Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79884 |
| ensemblid | ENSG00000164114.19 |
| hgncid | 26118 |
| symbol | MAP9 |
| name | microtubule associated protein 9 |
| refseq_nuc | NM_001039580.2 |
| refseq_prot | NP_001034669.1 |
| ensembl_nuc | ENST00000311277.9 |
| ensembl_prot | ENSP00000310593.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 155342658 |
| end | 155376965 |
| strand | - |
| ver | v1.2 |
| region | chr4:155342658-155376965 |
| region5000 | chr4:155337658-155381965 |
| regionname0 | MAP9_chr4_155342658_155376965 |
| regionname5000 | MAP9_chr4_155337658_155381965 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 647 | 191 | 53 | 26 | 103 | 1 | 8 | 78 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0002 | 1/1 | 647 | 72 | 2 | 24 | 22 | 5 | 17 | 20 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0003 | 0/0 | 647 | 69 | 4 | 10 | 44 | 3 | 8 | 40 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0004 | 0/0 | 647 | 46 | 18 | 0 | 26 | 0 | 2 | 20 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0005 | 0/0 | 647 | 18 | 4 | 9 | 3 | 1 | 1 | 3 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0006 | 0/0 | 647 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0007 | 0/0 | 647 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0008 | 0/0 | 617 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(612): Show |
chr4 | 155337658 | 155381965 |
| a0009 | 0/0 | 647 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0010 | 0/0 | 647 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0011 | 0/0 | 647 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0012 | 0/0 | 647 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| a0013 | 0/0 | 647 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | MSDEV others(642): Show |
chr4 | 155337658 | 155381965 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1941 | 97 | 11 | 17 | 67 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0001c0002 | 0/0 | 1941 | 93 | 42 | 9 | 35 | 1 | 6 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0001c0012 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0002c0003 | 1/1 | 1941 | 72 | 2 | 24 | 22 | 5 | 17 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0003c0004 | 0/0 | 1941 | 69 | 4 | 10 | 44 | 3 | 8 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0004c0005 | 0/0 | 1941 | 46 | 18 | 0 | 26 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0005c0006 | 0/0 | 1941 | 17 | 3 | 9 | 3 | 1 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0005c0011 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0006c0007 | 0/0 | 1941 | 8 | 8 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0006c0008 | 0/0 | 1941 | 3 | 3 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0007c0010 | 0/0 | 1941 | 2 | 0 | 0 | 0 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0008c0009 | 0/0 | 1941 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0009c0017 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0010c0016 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0011c0013 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0012c0015 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 | ||
| a0013c0014 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | ATGTC others(1936): Show |
chr4 | 155337658 | 155381965 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7323 | 87 | 6 | 15 | 64 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0001t0013 | 0/0 | 7323 | 4 | 4 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0001t0017 | 0/0 | 7323 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0001t0031 | 0/0 | 7323 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0001t0032 | 0/0 | 7323 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0001t0033 | 0/0 | 7323 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0001t0039 | 0/0 | 7323 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0001 | 0/0 | 7323 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0004 | 0/0 | 7323 | 54 | 9 | 8 | 32 | 1 | 4 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0007 | 0/0 | 7323 | 15 | 15 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0008 | 0/0 | 7323 | 6 | 6 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0009 | 0/0 | 7323 | 6 | 6 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0012 | 0/0 | 7323 | 4 | 4 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0019 | 0/0 | 7323 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0020 | 0/0 | 7323 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0021 | 0/0 | 7323 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0022 | 0/0 | 7323 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0023 | 0/0 | 7323 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0024 | 0/0 | 7323 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0002t0027 | 0/0 | 7323 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0001c0012t0001 | 0/0 | 7323 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0002c0003t0003 | 1/1 | 7328 | 64 | 2 | 24 | 18 | 4 | 14 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7323): Show |
chr4 | 155337658 | 155381965 |
| a0002c0003t0011 | 0/0 | 7329 | 5 | 0 | 0 | 4 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7324): Show |
chr4 | 155337658 | 155381965 |
| a0002c0003t0034 | 0/0 | 7328 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7323): Show |
chr4 | 155337658 | 155381965 |
| a0002c0003t0035 | 0/0 | 7328 | 1 | 0 | 0 | 0 | 1 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7323): Show |
chr4 | 155337658 | 155381965 |
| a0002c0003t0036 | 0/0 | 7328 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7323): Show |
chr4 | 155337658 | 155381965 |
| a0003c0004t0002 | 0/0 | 7319 | 68 | 4 | 10 | 43 | 3 | 8 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0003c0004t0026 | 0/0 | 7319 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0004c0005t0005 | 0/0 | 7324 | 33 | 9 | 0 | 22 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7319): Show |
chr4 | 155337658 | 155381965 |
| a0004c0005t0010 | 0/0 | 7326 | 6 | 6 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7321): Show |
chr4 | 155337658 | 155381965 |
| a0004c0005t0016 | 0/0 | 7324 | 3 | 0 | 0 | 3 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7319): Show |
chr4 | 155337658 | 155381965 |
| a0004c0005t0018 | 0/0 | 7324 | 2 | 2 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7319): Show |
chr4 | 155337658 | 155381965 |
| a0004c0005t0038 | 0/0 | 7323 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0004c0005t0040 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7321): Show |
chr4 | 155337658 | 155381965 |
| a0005c0006t0006 | 0/0 | 7319 | 17 | 3 | 9 | 3 | 1 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0005c0011t0015 | 0/0 | 7319 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0006c0007t0014 | 0/0 | 7319 | 4 | 4 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0006c0007t0025 | 0/0 | 7319 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0006c0007t0028 | 0/0 | 7319 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0006c0007t0029 | 0/0 | 7319 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0006c0007t0037 | 0/0 | 7319 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0006c0008t0015 | 0/0 | 7319 | 3 | 3 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0007c0010t0003 | 0/0 | 7328 | 2 | 0 | 0 | 0 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7323): Show |
chr4 | 155337658 | 155381965 |
| a0008c0009t0001 | 0/0 | 7323 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0009c0017t0005 | 0/0 | 7324 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7319): Show |
chr4 | 155337658 | 155381965 |
| a0010c0016t0030 | 0/0 | 7319 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0011c0013t0001 | 0/0 | 7323 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| a0012c0015t0002 | 0/0 | 7319 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7314): Show |
chr4 | 155337658 | 155381965 |
| a0013c0014t0001 | 0/0 | 7323 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | CTTCG others(7318): Show |
chr4 | 155337658 | 155381965 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0007 | 0/0 | 11 | 0 | 7 | 4 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0018 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0019 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0028 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0013g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0013g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0017g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0017g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0031g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0032g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0033g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0001t0039g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0009 | 0/0 | 10 | 0 | 3 | 5 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0010 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0011 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0013 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0014 | 0/0 | 6 | 0 | 3 | 2 | 1 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0007g0005 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0008g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0009g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0012g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0019g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0020g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0021g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0022g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0023g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0024g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0002t0027g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0001c0012t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0002 | 0/0 | 23 | 1 | 6 | 10 | 2 | 4 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0004 | 0/0 | 13 | 1 | 8 | 1 | 1 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0021 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0022 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0011g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0011g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0034g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0035g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0002c0003t0036g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0001 | 0/0 | 30 | 0 | 4 | 25 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0015 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0030 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0003c0004t0026g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0006 | 0/0 | 11 | 1 | 0 | 10 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0010g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0016g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0016g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0018g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0038g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0004c0005t0040g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0005c0006t0006g0008 | 0/0 | 11 | 3 | 7 | 0 | 0 | 1 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0005c0006t0006g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0005c0006t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0005c0006t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0005c0006t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0005c0006t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0005c0011t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0006c0007t0014g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0006c0007t0014g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0006c0007t0014g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0006c0007t0025g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0006c0007t0028g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0006c0007t0029g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0006c0007t0037g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0006c0008t0015g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0006c0008t0015g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0007c0010t0003g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0008c0009t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0009c0017t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0010c0016t0030g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0011c0013t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0012c0015t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| a0013c0014t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0002 | g0166 | EUR | GBR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00099 | hp2 | a0003 | c0004 | t0002 | g0160 | EUR | GBR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00280 | hp1 | a0002 | c0003 | t0003 | g0004 | EUR | FIN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00280 | hp2 | a0003 | c0004 | t0002 | g0161 | EUR | FIN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00408 | hp1 | a0001 | c0002 | t0004 | g0013 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00423 | hp2 | a0001 | c0002 | t0004 | g0182 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00438 | hp2 | a0004 | c0005 | t0005 | g0025 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00544 | hp2 | a0004 | c0005 | t0005 | g0006 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00558 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00597 | hp1 | a0003 | c0004 | t0002 | g0144 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00597 | hp2 | a0009 | c0017 | t0005 | g0087 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00621 | hp1 | a0004 | c0005 | t0005 | g0084 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0060 | EAS | CHS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00642 | hp1 | a0002 | c0003 | t0003 | g0021 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0014 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00733 | hp1 | a0003 | c0004 | t0002 | g0030 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00733 | hp2 | a0005 | c0006 | t0006 | g0008 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0009 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00735 | hp2 | a0003 | c0004 | t0002 | g0158 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00738 | hp1 | a0003 | c0004 | t0002 | g0001 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0009 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00741 | hp1 | a0002 | c0003 | t0003 | g0004 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01069 | hp1 | a0005 | c0006 | t0006 | g0187 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01069 | hp2 | a0002 | c0003 | t0003 | g0002 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01070 | hp1 | a0003 | c0004 | t0002 | g0001 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01070 | hp2 | a0005 | c0006 | t0006 | g0008 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01071 | hp1 | a0005 | c0006 | t0006 | g0008 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01071 | hp2 | a0003 | c0004 | t0002 | g0001 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01074 | hp1 | a0002 | c0003 | t0003 | g0004 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01081 | hp1 | a0002 | c0003 | t0003 | g0022 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01099 | hp1 | a0002 | c0003 | t0003 | g0143 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01099 | hp2 | a0003 | c0004 | t0002 | g0048 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01167 | hp1 | a0003 | c0004 | t0002 | g0149 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01167 | hp2 | a0005 | c0006 | t0006 | g0008 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01169 | hp1 | a0005 | c0006 | t0006 | g0008 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0066 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01175 | hp2 | a0002 | c0003 | t0003 | g0004 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01192 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01192 | hp2 | a0003 | c0004 | t0002 | g0030 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0009 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01243 | hp2 | a0002 | c0003 | t0003 | g0125 | AMR | PUR | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01255 | hp1 | a0010 | c0016 | t0030 | g0162 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01255 | hp2 | a0002 | c0003 | t0003 | g0022 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01257 | hp1 | a0001 | c0002 | t0023 | g0186 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01257 | hp2 | a0002 | c0003 | t0003 | g0172 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01261 | hp1 | a0002 | c0003 | t0003 | g0021 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01261 | hp2 | a0003 | c0004 | t0002 | g0159 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01346 | hp2 | a0003 | c0004 | t0002 | g0001 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01358 | hp2 | a0002 | c0003 | t0003 | g0002 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01361 | hp1 | a0002 | c0003 | t0003 | g0002 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01496 | hp1 | a0002 | c0003 | t0003 | g0127 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01496 | hp2 | a0001 | c0002 | t0004 | g0014 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0014 | EUR | IBS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01517 | hp2 | a0002 | c0003 | t0003 | g0002 | EUR | IBS | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01891 | hp1 | a0001 | c0002 | t0007 | g0005 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01891 | hp2 | a0001 | c0002 | t0012 | g0031 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01928 | hp1 | a0002 | c0003 | t0003 | g0002 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01934 | hp2 | a0005 | c0006 | t0006 | g0008 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01943 | hp1 | a0002 | c0003 | t0003 | g0004 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01943 | hp2 | a0001 | c0001 | t0039 | g0100 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0014 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01975 | hp2 | a0002 | c0003 | t0003 | g0004 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01978 | hp2 | a0002 | c0003 | t0003 | g0004 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01981 | hp1 | a0005 | c0006 | t0006 | g0008 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01993 | hp1 | a0002 | c0003 | t0003 | g0004 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02004 | hp2 | a0002 | c0003 | t0003 | g0140 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02015 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02027 | hp1 | a0004 | c0005 | t0005 | g0085 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02040 | hp2 | a0001 | c0002 | t0004 | g0032 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02055 | hp2 | a0001 | c0002 | t0008 | g0074 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02071 | hp1 | a0001 | c0002 | t0004 | g0013 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02132 | hp1 | a0004 | c0005 | t0005 | g0088 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02135 | hp1 | a0001 | c0001 | t0017 | g0107 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02135 | hp2 | a0003 | c0004 | t0002 | g0151 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0115 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02145 | hp2 | a0001 | c0002 | t0007 | g0005 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02155 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | CDX | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02155 | hp2 | a0003 | c0004 | t0002 | g0147 | EAS | CDX | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0069 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02257 | hp2 | a0006 | c0007 | t0014 | g0041 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02258 | hp1 | a0005 | c0011 | t0015 | g0170 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02258 | hp2 | a0001 | c0002 | t0008 | g0072 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02273 | hp1 | a0002 | c0003 | t0003 | g0002 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0026 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02280 | hp2 | a0005 | c0006 | t0006 | g0008 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02293 | hp1 | a0002 | c0003 | t0003 | g0004 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02293 | hp2 | a0001 | c0001 | t0032 | g0099 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02300 | hp2 | a0002 | c0003 | t0003 | g0002 | AMR | PEL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02451 | hp1 | a0006 | c0007 | t0037 | g0123 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02451 | hp2 | a0001 | c0002 | t0009 | g0176 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02523 | hp1 | a0004 | c0005 | t0038 | g0080 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02523 | hp2 | a0001 | c0002 | t0024 | g0185 | EAS | KHV | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02572 | hp1 | a0001 | c0002 | t0009 | g0052 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02572 | hp2 | a0001 | c0002 | t0012 | g0174 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0010 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02615 | hp2 | a0002 | c0003 | t0003 | g0002 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02622 | hp1 | a0004 | c0005 | t0010 | g0016 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02622 | hp2 | a0006 | c0007 | t0014 | g0091 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02630 | hp1 | a0004 | c0005 | t0005 | g0024 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02630 | hp2 | a0004 | c0005 | t0005 | g0058 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02647 | hp1 | a0003 | c0004 | t0002 | g0148 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02647 | hp2 | a0006 | c0007 | t0014 | g0090 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02683 | hp1 | a0002 | c0003 | t0034 | g0137 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02683 | hp2 | a0003 | c0004 | t0002 | g0015 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02698 | hp1 | a0003 | c0004 | t0002 | g0146 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02698 | hp2 | a0007 | c0010 | t0003 | g0047 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02717 | hp1 | a0004 | c0005 | t0005 | g0023 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02717 | hp2 | a0006 | c0007 | t0014 | g0041 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0010 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02723 | hp2 | a0001 | c0001 | t0013 | g0026 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02735 | hp1 | a0003 | c0004 | t0002 | g0167 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02735 | hp2 | a0002 | c0003 | t0003 | g0002 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02738 | hp1 | a0001 | c0002 | t0004 | g0009 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02738 | hp2 | a0002 | c0003 | t0003 | g0142 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02809 | hp2 | a0001 | c0002 | t0007 | g0005 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02818 | hp1 | a0006 | c0007 | t0028 | g0079 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02818 | hp2 | a0004 | c0005 | t0005 | g0006 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02886 | hp1 | a0001 | c0002 | t0007 | g0180 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02886 | hp2 | a0001 | c0002 | t0009 | g0177 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02895 | hp1 | a0001 | c0002 | t0007 | g0005 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02896 | hp1 | a0001 | c0002 | t0007 | g0005 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02896 | hp2 | a0004 | c0005 | t0018 | g0040 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02897 | hp1 | a0004 | c0005 | t0018 | g0040 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02922 | hp1 | a0001 | c0002 | t0007 | g0005 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02965 | hp1 | a0001 | c0002 | t0008 | g0035 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02965 | hp2 | a0001 | c0002 | t0012 | g0031 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02970 | hp1 | a0001 | c0002 | t0009 | g0052 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02970 | hp2 | a0006 | c0008 | t0015 | g0054 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02976 | hp1 | a0004 | c0005 | t0005 | g0024 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03041 | hp1 | a0003 | c0004 | t0002 | g0049 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03041 | hp2 | a0001 | c0002 | t0008 | g0071 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03130 | hp1 | a0004 | c0005 | t0010 | g0059 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0005 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03139 | hp2 | a0005 | c0006 | t0006 | g0008 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03195 | hp1 | a0001 | c0002 | t0007 | g0178 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03209 | hp1 | a0001 | c0002 | t0007 | g0005 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03225 | hp1 | a0001 | c0002 | t0007 | g0005 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03225 | hp2 | a0001 | c0002 | t0027 | g0181 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03453 | hp1 | a0006 | c0008 | t0015 | g0054 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0026 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03486 | hp1 | a0001 | c0001 | t0033 | g0122 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03486 | hp2 | a0001 | c0002 | t0007 | g0005 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03490 | hp1 | a0002 | c0003 | t0003 | g0021 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03490 | hp2 | a0007 | c0010 | t0003 | g0047 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03491 | hp1 | a0002 | c0003 | t0003 | g0129 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0009 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03492 | hp1 | a0002 | c0003 | t0003 | g0132 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03492 | hp2 | a0002 | c0003 | t0003 | g0021 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03516 | hp1 | a0004 | c0005 | t0005 | g0024 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03516 | hp2 | a0001 | c0002 | t0007 | g0005 | AFR | ESN | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03540 | hp1 | a0004 | c0005 | t0010 | g0016 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0005 | AFR | GWD | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03669 | hp1 | a0002 | c0003 | t0003 | g0002 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03669 | hp2 | a0001 | c0002 | t0004 | g0075 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03688 | hp1 | a0003 | c0004 | t0002 | g0164 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03688 | hp2 | a0002 | c0003 | t0003 | g0004 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03710 | hp1 | a0001 | c0002 | t0021 | g0184 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03710 | hp2 | a0002 | c0003 | t0003 | g0139 | SAS | PJL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03831 | hp1 | a0004 | c0005 | t0005 | g0086 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03831 | hp2 | a0002 | c0003 | t0003 | g0004 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03834 | hp1 | a0002 | c0003 | t0003 | g0126 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03834 | hp2 | a0004 | c0005 | t0005 | g0025 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03927 | hp1 | a0003 | c0004 | t0002 | g0048 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03927 | hp2 | a0002 | c0003 | t0011 | g0133 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03942 | hp1 | a0002 | c0003 | t0003 | g0141 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03942 | hp2 | a0001 | c0002 | t0020 | g0068 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04115 | hp1 | a0005 | c0006 | t0006 | g0008 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04115 | hp2 | a0003 | c0004 | t0002 | g0165 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04184 | hp1 | a0001 | c0002 | t0004 | g0067 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04199 | hp1 | a0002 | c0003 | t0003 | g0002 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04199 | hp2 | a0003 | c0004 | t0002 | g0015 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04204 | hp1 | a0002 | c0003 | t0036 | g0134 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0002 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG04228 | hp2 | a0003 | c0004 | t0002 | g0001 | SAS | STU | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18522 | hp1 | a0004 | c0005 | t0005 | g0082 | AFR | YRI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18522 | hp2 | a0004 | c0005 | t0005 | g0023 | AFR | YRI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18612 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | CHB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18612 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | CHB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18747 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | CHB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18906 | hp1 | a0004 | c0005 | t0010 | g0057 | AFR | YRI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18906 | hp2 | a0004 | c0005 | t0040 | g0193 | AFR | YRI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18940 | hp1 | a0011 | c0013 | t0001 | g0110 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18940 | hp2 | a0001 | c0002 | t0004 | g0073 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18941 | hp2 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18943 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18943 | hp2 | a0004 | c0005 | t0005 | g0025 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18944 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18946 | hp1 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18947 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18950 | hp1 | a0004 | c0005 | t0005 | g0039 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18952 | hp1 | a0008 | c0009 | t0001 | g0043 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18952 | hp2 | a0002 | c0003 | t0011 | g0020 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18953 | hp1 | a0002 | c0003 | t0003 | g0136 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18956 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18957 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18957 | hp2 | a0001 | c0002 | t0004 | g0065 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18959 