| chr11:75647529 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+19936G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647529 | |||||||
| chr11:75647561 | A | G | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG03516.hp1 HG06807.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+19904T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647561 | |||||||
| chr11:75647574 | A | C | 1 | a0006c0010t0001g0031 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.905+19891T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647574 | |||||||
| chr11:75647612 | G | A | 1 | a0001c0004t0001g0131 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.905+19853C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647612 | |||||||
| chr11:75647975 | A | T | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+19490T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647975 | |||||||
| chr11:75648006 | G | A | 1 | a0002c0002t0001g0303 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.905+19459C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648006 | |||||||
| chr11:75648074 | T | C | 2 | a0002c0002t0001g0255 a0002c0002t0001g0256 |
2 | HG02602.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.905+19391A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648074 | |||||||
| chr11:75648130 | T | C | 44 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
49 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.905+19335A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648130 | |||||||
| chr11:75648137 | C | T | 2 | a0002c0002t0001g0020 a0002c0002t0001g0265 |
3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.905+19328G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648137 | |||||||
| chr11:75648282 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+19183G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648282 | |||||||
| chr11:75648411 | T | C | 3 | a0002c0003t0001g0026 a0002c0003t0001g0314 a0002c0003t0001g0315 |
4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+19054A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648411 | |||||||
| chr11:75648454 | A | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+19011T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648454 | |||||||
| chr11:75648484 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+18981A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648484 | |||||||
| chr11:75648486 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+18979T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648486 | |||||||
| chr11:75648489 | C | A | 71 | a0002c0002t0001g0285 a0002c0002t0001g0302 a0002c0002t0001g0303 others(68): Show |
82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+18976G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648489 | |||||||
| chr11:75648498 | A | AAAAC | 13 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(10): Show |
15 | HG01928.hp1 HG02273.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+18963_905+1896 others(8): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648498 | |||||||
| chr11:75648498 | AAAAC | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(41): Show |
56 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.905+18963_905+1896 others(8): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648498 | |||||||
| chr11:75648564 | T | A | 3 | a0002c0003t0001g0025 a0002c0003t0001g0304 a0008c0017t0001g0308 |
4 | HG01243.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+18901A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648564 | |||||||
| chr11:75648575 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+18890T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648575 | |||||||
| chr11:75649190 | AT | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+18274delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649190 | |||||||
| chr11:75649461 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+18004C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649461 | |||||||
| chr11:75649464 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+18001C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649464 | |||||||
| chr11:75649473 | T | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+17992A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649473 | |||||||
| chr11:75649502 | A | G | 3 | a0002c0003t0001g0281 a0002c0003t0001g0282 a0002c0003t0001g0305 |
3 | HG02257.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.905+17963T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649502 | |||||||
| chr11:75649505 | A | G | 1 | a0002c0003t0001g0314 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.905+17960T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649505 | |||||||
| chr11:75649687 | C | T | 1 | a0002c0002t0001g0210 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905+17778G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649687 | |||||||
| chr11:75649827 | C | T | 2 | a0001c0001t0001g0059 a0001c0004t0001g0058 |
2 | HG01255.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.905+17638G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649827 | |||||||
| chr11:75649855 | G | A | 1 | a0001c0004t0001g0182 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.905+17610C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649855 | |||||||
| chr11:75649966 | G | C | 2 | a0002c0002t0001g0020 a0002c0002t0001g0265 |
3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.905+17499C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649966 | |||||||
| chr11:75649983 | C | T | 3 | a0002c0003t0001g0026 a0002c0003t0001g0314 a0002c0003t0001g0315 |
4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+17482G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649983 | |||||||
| chr11:75650080 | C | T | 15 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0038 others(12): Show |
16 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.905+17385G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650080 | |||||||
| chr11:75650108 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.905+17357T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650108 | |||||||
| chr11:75650525 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905+16940A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650525 | |||||||
| chr11:75650563 | G | C | 1 | a0002c0003t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.905+16902C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650563 | |||||||
| chr11:75650996 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(260): Show |
307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.905+16469A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650996 | |||||||
| chr11:75651060 | A | G | 1 | a0002c0003t0001g0310 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.905+16405T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651060 | |||||||
