Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4291 |
| ensemblid | ENSG00000178053.21 |
| hgncid | 7125 |
| symbol | MLF1 |
| name | myeloid leukemia factor 1 |
| refseq_nuc | NM_001369783.1 |
| refseq_prot | NP_001356712.1 |
| ensembl_nuc | ENST00000466246.7 |
| ensembl_prot | ENSP00000417278.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 158571194 |
| end | 158606456 |
| strand | + |
| ver | v1.2 |
| region | chr3:158571194-158606456 |
| region5000 | chr3:158566194-158611456 |
| regionname0 | MLF1_chr3_158571194_158606456 |
| regionname5000 | MLF1_chr3_158566194_158611456 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 283 | 235 | 58 | 47 | 91 | 11 | 26 | 68 | MLF1_chr3_158566194_158611456 | MLF1 | MFRML others(278): Show |
chr3 | 158566194 | 158611456 |
| a0002 | 0/0 | 283 | 129 | 18 | 19 | 73 | 7 | 12 | 58 | MLF1_chr3_158566194_158611456 | MLF1 | MFRML others(278): Show |
chr3 | 158566194 | 158611456 |
| a0003 | 0/0 | 283 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | MFRML others(278): Show |
chr3 | 158566194 | 158611456 |
| a0004 | 0/0 | 283 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | MFRML others(278): Show |
chr3 | 158566194 | 158611456 |
| a0005 | 0/0 | 283 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | MFRML others(278): Show |
chr3 | 158566194 | 158611456 |
| a0006 | 0/0 | 243 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | MFRML others(238): Show |
chr3 | 158566194 | 158611456 |
| a0007 | 0/0 | 283 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | MFRML others(278): Show |
chr3 | 158566194 | 158611456 |
| a0008 | 0/0 | 283 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | MFRML others(278): Show |
chr3 | 158566194 | 158611456 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 849 | 147 | 13 | 31 | 76 | 7 | 18 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 | ||
| a0001c0003 | 0/0 | 849 | 88 | 45 | 16 | 15 | 4 | 8 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 | ||
| a0002c0002 | 0/0 | 849 | 124 | 13 | 19 | 73 | 7 | 12 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 | ||
| a0002c0005 | 0/0 | 849 | 5 | 5 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 | ||
| a0003c0004 | 0/0 | 849 | 9 | 9 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 | ||
| a0004c0006 | 0/0 | 849 | 3 | 3 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 | ||
| a0005c0008 | 0/0 | 849 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 | ||
| a0006c0010 | 0/0 | 849 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 | ||
| a0007c0009 | 0/0 | 849 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 | ||
| a0008c0007 | 0/0 | 849 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | ATGTT others(844): Show |
chr3 | 158566194 | 158611456 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2213 | 132 | 11 | 22 | 75 | 7 | 15 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0001c0001t0006 | 0/0 | 2213 | 14 | 2 | 9 | 0 | 0 | 3 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0001c0001t0013 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0001c0003t0003 | 0/0 | 2213 | 67 | 26 | 14 | 15 | 4 | 8 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0001c0003t0004 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0001c0003t0005 | 0/0 | 2213 | 8 | 8 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0001c0003t0007 | 0/0 | 2213 | 7 | 7 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0001c0003t0008 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0001c0003t0010 | 0/0 | 2213 | 2 | 1 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0001c0003t0011 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0002c0002t0002 | 0/0 | 2213 | 71 | 4 | 10 | 44 | 4 | 9 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0002c0002t0004 | 0/0 | 2213 | 51 | 9 | 9 | 28 | 2 | 3 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0002c0002t0012 | 0/0 | 2213 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0002c0002t0014 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0002c0005t0002 | 0/0 | 2213 | 5 | 5 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0003c0004t0005 | 0/0 | 2213 | 9 | 9 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0004c0006t0004 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0004c0006t0009 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0005c0008t0002 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0006c0010t0001 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0007c0009t0002 | 0/0 | 2213 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| a0008c0007t0001 | 0/0 | 2213 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | GAGTG others(2208): Show |
chr3 | 158566194 | 158611456 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0004 | 0/0 | 6 | 1 | 0 | 4 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0007g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0007g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0010g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0010g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0001c0003t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0003 | 0/0 | 7 | 0 | 0 | 6 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0005 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0012g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0002t0014g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0005t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0005t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0005t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0002c0005t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0003c0004t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0003c0004t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0003c0004t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0003c0004t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0003c0004t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0003c0004t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0003c0004t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0003c0004t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0003c0004t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0004c0006t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0004c0006t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0004c0006t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0005c0008t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0006c0010t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0007c0009t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| a0008c0007t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0216 | EUR | GBR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0011 | EUR | GBR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0003 | EUR | FIN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00280 | hp2 | a0002 | c0002 | t0004 | g0060 | EUR | FIN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00323 | hp1 | a0001 | c0003 | t0003 | g0304 | EUR | FIN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00597 | hp2 | a0001 | c0003 | t0003 | g0267 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00609 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00642 | hp1 | a0001 | c0003 | t0003 | g0290 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00735 | hp1 | a0001 | c0003 | t0003 | g0250 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0023 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00738 | hp1 | a0001 | c0003 | t0003 | g0249 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0165 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0031 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01069 | hp2 | a0002 | c0002 | t0004 | g0308 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0031 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01071 | hp2 | a0002 | c0002 | t0004 | g0055 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01074 | hp1 | a0002 | c0002 | t0004 | g0007 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01081 | hp1 | a0002 | c0002 | t0004 | g0058 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01099 | hp2 | a0001 | c0003 | t0003 | g0268 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01106 | hp1 | a0002 | c0002 | t0004 | g0054 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0293 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0209 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01168 | hp1 | a0002 | c0002 | t0004 | g0064 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01175 | hp2 | a0001 | c0003 | t0003 | g0247 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0259 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01243 | hp2 | a0001 | c0003 | t0010 | g0271 | AMR | PUR | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0220 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01255 | hp2 | a0002 | c0002 | t0004 | g0018 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01257 | hp1 | a0002 | c0002 | t0004 | g0047 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0036 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0128 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01361 | hp2 | a0001 | c0003 | t0004 | g0048 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0264 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01515 | hp2 | a0002 | c0002 | t0012 | g0019 | EUR | IBS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01516 | hp1 | a0002 | c0002 | t0004 | g0065 | EUR | IBS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0292 | EUR | IBS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01517 | hp1 | a0001 | c0003 | t0003 | g0035 | EUR | IBS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01884 | hp1 | a0001 | c0003 | t0005 | g0254 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01891 | hp1 | a0001 | c0003 | t0005 | g0236 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01891 | hp2 | a0003 | c0004 | t0005 | g0231 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0012 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01981 | hp1 | a0001 | c0003 | t0003 | g0012 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01993 | hp1 | a0001 | c0001 | t0006 | g0092 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01993 | hp2 | a0001 | c0003 | t0003 | g0012 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0295 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02027 | hp1 | a0002 | c0002 | t0004 | g0043 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0126 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02055 | hp2 | a0001 | c0003 | t0005 | g0237 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02056 | hp2 | a0002 | c0002 | t0004 | g0075 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02074 | hp1 | a0005 | c0008 | t0002 | g0198 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02074 | hp2 | a0006 | c0010 | t0001 | g0091 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02129 | hp2 | a0002 | c0002 | t0004 | g0020 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02135 | hp2 | a0002 | c0002 | t0004 | g0076 | EAS | KHV | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02145 | hp2 | a0003 | c0004 | t0005 | g0239 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02257 | hp1 | a0001 | c0003 | t0007 | g0245 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02257 | hp2 | a0001 | c0003 | t0003 | g0253 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0242 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0261 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0270 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02280 | hp1 | a0003 | c0004 | t0005 | g0232 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0282 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02300 | hp1 | a0002 | c0002 | t0004 | g0019 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02451 | hp1 | a0002 | c0002 | t0004 | g0015 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02451 | hp2 | a0001 | c0003 | t0003 | g0285 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02572 | hp1 | a0001 | c0003 | t0003 | g0257 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02572 | hp2 | a0002 | c0002 | t0004 | g0052 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0248 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0255 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0279 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02622 | hp1 | a0001 | c0003 | t0005 | g0235 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02630 | hp1 | a0001 | c0003 | t0007 | g0244 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02630 | hp2 | a0001 | c0003 | t0003 | g0274 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02647 | hp1 | a0001 | c0003 | t0003 | g0251 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02647 | hp2 | a0001 | c0003 | t0010 | g0306 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02683 | hp1 | a0001 | c0003 | t0003 | g0294 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02698 | hp2 | a0001 | c0003 | t0003 | g0305 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02723 | hp1 | a0002 | c0002 | t0004 | g0018 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02723 | hp2 | a0001 | c0003 | t0003 | g0287 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0298 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0095 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02738 | hp2 | a0007 | c0009 | t0002 | g0204 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02809 | hp1 | a0003 | c0004 | t0005 | g0243 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0263 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0252 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02886 | hp1 | a0003 | c0004 | t0005 | g0234 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02886 | hp2 | a0001 | c0003 | t0005 | g0256 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02895 | hp1 | a0001 | c0003 | t0007 | g0277 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02895 | hp2 | a0004 | c0006 | t0009 | g0072 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02896 | hp2 | a0002 | c0002 | t0004 | g0059 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02897 | hp1 | a0002 | c0002 | t0004 | g0057 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02897 | hp2 | a0001 | c0003 | t0007 | g0303 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02965 | hp1 | a0002 | c0005 | t0002 | g0069 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0283 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02970 | hp1 | a0001 | c0003 | t0007 | g0014 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0302 | AFR | GWD | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03098 | hp1 | a0002 | c0002 | t0004 | g0015 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03098 | hp2 | a0001 | c0003 | t0008 | g0038 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03130 | hp1 | a0004 | c0006 | t0009 | g0073 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03130 | hp2 | a0001 | c0003 | t0007 | g0014 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0163 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0286 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03195 | hp1 | a0001 | c0003 | t0011 | g0229 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0301 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03209 | hp1 | a0001 | c0003 | t0005 | g0273 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0262 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03225 | hp1 | a0002 | c0002 | t0004 | g0041 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03225 | hp2 | a0002 | c0002 | t0004 | g0051 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0023 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03453 | hp1 | a0002 | c0005 | t0002 | g0017 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03453 | hp2 | a0001 | c0003 | t0003 | g0284 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03486 | hp1 | a0004 | c0006 | t0004 | g0074 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03486 | hp2 | a0001 | c0003 | t0008 | g0039 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0203 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0162 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03491 | hp1 | a0002 | c0002 | t0004 | g0049 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0205 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03516 | hp1 | a0003 | c0004 | t0005 | g0233 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03516 | hp2 | a0002 | c0005 | t0002 | g0063 | AFR | ESN | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0276 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0278 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03654 | hp1 | a0001 | c0003 | t0003 | g0265 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0195 | SAS | STU | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03688 | hp2 | a0001 | c0003 | t0003 | g0258 | SAS | STU | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0223 | SAS | PJL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | BEB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03831 | hp2 | a0002 | c0002 | t0004 | g0077 | SAS | BEB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03942 | hp1 | a0002 | c0002 | t0004 | g0056 | SAS | BEB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | BEB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG04184 | hp2 | a0008 | c0007 | t0001 | g0186 | SAS | BEB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG04199 | hp1 | a0001 | c0003 | t0003 | g0309 | SAS | STU | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0206 | SAS | STU | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | STU | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | CHB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0213 | AFR | YRI | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18906 | hp2 | a0003 | c0004 | t0005 | g0240 | AFR | YRI | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18944 | hp1 | a0001 | c0003 | t0003 | g0291 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18951 | hp1 | a0002 | c0002 | t0004 | g0067 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18951 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18953 | hp2 | a0001 | c0003 | t0003 | g0296 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18954 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18954 | hp2 | a0002 | c0002 | t0004 | g0182 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18956 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18964 | hp1 | a0001 | c0003 | t0003 | g0037 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18965 | hp2 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18966 | hp2 | a0002 | c0002 | t0004 | g0066 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18969 | hp1 | a0001 | c0003 | t0003 | g0299 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18970 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18971 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18972 | hp1 | a0002 | c0002 | t0014 | g0045 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18974 | hp2 | a0002 | c0002 | t0004 | g0061 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18977 | hp2 | a0002 | c0002 | t0004 | g0050 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0046 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18987 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18989 | hp2 | a0002 | c0002 | t0004 | g0068 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0269 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18991 | hp1 | a0001 | c0003 | t0003 | g0297 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18992 | hp2 | a0001 | c0003 | t0003 | g0035 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18999 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19003 | hp1 | a0002 | c0002 | t0004 | g0044 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19004 | hp2 | a0001 | c0003 | t0003 | g0266 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19007 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19043 | hp1 | a0001 | c0003 | t0007 | g0014 | AFR | LWK | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19043 | hp2 | a0001 | c0003 | t0003 | g0275 | AFR | LWK | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19054 | hp2 | a0001 | c0003 | t0003 | g0300 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19055 | hp2 | a0002 | c0002 | t0004 | g0071 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19056 | hp2 | a0002 | c0002 | t0004 | g0079 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19058 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19062 | hp2 | a0001 | c0003 | t0003 | g0288 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19063 | hp2 | a0001 | c0003 | t0003 | g0037 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19064 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19070 | hp2 | a0002 | c0002 | t0004 | g0020 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19077 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19080 | hp2 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19088 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19090 | hp2 | a0002 | c0002 | t0004 | g0070 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19240 | hp1 | a0003 | c0004 | t0005 | g0230 | AFR | YRI | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA19240 | hp2 | a0001 | c0003 | t0003 | g0280 | AFR | YRI | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0272 | AFR | ASW | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20752 | hp1 | a0001 | c0003 | t0003 | g0289 | EUR | TSI | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0210 | EUR | TSI | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20905 | hp2 | a0001 | c0003 | t0003 | g0036 | SAS | GIH | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02109 | hp2 | a0003 | c0004 | t0005 | g0241 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02486 | hp1 | a0002 | c0005 | t0002 | g0062 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0246 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0030 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG02559 | hp2 | a0002 | c0005 | t0002 | g0017 | AFR | ACB | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03471 | hp1 | a0002 | c0002 | t0004 | g0053 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG03471 | hp2 | a0001 | c0003 | t0005 | g0238 | AFR | MSL | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0224 | AFR | USA | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| HG06807 | hp2 | a0001 | c0003 | t0003 | g0260 | AFR | USA | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18955 | hp1 | a0002 | c0002 | t0004 | g0078 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0212 | AFR | USA | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0281 | AFR | LWK | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0117 | REF | REF | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0149 | REF | REF | MLF1_chr3_158566194_158611456 | MLF1 | chr3 | 158566194 | 158611456 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158596900 | G | A | 1 | a0004 | 3 | HG02895.hp2 HG03130.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.279G>A | p.Met93Ile | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/8 | 386/2213 | 279/852 | 93/283 | chr3 | 158596900 | |||
| chr3:158600032 | G | A | 1 | a0003 | 9 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
missense_variant | MODERATE | c.472G>A | p.Ala158Thr | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/8 | 579/2213 | 472/852 | 158/283 | chr3 | 158600032 | |||
| chr3:158600036 | T | C | 1 | a0008 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.476T>C | p.Met159Thr | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/8 | 583/2213 | 476/852 | 159/283 | chr3 | 158600036 | |||
| chr3:158602809 | G | A | 1 | a0005 | 1 | HG02074.hp1 | missense_variant&splice_region_variant | MODERATE | c.616G>A | p.Asp206Asn | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/8 | 723/2213 | 616/852 | 206/283 | chr3 | 158602809 | |||
| chr3:158602914 | C | A | 4 | a0002 a0004 a0005 others(1): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
missense_variant | MODERATE | c.721C>A | p.Pro241Thr | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/8 | 828/2213 | 721/852 | 241/283 | chr3 | 158602914 | |||
| chr3:158602921 | C | T | 1 | a0007 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.728C>T | p.Ser243Phe | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/8 | 835/2213 | 728/852 | 243/283 | chr3 | 158602921 | |||
| chr3:158602923 | C | T | 1 | a0006 | 1 | HG02074.hp2 | stop_gained | HIGH | c.730C>T | p.Arg244* | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/8 | 837/2213 | 730/852 | 244/283 | chr3 | 158602923 | |||
| chr3:158605145 | T | A | 1 | a0004 | 3 | HG02895.hp2 HG03130.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.795T>A | p.Asn265Lys | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 8/8 | 902/2213 | 795/852 | 265/283 | chr3 | 158605145 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158600160 | C | T | 1 | a0002c0005 | 5 | HG02486.hp1 HG02559.hp2 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.600C>T | p.Ile200Ile | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/8 | 707/2213 | 600/852 | 200/283 | chr3 | 158600160 | |||
| chr3:158602808 | T | C | 7 | a0001c0003 a0002c0002 a0002c0005 others(4): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
splice_region_variant&synonymous_variant | LOW | c.615T>C | p.Ser205Ser | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/8 | 722/2213 | 615/852 | 205/283 | chr3 | 158602808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158571220 | C | G | 1 | a0001c0003t0010 | 2 | HG01243.hp2 HG02647.hp2 |
5_prime_UTR_variant | MODIFIER | c.-81C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/8 | 81 | chr3 | 158571220 | ||||||
| chr3:158571246 | T | A | 3 | a0001c0003t0003 a0001c0003t0007 a0001c0003t0008 |
76 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(73): Show |
5_prime_UTR_variant | MODIFIER | c.-55T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/8 | 55 | chr3 | 158571246 | ||||||
| chr3:158571249 | A | G | 1 | a0001c0003t0007 | 7 | HG02257.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-52A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/8 | 52 | chr3 | 158571249 | ||||||
| chr3:158571279 | C | A | 1 | a0004c0006t0009 | 2 | HG02895.hp2 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-22C>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/8 | 22 | chr3 | 158571279 | ||||||
| chr3:158605207 | C | T | 1 | a0002c0002t0014 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 8/8 | 5 | chr3 | 158605207 | ||||||
| chr3:158605284 | C | G | 1 | a0001c0001t0013 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 8/8 | 82 | chr3 | 158605284 | ||||||
| chr3:158605423 | G | A | 17 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0005 others(14): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*221G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 8/8 | 221 | chr3 | 158605423 | ||||||
| chr3:158605843 | A | C | 1 | a0002c0002t0012 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*641A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 8/8 | 641 | chr3 | 158605843 | ||||||
| chr3:158605876 | A | G | 10 | a0001c0003t0004 a0002c0002t0002 a0002c0002t0004 others(7): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*674A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 8/8 | 674 | chr3 | 158605876 | ||||||
| chr3:158605927 | T | A | 4 | a0002c0002t0002 a0002c0005t0002 a0005c0008t0002 others(1): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*725T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 8/8 | 725 | chr3 | 158605927 | ||||||
| chr3:158606234 | A | G | 1 | a0001c0001t0006 | 14 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1032A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 8/8 | 1032 | chr3 | 158606234 | ||||||
| chr3:158606261 | T | G | 2 | a0001c0003t0008 a0001c0003t0011 |
3 | HG03098.hp2 HG03195.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1059T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 8/8 | 1059 | chr3 | 158606261 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158571563 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.47+216A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158571563 | |||||||
| chr3:158571615 | G | T | 1 | a0001c0003t0003g0309 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.47+268G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158571615 | |||||||
| chr3:158571701 | A | G | 1 | a0002c0002t0004g0308 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.47+354A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158571701 | |||||||
| chr3:158571782 | C | A | 2 | a0001c0003t0008g0038 a0001c0003t0008g0039 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.47+435C>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158571782 | |||||||
| chr3:158571782 | C | CGTGAGGT others(71): Show |
1 | a0001c0001t0001g0307 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.47+512_47+513insTG others(76): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158571782 | ||||||
| chr3:158571782 | CGTGAGGT others(19): Show |
C | 1 | a0001c0001t0001g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.47+461_47+486delTG others(24): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158571782 | ||||||
| chr3:158571808 | TGTGAGGT others(19): Show |
T | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.47+522_47+547delAG others(24): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158571808 | ||||||
| chr3:158571845 | G | A | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.47+498G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158571845 | |||||||
| chr3:158571919 | T | G | 1 | a0002c0002t0002g0042 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.47+572T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158571919 | |||||||
| chr3:158571961 | G | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | NA18946.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.47+614G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158571961 | |||||||
| chr3:158572002 | TG | T | 11 | a0001c0003t0004g0048 a0002c0002t0004g0007 a0002c0002t0004g0043 others(8): Show |