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18961 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18961 | hp2 | a0004 | c0005 | t0005 | g0038 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18963 | hp1 | a0003 | c0004 | t0002 | g0155 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18963 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18964 | hp1 | a0012 | c0015 | t0002 | g0157 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18964 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18965 | hp1 | a0004 | c0005 | t0005 | g0006 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18965 | hp2 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18966 | hp1 | a0001 | c0002 | t0004 | g0061 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18966 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18969 | hp2 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18970 | hp1 | a0002 | c0003 | t0003 | g0169 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18970 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18971 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18971 | hp2 | a0001 | c0001 | t0031 | g0106 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18972 | hp2 | a0005 | c0006 | t0006 | g0190 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18973 | hp1 | a0005 | c0006 | t0006 | g0189 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18973 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18975 | hp1 | a0001 | c0002 | t0019 | g0064 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18977 | hp1 | a0004 | c0005 | t0005 | g0006 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18977 | hp2 | a0002 | c0003 | t0003 | g0124 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18978 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18979 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18980 | hp1 | a0004 | c0005 | t0005 | g0081 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18981 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18981 | hp2 | a0003 | c0004 | t0002 | g0051 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18982 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18983 | hp1 | a0001 | c0012 | t0001 | g0120 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18984 | hp2 | a0004 | c0005 | t0016 | g0037 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18985 | hp2 | a0004 | c0005 | t0005 | g0006 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18986 | hp2 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18987 | hp1 | a0002 | c0003 | t0003 | g0131 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18987 | hp2 | a0004 | c0005 | t0005 | g0006 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18988 | hp2 | a0004 | c0005 | t0016 | g0037 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18990 | hp1 | a0004 | c0005 | t0005 | g0006 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18991 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18992 | hp1 | a0003 | c0004 | t0002 | g0050 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18992 | hp2 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18994 | hp1 | a0002 | c0003 | t0011 | g0020 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18998 | hp1 | a0004 | c0005 | t0005 | g0006 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18998 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18999 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19001 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19001 | hp2 | a0002 | c0003 | t0003 | g0130 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19002 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19002 | hp2 | a0013 | c0014 | t0001 | g0114 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19003 | hp1 | a0003 | c0004 | t0002 | g0150 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19004 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19005 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19006 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19007 | hp1 | a0003 | c0004 | t0002 | g0154 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19012 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19030 | hp1 | a0006 | c0008 | t0015 | g0191 | AFR | LWK | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19030 | hp2 | a0001 | c0002 | t0008 | g0035 | AFR | LWK | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19054 | hp1 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19054 | hp2 | a0003 | c0004 | t0002 | g0050 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19055 | hp1 | a0001 | c0002 | t0022 | g0062 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19055 | hp2 | a0002 | c0003 | t0003 | g0046 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19056 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19056 | hp2 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19057 | hp2 | a0003 | c0004 | t0002 | g0051 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19058 | hp1 | a0003 | c0004 | t0026 | g0156 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19058 | hp2 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19060 | hp1 | a0004 | c0005 | t0005 | g0036 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19060 | hp2 | a0008 | c0009 | t0001 | g0043 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19063 | hp2 | a0004 | c0005 | t0005 | g0036 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19064 | hp1 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19064 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19065 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19067 | hp2 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19068 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0183 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19070 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19070 | hp2 | a0003 | c0004 | t0002 | g0168 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19072 | hp1 | a0004 | c0005 | t0005 | g0039 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19072 | hp2 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19074 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19075 | hp2 | a0002 | c0003 | t0003 | g0046 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19076 | hp1 | a0004 | c0005 | t0005 | g0006 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19076 | hp2 | a0003 | c0004 | t0002 | g0152 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19078 | hp1 | a0003 | c0004 | t0002 | g0145 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19079 | hp1 | a0001 | c0001 | t0017 | g0092 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19079 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19080 | hp2 | a0004 | c0005 | t0005 | g0006 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19083 | hp2 | a0003 | c0004 | t0002 | g0153 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19084 | hp1 | a0005 | c0006 | t0006 | g0188 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19084 | hp2 | a0002 | c0003 | t0011 | g0020 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19085 | hp1 | a0002 | c0003 | t0011 | g0020 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19085 | hp2 | a0003 | c0004 | t0002 | g0163 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19086 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19087 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19088 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19089 | hp1 | a0004 | c0005 | t0016 | g0083 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19090 | hp1 | a0004 | c0005 | t0005 | g0038 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19090 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19240 | hp1 | a0006 | c0007 | t0029 | g0089 | AFR | YRI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | YRI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA20129 | hp1 | a0001 | c0002 | t0004 | g0010 | AFR | ASW | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA20129 | hp2 | a0003 | c0004 | t0002 | g0049 | AFR | ASW | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA20752 | hp1 | a0002 | c0003 | t0035 | g0135 | EUR | TSI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA20752 | hp2 | a0002 | c0003 | t0003 | g0022 | EUR | TSI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA20805 | hp1 | a0005 | c0006 | t0006 | g0053 | EUR | TSI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA20805 | hp2 | a0002 | c0003 | t0003 | g0002 | EUR | TSI | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01123 | hp1 | a0002 | c0003 | t0003 | g0022 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG01123 | hp2 | a0005 | c0006 | t0006 | g0053 | AMR | CLM | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02109 | hp1 | a0001 | c0002 | t0009 | g0175 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02109 | hp2 | a0004 | c0005 | t0010 | g0016 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02486 | hp1 | a0004 | c0005 | t0010 | g0016 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02486 | hp2 | a0005 | c0006 | t0006 | g0008 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02559 | hp1 | a0001 | c0002 | t0008 | g0070 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG02559 | hp2 | a0003 | c0004 | t0002 | g0030 | AFR | ACB | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03471 | hp1 | a0001 | c0002 | t0012 | g0031 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG03471 | hp2 | a0006 | c0007 | t0025 | g0078 | AFR | MSL | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG06807 | hp1 | a0004 | c0005 | t0005 | g0023 | AFR | USA | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| HG06807 | hp2 | a0001 | c0002 | t0009 | g0173 | AFR | USA | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18955 | hp1 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA18955 | hp2 | a0004 | c0005 | t0005 | g0006 | EAS | JPT | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA20300 | hp1 | a0002 | c0003 | t0003 | g0004 | AFR | USA | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0010 | AFR | USA | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA21309 | hp1 | a0001 | c0002 | t0007 | g0179 | AFR | LWK | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0003 | g0128 | REF | REF | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0003 | g0138 | REF | REF | MAP9_chr4_155337658_155381965 | MAP9 | chr4 | 155337658 | 155381965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:155347797 | C | T | 1 | a0009 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1930G>A | p.Ala644Thr | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2189/7328 | 1930/1944 | 644/647 | chr4 | 155347797 | |||
| chr4:155347875 | G | A | 1 | a0008 | 2 | NA18952.hp1 NA19060.hp2 |
stop_gained | HIGH | c.1852C>T | p.Arg618* | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2111/7328 | 1852/1944 | 618/647 | chr4 | 155347875 | |||
| chr4:155352616 | T | C | 9 | a0001 a0003 a0005 others(6): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
missense_variant | MODERATE | c.1801A>G | p.Asn601Asp | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/14 | 2060/7328 | 1801/1944 | 601/647 | chr4 | 155352616 | |||
| chr4:155352922 | C | G | 1 | a0007 | 2 | HG02698.hp2 HG03490.hp2 |
missense_variant | MODERATE | c.1678G>C | p.Val560Leu | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 12/14 | 1937/7328 | 1678/1944 | 560/647 | chr4 | 155352922 | |||
| chr4:155353225 | T | C | 4 | a0001 a0008 a0011 others(1): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
missense_variant | MODERATE | c.1496A>G | p.Lys499Arg | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 11/14 | 1755/7328 | 1496/1944 | 499/647 | chr4 | 155353225 | |||
| chr4:155355771 | T | A | 1 | a0012 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.1235A>T | p.Gln412Leu | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/14 | 1494/7328 | 1235/1944 | 412/647 | chr4 | 155355771 | |||
| chr4:155360262 | G | A | 1 | a0011 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.956C>T | p.Ala319Val | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/14 | 1215/7328 | 956/1944 | 319/647 | chr4 | 155360262 | |||
| chr4:155360388 | T | C | 2 | a0010 a0011 |
2 | HG01255.hp1 NA18940.hp1 |
missense_variant | MODERATE | c.830A>G | p.His277Arg | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/14 | 1089/7328 | 830/1944 | 277/647 | chr4 | 155360388 | |||
| chr4:155368632 | T | C | 1 | a0013 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.662A>G | p.Gln221Arg | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/14 | 921/7328 | 662/1944 | 221/647 | chr4 | 155368632 | |||
| chr4:155368651 | G | T | 1 | a0006 | 11 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
missense_variant | MODERATE | c.643C>A | p.Pro215Thr | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/14 | 902/7328 | 643/1944 | 215/647 | chr4 | 155368651 | |||
| chr4:155368765 | G | A | 3 | a0003 a0010 a0012 |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
missense_variant | MODERATE | c.529C>T | p.Arg177Trp | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/14 | 788/7328 | 529/1944 | 177/647 | chr4 | 155368765 | |||
| chr4:155373181 | T | C | 2 | a0004 a0009 |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
missense_variant | MODERATE | c.436A>G | p.Met146Val | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/14 | 695/7328 | 436/1944 | 146/647 | chr4 | 155373181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:155352674 | C | T | 1 | a0001c0012 | 1 | NA18983.hp1 | synonymous_variant | LOW | c.1743G>A | p.Glu581Glu | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/14 | 2002/7328 | 1743/1944 | 581/647 | chr4 | 155352674 | |||
| chr4:155355137 | C | T | 15 | a0001c0001 a0001c0002 a0001c0012 others(12): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
synonymous_variant | LOW | c.1314G>A | p.Val438Val | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/14 | 1573/7328 | 1314/1944 | 438/647 | chr4 | 155355137 | |||
| chr4:155355865 | A | G | 1 | a0005c0011 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1141T>C | p.Leu381Leu | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/14 | 1400/7328 | 1141/1944 | 381/647 | chr4 | 155355865 | |||
| chr4:155360219 | T | C | 5 | a0001c0001 a0001c0012 a0008c0009 others(2): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
synonymous_variant | LOW | c.999A>G | p.Leu333Leu | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/14 | 1258/7328 | 999/1944 | 333/647 | chr4 | 155360219 | |||
| chr4:155362112 | T | A | 1 | a0006c0008 | 3 | HG02970.hp2 HG03453.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.738A>T | p.Ser246Ser | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/14 | 997/7328 | 738/1944 | 246/647 | chr4 | 155362112 | |||
| chr4:155368748 | C | T | 10 | a0001c0001 a0001c0012 a0003c0004 others(7): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
synonymous_variant | LOW | c.546G>A | p.Leu182Leu | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/14 | 805/7328 | 546/1944 | 182/647 | chr4 | 155368748 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:155342695 | C | T | 1 | a0006c0007t0025 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5088G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 5088 | chr4 | 155342695 | ||||||
| chr4:155342719 | G | A | 43 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(40): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*5064C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 5064 | chr4 | 155342719 | ||||||
