Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 173 |
| ensemblid | ENSG00000079557.5 |
| hgncid | 316 |
| symbol | AFM |
| name | afamin |
| refseq_nuc | NM_001133.2 |
| refseq_prot | NP_001124.1 |
| ensembl_nuc | ENST00000226355.5 |
| ensembl_prot | ENSP00000226355.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 73481745 |
| end | 73504001 |
| strand | + |
| ver | v1.2 |
| region | chr4:73481745-73504001 |
| region5000 | chr4:73476745-73509001 |
| regionname0 | AFM_chr4_73481745_73504001 |
| regionname5000 | AFM_chr4_73476745_73509001 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 599 | 324 | 62 | 68 | 150 | 12 | 30 | 116 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0002 | 0/0 | 599 | 20 | 9 | 2 | 3 | 2 | 4 | 1 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0003 | 0/0 | 599 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0004 | 0/0 | 599 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0005 | 0/0 | 599 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0006 | 0/0 | 599 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0007 | 0/0 | 599 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0008 | 0/0 | 599 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0009 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0010 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0011 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0012 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0013 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| a0014 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | MKLLK others(594): Show |
chr4 | 73476745 | 73509001 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1797 | 322 | 62 | 68 | 148 | 12 | 30 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0001c0008 | 0/0 | 1797 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0002c0002 | 0/0 | 1797 | 19 | 8 | 2 | 3 | 2 | 4 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0002c0015 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0003c0003 | 0/0 | 1797 | 5 | 0 | 0 | 5 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0004c0004 | 0/0 | 1797 | 4 | 4 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0005c0005 | 0/0 | 1797 | 3 | 1 | 2 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0006c0009 | 0/0 | 1797 | 2 | 0 | 2 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0007c0007 | 0/0 | 1797 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0008c0006 | 0/0 | 1797 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0009c0016 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0010c0010 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0011c0012 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0012c0013 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0013c0014 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 | ||
| a0014c0011 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ATGAA others(1792): Show |
chr4 | 73476745 | 73509001 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1997 | 318 | 60 | 66 | 148 | 12 | 30 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0001c0001t0002 | 0/0 | 1997 | 2 | 1 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0001c0001t0003 | 0/0 | 1997 | 2 | 1 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0001c0008t0001 | 0/0 | 1997 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0002c0002t0001 | 0/0 | 1997 | 19 | 8 | 2 | 3 | 2 | 4 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0002c0015t0001 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0003c0003t0001 | 0/0 | 1997 | 5 | 0 | 0 | 5 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0004c0004t0001 | 0/0 | 1997 | 4 | 4 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0005c0005t0001 | 0/0 | 1997 | 3 | 1 | 2 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0006c0009t0001 | 0/0 | 1997 | 2 | 0 | 2 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0007c0007t0001 | 0/0 | 1997 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0008c0006t0001 | 0/0 | 1997 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0009c0016t0001 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0010c0010t0001 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0011c0012t0001 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0012c0013t0001 | 0/0 | 1997 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0013c0014t0001 | 0/0 | 1997 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| a0014c0011t0001 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | ACTTT others(1992): Show |
chr4 | 73476745 | 73509001 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 1 | 3 | 4 | 0 | 3 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 1 | 7 | 0 | 3 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0003 | 0/0 | 8 | 2 | 0 | 5 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 5 | 4 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 2 | 2 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 2 | 3 | 0 | 2 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0015 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0001c0008t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0002c0015t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0003c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0003c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0003c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0004c0004t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0004c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0004c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0005c0005t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0005c0005t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0005c0005t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0006c0009t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0007c0007t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0007c0007t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0008c0006t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0008c0006t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0009c0016t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0010c0010t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0011c0012t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0012c0013t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0013c0014t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| a0014c0011t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0073 | EUR | GBR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01070 | hp1 | a0005 | c0005 | t0001 | g0169 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01071 | hp1 | a0005 | c0005 | t0001 | g0170 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01257 | hp1 | a0006 | c0009 | t0001 | g0053 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01258 | hp1 | a0006 | c0009 | t0001 | g0053 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0026 | EUR | IBS | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01884 | hp1 | a0007 | c0007 | t0001 | g0149 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02258 | hp2 | a0004 | c0004 | t0001 | g0047 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02615 | hp2 | a0008 | c0006 | t0001 | g0106 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02717 | hp1 | a0010 | c0010 | t0001 | g0108 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0061 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02809 | hp1 | a0004 | c0004 | t0001 | g0166 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02818 | hp1 | a0005 | c0005 | t0001 | g0168 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03130 | hp2 | a0004 | c0004 | t0001 | g0159 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03139 | hp1 | a0008 | c0006 | t0001 | g0118 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03195 | hp1 | a0011 | c0012 | t0001 | g0001 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03195 | hp2 | a0007 | c0007 | t0001 | g0148 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03209 | hp2 | a0004 | c0004 | t0001 | g0047 | AFR | MSL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | MSL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0074 | SAS | STU | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | STU | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0062 | SAS | STU | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18961 | hp1 | a0001 | c0008 | t0001 | g0002 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18970 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18972 | hp1 | a0001 | c0008 | t0001 | g0082 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18981 | hp2 | a0012 | c0013 | t0001 | g0030 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18991 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19063 | hp2 | a0013 | c0014 | t0001 | g0146 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | YRI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20129 | hp1 | a0002 | c0015 | t0001 | g0070 | AFR | ASW | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02486 | hp1 | a0009 | c0016 | t0001 | g0201 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | USA | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | USA | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | USA | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| NA21309 | hp2 | a0014 | c0011 | t0001 | g0007 | AFR | LWK | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0192 | REF | REF | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0164 | REF | REF | AFM_chr4_73476745_73509001 | AFM | chr4 | 73476745 | 73509001 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73481815 | T | G | 1 | a0008 | 2 | HG02615.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.40T>G | p.Phe14Val | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/15 | 71/1997 | 40/1800 | 14/599 | chr4 | 73481815 | |||
| chr4:73481855 | G | A | 1 | a0007 | 2 | HG01884.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.80G>A | p.Arg27Gln | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/15 | 111/1997 | 80/1800 | 27/599 | chr4 | 73481855 | |||
| chr4:73485876 | G | T | 1 | a0006 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.285G>T | p.Gln95His | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/15 | 316/1997 | 285/1800 | 95/599 | chr4 | 73485876 | |||
| chr4:73486060 | T | A | 1 | a0005 | 3 | HG01070.hp1 HG01071.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.469T>A | p.Ser157Thr | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/15 | 500/1997 | 469/1800 | 157/599 | chr4 | 73486060 | |||
| chr4:73487082 | A | T | 1 | a0004 | 4 | HG02258.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
missense_variant | MODERATE | c.598A>T | p.Asn200Tyr | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 5/15 | 629/1997 | 598/1800 | 200/599 | chr4 | 73487082 | |||
| chr4:73487083 | A | T | 1 | a0004 | 4 | HG02258.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
missense_variant | MODERATE | c.599A>T | p.Asn200Ile | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 5/15 | 630/1997 | 599/1800 | 200/599 | chr4 | 73487083 | |||
| chr4:73487739 | C | A | 1 | a0010 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.631C>A | p.Gln211Lys | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 6/15 | 662/1997 | 631/1800 | 211/599 | chr4 | 73487739 | |||
| chr4:73488751 | C | T | 1 | a0009 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.835C>T | p.Arg279Cys | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/15 | 866/1997 | 835/1800 | 279/599 | chr4 | 73488751 | |||
| chr4:73492035 | G | C | 1 | a0014 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1007G>C | p.Ser336Thr | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/15 | 1038/1997 | 1007/1800 | 336/599 | chr4 | 73492035 | |||
| chr4:73492080 | T | C | 1 | a0011 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1052T>C | p.Phe351Ser | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/15 | 1083/1997 | 1052/1800 | 351/599 | chr4 | 73492080 | |||
| chr4:73495425 | G | A | 1 | a0002 | 20 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(17): Show |
missense_variant | MODERATE | c.1184G>A | p.Arg395His | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/15 | 1215/1997 | 1184/1800 | 395/599 | chr4 | 73495425 | |||
| chr4:73497670 | A | T | 1 | a0003 | 5 | NA18947.hp2 NA18970.hp1 NA18974.hp2 others(2): Show |
missense_variant | MODERATE | c.1210A>T | p.Thr404Ser | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/15 | 1241/1997 | 1210/1800 | 404/599 | chr4 | 73497670 | |||
| chr4:73499188 | T | A | 1 | a0012 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1364T>A | p.Val455Glu | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/15 | 1395/1997 | 1364/1800 | 455/599 | chr4 | 73499188 | |||
| chr4:73499229 | G | A | 1 | a0013 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.1405G>A | p.Ala469Thr | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/15 | 1436/1997 | 1405/1800 | 469/599 | chr4 | 73499229 | |||
| chr4:73503877 | G | A | 1 | a0001 | 2 | HG02004.hp2 HG02723.hp2 |
