Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55892 |
| ensemblid | ENSG00000085274.16 |
| hgncid | 14955 |
| symbol | MYNN |
| name | myoneurin |
| refseq_nuc | NM_018657.5 |
| refseq_prot | NP_061127.1 |
| ensembl_nuc | ENST00000349841.10 |
| ensembl_prot | ENSP00000326240.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 169773396 |
| end | 169789716 |
| strand | + |
| ver | v1.2 |
| region | chr3:169773396-169789716 |
| region5000 | chr3:169768396-169794716 |
| regionname0 | MYNN_chr3_169773396_169789716 |
| regionname5000 | MYNN_chr3_169768396_169794716 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 610 | 347 | 94 | 64 | 144 | 8 | 35 | 113 | MYNN_chr3_169768396_169794716 | MYNN | MQYSH others(605): Show |
chr3 | 169768396 | 169794716 |
| a0002 | 0/0 | 610 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | MQYSH others(605): Show |
chr3 | 169768396 | 169794716 |
| a0003 | 0/0 | 610 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYNN_chr3_169768396_169794716 | MYNN | MQYSH others(605): Show |
chr3 | 169768396 | 169794716 |
| a0004 | 0/0 | 610 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | MQYSH others(605): Show |
chr3 | 169768396 | 169794716 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1830 | 233 | 90 | 46 | 64 | 7 | 24 | MYNN_chr3_169768396_169794716 | MYNN | ATGCA others(1825): Show |
chr3 | 169768396 | 169794716 | ||
| a0001c0002 | 0/0 | 1830 | 112 | 4 | 18 | 78 | 1 | 11 | MYNN_chr3_169768396_169794716 | MYNN | ATGCA others(1825): Show |
chr3 | 169768396 | 169794716 | ||
| a0001c0004 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | ATGCA others(1825): Show |
chr3 | 169768396 | 169794716 | ||
| a0001c0007 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | ATGCA others(1825): Show |
chr3 | 169768396 | 169794716 | ||
| a0002c0006 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | ATGCA others(1825): Show |
chr3 | 169768396 | 169794716 | ||
| a0003c0003 | 0/0 | 1830 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | ATGCA others(1825): Show |
chr3 | 169768396 | 169794716 | ||
| a0004c0005 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | ATGCA others(1825): Show |
chr3 | 169768396 | 169794716 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4969 | 144 | 32 | 35 | 49 | 7 | 19 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0002 | 0/0 | 4969 | 22 | 15 | 3 | 1 | 0 | 3 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0003 | 0/0 | 4969 | 18 | 0 | 3 | 14 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0004 | 0/0 | 4969 | 15 | 13 | 2 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0005 | 0/0 | 4969 | 11 | 11 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0006 | 0/0 | 4969 | 6 | 6 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0007 | 0/0 | 4969 | 4 | 4 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0008 | 0/0 | 4969 | 3 | 1 | 2 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0009 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0010 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0011 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0012 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0013 | 0/0 | 4969 | 1 | 0 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0014 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0016 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0017 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0001t0021 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0002t0001 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0002t0002 | 0/0 | 4969 | 108 | 4 | 18 | 74 | 1 | 11 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0002t0015 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0002t0019 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0002t0020 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0004t0006 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0001c0007t0002 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0002c0006t0018 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0003c0003t0001 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| a0004c0005t0001 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | GGTGA others(4964): Show |
chr3 | 169768396 | 169794716 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/1 | 60 | 0 | 18 | 30 | 4 | 6 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0003 | 0/0 | 21 | 11 | 4 | 0 | 2 | 4 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0005 | 0/0 | 10 | 7 | 1 | 0 | 0 | 2 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0013 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0003g0009 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0004g0007 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0005g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0006g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0006g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0007g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0007g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0008g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0009g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0011g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0016g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0017g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0001t0021g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0002 | 0/0 | 41 | 1 | 6 | 29 | 1 | 4 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0004 | 0/0 | 21 | 2 | 4 | 13 | 0 | 2 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0006 | 0/0 | 11 | 0 | 3 | 5 | 0 | 3 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0008 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0014 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0015g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0019g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0002t0020g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0004t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0001c0007t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0002c0006t0018g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| a0004c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00544 | hp2 | a0001 | c0004 | t0006 | g0100 