| chr4:155342896 | T | G | 1 | a0001c0002t0020 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4887A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4887 | chr4 | 155342896 | ||||||
| chr4:155342899 | T | C | 1 | a0001c0001t0032 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4884A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4884 | chr4 | 155342899 | ||||||
| chr4:155342911 | G | A | 2 | a0001c0002t0021 a0004c0005t0016 |
4 | HG03710.hp1 NA18984.hp2 NA18988.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4872C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4872 | chr4 | 155342911 | ||||||
| chr4:155342942 | C | T | 4 | a0006c0007t0014 a0006c0007t0028 a0006c0007t0029 others(1): Show |
7 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4841G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4841 | chr4 | 155342942 | ||||||
| chr4:155342981 | T | C | 9 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0019 others(6): Show |
67 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*4802A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4802 | chr4 | 155342981 | ||||||
| chr4:155343204 | ACAT | A | 43 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(40): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*4576_*4578delATG | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4576 | chr4 | 155343204 | ||||||
| chr4:155343235 | T | TA | 1 | a0002c0003t0011 | 5 | HG03927.hp2 NA18952.hp2 NA18994.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4547dupT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4547 | chr4 | 155343235 | ||||||
| chr4:155343272 | GGAGA | G | 12 | a0003c0004t0002 a0003c0004t0026 a0005c0006t0006 others(9): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*4507_*4510delTCTC | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4507 | chr4 | 155343272 | ||||||
| chr4:155343292 | G | C | 1 | a0001c0001t0017 | 2 | HG02135.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4491C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4491 | chr4 | 155343292 | ||||||
| chr4:155343328 | G | A | 1 | a0001c0001t0033 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4455C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4455 | chr4 | 155343328 | ||||||
| chr4:155343469 | A | G | 1 | a0001c0001t0031 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4314T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4314 | chr4 | 155343469 | ||||||
| chr4:155343476 | T | C | 7 | a0004c0005t0005 a0004c0005t0010 a0004c0005t0016 others(4): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4307A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4307 | chr4 | 155343476 | ||||||
| chr4:155343703 | AAT | A | 43 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(40): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*4078_*4079delAT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 4078 | chr4 | 155343703 | ||||||
| chr4:155343790 | G | A | 43 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(40): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*3993C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3993 | chr4 | 155343790 | ||||||
| chr4:155343924 | G | T | 1 | a0010c0016t0030 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3859C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3859 | chr4 | 155343924 | ||||||
| chr4:155344087 | C | T | 4 | a0003c0004t0002 a0003c0004t0026 a0010c0016t0030 others(1): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*3696G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3696 | chr4 | 155344087 | ||||||
| chr4:155344184 | T | G | 1 | a0001c0002t0007 | 15 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3599A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3599 | chr4 | 155344184 | ||||||
| chr4:155344257 | G | A | 10 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0009 others(7): Show |
73 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*3526C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3526 | chr4 | 155344257 | ||||||
| chr4:155344280 | A | G | 1 | a0001c0002t0019 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3503T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3503 | chr4 | 155344280 | ||||||
| chr4:155344376 | T | A | 1 | a0006c0007t0029 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3407A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3407 | chr4 | 155344376 | ||||||
| chr4:155344482 | T | TAA | 2 | a0004c0005t0010 a0004c0005t0040 |
7 | HG02109.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3299_*3300dupTT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3300 | chr4 | 155344482 | ||||||
| chr4:155344585 | A | G | 37 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(34): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*3198T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3198 | chr4 | 155344585 | ||||||
| chr4:155344587 | A | G | 12 | a0003c0004t0002 a0003c0004t0026 a0005c0006t0006 others(9): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3196T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 3196 | chr4 | 155344587 | ||||||
| chr4:155344951 | C | T | 1 | a0005c0006t0006 | 17 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2832G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2832 | chr4 | 155344951 | ||||||
| chr4:155345086 | G | A | 1 | a0002c0003t0036 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2697C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2697 | chr4 | 155345086 | ||||||
| chr4:155345344 | C | T | 1 | a0002c0003t0035 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2439G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2439 | chr4 | 155345344 | ||||||
| chr4:155345459 | G | GT | 6 | a0004c0005t0005 a0004c0005t0010 a0004c0005t0016 others(3): Show |
46 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2323dupA | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2323 | chr4 | 155345459 | ||||||
| chr4:155345464 | G | T | 7 | a0004c0005t0005 a0004c0005t0010 a0004c0005t0016 others(4): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2319C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2319 | chr4 | 155345464 | ||||||
| chr4:155345464 | GT | G | 35 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(32): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
3_prime_UTR_variant | MODIFIER | c.*2318delA | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2318 | chr4 | 155345464 | ||||||
| chr4:155345465 | T | G | 1 | a0001c0002t0022 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2318A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2318 | chr4 | 155345465 | ||||||
| chr4:155345633 | A | C | 3 | a0006c0007t0014 a0006c0007t0029 a0006c0007t0037 |
6 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2150T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2150 | chr4 | 155345633 | ||||||
| chr4:155345709 | T | C | 36 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(33): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*2074A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 2074 | chr4 | 155345709 | ||||||
| chr4:155345981 | A | T | 7 | a0004c0005t0005 a0004c0005t0010 a0004c0005t0016 others(4): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1802T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 1802 | chr4 | 155345981 | ||||||
| chr4:155346002 | C | A | 1 | a0001c0002t0023 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1781G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 1781 | chr4 | 155346002 | ||||||
| chr4:155346157 | T | C | 43 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(40): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*1626A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 1626 | chr4 | 155346157 | ||||||
| chr4:155346329 | C | T | 1 | a0006c0007t0028 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 1454 | chr4 | 155346329 | ||||||
| chr4:155346362 | T | A | 1 | a0001c0002t0008 | 6 | HG02055.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1421A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 1421 | chr4 | 155346362 | ||||||
| chr4:155346560 | G | A | 36 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(33): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*1223C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 1223 | chr4 | 155346560 | ||||||
| chr4:155346579 | C | T | 1 | a0002c0003t0034 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1204G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 1204 | chr4 | 155346579 | ||||||
| chr4:155346701 | A | T | 36 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(33): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*1082T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 1082 | chr4 | 155346701 | ||||||
| chr4:155346913 | C | T | 9 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0019 others(6): Show |
67 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*870G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 870 | chr4 | 155346913 | ||||||
| chr4:155346940 | G | T | 1 | a0001c0001t0013 | 4 | HG02145.hp1 HG02280.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*843C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 843 | chr4 | 155346940 | ||||||
| chr4:155347031 | C | A | 1 | a0006c0007t0037 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*752G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 752 | chr4 | 155347031 | ||||||
| chr4:155347148 | G | C | 1 | a0001c0002t0024 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*635C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 635 | chr4 | 155347148 | ||||||
| chr4:155347343 | G | A | 7 | a0004c0005t0005 a0004c0005t0010 a0004c0005t0016 others(4): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*440C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 440 | chr4 | 155347343 | ||||||
| chr4:155347352 | C | G | 1 | a0003c0004t0026 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431G>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 431 | chr4 | 155347352 | ||||||
| chr4:155347460 | A | C | 1 | a0001c0002t0012 | 4 | HG01891.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*323T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 323 | chr4 | 155347460 | ||||||
| chr4:155347604 | T | C | 1 | a0001c0001t0039 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 179 | chr4 | 155347604 | ||||||
| chr4:155347701 | C | T | 1 | a0006c0007t0025 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 14/14 | 82 | chr4 | 155347701 | ||||||
| chr4:155375908 | A | G | 8 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0019 others(5): Show |
66 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
5_prime_UTR_variant | MODIFIER | c.-58T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 2/14 | 58 | chr4 | 155375908 | ||||||
| chr4:155376798 | G | C | 1 | a0004c0005t0040 | 1 | NA18906.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-92C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 1/14 | chr4 | 155376798 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:155347911 | G | A | 3 | a0001c0002t0004g0013 a0001c0002t0004g0183 a0001c0002t0024g0185 |
9 | HG00408.hp1 HG02015.hp2 HG02071.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1822-6C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155347911 | |||||||
| chr4:155348056 | C | T | 32 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(29): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1822-151G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348056 | |||||||
| chr4:155348241 | A | G | 2 | a0005c0006t0006g0188 a0005c0006t0006g0189 |
2 | NA18973.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1822-336T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348241 | |||||||
| chr4:155348242 | T | TG | 42 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(39): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1822-338dupC | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348242 | |||||||
| chr4:155348244 | G | GC | 6 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(3): Show |
17 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1822-340_1822-339i others(3): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348244 | |||||||
| chr4:155348285 | C | T | 2 | a0001c0002t0012g0031 a0001c0002t0012g0174 |
4 | HG01891.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1822-380G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348285 | |||||||
| chr4:155348286 | G | A | 1 | a0006c0007t0028g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1822-381C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348286 | |||||||
| chr4:155348377 | T | C | 1 | a0003c0004t0002g0160 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1822-472A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348377 | |||||||
| chr4:155348660 | C | T | 1 | a0003c0004t0002g0155 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1822-755G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348660 | |||||||
| chr4:155348701 | C | A | 48 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(45): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1822-796G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348701 | |||||||
| chr4:155348722 | T | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(90): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1822-817A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348722 | |||||||
| chr4:155348757 | G | A | 1 | a0006c0007t0028g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1822-852C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348757 | |||||||
| chr4:155348759 | A | G | 1 | a0003c0004t0002g0163 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1822-854T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348759 | |||||||
| chr4:155348989 | A | AAAC | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1822-1085_1822-108 others(7): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155348989 | |||||||
| chr4:155349027 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1822-1122A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349027 | |||||||
| chr4:155349110 | C | T | 1 | a0004c0005t0018g0040 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1822-1205G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349110 | |||||||
| chr4:155349147 | C | T | 1 | a0001c0002t0009g0173 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1822-1242G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349147 | |||||||
| chr4:155349247 | C | CATTGTGA others(895): Show |
1 | a0004c0005t0016g0083 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1822-1343_1822-134 others(906): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349247 | |||||||
| chr4:155349247 | C | CATTGTGA others(894): Show |
21 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(18): Show |
45 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1822-1343_1822-134 others(905): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349247 | |||||||
| chr4:155349247 | C | CATTGTGA others(894): Show |
2 | a0002c0003t0011g0020 a0002c0003t0011g0133 |
5 | HG03927.hp2 NA18952.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1822-1343_1822-134 others(905): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349247 | |||||||
| chr4:155349247 | C | CATTGTGA others(894): Show |
25 | a0002c0003t0003g0002 a0002c0003t0003g0004 a0002c0003t0003g0021 others(22): Show |