splice_region_variant | LOW | c.*42G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 15/15 | chr4 | 73503877 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73487006 | C | T | 1 | a0001c0008 | 2 | NA18961.hp1 NA18972.hp1 |
synonymous_variant | LOW | c.522C>T | p.Phe174Phe | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 5/15 | 553/1997 | 522/1800 | 174/599 | chr4 | 73487006 | |||
| chr4:73491958 | C | T | 1 | a0002c0015 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.930C>T | p.Arg310Arg | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/15 | 961/1997 | 930/1800 | 310/599 | chr4 | 73491958 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73481761 | G | A | 1 | a0001c0001t0002 | 2 | HG01243.hp2 HG03540.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-15G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/15 | chr4 | 73481761 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73481912 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.88+49T>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73481912 | |||||||
| chr4:73482020 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.88+157G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482020 | |||||||
| chr4:73482054 | A | G | 69 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(66): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.88+191A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482054 | |||||||
| chr4:73482292 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.88+429C>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482292 | |||||||
| chr4:73482382 | G | C | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.88+519G>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482382 | |||||||
| chr4:73482511 | C | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(8): Show |
14 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+648C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482511 | |||||||
| chr4:73482512 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG02965.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.88+649G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482512 | |||||||
| chr4:73482583 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.88+720T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482583 | |||||||
| chr4:73482604 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.88+741G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482604 | |||||||
| chr4:73482612 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.88+749C>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482612 | |||||||
| chr4:73482717 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.88+854G>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482717 | |||||||
| chr4:73482821 | T | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.88+958T>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482821 | |||||||
| chr4:73482889 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.88+1026A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482889 | |||||||
| chr4:73482912 | A | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
17 | HG01358.hp2 HG01496.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.89-1029A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73482912 | |||||||
| chr4:73483015 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.89-926T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73483015 | |||||||
| chr4:73483303 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.89-638T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73483303 | |||||||
| chr4:73483374 | C | G | 1 | a0007c0007t0001g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-567C>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73483374 | |||||||
| chr4:73483419 | A | G | 3 | a0001c0001t0003g0147 a0007c0007t0001g0148 a0007c0007t0001g0149 |
3 | HG01884.hp1 HG02004.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.89-522A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73483419 | |||||||
| chr4:73483441 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
119 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.89-500G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73483441 | |||||||
| chr4:73483456 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.89-485G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73483456 | |||||||
| chr4:73483582 | A | G | 1 | a0013c0014t0001g0146 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.89-359A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 1/14 | chr4 | 73483582 | |||||||
| chr4:73484149 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138-109T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 2/14 | chr4 | 73484149 | |||||||
| chr4:73484150 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
181 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.138-108A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 2/14 | chr4 | 73484150 | |||||||
| chr4:73484440 | C | CTCTT | 29 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(26): Show |
49 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.270+113_270+116dup others(4): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484440 | ||||||
| chr4:73484440 | C | CTCTTTCT others(1): Show |
11 | a0001c0001t0001g0043 a0001c0001t0001g0119 a0001c0001t0001g0120 others(8): Show |
12 | HG00642.hp1 HG01993.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.270+109_270+116dup others(8): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484440 | ||||||
| chr4:73484440 | C | CTCTTTCT others(5): Show |
4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0155 others(1): Show |
4 | HG01109.hp1 NA18950.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+105_270+116dup others(12): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484440 | ||||||
| chr4:73484440 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.270+50C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73484440 | |||||||
| chr4:73484440 | CTCTT | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0017 others(67): Show |
102 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.270+113_270+116del others(4): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484440 | ||||||
| chr4:73484440 | CTCTTTCT others(1): Show |
C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(29): Show |
59 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.270+109_270+116del others(8): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484440 | ||||||
| chr4:73484440 | CTCTTTCT others(5): Show |