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00597 | hp1 | a0001 | c0007 | t0002 | g0014 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0090 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0019 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0019 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02055 | hp1 | a0001 | c0001 | t0014 | g0039 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02129 | hp1 | a0002 | c0006 | t0018 | g0002 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02148 | hp2 | a0001 | c0001 | t0013 | g0001 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CDX | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0085 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0070 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02717 | hp1 | a0001 | c0001 | t0016 | g0015 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0096 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0063 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0059 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0064 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0014 | SAS | BEB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | BEB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | BEB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04184 | hp2 | a0001 | c0001 | t0021 | g0043 | SAS | BEB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | STU | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | YRI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | YRI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | CHB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18952 | hp2 | a0001 | c0002 | t0015 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18963 | hp1 | a0001 | c0002 | t0019 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19001 | hp2 | a0001 | c0002 | t0020 | g0022 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | LWK | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | LWK | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19043 | hp2 | a0001 | c0001 | t0017 | g0017 | AFR | LWK | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19083 | hp1 | a0004 | c0005 | t0001 | g0089 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0093 | AFR | ASW | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0087 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | USA | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | USA | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | LWK | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | LWK | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | MYNN_chr3_169768396_169794716 | MYNN | chr3 | 169768396 | 169794716 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:169778926 | C | T | 1 | a0002 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.425C>T | p.Thr142Ile | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/8 | 523/4969 | 425/1833 | 142/610 | chr3 | 169778926 | |||
| chr3:169779141 | G | A | 1 | a0003 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.640G>A | p.Asp214Asn | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/8 | 738/4969 | 640/1833 | 214/610 | chr3 | 169779141 | |||
| chr3:169786539 | C | T | 1 | a0004 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.1694C>T | p.Ala565Val | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1792/4969 | 1694/1833 | 565/610 | chr3 | 169786539 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:169774313 | C | T | 3 | a0001c0002 a0001c0007 a0002c0006 |
114 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
synonymous_variant | LOW | c.18C>T | p.His6His | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/8 | 116/4969 | 18/1833 | 6/610 | chr3 | 169774313 | |||
| chr3:169778882 | A | G | 1 | a0001c0007 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.381A>G | p.Thr127Thr | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/8 | 479/4969 | 381/1833 | 127/610 | chr3 | 169778882 | |||
| chr3:169782609 | T | C | 1 | a0001c0004 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.1365T>C | p.Ser455Ser | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 5/8 | 1463/4969 | 1365/1833 | 455/610 | chr3 | 169782609 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:169786795 | C | T | 1 | a0001c0001t0021 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 117 | chr3 | 169786795 | ||||||
| chr3:169786977 | C | T | 1 | a0001c0001t0008 | 3 | HG01167.hp2 HG01169.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*299C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 299 | chr3 | 169786977 | ||||||
| chr3:169787130 | T | C | 1 | a0001c0001t0010 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*452T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 452 | chr3 | 169787130 | ||||||
| chr3:169787159 | G | A | 1 | a0001c0001t0003 | 18 | HG00673.hp1 HG00738.hp2 HG01981.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*481G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 481 | chr3 | 169787159 | ||||||
| chr3:169787377 | G | A | 2 | a0001c0001t0004 a0001c0001t0011 |
16 | HG00639.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*699G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 699 | chr3 | 169787377 | ||||||
| chr3:169787442 | G | T | 1 | a0001c0001t0008 | 3 | HG01167.hp2 HG01169.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*764G>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 764 | chr3 | 169787442 | ||||||
| chr3:169787570 | T | C | 1 | a0001c0001t0011 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*892T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 892 | chr3 | 169787570 | ||||||
| chr3:169787865 | A | G | 1 | a0001c0001t0003 | 18 | HG00673.hp1 HG00738.hp2 HG01981.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1187A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1187 | chr3 | 169787865 | ||||||
| chr3:169787975 | T | C | 1 | a0001c0001t0007 | 4 | HG02615.hp2 HG02723.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1297T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1297 | chr3 | 169787975 | ||||||
| chr3:169788007 | G | T | 1 | a0001c0002t0020 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1329G>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1329 | chr3 | 169788007 | ||||||