67 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1822-1343_1822-134 others(905): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349247 | |||||||
| chr4:155349247 | C | CATTGTGA others(894): Show |
1 | a0004c0005t0005g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1822-1343_1822-134 others(905): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349247 | |||||||
| chr4:155349248 | A | ATTGTGAC others(893): Show |
1 | a0001c0001t0001g0076 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1822-1344_1822-134 others(904): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349248 | |||||||
| chr4:155349248 | A | ATTGTGAC others(894): Show |
2 | a0001c0002t0009g0052 a0001c0002t0009g0173 |
3 | HG02572.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1822-1344_1822-134 others(905): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349248 | |||||||
| chr4:155349248 | A | ATTGTGAC others(895): Show |
1 | a0011c0013t0001g0110 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1822-1344_1822-134 others(906): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349248 | |||||||
| chr4:155349248 | A | ATTGTGAC others(894): Show |
38 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(35): Show |
88 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1822-1344_1822-134 others(905): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349248 | |||||||
| chr4:155349248 | A | ATTGTGAC others(894): Show |
93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0017 others(90): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1822-1344_1822-134 others(905): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349248 | |||||||
| chr4:155349248 | A | ATTGTGAC others(918): Show |
1 | a0001c0002t0004g0065 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1822-1344_1822-134 others(929): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349248 | |||||||
| chr4:155349248 | A | ATTGTGAC others(894): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0095 |
2 | NA18959.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1822-1344_1822-134 others(905): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349248 | |||||||
| chr4:155349248 | A | ATTGTGAC others(894): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0171 |
8 | NA18960.hp2 NA18962.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.1822-1344_1822-134 others(905): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349248 | |||||||
| chr4:155349287 | T | C | 1 | a0001c0002t0022g0062 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1822-1382A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349287 | |||||||
| chr4:155349288 | G | GGAAGAGG others(891): Show |
1 | a0001c0002t0022g0062 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1822-1384_1822-138 others(902): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349288 | |||||||
| chr4:155349312 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1822-1407A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349312 | |||||||
| chr4:155349381 | G | A | 1 | a0005c0011t0015g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1822-1476C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349381 | |||||||
| chr4:155349383 | G | A | 22 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(19): Show |
45 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1822-1478C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349383 | |||||||
| chr4:155349559 | G | A | 48 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(45): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1822-1654C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349559 | |||||||
| chr4:155349603 | A | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1822-1698T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349603 | |||||||
| chr4:155349656 | G | A | 16 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(13): Show |
29 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1822-1751C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349656 | |||||||
| chr4:155349668 | C | T | 6 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(3): Show |
17 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1822-1763G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349668 | |||||||
| chr4:155349669 | T | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1822-1764A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349669 | |||||||
| chr4:155349681 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1822-1776A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349681 | |||||||
| chr4:155349837 | A | T | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1822-1932T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349837 | |||||||
| chr4:155349922 | A | C | 1 | a0003c0004t0002g0158 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1822-2017T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349922 | |||||||
| chr4:155349929 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1822-2024C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155349929 | |||||||
| chr4:155350000 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(161): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1822-2095A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155350000 | |||||||
| chr4:155350062 | A | T | 1 | a0005c0011t0015g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1822-2157T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155350062 | |||||||
| chr4:155350117 | A | G | 30 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0011 others(27): Show |
67 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1822-2212T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155350117 | |||||||
| chr4:155350228 | TTTCTA | T | 4 | a0001c0002t0007g0005 a0001c0002t0007g0178 a0001c0002t0007g0179 others(1): Show |
15 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.1822-2328_1822-232 others(9): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155350228 | |||||||
| chr4:155350404 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1821+2192T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155350404 | |||||||
| chr4:155350458 | C | T | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1821+2138G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155350458 | |||||||
| chr4:155350583 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0104 a0011c0013t0001g0110 |
4 | NA18940.hp1 NA18988.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821+2013G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155350583 | |||||||
| chr4:155351029 | T | C | 6 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(3): Show |
17 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1821+1567A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351029 | |||||||
| chr4:155351141 | G | C | 1 | a0002c0003t0003g0130 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1821+1455C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351141 | |||||||
| chr4:155351240 | A | G | 1 | a0001c0002t0007g0179 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1821+1356T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351240 | |||||||
| chr4:155351258 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1821+1338G>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351258 | |||||||
| chr4:155351393 | T | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1821+1203A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351393 | |||||||
| chr4:155351406 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1821+1190A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351406 | |||||||
| chr4:155351452 | C | CA | 28 | a0001c0001t0001g0113 a0002c0003t0035g0135 a0004c0005t0005g0006 others(25): Show |
63 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1821+1143dupT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351452 | |||||||
| chr4:155351467 | G | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(161): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1821+1129C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351467 | |||||||
| chr4:155351504 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1821+1092C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351504 | |||||||
| chr4:155351562 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1821+1034G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351562 | |||||||
| chr4:155351617 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1821+979G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351617 | |||||||
| chr4:155351766 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1821+830G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351766 | |||||||
| chr4:155351919 | A | G | 1 | a0004c0005t0005g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1821+677T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155351919 | |||||||
| chr4:155352250 | C | T | 2 | a0003c0004t0002g0050 a0003c0004t0002g0153 |
3 | NA18992.hp1 NA19054.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1821+346G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155352250 | |||||||
| chr4:155352284 | T | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1821+312A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155352284 | |||||||
| chr4:155352431 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1821+165C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155352431 | |||||||
| chr4:155352590 | A | C | 1 | a0001c0002t0007g0179 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.1821+6T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 13/13 | chr4 | 155352590 | |||||||
| chr4:155353081 | C | T | 1 | a0001c0002t0008g0072 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1543-24G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 11/13 | chr4 | 155353081 | |||||||
| chr4:155353432 | T | G | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1381-92A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155353432 | |||||||
| chr4:155353435 | T | C | 1 | a0005c0011t0015g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1381-95A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155353435 | |||||||
| chr4:155353454 | CATT | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1381-117_1381-115d others(5): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155353454 | |||||||
| chr4:155353554 | G | A | 6 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(3): Show |
17 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1381-214C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155353554 | |||||||
| chr4:155353668 | T | C | 1 | a0006c0007t0025g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1381-328A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155353668 | |||||||
| chr4:155353996 | G | C | 2 | a0004c0005t0005g0038 a0004c0005t0005g0088 |
3 | HG02132.hp1 NA18961.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1381-656C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155353996 | |||||||
| chr4:155354017 | A | G | 2 | a0006c0007t0014g0090 a0006c0007t0014g0091 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1381-677T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354017 | |||||||
| chr4:155354098 | C | T | 1 | a0003c0004t0002g0154 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1381-758G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354098 | |||||||
| chr4:155354099 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(90): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1381-759C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354099 | |||||||
| chr4:155354174 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1381-834G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354174 | |||||||
| chr4:155354182 | AT | A | 2 | a0004c0005t0005g0023 a0004c0005t0010g0057 |
4 | HG02717.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-843delA | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354182 | |||||||
| chr4:155354183 | T | A | 21 | a0004c0005t0005g0006 a0004c0005t0005g0024 a0004c0005t0005g0025 others(18): Show |
43 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1381-843A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354183 | |||||||
| chr4:155354251 | T | C | 1 | a0006c0007t0037g0123 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1380+820A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354251 | |||||||
| chr4:155354278 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1380+793A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354278 | |||||||
| chr4:155354470 | C | CT | 22 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(19): Show |
46 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1380+600dupA | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354470 | |||||||
| chr4:155354470 | C | CTTTT | 5 | a0003c0004t0002g0149 a0003c0004t0026g0156 a0006c0007t0014g0041 others(2): Show |
6 | HG01167.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1380+597_1380+600d others(6): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354470 | |||||||
| chr4:155354470 | C | CTTTTT | 34 | a0001c0002t0009g0175 a0001c0002t0009g0177 a0003c0004t0002g0001 others(31): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1380+596_1380+600d others(7): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354470 | |||||||
| chr4:155354470 | C | CTTTTTT | 85 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(82): Show |
198 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.1380+595_1380+600d others(8): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354470 | |||||||
| chr4:155354470 | C | CTTTTTTT | 17 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0093 others(14): Show |
22 | HG00408.hp2 HG00423.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1380+594_1380+600d others(9): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354470 | |||||||
| chr4:155354704 | T | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(90): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1380+367A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354704 | |||||||
| chr4:155354745 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1380+326T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354745 | |||||||
| chr4:155354762 | G | A | 1 | a0001c0002t0007g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1380+309C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354762 | |||||||
| chr4:155354924 | A | G | 48 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(45): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1380+147T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354924 | |||||||
| chr4:155354944 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1380+127C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354944 | |||||||
| chr4:155354948 | A | G | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1380+123T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 10/13 | chr4 | 155354948 | |||||||
| chr4:155355165 | A | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(161): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
splice_region_variant&intron_variant | LOW | c.1291-5T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355165 | |||||||
| chr4:155355184 | T | C | 1 | a0003c0004t0002g0163 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1291-24A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355184 | |||||||
| chr4:155355266 | G | A | 1 | a0002c0003t0003g0136 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1291-106C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355266 | |||||||