| chr11:75651244 | G | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0193 a0001c0004t0001g0035 others(1): Show |
4 | HG02886.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+16221C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651244 | |||||||
| chr11:75651483 | G | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
67 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.905+15982C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651483 | |||||||
| chr11:75651530 | T | TA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+15934dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651530 | |||||||
| chr11:75651759 | G | A | 1 | a0002c0002t0001g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.905+15706C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651759 | |||||||
| chr11:75651788 | C | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0193 others(5): Show |
9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+15677G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651788 | |||||||
| chr11:75651938 | G | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+15527C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651938 | |||||||
| chr11:75652024 | C | T | 1 | a0001c0012t0001g0050 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905+15441G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652024 | |||||||
| chr11:75652056 | T | A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.905+15409A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652056 | |||||||
| chr11:75652074 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0159 |
3 | HG03516.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.905+15391G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652074 | |||||||
| chr11:75652167 | T | G | 1 | a0002c0003t0001g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.905+15298A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652167 | |||||||
| chr11:75652273 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+15192C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652273 | |||||||
| chr11:75652365 | T | C | 1 | a0001c0004t0001g0132 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.905+15100A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652365 | |||||||
| chr11:75652408 | C | A | 1 | a0002c0002t0001g0216 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.905+15057G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652408 | |||||||
| chr11:75652580 | G | A | 7 | a0001c0001t0001g0038 a0002c0002t0001g0201 a0002c0002t0001g0202 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+14885C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652580 | |||||||
| chr11:75652632 | T | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+14833A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652632 | |||||||
| chr11:75652836 | G | GA | 39 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(36): Show |
51 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+14628dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652836 | |||||||
| chr11:75652849 | A | G | 2 | a0002c0003t0001g0279 a0002c0003t0001g0280 |
2 | NA18959.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.905+14616T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652849 | |||||||
| chr11:75652973 | A | G | 2 | a0002c0002t0001g0215 a0002c0002t0001g0216 |
2 | NA19054.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.905+14492T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652973 | |||||||
| chr11:75653026 | C | A | 2 | a0001c0001t0001g0043 a0001c0004t0001g0042 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.905+14439G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653026 | |||||||
| chr11:75653168 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+14297G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653168 | |||||||
| chr11:75653264 | C | A | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+14201G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653264 | |||||||
| chr11:75653269 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+14196A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653269 | |||||||
| chr11:75653290 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.905+14175G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653290 | |||||||
| chr11:75653312 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.905+14153A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653312 | |||||||
| chr11:75653567 | T | C | 2 | a0001c0001t0001g0133 a0001c0004t0001g0134 |
2 | HG01255.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.905+13898A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653567 | |||||||
| chr11:75653729 | T | C | 1 | a0002c0002t0001g0258 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.905+13736A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653729 | |||||||
| chr11:75653962 | C | T | 2 | a0002c0002t0001g0213 a0002c0002t0001g0214 |
2 | HG03927.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.905+13503G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653962 | |||||||
| chr11:75653994 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.905+13471A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653994 | |||||||
| chr11:75654377 | T | A | 1 | a0001c0001t0001g0103 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.905+13088A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654377 | |||||||
| chr11:75654489 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+12976A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654489 | |||||||
| chr11:75654728 | G | A | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+12737C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654728 | |||||||
| chr11:75654755 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.905+12710G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654755 | |||||||
| chr11:75654864 | G | A | 1 | a0001c0004t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.905+12601C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654864 | |||||||
| chr11:75655165 | T | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+12300A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655165 | |||||||
| chr11:75655240 | C | T | 1 | a0002c0003t0001g0278 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.905+12225G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655240 | |||||||
| chr11:75655344 | A | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.905+12121T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655344 | |||||||
| chr11:75655517 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(32): Show |
47 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.905+11948G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655517 | |||||||
| chr11:75655556 | C | A | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+11909G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655556 | |||||||
| chr11:75655606 | G | C | 2 | a0002c0002t0001g0306 a0002c0002t0001g0307 |