| chr3:169788136 | C | A | 1 | a0001c0001t0012 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1458C>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1458 | chr3 | 169788136 | ||||||
| chr3:169788307 | C | T | 1 | a0001c0001t0005 | 11 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1629C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1629 | chr3 | 169788307 | ||||||
| chr3:169788312 | A | G | 3 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0010 |
7 | HG01884.hp2 HG02615.hp2 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1634A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1634 | chr3 | 169788312 | ||||||
| chr3:169788353 | C | T | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(14): Show |
179 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1675C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1675 | chr3 | 169788353 | ||||||
| chr3:169788385 | C | T | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(14): Show |
179 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1707C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1707 | chr3 | 169788385 | ||||||
| chr3:169788535 | T | C | 1 | a0001c0001t0014 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1857T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1857 | chr3 | 169788535 | ||||||
| chr3:169788600 | T | C | 1 | a0001c0002t0015 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1922T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 1922 | chr3 | 169788600 | ||||||
| chr3:169788898 | G | A | 1 | a0001c0001t0016 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2220G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 2220 | chr3 | 169788898 | ||||||
| chr3:169789019 | T | C | 1 | a0001c0001t0013 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2341T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 2341 | chr3 | 169789019 | ||||||
| chr3:169789160 | T | A | 1 | a0001c0001t0017 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2482T>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 2482 | chr3 | 169789160 | ||||||
| chr3:169789630 | G | A | 1 | a0002c0006t0018 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2952G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 2952 | chr3 | 169789630 | ||||||
| chr3:169789636 | G | A | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(2): Show |
37 | HG00544.hp2 HG00673.hp1 HG00738.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2958G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 2958 | chr3 | 169789636 | ||||||
| chr3:169789705 | C | A | 1 | a0001c0002t0019 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3027C>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 8/8 | 3027 | chr3 | 169789705 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:169773516 | C | T | 1 | a0001c0001t0003g0101 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-32+54C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 1/7 | chr3 | 169773516 | |||||||
| chr3:169773646 | A | G | 1 | a0001c0001t0002g0042 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-32+184A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 1/7 | chr3 | 169773646 | |||||||
| chr3:169773797 | G | A | 1 | a0001c0001t0021g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-32+335G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 1/7 | chr3 | 169773797 | |||||||
| chr3:169773905 | C | G | 1 | a0001c0004t0006g0100 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-31-360C>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 1/7 | chr3 | 169773905 | |||||||
| chr3:169773941 | T | A | 27 | a0001c0001t0001g0023 a0001c0002t0001g0044 a0001c0002t0002g0002 others(24): Show |
116 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-31-324T>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 1/7 | chr3 | 169773941 | |||||||
| chr3:169774228 | T | TA | 26 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0004 others(23): Show |
114 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-31-36dupA | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169774228 | ||||||
| chr3:169774702 | A | G | 10 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0039 others(7): Show |
19 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.266+141A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169774702 | |||||||
| chr3:169774907 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.266+346C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169774907 | |||||||
| chr3:169774932 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.266+371G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169774932 | |||||||
| chr3:169774939 | A | G | 6 | a0001c0001t0002g0042 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
7 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.266+378A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169774939 | |||||||
| chr3:169774982 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | NA19004.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.266+421G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169774982 | |||||||
| chr3:169775079 | C | T | 1 | a0001c0001t0007g0038 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.266+518C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169775079 | |||||||
| chr3:169775223 | A | G | 1 | a0001c0001t0021g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.266+662A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169775223 | |||||||
| chr3:169775365 | CAA | C | 1 | a0001c0001t0008g0019 | 3 | HG01167.hp2 HG01169.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.266+806_266+807del others(2): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169775365 | ||||||
| chr3:169775495 | C | G | 25 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0006 others(22): Show |
113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.266+934C>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169775495 | |||||||
| chr3:169775505 | C | T | 4 | a0001c0001t0006g0036 a0001c0001t0006g0037 a0001c0001t0006g0092 others(1): Show |
6 | HG02451.hp2 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.266+944C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169775505 | |||||||