| chr4:155355281 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1291-121G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355281 | |||||||
| chr4:155355395 | A | G | 1 | a0006c0007t0028g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1291-235T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355395 | |||||||
| chr4:155355430 | A | T | 1 | a0002c0003t0011g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1291-270T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355430 | |||||||
| chr4:155355496 | G | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1290+220C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355496 | |||||||
| chr4:155355590 | ACT | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1290+124_1290+125d others(4): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355590 | |||||||
| chr4:155355636 | G | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1290+80C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355636 | |||||||
| chr4:155355670 | T | C | 5 | a0006c0007t0014g0041 a0006c0007t0014g0090 a0006c0007t0014g0091 others(2): Show |
6 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1290+46A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355670 | |||||||
| chr4:155355689 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1290+27A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 9/13 | chr4 | 155355689 | |||||||
| chr4:155355960 | C | T | 2 | a0002c0003t0003g0127 a0004c0005t0005g0084 |
2 | HG00621.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1122-76G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155355960 | |||||||
| chr4:155355970 | T | C | 1 | a0001c0002t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1122-86A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155355970 | |||||||
| chr4:155356008 | C | T | 1 | a0002c0003t0003g0125 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1122-124G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155356008 | |||||||
| chr4:155356179 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1122-295T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155356179 | |||||||
| chr4:155356228 | C | T | 1 | a0001c0001t0001g0029 | 3 | NA19010.hp1 NA19063.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1122-344G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155356228 | |||||||
| chr4:155356479 | A | C | 5 | a0001c0002t0001g0192 a0001c0002t0007g0005 a0001c0002t0007g0178 others(2): Show |
16 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.1122-595T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155356479 | |||||||
| chr4:155356614 | C | A | 3 | a0001c0002t0004g0034 a0001c0002t0004g0061 a0001c0002t0022g0062 |
4 | NA18954.hp1 NA18966.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1122-730G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155356614 | |||||||
| chr4:155356684 | A | G | 2 | a0004c0005t0005g0023 a0004c0005t0010g0057 |
4 | HG02717.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+765T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155356684 | |||||||
| chr4:155356795 | C | T | 48 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(45): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1121+654G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155356795 | |||||||
| chr4:155356861 | C | T | 1 | a0003c0004t0002g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1121+588G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155356861 | |||||||
| chr4:155357117 | A | C | 6 | a0004c0005t0005g0023 a0004c0005t0005g0058 a0004c0005t0010g0016 others(3): Show |
11 | HG02109.hp2 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1121+332T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155357117 | |||||||
| chr4:155357132 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0033g0122 |
5 | HG01081.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+317G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155357132 | |||||||
| chr4:155357185 | C | T | 1 | a0001c0002t0004g0067 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1121+264G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155357185 | |||||||
| chr4:155357211 | T | C | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1121+238A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 8/13 | chr4 | 155357211 | |||||||
| chr4:155357695 | C | T | 1 | a0003c0004t0002g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1051-176G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155357695 | |||||||
| chr4:155357804 | T | C | 1 | a0001c0002t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1051-285A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155357804 | |||||||
| chr4:155357907 | T | G | 1 | a0005c0011t0015g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1051-388A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155357907 | |||||||
| chr4:155358258 | C | T | 9 | a0006c0007t0014g0041 a0006c0007t0014g0090 a0006c0007t0014g0091 others(6): Show |
11 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1051-739G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155358258 | |||||||
| chr4:155358518 | C | T | 1 | a0001c0002t0004g0183 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1051-999G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155358518 | |||||||
| chr4:155358617 | T | G | 1 | a0001c0002t0008g0072 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1051-1098A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155358617 | |||||||
| chr4:155358720 | A | G | 1 | a0005c0011t0015g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1051-1201T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155358720 | |||||||
| chr4:155358886 | A | G | 32 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(29): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1050+1282T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155358886 | |||||||
| chr4:155358968 | T | C | 48 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(45): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1050+1200A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155358968 | |||||||
| chr4:155359174 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1050+994C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359174 | |||||||
| chr4:155359210 | T | TAC | 15 | a0001c0001t0001g0027 a0001c0001t0001g0097 a0001c0001t0001g0103 others(12): Show |
30 | HG00408.hp2 HG00733.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1050+956_1050+957d others(4): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359210 | T | TACAC | 79 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(76): Show |
187 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1050+954_1050+957d others(6): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359210 | T | TACACAC | 20 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0055 others(17): Show |
28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.1050+952_1050+957d others(8): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359210 | T | TACACACA others(1): Show |
8 | a0001c0001t0001g0109 a0003c0004t0002g0030 a0003c0004t0002g0161 others(5): Show |
10 | HG00280.hp2 HG00733.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1050+950_1050+957d others(10): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359210 | T | TACACACA others(3): Show |
5 | a0001c0002t0001g0192 a0001c0002t0004g0069 a0001c0002t0009g0177 others(2): Show |
6 | HG02257.hp1 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050+948_1050+957d others(12): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359210 | T | TACACACA others(7): Show |
1 | a0006c0007t0028g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1050+944_1050+957d others(16): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359210 | TAC | T | 31 | a0002c0003t0003g0002 a0002c0003t0003g0021 a0002c0003t0003g0022 others(28): Show |
82 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1050+956_1050+957d others(4): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359210 | TACAC | T | 9 | a0001c0002t0008g0070 a0001c0002t0012g0174 a0002c0003t0003g0127 others(6): Show |
12 | HG01496.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1050+954_1050+957d others(6): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359210 | TACACAC | T | 7 | a0001c0001t0001g0056 a0001c0002t0007g0005 a0001c0002t0007g0178 others(4): Show |
20 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1050+952_1050+957d others(8): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359210 | TACACACA others(3): Show |
T | 2 | a0002c0003t0003g0046 a0002c0003t0003g0130 |
3 | NA19001.hp2 NA19055.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1050+948_1050+957d others(12): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359210 | |||||||
| chr4:155359248 | G | C | 3 | a0001c0002t0001g0192 a0006c0008t0015g0054 a0006c0008t0015g0191 |
4 | HG02970.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1050+920C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359248 | |||||||
| chr4:155359322 | A | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(90): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1050+846T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359322 | |||||||
| chr4:155359387 | A | C | 1 | a0002c0003t0003g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1050+781T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359387 | |||||||
| chr4:155359409 | G | A | 1 | a0005c0011t0015g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1050+759C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359409 | |||||||
| chr4:155359680 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1050+488G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359680 | |||||||
| chr4:155359684 | T | C | 1 | a0004c0005t0005g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1050+484A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359684 | |||||||
| chr4:155359711 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1050+457G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359711 | |||||||
| chr4:155359727 | A | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1050+441T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155359727 | |||||||
| chr4:155360159 | T | G | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1050+9A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 7/13 | chr4 | 155360159 | |||||||
| chr4:155360514 | ACT | A | 44 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(41): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.803-101_803-100del others(2): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155360514 | |||||||
| chr4:155360588 | CA | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(90): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.803-174delT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155360588 | |||||||
| chr4:155360782 | C | T | 1 | a0004c0005t0005g0088 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.803-367G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155360782 | |||||||
| chr4:155360869 | A | T | 8 | a0001c0002t0004g0011 a0001c0002t0004g0034 a0001c0002t0004g0060 others(5): Show |
15 | HG00621.hp2 HG01192.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.803-454T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155360869 | |||||||
| chr4:155360970 | T | C | 6 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(3): Show |
17 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-555A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155360970 | |||||||
| chr4:155361001 | G | A | 48 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(45): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.803-586C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155361001 | |||||||
| chr4:155361052 | T | C | 1 | a0009c0017t0005g0087 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.803-637A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155361052 | |||||||
| chr4:155361276 | G | A | 1 | a0002c0003t0003g0139 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.802+772C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155361276 | |||||||
| chr4:155361520 | A | G | 1 | a0004c0005t0018g0040 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.802+528T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155361520 | |||||||
| chr4:155361528 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.802+520C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 6/13 | chr4 | 155361528 | |||||||
| chr4:155362150 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.709-9C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155362150 | |||||||
| chr4:155362436 | A | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(161): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.709-295T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155362436 | |||||||
| chr4:155362454 | A | G | 3 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 |
14 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.709-313T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155362454 | |||||||
| chr4:155362706 | C | T | 1 | a0003c0004t0002g0167 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.709-565G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155362706 | |||||||
| chr4:155362765 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.709-624A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155362765 | |||||||
| chr4:155362798 | T | C | 1 | a0003c0004t0002g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.709-657A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155362798 | |||||||
| chr4:155362815 | AGTATTTT others(3): Show |
A | 3 | a0001c0002t0009g0175 a0001c0002t0009g0176 a0001c0002t0009g0177 |
3 | HG02109.hp1 HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.709-684_709-675del others(10): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155362815 | |||||||
| chr4:155362841 | A | G | 1 | a0001c0002t0009g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.709-700T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155362841 | |||||||
| chr4:155363009 | C | T | 3 | a0003c0004t0002g0049 a0003c0004t0002g0148 a0003c0004t0002g0149 |
4 | HG01167.hp1 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.709-868G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363009 | |||||||
| chr4:155363017 | G | T | 2 | a0002c0003t0003g0022 a0002c0003t0003g0172 |
5 | HG01081.hp1 HG01123.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.709-876C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363017 | |||||||
| chr4:155363044 | G | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(90): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.709-903C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363044 | |||||||
| chr4:155363116 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.709-975C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363116 | |||||||
| chr4:155363117 | A | C | 1 | a0003c0004t0002g0147 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.709-976T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363117 | |||||||
| chr4:155363140 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.709-999G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363140 | |||||||
| chr4:155363254 | T | G | 48 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(45): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.709-1113A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363254 | |||||||