13 | HG01074.hp1 HG01257.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.47+657delG | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158572002 | ||||||
| chr3:158572013 | G | T | 2 | a0002c0002t0004g0051 a0002c0002t0004g0052 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.47+666G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572013 | |||||||
| chr3:158572081 | G | A | 49 | a0001c0003t0004g0048 a0002c0002t0004g0006 a0002c0002t0004g0007 others(46): Show |
61 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.47+734G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572081 | |||||||
| chr3:158572137 | G | T | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.47+790G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572137 | |||||||
| chr3:158572242 | G | A | 1 | a0002c0002t0002g0080 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.47+895G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572242 | |||||||
| chr3:158572341 | G | GTTGAGGG others(46): Show |
1 | a0002c0002t0002g0226 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.47+1003_47+1055dup others(53): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158572341 | ||||||
| chr3:158572355 | TTGG | T | 15 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(12): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.47+1012_47+1014del others(3): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158572355 | ||||||
| chr3:158572430 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.47+1083G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572430 | |||||||
| chr3:158572439 | C | G | 193 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0184 others(190): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.47+1092C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572439 | |||||||
| chr3:158572488 | G | A | 1 | a0001c0003t0011g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.47+1141G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572488 | |||||||
| chr3:158572516 | G | A | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.47+1169G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572516 | |||||||
| chr3:158572563 | C | T | 184 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(181): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.47+1216C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572563 | |||||||
| chr3:158572597 | G | A | 2 | a0003c0004t0005g0230 a0003c0004t0005g0231 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.47+1250G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572597 | |||||||
| chr3:158572609 | G | A | 1 | a0002c0002t0004g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.47+1262G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572609 | |||||||
| chr3:158572640 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG00323.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.47+1293G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572640 | |||||||
| chr3:158572714 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+1367A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572714 | |||||||
| chr3:158572724 | G | T | 1 | a0002c0002t0002g0225 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.47+1377G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572724 | |||||||
| chr3:158572732 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+1385A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572732 | |||||||
| chr3:158572737 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+1390T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572737 | |||||||
| chr3:158572752 | G | C | 1 | a0001c0001t0001g0183 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+1405G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572752 | |||||||
| chr3:158572753 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+1406A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572753 | |||||||
| chr3:158572754 | C | G | 1 | a0001c0001t0001g0183 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+1407C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572754 | |||||||
| chr3:158572763 | G | A | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.47+1416G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572763 | |||||||
| chr3:158572776 | A | G | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.47+1429A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572776 | |||||||
| chr3:158572805 | G | A | 1 | a0002c0002t0002g0011 | 3 | HG00140.hp2 HG01261.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.47+1458G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572805 | |||||||
| chr3:158572817 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+1470A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572817 | |||||||
| chr3:158572818 | T | G | 184 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(181): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.47+1471T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572818 | |||||||
| chr3:158572849 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.47+1502C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572849 | |||||||
| chr3:158572858 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.47+1511G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572858 | |||||||
| chr3:158572926 | C | T | 6 | a0002c0002t0004g0020 a0002c0002t0004g0075 a0002c0002t0004g0076 others(3): Show |
7 | HG02056.hp2 HG02129.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+1579C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572926 | |||||||
| chr3:158572928 | T | C | 184 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(181): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.47+1581T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572928 | |||||||
| chr3:158572940 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.47+1593G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572940 | |||||||
| chr3:158572944 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+1597T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158572944 | |||||||
| chr3:158573038 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.47+1691T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573038 | |||||||
| chr3:158573078 | GAATATTT others(35): Show |
G | 2 | a0001c0003t0007g0244 a0001c0003t0007g0245 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.47+1745_47+1786del others(42): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158573078 | ||||||
| chr3:158573266 | T | G | 184 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(181): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.47+1919T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573266 | |||||||
| chr3:158573373 | C | CG | 15 | a0001c0001t0001g0024 a0001c0001t0001g0088 a0001c0001t0001g0129 others(12): Show |
16 | HG00741.hp1 HG01192.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.47+2032dupG | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158573373 | ||||||
| chr3:158573377 | G | A | 1 | a0002c0002t0004g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.47+2030G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573377 | |||||||
| chr3:158573378 | G | T | 3 | a0004c0006t0004g0074 a0004c0006t0009g0072 a0004c0006t0009g0073 |
3 | HG02895.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.47+2031G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573378 | |||||||
| chr3:158573380 | A | G | 2 | a0001c0001t0001g0180 a0002c0002t0004g0079 |
2 | NA19056.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.47+2033A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573380 | |||||||
| chr3:158573401 | C | CG | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(93): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.47+2067dupG | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158573401 | ||||||
| chr3:158573401 | C | CGG | 21 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(18): Show |
22 | HG00408.hp1 HG00609.hp2 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.47+2066_47+2067dup others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158573401 | ||||||
| chr3:158573401 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.47+2054C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573401 | |||||||
| chr3:158573401 | CG | C | 61 | a0001c0001t0001g0040 a0001c0001t0001g0173 a0001c0001t0001g0174 others(58): Show |
72 | HG00642.hp1 HG01074.hp1 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.47+2067delG | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158573401 | ||||||
| chr3:158573401 | CGG | C | 16 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0003t0003g0302 others(13): Show |
20 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.47+2066_47+2067del others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158573401 | ||||||
| chr3:158573405 | G | C | 2 | a0004c0006t0009g0072 a0004c0006t0009g0073 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.47+2058G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573405 | |||||||
| chr3:158573408 | G | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.47+2061G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573408 | |||||||
| chr3:158573627 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.47+2280G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573627 | |||||||
| chr3:158573711 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.47+2364G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573711 | |||||||
| chr3:158573810 | TG | T | 97 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(94): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.47+2464delG | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573810 | |||||||
| chr3:158573835 | C | T | 1 | a0001c0003t0003g0301 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.47+2488C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158573835 | |||||||
| chr3:158574298 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.47+2951G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574298 | |||||||
| chr3:158574361 | G | A | 71 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(68): Show |
80 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.47+3014G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574361 | |||||||
| chr3:158574406 | G | A | 1 | a0001c0003t0003g0250 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.47+3059G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574406 | |||||||
| chr3:158574505 | T | TA | 15 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0098 others(12): Show |
17 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.47+3180dupA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574505 | ||||||
| chr3:158574505 | T | TAA | 42 | a0001c0001t0001g0097 a0001c0001t0001g0143 a0001c0001t0001g0189 others(39): Show |
51 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.47+3179_47+3180dup others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574505 | ||||||
| chr3:158574505 | T | TAAA | 4 | a0002c0002t0004g0015 a0002c0002t0004g0018 a0002c0002t0004g0043 others(1): Show |
6 | HG01255.hp2 HG02027.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.47+3178_47+3180dup others(3): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574505 | ||||||
| chr3:158574505 | T | TAAAAAAA others(3): Show |
1 | a0001c0003t0010g0271 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.47+3171_47+3180dup others(10): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574505 | ||||||
| chr3:158574505 | T | TAAAAAAA others(4): Show |
2 | a0001c0003t0005g0238 a0001c0003t0011g0229 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.47+3170_47+3180dup others(11): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574505 | ||||||
| chr3:158574505 | T | TAAAAAAA others(5): Show |
2 | a0001c0003t0005g0236 a0001c0003t0005g0237 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.47+3169_47+3180dup others(12): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574505 | ||||||
| chr3:158574505 | T | TAAAAAAA others(6): Show |
1 | a0001c0003t0005g0235 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.47+3168_47+3180dup others(13): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574505 | ||||||
| chr3:158574505 | TAAAA | T | 48 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0005 others(45): Show |
74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.47+3177_47+3180del others(4): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574505 | ||||||
| chr3:158574516 | A | AAAAAAAC | 31 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(28): Show |
38 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.47+3175_47+3176ins others(7): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574516 | ||||||
| chr3:158574523 | A | AAAAAAAC | 20 | a0001c0003t0003g0246 a0001c0003t0003g0247 a0001c0003t0003g0251 others(17): Show |
22 | HG01175.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.47+3180_47+3181ins others(7): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574523 | ||||||
| chr3:158574523 | A | ACAAAAAC | 15 | a0001c0003t0003g0259 a0001c0003t0003g0260 a0001c0003t0003g0261 others(12): Show |
15 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.47+3176_47+3177ins others(7): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574523 | |||||||
| chr3:158574523 | A | C | 31 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(28): Show |
38 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.47+3176A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574523 | |||||||
| chr3:158574528 | T | A | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.47+3181T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574528 | |||||||
| chr3:158574530 | C | A | 3 | a0001c0003t0010g0271 a0001c0003t0010g0306 a0003c0004t0005g0232 |
3 | HG01243.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.47+3183C>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574530 | |||||||
| chr3:158574589 | C | T | 1 | a0001c0003t0003g0287 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.47+3242C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574589 | |||||||
| chr3:158574613 | G | A | 2 | a0002c0002t0004g0054 a0002c0002t0004g0064 |
2 | HG01106.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.47+3266G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574613 | |||||||
| chr3:158574684 | C | CA | 11 | a0001c0001t0001g0098 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG01358.hp2 HG02027.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.47+3355dupA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574684 | ||||||
| chr3:158574684 | CA | C | 81 | a0001c0001t0001g0028 a0001c0001t0001g0171 a0001c0001t0001g0172 others(78): Show |
89 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.47+3355delA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574684 | ||||||
| chr3:158574684 | CAA | C | 104 | a0001c0003t0003g0270 a0001c0003t0003g0276 a0001c0003t0003g0285 others(101): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.47+3354_47+3355del others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158574684 | ||||||
| chr3:158574738 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.47+3391C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574738 | |||||||