| chr3:169775681 | C | T | 1 | a0001c0001t0021g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.266+1120C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169775681 | |||||||
| chr3:169775931 | T | C | 2 | a0001c0001t0006g0036 a0001c0001t0006g0037 |
4 | HG02451.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.266+1370T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169775931 | |||||||
| chr3:169776084 | A | T | 3 | a0001c0002t0002g0011 a0001c0002t0002g0022 a0001c0002t0020g0022 |
8 | NA18943.hp1 NA18946.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.266+1523A>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169776084 | |||||||
| chr3:169776415 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.266+1854C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169776415 | |||||||
| chr3:169776681 | C | A | 2 | a0001c0001t0003g0024 a0001c0001t0003g0025 |
4 | HG01981.hp2 HG02293.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.267-2087C>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169776681 | |||||||
| chr3:169776694 | A | AT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(14): Show |
33 | HG00544.hp2 HG00639.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.267-2047dupT | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169776694 | ||||||
| chr3:169776694 | A | ATT | 6 | a0001c0001t0002g0041 a0001c0001t0006g0037 a0001c0002t0002g0020 others(3): Show |
9 | HG01257.hp1 HG02258.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.267-2048_267-2047d others(4): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169776694 | ||||||
| chr3:169776694 | A | ATTT | 15 | a0001c0001t0002g0099 a0001c0002t0002g0002 a0001c0002t0002g0004 others(12): Show |
90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.267-2049_267-2047d others(5): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169776694 | ||||||
| chr3:169776694 | A | ATTTT | 6 | a0001c0002t0002g0008 a0001c0002t0002g0014 a0001c0002t0002g0021 others(3): Show |
16 | HG00597.hp1 HG01071.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.267-2050_267-2047d others(6): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169776694 | ||||||
| chr3:169776694 | AT | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0002g0094 others(15): Show |
34 | HG00558.hp2 HG00673.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.267-2047delT | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169776694 | ||||||
| chr3:169776764 | C | T | 1 | a0001c0001t0011g0087 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.267-2004C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169776764 | |||||||
| chr3:169776828 | C | T | 1 | a0001c0002t0002g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.267-1940C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169776828 | |||||||
| chr3:169776839 | A | G | 69 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0039 others(66): Show |
193 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.267-1929A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169776839 | |||||||
| chr3:169776998 | T | C | 1 | a0001c0002t0002g0046 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.267-1770T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169776998 | |||||||
| chr3:169777102 | G | T | 1 | a0001c0001t0008g0019 | 3 | HG01167.hp2 HG01169.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.267-1666G>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169777102 | |||||||
| chr3:169777323 | T | G | 1 | a0001c0001t0002g0094 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.267-1445T>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169777323 | |||||||
| chr3:169777391 | T | C | 1 | a0001c0001t0006g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.267-1377T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169777391 | |||||||
| chr3:169777480 | G | GGT | 15 | a0001c0001t0001g0088 a0001c0001t0002g0095 a0001c0001t0002g0098 others(12): Show |
25 | HG00544.hp2 HG00639.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.267-1267_267-1266d others(4): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169777480 | ||||||
| chr3:169777762 | G | A | 6 | a0001c0001t0002g0042 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
7 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.267-1006G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169777762 | |||||||
| chr3:169777803 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.267-965C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169777803 | |||||||
| chr3:169777980 | G | A | 1 | a0001c0001t0006g0036 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.267-788G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169777980 | |||||||
| chr3:169778077 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.267-691C>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169778077 | |||||||
| chr3:169778152 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(90): Show |
253 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.267-616G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169778152 | |||||||
| chr3:169778159 | TATC | T | 25 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0006 others(22): Show |
113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.267-606_267-604del others(3): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169778159 | ||||||
| chr3:169778187 | G | C | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.267-581G>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169778187 | |||||||
| chr3:169778208 | C | T | 1 | a0001c0001t0006g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.267-560C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169778208 | |||||||
| chr3:169778267 | T | TC | 4 | a0001c0001t0006g0036 a0001c0001t0006g0037 a0001c0001t0006g0092 others(1): Show |
6 | HG02451.hp2 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.267-500dupC | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169778267 | ||||||
| chr3:169778425 | A | T | 1 | a0001c0001t0008g0019 | 3 | HG01167.hp2 HG01169.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.267-343A>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169778425 | |||||||
| chr3:169778487 | T | TA | 20 | a0001c0001t0001g0033 a0001c0001t0003g0009 a0001c0001t0003g0024 others(17): Show |