| chr4:155363255 | T | C | 1 | a0002c0003t0003g0021 | 4 | HG00642.hp1 HG01261.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.709-1114A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363255 | |||||||
| chr4:155363760 | C | T | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.709-1619G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363760 | |||||||
| chr4:155363811 | TAAAAAC | T | 1 | a0003c0004t0002g0030 | 3 | HG00733.hp1 HG01192.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.709-1676_709-1671d others(8): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363811 | |||||||
| chr4:155363895 | G | T | 1 | a0001c0002t0004g0063 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.709-1754C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363895 | |||||||
| chr4:155363967 | A | G | 1 | a0005c0011t0015g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.709-1826T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155363967 | |||||||
| chr4:155364018 | A | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.709-1877T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364018 | |||||||
| chr4:155364117 | A | G | 4 | a0001c0002t0004g0034 a0001c0002t0004g0060 a0001c0002t0004g0061 others(1): Show |
5 | HG00621.hp2 NA18954.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.709-1976T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364117 | |||||||
| chr4:155364239 | C | A | 5 | a0004c0005t0005g0025 a0004c0005t0005g0036 a0004c0005t0005g0039 others(2): Show |
9 | HG00438.hp2 HG00597.hp2 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.709-2098G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364239 | |||||||
| chr4:155364417 | T | C | 2 | a0004c0005t0005g0038 a0004c0005t0005g0088 |
3 | HG02132.hp1 NA18961.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.709-2276A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364417 | |||||||
| chr4:155364478 | A | G | 2 | a0001c0002t0009g0052 a0001c0002t0009g0173 |
3 | HG02572.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.709-2337T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364478 | |||||||
| chr4:155364529 | A | G | 37 | a0001c0001t0013g0026 a0001c0001t0013g0115 a0001c0002t0004g0009 others(34): Show |
77 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.709-2388T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364529 | |||||||
| chr4:155364536 | C | CTATAA | 141 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.709-2396_709-2395i others(7): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364536 | |||||||
| chr4:155364549 | T | C | 7 | a0001c0002t0004g0010 a0001c0002t0008g0035 a0001c0002t0008g0070 others(4): Show |
15 | HG02055.hp2 HG02258.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.709-2408A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364549 | |||||||
| chr4:155364559 | T | C | 1 | a0004c0005t0018g0040 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.709-2418A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364559 | |||||||
| chr4:155364732 | T | G | 1 | a0002c0003t0003g0140 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.709-2591A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364732 | |||||||
| chr4:155364784 | T | G | 1 | a0001c0001t0001g0044 | 2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.709-2643A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364784 | |||||||
| chr4:155364806 | T | C | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.709-2665A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364806 | |||||||
| chr4:155364916 | G | T | 6 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(3): Show |
17 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.709-2775C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364916 | |||||||
| chr4:155364937 | A | G | 1 | a0001c0001t0001g0029 | 3 | NA19010.hp1 NA19063.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.709-2796T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155364937 | |||||||
| chr4:155365294 | A | G | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.709-3153T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155365294 | |||||||
| chr4:155365299 | C | T | 22 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(19): Show |
45 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.709-3158G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155365299 | |||||||
| chr4:155365439 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(89): Show |
194 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.708+3147G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155365439 | |||||||
| chr4:155365494 | T | C | 3 | a0005c0006t0006g0188 a0005c0006t0006g0189 a0005c0006t0006g0190 |
3 | NA18972.hp2 NA18973.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.708+3092A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155365494 | |||||||
| chr4:155365823 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.708+2763G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155365823 | |||||||
| chr4:155366098 | C | T | 1 | a0002c0003t0003g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.708+2488G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155366098 | |||||||
| chr4:155366183 | A | G | 32 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(29): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.708+2403T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155366183 | |||||||
| chr4:155366231 | T | C | 25 | a0001c0001t0001g0019 a0001c0001t0033g0122 a0004c0005t0005g0006 others(22): Show |
52 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.708+2355A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155366231 | |||||||
| chr4:155366252 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.708+2334C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155366252 | |||||||
| chr4:155366338 | G | A | 1 | a0006c0007t0025g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.708+2248C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155366338 | |||||||
| chr4:155366358 | C | CA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(90): Show |
195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.708+2227dupT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155366358 | |||||||
| chr4:155366937 | C | T | 1 | a0002c0003t0003g0172 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.708+1649G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155366937 | |||||||
| chr4:155367063 | A | C | 6 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(3): Show |
17 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.708+1523T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155367063 | |||||||
| chr4:155367295 | C | T | 1 | a0004c0005t0005g0036 | 2 | NA19060.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.708+1291G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155367295 | |||||||
| chr4:155367314 | A | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(86): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.708+1272T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155367314 | |||||||
| chr4:155367414 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0112 others(2): Show |
8 | HG02056.hp2 NA18960.hp1 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.708+1172C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155367414 | |||||||
| chr4:155367457 | T | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(87): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.708+1129A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155367457 | |||||||
| chr4:155367594 | T | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(87): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.708+992A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155367594 | |||||||
| chr4:155367780 | T | C | 32 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(29): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.708+806A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155367780 | |||||||
| chr4:155367849 | C | A | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.708+737G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155367849 | |||||||
| chr4:155368438 | T | A | 1 | a0003c0004t0002g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.708+148A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155368438 | |||||||
| chr4:155368446 | A | G | 1 | a0004c0005t0005g0081 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.708+140T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155368446 | |||||||
| chr4:155368539 | A | C | 1 | a0001c0012t0001g0120 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.708+47T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155368539 | |||||||
| chr4:155368545 | A | C | 1 | a0006c0007t0025g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.708+41T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 5/13 | chr4 | 155368545 | |||||||
| chr4:155368823 | A | T | 1 | a0003c0004t0002g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.482-11T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155368823 | |||||||
| chr4:155368852 | G | A | 1 | a0004c0005t0005g0039 | 2 | NA18950.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.482-40C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155368852 | |||||||
| chr4:155368864 | A | T | 1 | a0001c0002t0012g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.482-52T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155368864 | |||||||
| chr4:155368880 | G | C | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.482-68C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155368880 | |||||||
| chr4:155369013 | G | A | 6 | a0006c0007t0014g0041 a0006c0007t0014g0090 a0006c0007t0014g0091 others(3): Show |
7 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-201C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369013 | |||||||
| chr4:155369070 | C | T | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.482-258G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369070 | |||||||
| chr4:155369139 | G | A | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.482-327C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369139 | |||||||
| chr4:155369191 | C | T | 1 | a0006c0007t0028g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.482-379G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369191 | |||||||
| chr4:155369325 | A | G | 1 | a0001c0002t0007g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.482-513T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369325 | |||||||
| chr4:155369328 | T | TA | 7 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(4): Show |
7 | HG02027.hp2 HG02145.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-517dupT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369328 | |||||||
| chr4:155369328 | TA | T | 73 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(70): Show |
160 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.482-517delT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369328 | |||||||
| chr4:155369339 | A | C | 1 | a0006c0008t0015g0054 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.482-527T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369339 | |||||||
| chr4:155369344 | AC | A | 30 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(27): Show |
68 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.482-533delG | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369344 | |||||||
| chr4:155369345 | C | A | 2 | a0003c0004t0002g0048 a0003c0004t0002g0145 |
3 | HG01099.hp2 HG03927.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.482-533G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369345 | |||||||
| chr4:155369362 | CA | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.482-551delT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369362 | |||||||
| chr4:155369365 | A | C | 10 | a0001c0002t0004g0034 a0006c0007t0014g0041 a0006c0007t0014g0090 others(7): Show |
13 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.482-553T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369365 | |||||||
| chr4:155369454 | T | TA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.482-643dupT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369454 | |||||||
| chr4:155369454 | TA | T | 73 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(70): Show |
149 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.482-643delT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369454 | |||||||
| chr4:155369456 | A | C | 1 | a0002c0003t0003g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.482-644T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369456 | |||||||
| chr4:155369477 | AAAAAC | A | 74 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(71): Show |
151 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.482-670_482-666del others(5): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369477 | |||||||
| chr4:155369542 | C | T | 1 | a0001c0002t0004g0183 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.482-730G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369542 | |||||||
| chr4:155369565 | C | T | 3 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 |
14 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-753G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369565 | |||||||
| chr4:155369643 | T | G | 1 | a0002c0003t0003g0125 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.482-831A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369643 | |||||||
| chr4:155369686 | A | G | 6 | a0006c0007t0014g0041 a0006c0007t0014g0090 a0006c0007t0014g0091 others(3): Show |
7 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-874T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369686 | |||||||
| chr4:155369718 | A | C | 2 | a0006c0008t0015g0054 a0006c0008t0015g0191 |
3 | HG02970.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.482-906T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369718 | |||||||
| chr4:155369847 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.482-1035C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369847 | |||||||
| chr4:155369972 | T | C | 1 | a0002c0003t0003g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.482-1160A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369972 | |||||||
| chr4:155369973 | T | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.482-1161A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155369973 | |||||||
| chr4:155370063 | T | C | 32 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(29): Show |
58 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.482-1251A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370063 | |||||||
| chr4:155370108 | T | C | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.482-1296A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370108 | |||||||
| chr4:155370308 | T | A | 5 | a0001c0002t0001g0192 a0001c0002t0007g0005 a0001c0002t0007g0178 others(2): Show |
16 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.482-1496A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370308 | |||||||
| chr4:155370310 | C | T | 1 | a0003c0004t0002g0144 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.482-1498G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370310 | |||||||
| chr4:155370347 | A | G | 1 | a0001c0002t0004g0182 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.482-1535T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370347 | |||||||