| chr3:158574769 | C | G | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.47+3422C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574769 | |||||||
| chr3:158574858 | G | T | 1 | a0001c0003t0003g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.47+3511G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158574858 | |||||||
| chr3:158575060 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.47+3713G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575060 | |||||||
| chr3:158575080 | AAC | A | 17 | a0002c0002t0004g0006 a0002c0002t0004g0008 a0002c0002t0004g0016 others(14): Show |
24 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.47+3735_47+3736del others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158575080 | ||||||
| chr3:158575194 | A | T | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.47+3847A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575194 | |||||||
| chr3:158575252 | C | T | 4 | a0001c0003t0003g0278 a0001c0003t0003g0302 a0001c0003t0008g0038 others(1): Show |
4 | HG03041.hp2 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+3905C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575252 | |||||||
| chr3:158575313 | A | G | 1 | a0001c0001t0006g0025 | 2 | HG00639.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.47+3966A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575313 | |||||||
| chr3:158575329 | A | G | 4 | a0001c0003t0003g0261 a0001c0003t0003g0262 a0001c0003t0003g0263 others(1): Show |
4 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+3982A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575329 | |||||||
| chr3:158575365 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.47+4018A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575365 | |||||||
| chr3:158575366 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.47+4019T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575366 | |||||||
| chr3:158575367 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.47+4020A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575367 | |||||||
| chr3:158575469 | G | A | 195 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0184 others(192): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.47+4122G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575469 | |||||||
| chr3:158575649 | T | C | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0146 others(1): Show |
4 | HG02015.hp2 NA18988.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+4302T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575649 | |||||||
| chr3:158575835 | G | C | 195 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0184 others(192): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.47+4488G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575835 | |||||||
| chr3:158575865 | A | G | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.47+4518A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158575865 | |||||||
| chr3:158576010 | G | T | 9 | a0003c0004t0005g0230 a0003c0004t0005g0231 a0003c0004t0005g0232 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.47+4663G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576010 | |||||||
| chr3:158576104 | T | G | 52 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0005 others(49): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.47+4757T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576104 | |||||||
| chr3:158576358 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18964.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.47+5011C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576358 | |||||||
| chr3:158576506 | G | A | 71 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(68): Show |
80 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.47+5159G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576506 | |||||||
| chr3:158576529 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0146 others(1): Show |
4 | HG02015.hp2 NA18988.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+5182C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576529 | |||||||
| chr3:158576577 | C | T | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.47+5230C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576577 | |||||||
| chr3:158576665 | A | T | 14 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(11): Show |
14 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.47+5318A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576665 | |||||||
| chr3:158576671 | A | AT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
124 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.47+5343dupT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158576671 | ||||||
| chr3:158576671 | A | ATT | 7 | a0001c0001t0001g0107 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG00597.hp1 HG02145.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+5342_47+5343dup others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158576671 | ||||||
| chr3:158576671 | AT | A | 111 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(108): Show |
131 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.47+5343delT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158576671 | ||||||
| chr3:158576687 | T | G | 1 | a0002c0002t0004g0044 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.47+5340T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576687 | |||||||
| chr3:158576834 | G | A | 1 | a0001c0003t0003g0288 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.47+5487G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576834 | |||||||
| chr3:158576900 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.47+5553C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576900 | |||||||
| chr3:158576954 | A | C | 4 | a0003c0004t0005g0230 a0003c0004t0005g0231 a0003c0004t0005g0233 others(1): Show |
4 | HG01891.hp2 HG02886.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+5607A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158576954 | |||||||
| chr3:158577091 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.47+5744G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577091 | |||||||
| chr3:158577135 | A | T | 2 | a0002c0002t0002g0212 a0002c0002t0002g0213 |
2 | NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.47+5788A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577135 | |||||||
| chr3:158577214 | T | G | 1 | a0001c0001t0001g0152 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.47+5867T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577214 | |||||||
| chr3:158577247 | A | T | 1 | a0001c0003t0010g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.47+5900A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577247 | |||||||
| chr3:158577381 | C | T | 186 | a0001c0001t0001g0184 a0001c0003t0003g0012 a0001c0003t0003g0013 others(183): Show |
232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.47+6034C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577381 | |||||||
| chr3:158577382 | T | C | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.47+6035T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577382 | |||||||
| chr3:158577491 | T | G | 195 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0184 others(192): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.47+6144T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577491 | |||||||
| chr3:158577582 | A | G | 14 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(11): Show |
14 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.47+6235A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577582 | |||||||
| chr3:158577891 | A | G | 1 | a0001c0003t0003g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.47+6544A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577891 | |||||||
| chr3:158577986 | T | A | 1 | a0001c0003t0003g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.47+6639T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158577986 | |||||||
| chr3:158578013 | G | A | 1 | a0001c0003t0003g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.47+6666G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158578013 | |||||||
| chr3:158578380 | A | AGT | 6 | a0001c0001t0001g0135 a0002c0002t0004g0041 a0002c0005t0002g0017 others(3): Show |
7 | HG00558.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+7054_47+7055dup others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158578380 | ||||||
| chr3:158578380 | A | AGTGT | 6 | a0001c0003t0003g0261 a0001c0003t0003g0262 a0001c0003t0003g0263 others(3): Show |
6 | HG02258.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+7052_47+7055dup others(4): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158578380 | ||||||
| chr3:158578380 | A | AGTGTGT | 8 | a0001c0003t0003g0289 a0001c0003t0003g0309 a0001c0003t0005g0235 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.47+7050_47+7055dup others(6): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158578380 | ||||||
| chr3:158578380 | A | AGTGTGTG others(1): Show |
27 | a0001c0003t0003g0246 a0001c0003t0003g0247 a0001c0003t0003g0251 others(24): Show |
27 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.47+7048_47+7055dup others(8): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158578380 | ||||||
| chr3:158578380 | A | AGTGTGTG others(3): Show |
38 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(35): Show |
45 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.47+7046_47+7055dup others(10): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158578380 | ||||||
| chr3:158578380 | A | AGTGTGTG others(5): Show |
7 | a0001c0003t0003g0275 a0001c0003t0005g0242 a0001c0003t0007g0014 others(4): Show |
9 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+7044_47+7055dup others(12): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158578380 | ||||||
| chr3:158578380 | A | AGTGTGTG others(7): Show |
1 | a0001c0003t0003g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.47+7042_47+7055dup others(14): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158578380 | ||||||
| chr3:158578467 | T | C | 9 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0086 others(6): Show |
11 | HG00597.hp1 HG02040.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+7120T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158578467 | |||||||
| chr3:158578505 | A | AAC | 5 | a0002c0002t0002g0201 a0002c0002t0004g0041 a0002c0002t0004g0068 others(2): Show |
5 | HG02895.hp2 HG03225.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.47+7181_47+7182dup others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158578505 | ||||||
| chr3:158578505 | A | C | 1 | a0001c0003t0010g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.47+7158A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158578505 | |||||||
| chr3:158578505 | AACAC | A | 13 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.47+7179_47+7182del others(4): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158578505 | ||||||
| chr3:158578530 | G | A | 2 | a0001c0003t0003g0258 a0001c0003t0003g0309 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.47+7183G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158578530 | |||||||
| chr3:158578634 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.47+7287C>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158578634 | |||||||
| chr3:158578855 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0024 others(22): Show |
33 | HG00609.hp2 HG00621.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.47+7508A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158578855 | |||||||
| chr3:158579034 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0138 |
2 | NA18947.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.47+7687C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579034 | |||||||
| chr3:158579055 | A | G | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.47+7708A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579055 | |||||||
| chr3:158579127 | C | T | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.47+7780C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579127 | |||||||
| chr3:158579225 | T | A | 1 | a0002c0002t0002g0196 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.47+7878T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579225 | |||||||
| chr3:158579286 | A | AT | 97 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(94): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.47+7946dupT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158579286 | ||||||
| chr3:158579356 | G | C | 2 | a0002c0002t0002g0222 a0002c0002t0002g0223 |
2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.47+8009G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579356 | |||||||
| chr3:158579471 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.47+8124T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579471 | |||||||
| chr3:158579510 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(298): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.47+8163G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579510 | |||||||
| chr3:158579587 | A | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02027.hp2 HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.47+8240A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579587 | |||||||
| chr3:158579638 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.47+8291T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579638 | |||||||
| chr3:158579648 | A | G | 14 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0033 others(11): Show |
27 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.47+8301A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579648 | |||||||
| chr3:158579844 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.47+8497C>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158579844 | |||||||
| chr3:158580019 | T | C | 2 | a0001c0003t0003g0279 a0001c0003t0003g0285 |
2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.47+8672T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580019 | |||||||
| chr3:158580079 | G | A | 1 | a0002c0002t0004g0055 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.47+8732G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580079 | |||||||
| chr3:158580129 | A | T | 2 | a0002c0002t0004g0054 a0002c0002t0004g0064 |
2 | HG01106.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.47+8782A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580129 | |||||||
| chr3:158580151 | T | G | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.47+8804T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580151 | |||||||
| chr3:158580216 | C | G | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.47+8869C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580216 | |||||||
| chr3:158580290 | TA | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0142 others(4): Show |
7 | HG02896.hp2 HG03239.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+8955delA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158580290 | ||||||
| chr3:158580342 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0310 |
2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.47+8995C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580342 | |||||||