2 | NA18941.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.905+11859C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655606 | |||||||
| chr11:75655621 | G | T | 1 | a0002c0003t0001g0309 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.905+11844C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655621 | |||||||
| chr11:75655653 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.905+11812C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655653 | |||||||
| chr11:75655976 | T | C | 1 | a0001c0012t0001g0050 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905+11489A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655976 | |||||||
| chr11:75656184 | G | T | 7 | a0001c0001t0001g0038 a0002c0002t0001g0201 a0002c0002t0001g0202 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+11281C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75656184 | |||||||
| chr11:75656244 | C | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0193 others(6): Show |
10 | HG00639.hp2 HG02630.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.905+11221G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75656244 | |||||||
| chr11:75656694 | T | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+10771A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75656694 | |||||||
| chr11:75657108 | CTAT | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
44 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.905+10354_905+1035 others(7): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657108 | |||||||
| chr11:75657110 | AT | A | 9 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0198 others(6): Show |
10 | HG02055.hp2 HG02630.hp1 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.905+10354delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657110 | |||||||
| chr11:75657110 | ATT | A | 9 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 others(6): Show |
9 | HG02109.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.905+10353_905+1035 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657110 | |||||||
| chr11:75657110 | ATTTT | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+10351_905+1035 others(8): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657110 | |||||||
| chr11:75657300 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+10165G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657300 | |||||||
| chr11:75657311 | C | T | 4 | a0002c0002t0001g0205 a0002c0002t0001g0210 a0002c0002t0001g0212 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+10154G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657311 | |||||||
| chr11:75657366 | G | A | 1 | a0002c0002t0001g0259 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.905+10099C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657366 | |||||||
| chr11:75657959 | A | G | 15 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(12): Show |
15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+9506T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657959 | |||||||
| chr11:75658308 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(32): Show |
47 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.905+9157G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658308 | |||||||
| chr11:75658397 | C | CA | 71 | a0002c0002t0001g0285 a0002c0002t0001g0302 a0002c0002t0001g0303 others(68): Show |
82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+9067_905+9068i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658397 | |||||||
| chr11:75658399 | C | CA | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0160 |
3 | HG00423.hp1 HG00609.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.905+9065_905+9066i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658399 | |||||||
| chr11:75658399 | C | CT | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+9065_905+9066i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658399 | |||||||
| chr11:75658399 | C | T | 2 | a0002c0003t0001g0275 a0002c0003t0001g0276 |
2 | NA19072.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.905+9066G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658399 | |||||||
| chr11:75658400 | C | CG | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+9064_905+9065i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658400 | |||||||
| chr11:75658404 | C | CT | 173 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(170): Show |
205 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.905+9060_905+9061i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658404 | |||||||
| chr11:75658404 | C | G | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+9061G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658404 | |||||||
| chr11:75658404 | C | T | 87 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(84): Show |
99 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.905+9061G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658404 | |||||||
| chr11:75658405 | G | A | 1 | a0008c0017t0001g0308 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.905+9060C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658405 | |||||||
| chr11:75658406 | C | T | 1 | a0002c0003t0001g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.905+9059G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658406 | |||||||
| chr11:75658411 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.905+9054C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658411 | |||||||
| chr11:75658830 | C | A | 3 | a0002c0003t0001g0026 a0002c0003t0001g0314 a0002c0003t0001g0315 |
4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+8635G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658830 | |||||||
| chr11:75658900 | A | C | 15 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(12): Show |
15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+8565T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658900 | |||||||
| chr11:75658938 | T | C | 1 | a0001c0004t0001g0135 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.905+8527A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658938 | |||||||
| chr11:75659003 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.905+8462T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659003 | |||||||
| chr11:75659264 | C | A | 1 | a0002c0002t0001g0260 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.905+8201G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659264 | |||||||
| chr11:75659274 | G | A | 4 | a0001c0001t0001g0136 a0001c0004t0001g0137 a0001c0004t0001g0138 others(1): Show |
4 | HG00140.hp2 HG00738.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+8191C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659274 | |||||||
| chr11:75659352 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.905+8113G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659352 | |||||||
| chr11:75659475 | A | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(50): Show |