C | 16 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(13): Show |
26 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.270+105_270+116del others(12): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484440 | ||||||
| chr4:73484440 | CTCTTTCT others(9): Show |
C | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0181 others(3): Show |
8 | HG00741.hp1 HG01496.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.270+101_270+116del others(16): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484440 | ||||||
| chr4:73484440 | CTCTTTCT others(13): Show |
C | 1 | a0001c0001t0001g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.270+97_270+116delT others(19): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484440 | ||||||
| chr4:73484440 | CTCTTTCT others(17): Show |
C | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.270+93_270+116delT others(23): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484440 | ||||||
| chr4:73484471 | T | C | 1 | a0001c0008t0001g0082 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.270+81T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73484471 | |||||||
| chr4:73484495 | TTTCTTTC others(5): Show |
T | 1 | a0001c0001t0001g0216 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.270+117_270+128del others(12): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484495 | ||||||
| chr4:73484495 | TTTCTTTC others(16): Show |
T | 1 | a0001c0001t0001g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.270+117_270+139del others(23): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484495 | ||||||
| chr4:73484499 | TTTCTTTC others(12): Show |
T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0203 a0001c0001t0003g0205 |
3 | HG02630.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.270+117_270+135del others(19): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73484499 | ||||||
| chr4:73484506 | CATTCTTT others(4): Show |
C | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+117_270+127del others(11): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73484506 | |||||||
| chr4:73484507 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.270+117A>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73484507 | |||||||
| chr4:73484507 | A | T | 1 | a0009c0016t0001g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.270+117A>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73484507 | |||||||
| chr4:73484511 | TTTCTTTC others(19): Show |
T | 1 | a0009c0016t0001g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.270+122_270+147del others(26): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73484511 | |||||||
| chr4:73484518 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+128C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73484518 | |||||||
| chr4:73484928 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.270+538G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73484928 | |||||||
| chr4:73484961 | A | G | 1 | a0001c0001t0001g0054 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.270+571A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73484961 | |||||||
| chr4:73485038 | T | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(8): Show |
14 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.270+648T>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73485038 | |||||||
| chr4:73485099 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(69): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.270+709A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73485099 | |||||||
| chr4:73485123 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.270+733A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73485123 | |||||||
| chr4:73485487 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.271-375G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73485487 | |||||||
| chr4:73485590 | A | AGAAGAG | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.271-248_271-243dup others(6): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73485590 | ||||||
| chr4:73485590 | A | AGAAGGAG others(5): Show |
1 | a0008c0006t0001g0106 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271-268_271-267ins others(12): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73485590 | ||||||
| chr4:73485590 | A | AGACGAG | 5 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0122 others(2): Show |
7 | NA18964.hp2 NA18971.hp1 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-270_271-269ins others(6): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73485590 | ||||||
| chr4:73485599 | A | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(7): Show |
13 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.271-263A>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73485599 | |||||||
| chr4:73485605 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.271-257A>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73485605 | |||||||
| chr4:73485638 | G | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(8): Show |
13 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.271-224G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73485638 | |||||||
| chr4:73485655 | GGGA | G | 4 | a0001c0001t0001g0038 a0005c0005t0001g0168 a0005c0005t0001g0169 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-186_271-184del others(3): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73485655 | ||||||
| chr4:73485702 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.271-160G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 3/14 | chr4 | 73485702 | |||||||
| chr4:73486158 | G | A | 2 | a0007c0007t0001g0148 a0007c0007t0001g0149 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.482+85G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | chr4 | 73486158 | |||||||
| chr4:73486164 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.482+91A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | chr4 | 73486164 | |||||||
| chr4:73486191 | C | T | 2 | a0001c0001t0001g0054 a0006c0009t0001g0053 |
4 | HG01257.hp1 HG01258.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+118C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | chr4 | 73486191 | |||||||
| chr4:73486236 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.482+163A>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | chr4 | 73486236 | |||||||
| chr4:73486305 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.482+232G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | chr4 | 73486305 | |||||||