| chr3:158580459 | C | T | 1 | a0002c0002t0002g0032 | 2 | HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.47+9112C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580459 | |||||||
| chr3:158580489 | A | T | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.47+9142A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580489 | |||||||
| chr3:158580531 | A | G | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.47+9184A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580531 | |||||||
| chr3:158580622 | T | G | 52 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0005 others(49): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.47+9275T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580622 | |||||||
| chr3:158580643 | A | G | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.47+9296A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580643 | |||||||
| chr3:158580745 | C | T | 5 | a0001c0003t0003g0246 a0001c0003t0003g0247 a0001c0003t0003g0252 others(2): Show |
5 | HG01175.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+9398C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580745 | |||||||
| chr3:158580773 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.47+9426T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580773 | |||||||
| chr3:158580787 | G | GA | 74 | a0001c0001t0001g0110 a0001c0001t0001g0180 a0001c0003t0003g0012 others(71): Show |
83 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.47+9457dupA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158580787 | ||||||
| chr3:158580787 | GA | G | 98 | a0001c0001t0001g0104 a0001c0001t0001g0143 a0001c0001t0001g0166 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.47+9457delA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158580787 | ||||||
| chr3:158580816 | T | TG | 52 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0005 others(49): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.47+9471dupG | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158580816 | ||||||
| chr3:158580826 | C | T | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.47+9479C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580826 | |||||||
| chr3:158580914 | T | C | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.47+9567T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580914 | |||||||
| chr3:158580988 | T | C | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.47+9641T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580988 | |||||||
| chr3:158580990 | C | G | 1 | a0001c0003t0003g0269 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.47+9643C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158580990 | |||||||
| chr3:158581094 | G | C | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.47+9747G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158581094 | |||||||
| chr3:158581238 | GTCCCCCA others(3): Show |
G | 1 | a0002c0002t0004g0049 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.47+9893_47+9902del others(10): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158581238 | ||||||
| chr3:158581298 | T | C | 1 | a0001c0003t0003g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.47+9951T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158581298 | |||||||
| chr3:158581471 | T | G | 6 | a0001c0003t0003g0251 a0001c0003t0003g0255 a0001c0003t0003g0272 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.47+10124T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158581471 | |||||||
| chr3:158581612 | C | G | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.47+10265C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158581612 | |||||||
| chr3:158581656 | C | G | 3 | a0004c0006t0004g0074 a0004c0006t0009g0072 a0004c0006t0009g0073 |
3 | HG02895.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.47+10309C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158581656 | |||||||
| chr3:158581719 | C | T | 13 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.47+10372C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158581719 | |||||||
| chr3:158581766 | T | A | 42 | a0001c0003t0004g0048 a0002c0002t0004g0006 a0002c0002t0004g0007 others(39): Show |
53 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.47+10419T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158581766 | |||||||
| chr3:158581962 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0146 others(1): Show |
4 | HG02015.hp2 NA18988.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-10472C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158581962 | |||||||
| chr3:158581985 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.48-10449G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158581985 | |||||||
| chr3:158582289 | C | T | 14 | a0001c0001t0001g0129 a0001c0001t0001g0161 a0001c0001t0001g0164 others(11): Show |
17 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.48-10145C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158582289 | |||||||
| chr3:158582315 | GA | G | 96 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(93): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.48-10109delA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158582315 | ||||||
| chr3:158582325 | A | C | 1 | a0001c0003t0008g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.48-10109A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158582325 | |||||||
| chr3:158582351 | A | G | 1 | a0001c0003t0003g0287 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.48-10083A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158582351 | |||||||
| chr3:158582382 | C | A | 1 | a0001c0003t0011g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.48-10052C>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158582382 | |||||||
| chr3:158582432 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.48-10002A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158582432 | |||||||
| chr3:158582544 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.48-9890G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158582544 | |||||||
| chr3:158582943 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(298): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.48-9491A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158582943 | |||||||
| chr3:158582957 | T | C | 1 | a0001c0003t0010g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.48-9477T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158582957 | |||||||
| chr3:158582998 | A | G | 1 | a0001c0003t0003g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.48-9436A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158582998 | |||||||
| chr3:158583044 | T | C | 1 | a0002c0005t0002g0062 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.48-9390T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583044 | |||||||
| chr3:158583182 | G | A | 186 | a0001c0001t0001g0184 a0001c0003t0003g0012 a0001c0003t0003g0013 others(183): Show |
232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.48-9252G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583182 | |||||||
| chr3:158583184 | A | T | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.48-9250A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583184 | |||||||
| chr3:158583302 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.48-9132A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583302 | |||||||
| chr3:158583361 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.48-9073T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583361 | |||||||
| chr3:158583371 | T | C | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.48-9063T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583371 | |||||||
| chr3:158583543 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | NA18946.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.48-8891A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583543 | |||||||
| chr3:158583583 | T | G | 1 | a0001c0003t0003g0287 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.48-8851T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583583 | |||||||
| chr3:158583712 | C | T | 1 | a0001c0003t0003g0302 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.48-8722C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583712 | |||||||
| chr3:158583835 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.48-8599G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583835 | |||||||
| chr3:158583893 | C | A | 61 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(58): Show |
70 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.48-8541C>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158583893 | |||||||
| chr3:158584264 | A | G | 2 | a0001c0003t0003g0279 a0001c0003t0003g0285 |
2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.48-8170A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584264 | |||||||
| chr3:158584282 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.48-8152A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584282 | |||||||
| chr3:158584360 | C | T | 1 | a0002c0002t0002g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.48-8074C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584360 | |||||||
| chr3:158584658 | A | AGT | 16 | a0001c0001t0001g0134 a0001c0001t0001g0160 a0001c0001t0001g0187 others(13): Show |
17 | HG00642.hp1 HG01192.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.48-7735_48-7734dup others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584658 | ||||||
| chr3:158584658 | A | AGTGT | 3 | a0001c0001t0001g0125 a0001c0001t0001g0184 a0001c0001t0001g0190 |
3 | HG00733.hp2 HG01123.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.48-7737_48-7734dup others(4): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584658 | ||||||
| chr3:158584658 | AGT | A | 81 | a0001c0001t0001g0022 a0001c0001t0001g0081 a0001c0001t0001g0085 others(78): Show |
95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.48-7735_48-7734del others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584658 | ||||||
| chr3:158584658 | AGTGT | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(69): Show |
88 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.48-7737_48-7734del others(4): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584658 | ||||||
| chr3:158584658 | AGTGTGT | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0108 a0001c0001t0001g0110 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.48-7739_48-7734del others(6): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584658 | ||||||
| chr3:158584658 | AGTGTGTG others(1): Show |
A | 10 | a0001c0001t0001g0100 a0001c0001t0001g0109 a0001c0001t0001g0113 others(7): Show |
10 | HG00099.hp2 HG01261.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.48-7741_48-7734del others(8): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584658 | ||||||
| chr3:158584661 | G | GTGTGTGT others(3): Show |
1 | a0002c0002t0002g0200 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.48-7764_48-7763ins others(10): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584661 | ||||||
| chr3:158584665 | G | GTGTGTT | 8 | a0002c0002t0002g0031 a0002c0002t0002g0210 a0002c0002t0002g0216 others(5): Show |
9 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.48-7764_48-7763ins others(6): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584665 | ||||||
| chr3:158584667 | G | GTGTT | 41 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0005 others(38): Show |
66 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.48-7764_48-7763ins others(4): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584667 | ||||||
| chr3:158584669 | G | GTT | 24 | a0001c0003t0004g0048 a0002c0002t0002g0203 a0002c0002t0002g0205 others(21): Show |
28 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.48-7764_48-7763ins others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158584669 | ||||||
| chr3:158584671 | G | T | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-7763G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584671 | |||||||
| chr3:158584673 | G | T | 20 | a0002c0002t0002g0217 a0002c0002t0002g0218 a0002c0002t0004g0006 others(17): Show |
27 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.48-7761G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584673 | |||||||
| chr3:158584722 | C | T | 9 | a0003c0004t0005g0230 a0003c0004t0005g0231 a0003c0004t0005g0232 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.48-7712C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584722 | |||||||
| chr3:158584728 | T | A | 1 | a0002c0002t0004g0075 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.48-7706T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584728 | |||||||
| chr3:158584728 | T | C | 184 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(181): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.48-7706T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584728 | |||||||
| chr3:158584757 | A | G | 1 | a0002c0002t0002g0032 | 2 | HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.48-7677A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584757 | |||||||
| chr3:158584888 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.48-7546A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584888 | |||||||
| chr3:158584922 | C | T | 1 | a0002c0002t0002g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.48-7512C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584922 | |||||||
| chr3:158584954 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(298): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.48-7480T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584954 | |||||||
| chr3:158584970 | T | C | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.48-7464T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158584970 | |||||||
| chr3:158585037 | GA | G | 7 | a0001c0001t0001g0040 a0001c0001t0001g0168 a0001c0001t0001g0176 others(4): Show |
7 | HG01358.hp1 HG01516.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.48-7379delA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158585037 | ||||||
| chr3:158585037 | GAA | G | 83 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(80): Show |
92 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.48-7380_48-7379del others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158585037 | ||||||
| chr3:158585041 | AAAAAAAA others(8): Show |
A | 1 | a0005c0008t0002g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.48-7387_48-7373del others(15): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158585041 | ||||||
| chr3:158585054 | AAG | A | 13 | a0002c0002t0002g0003 a0002c0002t0002g0207 a0002c0002t0002g0214 others(10): Show |
13 | HG00609.hp1 HG01074.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.48-7378_48-7377del others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158585054 | ||||||
| chr3:158585055 | AG | A | 82 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(79): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.48-7378delG | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158585055 | |||||||
| chr3:158585056 | G | A | 11 | a0002c0002t0002g0005 a0002c0002t0002g0029 a0002c0002t0002g0030 others(8): Show |
12 | HG01069.hp1 HG01071.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.48-7378G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158585056 | |||||||