66 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.905+7990T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659475 | |||||||
| chr11:75659883 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.905+7582A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659883 | |||||||
| chr11:75659943 | C | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(260): Show |
307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.905+7522G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659943 | |||||||
| chr11:75659991 | T | C | 4 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+7474A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659991 | |||||||
| chr11:75659996 | C | T | 3 | a0001c0001t0001g0037 a0001c0004t0001g0035 a0001c0004t0001g0036 |
3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+7469G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659996 | |||||||
| chr11:75660137 | T | C | 39 | a0001c0001t0001g0119 a0001c0001t0001g0133 a0001c0001t0001g0136 others(36): Show |
52 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.905+7328A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660137 | |||||||
| chr11:75660142 | T | C | 1 | a0002c0002t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.905+7323A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660142 | |||||||
| chr11:75660309 | C | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
29 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.905+7156G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660309 | |||||||
| chr11:75660312 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+7153G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660312 | |||||||
| chr11:75660412 | A | G | 1 | a0001c0012t0001g0050 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905+7053T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660412 | |||||||
| chr11:75660534 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+6931A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660534 | |||||||
| chr11:75660659 | C | T | 4 | a0001c0004t0001g0046 a0001c0004t0001g0047 a0001c0004t0001g0048 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+6806G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660659 | |||||||
| chr11:75660809 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+6656G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660809 | |||||||
| chr11:75660882 | T | G | 3 | a0002c0003t0001g0026 a0002c0003t0001g0314 a0002c0003t0001g0315 |
4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+6583A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660882 | |||||||
| chr11:75660966 | T | C | 18 | a0002c0002t0001g0311 a0002c0002t0001g0319 a0002c0002t0001g0320 others(15): Show |
19 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.905+6499A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660966 | |||||||
| chr11:75661009 | T | C | 15 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(12): Show |
15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+6456A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661009 | |||||||
| chr11:75661019 | GA | G | 4 | a0002c0003t0001g0021 a0002c0003t0001g0266 a0002c0003t0001g0267 others(1): Show |
5 | NA18942.hp1 NA18975.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.905+6445delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661019 | |||||||
| chr11:75661178 | G | C | 2 | a0002c0003t0001g0316 a0002c0003t0001g0317 |
2 | NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.905+6287C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661178 | |||||||
| chr11:75661212 | T | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.905+6253A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661212 | |||||||
| chr11:75661421 | A | G | 71 | a0002c0002t0001g0285 a0002c0002t0001g0302 a0002c0002t0001g0303 others(68): Show |
82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+6044T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661421 | |||||||
| chr11:75661512 | A | C | 4 | a0002c0002t0001g0205 a0002c0002t0001g0210 a0002c0002t0001g0212 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+5953T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661512 | |||||||
| chr11:75661669 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+5796T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661669 | |||||||
| chr11:75661730 | T | A | 1 | a0001c0004t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.905+5735A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661730 | |||||||
| chr11:75661779 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.905+5686T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661779 | |||||||
| chr11:75661833 | CA | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+5631delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661833 | |||||||
| chr11:75661835 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.905+5630T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661835 | |||||||
| chr11:75662071 | A | C | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+5394T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662071 | |||||||
| chr11:75662174 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+5291A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662174 | |||||||
| chr11:75662391 | C | T | 1 | a0002c0002t0001g0324 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905+5074G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662391 | |||||||
| chr11:75662571 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.905+4894C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662571 | |||||||
| chr11:75662646 | G | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG03516.hp1 HG06807.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+4819C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662646 | |||||||
| chr11:75662962 | CT | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(117): Show |
143 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.905+4502delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662962 | |||||||
| chr11:75663001 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.905+4464T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663001 | |||||||
| chr11:75663120 | C | T | 4 | a0002c0002t0001g0206 a0002c0002t0001g0207 a0002c0002t0001g0208 others(1): Show |
4 | NA18955.hp2 NA18962.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+4345G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663120 | |||||||
| chr11:75663394 | A | ATTTTCTG others(39): Show |
1 | a0001c0001t0001g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.905+4025_905+4070d others(48): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663394 | |||||||
| chr11:75663531 | C | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(43): Show |
59 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.905+3934G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663531 | |||||||
| chr11:75663688 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