38 | HG00544.hp2 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.267-272dupA | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169778487 | ||||||
| chr3:169778707 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.267-61G>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169778707 | |||||||
| chr3:169778743 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0016g0015 |
5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.267-25G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 2/7 | chr3 | 169778743 | |||||||
| chr3:169779766 | A | ACT | 6 | a0001c0001t0002g0042 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
7 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060+207_1060+208d others(4): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 169779766 | ||||||
| chr3:169779797 | A | G | 25 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0006 others(22): Show |
113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1060+236A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/7 | chr3 | 169779797 | |||||||
| chr3:169780035 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0074 |
3 | HG00735.hp1 HG01256.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1060+474A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/7 | chr3 | 169780035 | |||||||
| chr3:169780092 | G | C | 1 | a0001c0002t0002g0047 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1061-498G>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/7 | chr3 | 169780092 | |||||||
| chr3:169780257 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1061-333A>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/7 | chr3 | 169780257 | |||||||
| chr3:169780301 | G | A | 6 | a0001c0001t0002g0042 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
7 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1061-289G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/7 | chr3 | 169780301 | |||||||
| chr3:169780305 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1061-285G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/7 | chr3 | 169780305 | |||||||
| chr3:169780337 | C | G | 1 | a0001c0001t0005g0064 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1061-253C>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 3/7 | chr3 | 169780337 | |||||||
| chr3:169780878 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1220+129T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169780878 | |||||||
| chr3:169781113 | GAAAT | G | 4 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0098 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220+367_1220+370d others(6): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 169781113 | ||||||
| chr3:169781203 | A | G | 2 | a0001c0002t0002g0049 a0001c0002t0002g0050 |
2 | HG00423.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1220+454A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169781203 | |||||||
| chr3:169781217 | G | A | 6 | a0001c0001t0002g0042 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
7 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1220+468G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169781217 | |||||||
| chr3:169781577 | A | G | 3 | a0001c0001t0002g0095 a0001c0001t0002g0098 a0001c0001t0012g0096 |
3 | HG01109.hp1 HG02809.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1220+828A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169781577 | |||||||
| chr3:169781911 | G | T | 2 | a0001c0001t0006g0036 a0001c0001t0006g0037 |
4 | HG02451.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221-554G>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169781911 | |||||||
| chr3:169781936 | A | G | 1 | a0001c0002t0002g0048 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1221-529A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169781936 | |||||||
| chr3:169782058 | G | A | 1 | a0001c0002t0002g0052 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1221-407G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169782058 | |||||||
| chr3:169782170 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1221-295C>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169782170 | |||||||
| chr3:169782212 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1221-253C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169782212 | |||||||
| chr3:169782269 | A | T | 1 | a0001c0001t0001g0030 | 2 | HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1221-196A>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169782269 | |||||||
| chr3:169782301 | A | T | 4 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0098 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221-164A>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 4/7 | chr3 | 169782301 | |||||||
| chr3:169782699 | G | A | 25 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0006 others(22): Show |
113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1399+56G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 5/7 | chr3 | 169782699 | |||||||
| chr3:169782813 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1399+170T>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 5/7 | chr3 | 169782813 | |||||||
| chr3:169782838 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1399+195G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 5/7 | chr3 | 169782838 | |||||||
| chr3:169782940 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1399+297T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 5/7 | chr3 | 169782940 | |||||||
| chr3:169783053 | A | G | 1 | a0001c0002t0002g0045 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1399+410A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 5/7 | chr3 | 169783053 | |||||||
| chr3:169783159 | A | C | 5 | a0001c0001t0005g0012 a0001c0001t0005g0032 a0001c0001t0005g0063 others(2): Show |
11 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1400-318A>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 5/7 | chr3 | 169783159 | |||||||
| chr3:169783224 | A | G | 1 | a0001c0001t0008g0019 | 3 | HG01167.hp2 HG01169.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1400-253A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 5/7 | chr3 | 169783224 | |||||||
| chr3:169783337 | C | T | 8 | a0001c0001t0003g0009 a0001c0001t0003g0024 a0001c0001t0003g0025 others(5): Show |