| chr3:158585069 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.48-7365A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158585069 | |||||||
| chr3:158585788 | T | G | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.48-6646T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158585788 | |||||||
| chr3:158585795 | T | C | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.48-6639T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158585795 | |||||||
| chr3:158585797 | C | T | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-6637C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158585797 | |||||||
| chr3:158585948 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.48-6486G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158585948 | |||||||
| chr3:158586007 | C | CA | 4 | a0001c0003t0003g0278 a0001c0003t0003g0302 a0001c0003t0008g0038 others(1): Show |
4 | HG03041.hp2 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-6420dupA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158586007 | ||||||
| chr3:158586075 | A | T | 1 | a0001c0003t0003g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.48-6359A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586075 | |||||||
| chr3:158586077 | T | C | 1 | a0001c0003t0003g0304 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.48-6357T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586077 | |||||||
| chr3:158586095 | C | T | 13 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.48-6339C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586095 | |||||||
| chr3:158586106 | G | A | 11 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0027 others(8): Show |
14 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.48-6328G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586106 | |||||||
| chr3:158586120 | C | T | 99 | a0001c0001t0001g0124 a0001c0003t0004g0048 a0002c0002t0002g0002 others(96): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.48-6314C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586120 | |||||||
| chr3:158586164 | CA | C | 136 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0142 others(133): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.48-6256delA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158586164 | ||||||
| chr3:158586251 | A | G | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.48-6183A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586251 | |||||||
| chr3:158586276 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.48-6158T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586276 | |||||||
| chr3:158586502 | A | C | 1 | a0001c0003t0003g0268 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.48-5932A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586502 | |||||||
| chr3:158586742 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.48-5692G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586742 | |||||||
| chr3:158586811 | A | AAATAT | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.48-5619_48-5618ins others(5): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158586811 | ||||||
| chr3:158586982 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.48-5452T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158586982 | |||||||
| chr3:158587161 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.48-5273A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587161 | |||||||
| chr3:158587185 | A | G | 1 | a0002c0002t0004g0078 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.48-5249A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587185 | |||||||
| chr3:158587258 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.48-5176A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587258 | |||||||
| chr3:158587378 | G | C | 1 | a0001c0003t0003g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.48-5056G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587378 | |||||||
| chr3:158587419 | G | T | 1 | a0008c0007t0001g0186 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.48-5015G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587419 | |||||||
| chr3:158587455 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.48-4979A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587455 | |||||||
| chr3:158587615 | C | T | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.48-4819C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587615 | |||||||
| chr3:158587658 | G | A | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.48-4776G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587658 | |||||||
| chr3:158587704 | A | T | 1 | a0001c0003t0003g0294 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.48-4730A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587704 | |||||||
| chr3:158587852 | T | A | 1 | a0001c0001t0006g0162 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.48-4582T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587852 | |||||||
| chr3:158587870 | G | A | 13 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.48-4564G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587870 | |||||||
| chr3:158587873 | C | T | 1 | a0001c0003t0003g0301 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.48-4561C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587873 | |||||||
| chr3:158587957 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(298): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.48-4477T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158587957 | |||||||
| chr3:158588105 | G | A | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.48-4329G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588105 | |||||||
| chr3:158588168 | T | C | 1 | a0001c0003t0003g0264 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.48-4266T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588168 | |||||||
| chr3:158588399 | T | C | 1 | a0002c0002t0004g0060 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.48-4035T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588399 | |||||||
| chr3:158588464 | G | T | 1 | a0001c0003t0003g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.48-3970G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588464 | |||||||
| chr3:158588600 | CA | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(88): Show |
106 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.48-3810delA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158588600 | ||||||
| chr3:158588612 | A | C | 74 | a0001c0003t0003g0013 a0001c0003t0003g0035 a0001c0003t0003g0036 others(71): Show |
80 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.48-3822A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588612 | |||||||
| chr3:158588613 | A | C | 13 | a0001c0003t0003g0012 a0001c0003t0003g0037 a0001c0003t0003g0249 others(10): Show |
16 | HG00738.hp1 HG01934.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.48-3821A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588613 | |||||||
| chr3:158588615 | A | AC | 8 | a0002c0002t0004g0019 a0002c0002t0004g0054 a0002c0002t0004g0055 others(5): Show |
8 | HG01071.hp2 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.48-3819_48-3818ins others(1): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588615 | |||||||
| chr3:158588617 | A | C | 152 | a0001c0003t0003g0013 a0001c0003t0003g0035 a0001c0003t0003g0036 others(149): Show |
192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.48-3817A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588617 | |||||||
| chr3:158588618 | A | C | 25 | a0001c0003t0003g0012 a0001c0003t0003g0037 a0001c0003t0003g0249 others(22): Show |
31 | HG00738.hp1 HG00741.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.48-3816A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588618 | |||||||
| chr3:158588621 | A | G | 8 | a0002c0002t0004g0019 a0002c0002t0004g0054 a0002c0002t0004g0055 others(5): Show |
8 | HG01071.hp2 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.48-3813A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588621 | |||||||
| chr3:158588622 | A | AAGC | 25 | a0001c0003t0003g0012 a0001c0003t0003g0037 a0001c0003t0003g0249 others(22): Show |
31 | HG00738.hp1 HG00741.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.48-3811_48-3810ins others(3): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158588622 | ||||||
| chr3:158588622 | A | AGC | 152 | a0001c0003t0003g0013 a0001c0003t0003g0035 a0001c0003t0003g0036 others(149): Show |
192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.48-3812_48-3811ins others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588622 | |||||||
| chr3:158588622 | A | C | 8 | a0002c0002t0004g0019 a0002c0002t0004g0054 a0002c0002t0004g0055 others(5): Show |
8 | HG01071.hp2 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.48-3812A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588622 | |||||||
| chr3:158588625 | G | A | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.48-3809G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588625 | |||||||
| chr3:158588788 | G | T | 1 | a0001c0003t0003g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.48-3646G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588788 | |||||||
| chr3:158588838 | A | G | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.48-3596A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588838 | |||||||
| chr3:158588841 | T | G | 71 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(68): Show |
80 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.48-3593T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588841 | |||||||
| chr3:158588906 | G | A | 1 | a0002c0002t0002g0207 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.48-3528G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158588906 | |||||||
| chr3:158589092 | C | T | 1 | a0002c0002t0002g0194 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.48-3342C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589092 | |||||||
| chr3:158589232 | G | A | 42 | a0001c0003t0004g0048 a0002c0002t0004g0006 a0002c0002t0004g0007 others(39): Show |
53 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.48-3202G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589232 | |||||||
| chr3:158589235 | G | A | 42 | a0001c0003t0004g0048 a0002c0002t0004g0006 a0002c0002t0004g0007 others(39): Show |
53 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.48-3199G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589235 | |||||||
| chr3:158589253 | C | T | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.48-3181C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589253 | |||||||
| chr3:158589319 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.48-3115C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589319 | |||||||
| chr3:158589401 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0183 |
2 | NA18956.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.48-3033G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589401 | |||||||
| chr3:158589499 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.48-2935C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589499 | |||||||
| chr3:158589581 | G | A | 4 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-2853G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589581 | |||||||
| chr3:158589701 | T | G | 1 | a0001c0003t0011g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.48-2733T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589701 | |||||||
| chr3:158589722 | C | T | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.48-2712C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589722 | |||||||
| chr3:158589723 | A | G | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.48-2711A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589723 | |||||||
| chr3:158589791 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.48-2643A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589791 | |||||||
| chr3:158589841 | G | A | 1 | a0002c0002t0002g0042 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.48-2593G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589841 | |||||||
| chr3:158589942 | A | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.48-2492A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158589942 | |||||||
| chr3:158590012 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0173 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.48-2422A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590012 | |||||||
| chr3:158590017 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.48-2417C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590017 | |||||||
| chr3:158590018 | A | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.48-2416A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590018 | |||||||
| chr3:158590093 | G | A | 2 | a0001c0003t0003g0278 a0001c0003t0003g0302 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.48-2341G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590093 | |||||||
| chr3:158590099 | A | G | 71 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(68): Show |
80 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.48-2335A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590099 | |||||||
| chr3:158590128 | T | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0144 a0001c0001t0001g0154 others(3): Show |
7 | HG02074.hp2 HG02155.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.48-2306T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590128 | |||||||
| chr3:158590221 | G | A | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-2213G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590221 | |||||||
| chr3:158590250 | A | G | 4 | a0001c0003t0003g0278 a0001c0003t0003g0302 a0001c0003t0008g0038 others(1): Show |
4 | HG03041.hp2 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-2184A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590250 | |||||||
| chr3:158590363 | C | G | 1 | a0001c0003t0011g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.48-2071C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590363 | |||||||
| chr3:158590382 | A | T | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-2052A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590382 | |||||||
| chr3:158590595 | A | C | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-1839A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590595 | |||||||
| chr3:158590752 | C | T | 1 | a0001c0003t0011g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.48-1682C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590752 | |||||||
| chr3:158590930 | G | C | 1 | a0002c0002t0002g0210 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.48-1504G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158590930 | |||||||
| chr3:158591038 | T | C | 1 | a0001c0003t0010g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.48-1396T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591038 | |||||||
| chr3:158591048 | A | G | 4 | a0001c0003t0003g0259 a0001c0003t0003g0281 a0001c0003t0003g0282 others(1): Show |
4 | HG01243.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-1386A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591048 | |||||||