| chr4:155370355 | G | C | 1 | a0003c0004t0002g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.482-1543C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370355 | |||||||
| chr4:155370390 | C | T | 32 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(29): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.482-1578G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370390 | |||||||
| chr4:155370391 | G | A | 1 | a0007c0010t0003g0047 | 2 | HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.482-1579C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370391 | |||||||
| chr4:155370552 | C | T | 2 | a0006c0008t0015g0054 a0006c0008t0015g0191 |
3 | HG02970.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.482-1740G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370552 | |||||||
| chr4:155370640 | T | G | 32 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(29): Show |
58 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.482-1828A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370640 | |||||||
| chr4:155370648 | AT | A | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.482-1837delA | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370648 | |||||||
| chr4:155370730 | T | A | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.482-1918A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370730 | |||||||
| chr4:155370766 | A | G | 9 | a0006c0007t0014g0041 a0006c0007t0014g0090 a0006c0007t0014g0091 others(6): Show |
11 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-1954T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155370766 | |||||||
| chr4:155371013 | G | A | 1 | a0001c0012t0001g0120 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.481+2123C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371013 | |||||||
| chr4:155371067 | C | T | 23 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(20): Show |
47 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.481+2069G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371067 | |||||||
| chr4:155371165 | C | A | 32 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(29): Show |
58 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.481+1971G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371165 | |||||||
| chr4:155371189 | C | T | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.481+1947G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371189 | |||||||
| chr4:155371249 | T | G | 1 | a0003c0004t0002g0167 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.481+1887A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371249 | |||||||
| chr4:155371256 | A | G | 2 | a0001c0002t0009g0052 a0001c0002t0009g0173 |
3 | HG02572.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.481+1880T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371256 | |||||||
| chr4:155371523 | G | GA | 32 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(29): Show |
58 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.481+1612dupT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371523 | |||||||
| chr4:155371523 | G | GAA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.481+1611_481+1612d others(4): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371523 | |||||||
| chr4:155371821 | T | G | 74 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(71): Show |
151 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.481+1315A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371821 | |||||||
| chr4:155371845 | T | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0097 others(5): Show |
18 | HG01175.hp1 HG01346.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.481+1291A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371845 | |||||||
| chr4:155371877 | T | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.481+1259A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371877 | |||||||
| chr4:155371960 | T | C | 1 | a0005c0011t0015g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.481+1176A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155371960 | |||||||
| chr4:155372152 | A | G | 32 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(29): Show |
58 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.481+984T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155372152 | |||||||
| chr4:155372221 | C | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.481+915G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155372221 | |||||||
| chr4:155372306 | T | C | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.481+830A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155372306 | |||||||
| chr4:155372309 | G | A | 1 | a0005c0006t0006g0190 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.481+827C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155372309 | |||||||
| chr4:155372317 | A | C | 1 | a0004c0005t0038g0080 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.481+819T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155372317 | |||||||
| chr4:155372407 | C | A | 1 | a0004c0005t0018g0040 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.481+729G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155372407 | |||||||
| chr4:155372529 | G | A | 32 | a0004c0005t0005g0006 a0004c0005t0005g0023 a0004c0005t0005g0024 others(29): Show |
58 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.481+607C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155372529 | |||||||
| chr4:155373081 | A | T | 1 | a0006c0007t0029g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.481+55T>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155373081 | |||||||
| chr4:155373107 | A | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0077 others(10): Show |
26 | HG00438.hp1 HG01175.hp1 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.481+29T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 4/13 | chr4 | 155373107 | |||||||
| chr4:155373472 | G | GA | 124 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(121): Show |
252 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.161-17dupT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373472 | |||||||
| chr4:155373478 | T | A | 1 | a0001c0002t0004g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161-22A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373478 | |||||||
| chr4:155373479 | G | T | 1 | a0001c0002t0004g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161-23C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373479 | |||||||
| chr4:155373480 | T | G | 1 | a0001c0002t0004g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161-24A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373480 | |||||||
| chr4:155373514 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.161-58G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373514 | |||||||
| chr4:155373588 | TA | T | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.161-133delT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373588 | |||||||
| chr4:155373646 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.161-190A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373646 | |||||||
| chr4:155373732 | C | T | 1 | a0002c0003t0003g0125 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.161-276G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373732 | |||||||
| chr4:155373737 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-281C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373737 | |||||||
| chr4:155373762 | C | G | 1 | a0001c0001t0017g0092 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.161-306G>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373762 | |||||||
| chr4:155373764 | A | G | 1 | a0001c0001t0017g0092 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.161-308T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373764 | |||||||
| chr4:155373765 | T | A | 1 | a0001c0001t0017g0092 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.161-309A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373765 | |||||||
| chr4:155373766 | C | T | 1 | a0001c0001t0017g0092 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.161-310G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373766 | |||||||
| chr4:155373769 | T | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(121): Show |
252 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.161-313A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373769 | |||||||
| chr4:155373779 | T | A | 9 | a0006c0007t0014g0041 a0006c0007t0014g0090 a0006c0007t0014g0091 others(6): Show |
11 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-323A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155373779 | |||||||
| chr4:155374091 | A | C | 2 | a0006c0008t0015g0054 a0006c0008t0015g0191 |
3 | HG02970.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.161-635T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374091 | |||||||
| chr4:155374111 | C | T | 1 | a0006c0007t0028g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.161-655G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374111 | |||||||
| chr4:155374112 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.161-656C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374112 | |||||||
| chr4:155374115 | C | T | 1 | a0002c0003t0003g0124 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.161-659G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374115 | |||||||
| chr4:155374234 | G | C | 1 | a0001c0001t0033g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+703C>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374234 | |||||||
| chr4:155374246 | G | A | 32 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(29): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.160+691C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374246 | |||||||
| chr4:155374290 | G | A | 2 | a0003c0004t0002g0051 a0003c0004t0002g0168 |
3 | NA18981.hp2 NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.160+647C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374290 | |||||||
| chr4:155374337 | T | TCAAAAA | 39 | a0003c0004t0002g0001 a0003c0004t0002g0015 a0003c0004t0002g0030 others(36): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.160+594_160+599dup others(6): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374337 | |||||||
| chr4:155374346 | A | AAAACAAA others(3): Show |
125 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(122): Show |
253 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.160+590_160+591ins others(10): Show |
MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374346 | |||||||
| chr4:155374466 | C | T | 1 | a0006c0007t0025g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.160+471G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374466 | |||||||
| chr4:155374467 | G | A | 3 | a0005c0006t0006g0188 a0005c0006t0006g0189 a0005c0006t0006g0190 |
3 | NA18972.hp2 NA18973.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.160+470C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374467 | |||||||
| chr4:155374553 | T | G | 1 | a0002c0003t0003g0169 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.160+384A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374553 | |||||||
| chr4:155374664 | T | C | 1 | a0005c0011t0015g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.160+273A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374664 | |||||||
| chr4:155374717 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.160+220T>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374717 | |||||||
| chr4:155374747 | T | G | 4 | a0001c0002t0007g0005 a0001c0002t0007g0178 a0001c0002t0007g0179 others(1): Show |
15 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.160+190A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374747 | |||||||
| chr4:155374813 | T | C | 42 | a0001c0002t0001g0192 a0001c0002t0004g0009 a0001c0002t0004g0010 others(39): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.160+124A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374813 | |||||||
| chr4:155374881 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.160+56T>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 3/13 | chr4 | 155374881 | |||||||
| chr4:155375141 | T | A | 1 | a0006c0007t0037g0123 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.76-120A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 2/13 | chr4 | 155375141 | |||||||
| chr4:155375241 | C | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(122): Show |
253 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.76-220G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 2/13 | chr4 | 155375241 | |||||||
| chr4:155375610 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.75+166C>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 2/13 | chr4 | 155375610 | |||||||
| chr4:155375669 | T | C | 2 | a0002c0003t0003g0022 a0002c0003t0003g0172 |
5 | HG01081.hp1 HG01123.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+107A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 2/13 | chr4 | 155375669 | |||||||
| chr4:155375716 | T | A | 40 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0011 others(37): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.75+60A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 2/13 | chr4 | 155375716 | |||||||
| chr4:155375758 | C | T | 6 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(3): Show |
17 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.75+18G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 2/13 | chr4 | 155375758 | |||||||
| chr4:155375946 | T | G | 1 | a0001c0002t0027g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-64-32A>C | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 1/13 | chr4 | 155375946 | |||||||
| chr4:155376021 | T | C | 8 | a0001c0002t0004g0009 a0001c0002t0004g0013 a0001c0002t0004g0032 others(5): Show |
25 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.-64-107A>G | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 1/13 | chr4 | 155376021 | |||||||
| chr4:155376235 | C | A | 3 | a0005c0006t0006g0188 a0005c0006t0006g0189 a0005c0006t0006g0190 |
3 | NA18972.hp2 NA18973.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-64-321G>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 1/13 | chr4 | 155376235 | |||||||
| chr4:155376310 | C | CA | 7 | a0005c0006t0006g0008 a0005c0006t0006g0053 a0005c0006t0006g0187 others(4): Show |
19 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.-64-397dupT | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 1/13 | chr4 | 155376310 | |||||||
| chr4:155376321 | T | A | 1 | a0006c0008t0015g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-64-407A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 1/13 | chr4 | 155376321 | |||||||
| chr4:155376334 | T | A | 1 | a0001c0002t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-64-420A>T | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 1/13 | chr4 | 155376334 | |||||||
| chr4:155376493 | C | T | 6 | a0004c0005t0005g0023 a0004c0005t0005g0058 a0004c0005t0010g0016 others(3): Show |
11 | HG02109.hp2 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-65+278G>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 1/13 | chr4 | 155376493 | |||||||
| chr4:155376550 | G | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0056 |
4 | HG00558.hp1 NA18950.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-65+221C>A | MAP9 | ENSG00000164114.19 | transcript | ENST00000311277.9 | protein_coding | 1/13 | chr4 | 155376550 |