50 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.905+3777C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663688 | |||||||
| chr11:75664081 | A | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(43): Show |
59 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.905+3384T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664081 | |||||||
| chr11:75664097 | C | T | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+3368G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664097 | |||||||
| chr11:75664134 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(117): Show |
144 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.905+3331G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664134 | |||||||
| chr11:75664185 | A | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0197 others(1): Show |
4 | HG02717.hp2 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+3280T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664185 | |||||||
| chr11:75664256 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.905+3209G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664256 | |||||||
| chr11:75664261 | T | C | 2 | a0002c0002t0001g0263 a0002c0002t0001g0264 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.905+3204A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664261 | |||||||
| chr11:75664711 | A | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(43): Show |
59 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.905+2754T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664711 | |||||||
| chr11:75664865 | T | A | 1 | a0001c0001t0001g0161 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.905+2600A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664865 | |||||||
| chr11:75664889 | C | CA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0192 others(7): Show |
11 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.905+2575dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664889 | |||||||
| chr11:75664903 | G | A | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+2562C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664903 | |||||||
| chr11:75665093 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+2372C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665093 | |||||||
| chr11:75665286 | G | C | 5 | a0002c0002t0001g0319 a0002c0002t0001g0320 a0002c0002t0001g0321 others(2): Show |
5 | HG02451.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.905+2179C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665286 | |||||||
| chr11:75665288 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.905+2177T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665288 | |||||||
| chr11:75665590 | G | C | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+1875C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665590 | |||||||
| chr11:75665702 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+1763A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665702 | |||||||
| chr11:75665825 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+1640C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665825 | |||||||
| chr11:75666115 | G | A | 2 | a0002c0002t0001g0020 a0002c0002t0001g0265 |
3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.905+1350C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666115 | |||||||
| chr11:75666181 | T | A | 72 | a0002c0002t0001g0272 a0002c0002t0001g0285 a0002c0002t0001g0302 others(69): Show |
83 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.905+1284A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666181 | |||||||
| chr11:75666358 | AGCT | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+1104_905+1106d others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666358 | |||||||
| chr11:75666388 | AAG | A | 3 | a0001c0007t0001g0028 a0001c0007t0001g0030 a0001c0009t0001g0029 |
3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+1075_905+1076d others(4): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666388 | |||||||
| chr11:75666396 | G | A | 1 | a0002c0002t0001g0324 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905+1069C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666396 | |||||||
| chr11:75666472 | G | A | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+993C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666472 | |||||||
| chr11:75666490 | GAACATGT others(40): Show |
G | 1 | a0001c0001t0001g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.905+928_905+974del others(47): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666490 | |||||||
| chr11:75666495 | T | A | 7 | a0001c0001t0001g0133 a0001c0004t0001g0001 a0001c0004t0001g0122 others(4): Show |
12 | HG00099.hp2 HG00735.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.905+970A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666495 | |||||||
| chr11:75666632 | G | C | 2 | a0002c0002t0001g0325 a0002c0002t0001g0326 |
2 | NA18983.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.905+833C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666632 | |||||||
| chr11:75666684 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.905+781G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666684 | |||||||
| chr11:75666708 | A | G | 1 | a0002c0003t0001g0327 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905+757T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666708 | |||||||
| chr11:75666725 | T | C | 1 | a0002c0002t0001g0205 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.905+740A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666725 | |||||||
| chr11:75666793 | C | G | 1 | a0002c0002t0001g0205 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.905+672G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666793 | |||||||
| chr11:75666891 | A | T | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+574T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666891 | |||||||
| chr11:75666958 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+507C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666958 | |||||||
| chr11:75667101 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
53 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.905+364A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667101 | |||||||
| chr11:75667134 | G | A | 2 | a0002c0003t0001g0027 a0002c0003t0001g0327 |
3 | HG02280.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.905+331C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667134 | |||||||
| chr11:75667278 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905+187G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667278 | |||||||
| chr11:75667308 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.905+157C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667308 | |||||||
| chr11:75667403 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+62C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667403 |