| chr3:158591086 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(296): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.48-1348T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591086 | |||||||
| chr3:158591086 | T | G | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.48-1348T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591086 | |||||||
| chr3:158591103 | TTTTGAGC others(7): Show |
T | 2 | a0001c0001t0001g0175 a0002c0002t0004g0049 |
2 | HG02683.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.48-1308_48-1295del others(14): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158591103 | ||||||
| chr3:158591159 | C | CT | 13 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0120 others(10): Show |
13 | HG00408.hp1 HG00408.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.48-1257dupT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158591159 | ||||||
| chr3:158591159 | CT | C | 121 | a0001c0001t0001g0108 a0001c0001t0001g0133 a0001c0001t0001g0155 others(118): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.48-1257delT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158591159 | ||||||
| chr3:158591388 | G | T | 71 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(68): Show |
80 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.48-1046G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591388 | |||||||
| chr3:158591400 | T | C | 3 | a0004c0006t0004g0074 a0004c0006t0009g0072 a0004c0006t0009g0073 |
3 | HG02895.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.48-1034T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591400 | |||||||
| chr3:158591427 | G | A | 1 | a0001c0003t0010g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.48-1007G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591427 | |||||||
| chr3:158591671 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.48-763C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591671 | |||||||
| chr3:158591681 | G | A | 2 | a0002c0002t0002g0222 a0002c0002t0002g0223 |
2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.48-753G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591681 | |||||||
| chr3:158591845 | TG | T | 5 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.48-588delG | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591845 | |||||||
| chr3:158591846 | GT | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(115): Show |
138 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.48-580delT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 158591846 | ||||||
| chr3:158591893 | G | T | 13 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.48-541G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591893 | |||||||
| chr3:158591968 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.48-466G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158591968 | |||||||
| chr3:158592117 | T | C | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.48-317T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158592117 | |||||||
| chr3:158592364 | A | G | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.48-70A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158592364 | |||||||
| chr3:158592367 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.48-67T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 1/7 | chr3 | 158592367 | |||||||
| chr3:158592602 | CAGTT | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.195+25_195+28delTA others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 158592602 | ||||||
| chr3:158592666 | A | G | 6 | a0001c0003t0005g0242 a0001c0003t0007g0014 a0001c0003t0007g0244 others(3): Show |
8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+85A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | chr3 | 158592666 | |||||||
| chr3:158592691 | C | G | 2 | a0002c0002t0004g0015 a0002c0002t0004g0018 |
4 | HG01255.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+110C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | chr3 | 158592691 | |||||||
| chr3:158592694 | G | T | 94 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(91): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.195+113G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | chr3 | 158592694 | |||||||
| chr3:158592955 | C | T | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.195+374C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | chr3 | 158592955 | |||||||
| chr3:158593057 | A | G | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.196-325A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | chr3 | 158593057 | |||||||
| chr3:158593139 | T | TA | 80 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(77): Show |
89 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.196-233dupA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 158593139 | ||||||
| chr3:158593140 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.196-242A>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | chr3 | 158593140 | |||||||
| chr3:158593144 | A | G | 1 | a0001c0001t0006g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.196-238A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | chr3 | 158593144 | |||||||
| chr3:158593152 | G | A | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.196-230G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 2/7 | chr3 | 158593152 | |||||||
| chr3:158593430 | C | T | 1 | a0001c0003t0011g0229 | 1 | HG03195.hp1 | splice_region_variant&intron_variant | LOW | c.240+4C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158593430 | |||||||
| chr3:158593657 | G | A | 21 | a0001c0003t0003g0251 a0001c0003t0003g0255 a0001c0003t0003g0259 others(18): Show |
23 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.240+231G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158593657 | |||||||
| chr3:158593758 | A | G | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.240+332A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158593758 | |||||||
| chr3:158593791 | TAAGCACA others(10): Show |
T | 67 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(64): Show |
76 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.240+373_240+389del others(17): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 158593791 | ||||||
| chr3:158593971 | A | C | 1 | a0001c0003t0008g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.240+545A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158593971 | |||||||
| chr3:158594039 | G | GT | 20 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0006g0027 others(17): Show |
21 | HG00408.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.240+622dupT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 158594039 | ||||||
| chr3:158594048 | T | A | 1 | a0001c0003t0003g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.240+622T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158594048 | |||||||
| chr3:158594161 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.240+735G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158594161 | |||||||
| chr3:158594365 | C | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(298): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.240+939C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158594365 | |||||||
| chr3:158594473 | G | GT | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.240+1047_240+1048i others(3): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158594473 | |||||||
| chr3:158594878 | T | C | 48 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0005 others(45): Show |
73 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.240+1452T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158594878 | |||||||
| chr3:158595065 | C | T | 4 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+1639C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595065 | |||||||
| chr3:158595214 | C | T | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.241-1648C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595214 | |||||||
| chr3:158595393 | T | C | 1 | a0001c0003t0003g0264 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.241-1469T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595393 | |||||||
| chr3:158595417 | A | G | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.241-1445A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595417 | |||||||
| chr3:158595576 | T | C | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0146 others(1): Show |
4 | HG02015.hp2 NA18988.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-1286T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595576 | |||||||
| chr3:158595673 | T | C | 1 | a0001c0003t0003g0263 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.241-1189T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595673 | |||||||
| chr3:158595787 | A | G | 1 | a0002c0002t0002g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.241-1075A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595787 | |||||||
| chr3:158595794 | T | C | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.241-1068T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595794 | |||||||
| chr3:158595862 | C | G | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.241-1000C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595862 | |||||||
| chr3:158595899 | G | A | 6 | a0002c0002t0004g0019 a0002c0002t0004g0054 a0002c0002t0004g0055 others(3): Show |
6 | HG01071.hp2 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-963G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595899 | |||||||
| chr3:158595930 | G | A | 3 | a0004c0006t0004g0074 a0004c0006t0009g0072 a0004c0006t0009g0073 |
3 | HG02895.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.241-932G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595930 | |||||||
| chr3:158595989 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.241-873G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158595989 | |||||||
| chr3:158596238 | CT | C | 4 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-623delT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158596238 | |||||||
| chr3:158596357 | A | G | 1 | a0004c0006t0004g0074 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.241-505A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158596357 | |||||||
| chr3:158596399 | T | C | 40 | a0001c0003t0004g0048 a0001c0003t0010g0271 a0001c0003t0010g0306 others(37): Show |
49 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.241-463T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158596399 | |||||||
| chr3:158596504 | G | A | 2 | a0002c0002t0004g0057 a0002c0002t0004g0059 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.241-358G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158596504 | |||||||
| chr3:158596602 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.241-260T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158596602 | |||||||
| chr3:158596766 | G | T | 2 | a0001c0003t0008g0038 a0001c0003t0008g0039 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.241-96G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 3/7 | chr3 | 158596766 | |||||||
| chr3:158597021 | C | G | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.324+76C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597021 | |||||||
| chr3:158597057 | A | G | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.324+112A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597057 | |||||||
| chr3:158597091 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.324+146A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597091 | |||||||
| chr3:158597291 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.324+346G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597291 | |||||||
| chr3:158597338 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0118 |
2 | HG02083.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.324+393G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597338 | |||||||
| chr3:158597675 | C | T | 1 | a0001c0001t0006g0092 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.325-405C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597675 | |||||||
| chr3:158597814 | G | A | 5 | a0001c0001t0001g0130 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG00733.hp1 HG03239.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-266G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597814 | |||||||
| chr3:158597848 | A | G | 1 | a0001c0003t0011g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.325-232A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597848 | |||||||
| chr3:158597869 | C | T | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.325-211C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597869 | |||||||
| chr3:158597873 | A | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0125 a0001c0001t0001g0181 |
3 | HG01109.hp2 HG01123.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.325-207A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597873 | |||||||
| chr3:158597902 | C | T | 1 | a0001c0003t0003g0285 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.325-178C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597902 | |||||||
| chr3:158597974 | T | G | 1 | a0001c0003t0011g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.325-106T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158597974 | |||||||
| chr3:158598021 | T | A | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.325-59T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 4/7 | chr3 | 158598021 | |||||||
| chr3:158598258 | A | G | 1 | a0002c0002t0002g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.453+50A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158598258 | |||||||
| chr3:158598403 | AT | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.453+203delT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 158598403 | ||||||
| chr3:158598431 | G | A | 1 | a0001c0003t0010g0271 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.453+223G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158598431 | |||||||
| chr3:158598493 | G | A | 2 | a0002c0002t0002g0203 a0002c0002t0002g0205 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.453+285G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158598493 | |||||||
| chr3:158598505 | C | T | 11 | a0001c0003t0003g0251 a0001c0003t0003g0255 a0001c0003t0003g0260 others(8): Show |
11 | HG01884.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.453+297C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158598505 | |||||||
| chr3:158598689 | A | G | 12 | a0002c0002t0002g0030 a0002c0002t0002g0034 a0002c0002t0002g0042 others(9): Show |
14 | HG02074.hp1 HG02559.hp1 NA18747.hp2 others(11): Show |
intron_variant | MODIFIER | c.453+481A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158598689 | |||||||
| chr3:158598854 | A | G | 66 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(63): Show |
75 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.453+646A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158598854 | |||||||
| chr3:158598861 | G | A | 184 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(181): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.453+653G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158598861 | |||||||
| chr3:158598937 | T | C | 49 | a0001c0003t0003g0266 a0001c0003t0003g0288 a0001c0003t0003g0296 others(46): Show |