17 | HG00673.hp1 HG00738.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.1400-140C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 5/7 | chr3 | 169783337 | |||||||
| chr3:169783865 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1483+305C>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 6/7 | chr3 | 169783865 | |||||||
| chr3:169783904 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1483+344T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 6/7 | chr3 | 169783904 | |||||||
| chr3:169784141 | G | A | 5 | a0001c0001t0005g0012 a0001c0001t0005g0032 a0001c0001t0005g0063 others(2): Show |
11 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1484-481G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 6/7 | chr3 | 169784141 | |||||||
| chr3:169784375 | G | T | 7 | a0001c0001t0004g0007 a0001c0001t0004g0080 a0001c0001t0004g0081 others(4): Show |
16 | HG00639.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1484-247G>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 6/7 | chr3 | 169784375 | |||||||
| chr3:169784392 | T | C | 62 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0039 others(59): Show |
177 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1484-230T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 6/7 | chr3 | 169784392 | |||||||
| chr3:169784515 | T | A | 1 | a0001c0002t0002g0053 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1484-107T>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 6/7 | chr3 | 169784515 | |||||||
| chr3:169784524 | TATA | T | 6 | a0001c0001t0002g0042 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
7 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1484-92_1484-90del others(3): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 169784524 | ||||||
| chr3:169784879 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1570+171T>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169784879 | |||||||
| chr3:169784912 | T | TA | 50 | a0001c0001t0002g0015 a0001c0001t0002g0095 a0001c0001t0002g0097 others(47): Show |
150 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1570+222dupA | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169784912 | ||||||
| chr3:169784912 | TA | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0088 others(6): Show |
18 | HG01433.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1570+222delA | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169784912 | ||||||
| chr3:169785062 | G | GA | 4 | a0001c0001t0004g0080 a0001c0001t0005g0012 a0001c0001t0005g0032 others(1): Show |
10 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1570+362dupA | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169785062 | ||||||
| chr3:169785070 | A | AG | 36 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0034 others(33): Show |
115 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1570+373dupG | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169785070 | ||||||
| chr3:169785070 | A | AGG | 9 | a0001c0001t0002g0039 a0001c0001t0003g0024 a0001c0001t0003g0061 others(6): Show |
23 | HG00544.hp1 HG00597.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.1570+372_1570+373d others(4): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169785070 | ||||||
| chr3:169785071 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0005g0063 |
2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1570+363G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785071 | |||||||
| chr3:169785075 | G | C | 2 | a0001c0001t0001g0066 a0001c0001t0004g0081 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1570+367G>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785075 | |||||||
| chr3:169785079 | G | GT | 2 | a0001c0001t0002g0015 a0001c0001t0016g0015 |
5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1570+371_1570+372i others(3): Show |
MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785079 | |||||||
| chr3:169785079 | G | T | 1 | a0001c0001t0006g0093 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1570+371G>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785079 | |||||||
| chr3:169785280 | G | C | 4 | a0001c0001t0006g0036 a0001c0001t0006g0037 a0001c0001t0006g0092 others(1): Show |
6 | HG02451.hp2 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1570+572G>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785280 | |||||||
| chr3:169785428 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1570+720A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785428 | |||||||
| chr3:169785532 | A | G | 1 | a0001c0001t0004g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1570+824A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785532 | |||||||
| chr3:169785644 | C | T | 69 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0039 others(66): Show |
193 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.1571-772C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785644 | |||||||
| chr3:169785750 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1571-666G>A | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785750 | |||||||
| chr3:169785788 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0079 |
3 | HG01175.hp1 HG01952.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1571-628T>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785788 | |||||||
| chr3:169785906 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1571-510A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785906 | |||||||
| chr3:169785914 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1571-502A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169785914 | |||||||
| chr3:169786165 | A | G | 5 | a0001c0001t0005g0012 a0001c0001t0005g0032 a0001c0001t0005g0063 others(2): Show |
11 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1571-251A>G | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169786165 | |||||||
| chr3:169786188 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1571-228C>T | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169786188 | |||||||
| chr3:169786216 | G | C | 1 | a0001c0004t0006g0100 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1571-200G>C | MYNN | ENSG00000085274.16 | transcript | ENST00000349841.10 | protein_coding | 7/7 | chr3 | 169786216 |