74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.453+729T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158598937 | |||||||
| chr3:158599139 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0167 |
2 | NA19003.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.454-875A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599139 | |||||||
| chr3:158599168 | T | A | 1 | a0002c0002t0004g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.454-846T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599168 | |||||||
| chr3:158599279 | C | T | 68 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(65): Show |
77 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.454-735C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599279 | |||||||
| chr3:158599377 | A | G | 6 | a0001c0003t0005g0242 a0001c0003t0007g0014 a0001c0003t0007g0244 others(3): Show |
8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.454-637A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599377 | |||||||
| chr3:158599382 | T | G | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.454-632T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599382 | |||||||
| chr3:158599526 | A | C | 13 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.454-488A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599526 | |||||||
| chr3:158599576 | T | A | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.454-438T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599576 | |||||||
| chr3:158599737 | A | G | 16 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(13): Show |
16 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.454-277A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599737 | |||||||
| chr3:158599851 | T | C | 1 | a0001c0003t0003g0280 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.454-163T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599851 | |||||||
| chr3:158599876 | C | G | 4 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.454-138C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 5/7 | chr3 | 158599876 | |||||||
| chr3:158600226 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(298): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.613+53C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158600226 | |||||||
| chr3:158600359 | T | A | 6 | a0001c0003t0003g0251 a0001c0003t0003g0255 a0001c0003t0003g0272 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+186T>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158600359 | |||||||
| chr3:158600364 | G | T | 1 | a0002c0002t0002g0208 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.613+191G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158600364 | |||||||
| chr3:158600428 | T | C | 69 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(66): Show |
78 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.613+255T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158600428 | |||||||
| chr3:158600433 | A | ATAT | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.613+261_613+263dup others(3): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 158600433 | ||||||
| chr3:158600454 | CT | C | 69 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(66): Show |
78 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.613+284delT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 158600454 | ||||||
| chr3:158600530 | CA | C | 61 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(58): Show |
70 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.613+361delA | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 158600530 | ||||||
| chr3:158600572 | T | TTA | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.613+408_613+409dup others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 158600572 | ||||||
| chr3:158600702 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0135 |
2 | HG00438.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.613+529T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158600702 | |||||||
| chr3:158600762 | CAGT | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(298): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.613+594_613+596del others(3): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 158600762 | ||||||
| chr3:158600833 | C | T | 1 | a0002c0002t0004g0067 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.613+660C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158600833 | |||||||
| chr3:158600892 | A | G | 16 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(13): Show |
16 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.613+719A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158600892 | |||||||
| chr3:158600952 | A | C | 1 | a0001c0003t0003g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.613+779A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158600952 | |||||||
| chr3:158601073 | G | C | 13 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.613+900G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601073 | |||||||
| chr3:158601437 | G | A | 2 | a0001c0003t0003g0246 a0001c0003t0003g0247 |
2 | HG01175.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.613+1264G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601437 | |||||||
| chr3:158601485 | G | A | 1 | a0001c0003t0003g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.613+1312G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601485 | |||||||
| chr3:158601501 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.614-1306C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601501 | |||||||
| chr3:158601502 | G | A | 1 | a0002c0002t0002g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.614-1305G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601502 | |||||||
| chr3:158601629 | C | T | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.614-1178C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601629 | |||||||
| chr3:158601630 | G | T | 9 | a0003c0004t0005g0230 a0003c0004t0005g0231 a0003c0004t0005g0232 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.614-1177G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601630 | |||||||
| chr3:158601673 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.614-1134C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601673 | |||||||
| chr3:158601679 | C | T | 1 | a0002c0002t0002g0219 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.614-1128C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601679 | |||||||
| chr3:158601708 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.614-1099G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601708 | |||||||
| chr3:158601713 | C | G | 1 | a0002c0002t0002g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.614-1094C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601713 | |||||||
| chr3:158601713 | C | T | 10 | a0002c0002t0004g0006 a0002c0002t0004g0008 a0002c0002t0004g0016 others(7): Show |
16 | HG00423.hp2 HG00609.hp1 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.614-1094C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601713 | |||||||
| chr3:158601719 | G | A | 1 | a0002c0002t0002g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.614-1088G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601719 | |||||||
| chr3:158601746 | A | ACT | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.614-1060_614-1059d others(4): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 158601746 | ||||||
| chr3:158601806 | C | CT | 108 | a0001c0001t0001g0190 a0001c0001t0001g0228 a0001c0003t0003g0296 others(105): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.614-981dupT | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 158601806 | ||||||
| chr3:158601806 | C | CTT | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(173): Show |
205 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.614-982_614-981dup others(2): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 158601806 | ||||||
| chr3:158601806 | C | CTTT | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0138 others(10): Show |
13 | HG00597.hp2 HG00738.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.614-983_614-981dup others(3): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 158601806 | ||||||
| chr3:158601840 | G | A | 3 | a0001c0003t0003g0257 a0002c0002t0004g0044 a0002c0002t0014g0045 |
3 | HG02572.hp1 NA18972.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.614-967G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601840 | |||||||
| chr3:158601913 | T | C | 70 | a0001c0001t0001g0102 a0001c0003t0003g0012 a0001c0003t0003g0013 others(67): Show |
79 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.614-894T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601913 | |||||||
| chr3:158601931 | C | T | 3 | a0004c0006t0004g0074 a0004c0006t0009g0072 a0004c0006t0009g0073 |
3 | HG02895.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.614-876C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158601931 | |||||||
| chr3:158602076 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.614-731A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158602076 | |||||||
| chr3:158602266 | A | G | 3 | a0001c0003t0008g0038 a0001c0003t0008g0039 a0001c0003t0011g0229 |
3 | HG03098.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.614-541A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158602266 | |||||||
| chr3:158602313 | G | A | 4 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-494G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158602313 | |||||||
| chr3:158602387 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.614-420A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158602387 | |||||||
| chr3:158602635 | G | A | 1 | a0001c0003t0003g0293 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.614-172G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158602635 | |||||||
| chr3:158602660 | G | T | 1 | a0002c0002t0002g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.614-147G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158602660 | |||||||
| chr3:158602680 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.614-127C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158602680 | |||||||
| chr3:158602751 | G | C | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.614-56G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 6/7 | chr3 | 158602751 | |||||||
| chr3:158602996 | T | C | 1 | a0001c0003t0003g0037 | 2 | NA18964.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.746+57T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158602996 | |||||||
| chr3:158603091 | G | C | 42 | a0001c0003t0004g0048 a0002c0002t0004g0006 a0002c0002t0004g0007 others(39): Show |
53 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.746+152G>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603091 | |||||||
| chr3:158603103 | C | G | 87 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(84): Show |
96 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.746+164C>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603103 | |||||||
| chr3:158603134 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.746+195T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603134 | |||||||
| chr3:158603176 | C | T | 1 | a0001c0003t0003g0287 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.746+237C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603176 | |||||||
| chr3:158603186 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(298): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.746+247C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603186 | |||||||
| chr3:158603199 | C | T | 46 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0005 others(43): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.746+260C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603199 | |||||||
| chr3:158603411 | C | T | 1 | a0003c0004t0005g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.746+472C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603411 | |||||||
| chr3:158603473 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.746+534T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603473 | |||||||
| chr3:158603596 | C | T | 2 | a0001c0003t0010g0271 a0001c0003t0010g0306 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.746+657C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603596 | |||||||
| chr3:158603671 | C | T | 1 | a0002c0002t0002g0215 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.746+732C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603671 | |||||||
| chr3:158603804 | A | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.746+865A>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603804 | |||||||
| chr3:158603861 | T | C | 13 | a0001c0003t0005g0235 a0001c0003t0005g0236 a0001c0003t0005g0237 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.746+922T>C | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158603861 | |||||||
| chr3:158604280 | C | T | 46 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0005 others(43): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.747-817C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604280 | |||||||
| chr3:158604286 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.747-811G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604286 | |||||||
| chr3:158604385 | G | A | 185 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(182): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.747-712G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604385 | |||||||
| chr3:158604426 | G | T | 72 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(69): Show |
81 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.747-671G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604426 | |||||||
| chr3:158604567 | A | ATAAACAG others(7): Show |
1 | a0001c0001t0001g0170 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.747-526_747-513dup others(14): Show |
MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 158604567 | ||||||
| chr3:158604633 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(305): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.747-464A>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604633 | |||||||
| chr3:158604641 | G | T | 19 | a0001c0001t0001g0114 a0001c0003t0005g0235 a0001c0003t0005g0236 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.747-456G>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604641 | |||||||
| chr3:158604642 | T | G | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.747-455T>G | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604642 | |||||||
| chr3:158604696 | G | A | 98 | a0001c0003t0004g0048 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.747-401G>A | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604696 | |||||||
| chr3:158604719 | C | T | 69 | a0001c0003t0003g0012 a0001c0003t0003g0013 a0001c0003t0003g0035 others(66): Show |
78 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.747-378C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604719 | |||||||
| chr3:158604781 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.747-316C>T | MLF1 | ENSG00000178053.21 | transcript | ENST00000466246.7 | protein_coding | 7/7 | chr3 | 158604781 |