| chr4:73486748 | G | A | 1 | a0002c0002t0001g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.483-219G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | chr4 | 73486748 | |||||||
| chr4:73486845 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.483-122T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | chr4 | 73486845 | |||||||
| chr4:73486873 | C | CTCCCT | 19 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(16): Show |
32 | HG00323.hp2 HG00408.hp1 HG02486.hp1 others(29): Show |
intron_variant | MODIFIER | c.483-72_483-68dupCC others(3): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 73486873 | ||||||
| chr4:73486873 | C | CTCCCTTC others(3): Show |
2 | a0001c0001t0001g0052 a0001c0001t0001g0203 |
3 | HG00558.hp1 HG00597.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.483-77_483-68dupCC others(8): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 73486873 | ||||||
| chr4:73486873 | CTCCCT | C | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.483-72_483-68delCC others(3): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 73486873 | ||||||
| chr4:73486914 | C | T | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.483-53C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | chr4 | 73486914 | |||||||
| chr4:73486945 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.483-22C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 4/14 | chr4 | 73486945 | |||||||
| chr4:73487138 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.615+39C>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 5/14 | chr4 | 73487138 | |||||||
| chr4:73487199 | A | G | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.615+100A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 5/14 | chr4 | 73487199 | |||||||
| chr4:73487381 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0172 a0001c0001t0001g0174 others(2): Show |
7 | HG00733.hp1 HG01361.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.615+282G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 5/14 | chr4 | 73487381 | |||||||
| chr4:73487565 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.616-159G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 5/14 | chr4 | 73487565 | |||||||
| chr4:73487666 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0217 |
2 | HG00323.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.616-58A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 5/14 | chr4 | 73487666 | |||||||
| chr4:73488212 | A | G | 1 | a0007c0007t0001g0148 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.713+391A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 6/14 | chr4 | 73488212 | |||||||
| chr4:73488233 | G | A | 1 | a0005c0005t0001g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.714-397G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 6/14 | chr4 | 73488233 | |||||||
| chr4:73488236 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.714-394T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 6/14 | chr4 | 73488236 | |||||||
| chr4:73488245 | T | C | 3 | a0001c0001t0001g0183 a0001c0001t0001g0194 a0001c0001t0001g0204 |
3 | HG06807.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.714-385T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 6/14 | chr4 | 73488245 | |||||||
| chr4:73488323 | G | A | 3 | a0005c0005t0001g0168 a0005c0005t0001g0169 a0005c0005t0001g0170 |
3 | HG01070.hp1 HG01071.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.714-307G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 6/14 | chr4 | 73488323 | |||||||
| chr4:73488334 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.714-296G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 6/14 | chr4 | 73488334 | |||||||
| chr4:73488401 | GT | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(68): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.714-221delT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 73488401 | ||||||
| chr4:73488803 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(7): Show |
23 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.843+44A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73488803 | |||||||
| chr4:73488839 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.843+80T>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73488839 | |||||||
| chr4:73488890 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.843+131G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73488890 | |||||||
| chr4:73488915 | T | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.843+156T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73488915 | |||||||
| chr4:73489198 | G | T | 3 | a0005c0005t0001g0168 a0005c0005t0001g0169 a0005c0005t0001g0170 |
3 | HG01070.hp1 HG01071.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.843+439G>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73489198 | |||||||
| chr4:73489289 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.843+530C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73489289 | |||||||
| chr4:73489491 | A | AT | 12 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(9): Show |
15 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.843+739dupT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 73489491 | ||||||
| chr4:73489531 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0217 |
2 | HG00323.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.843+772A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73489531 | |||||||
| chr4:73489650 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.843+891A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73489650 | |||||||
| chr4:73489785 | C | G | 13 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
19 | HG01109.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.843+1026C>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73489785 | |||||||
| chr4:73489870 | G | A | 2 | a0005c0005t0001g0169 a0005c0005t0001g0170 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.843+1111G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73489870 | |||||||
| chr4:73489884 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.843+1125A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73489884 | |||||||
| chr4:73489925 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0097 |
2 | HG00323.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.843+1166G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73489925 | |||||||
| chr4:73489986 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.843+1227G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73489986 | |||||||
| chr4:73490092 | C | T | 1 | a0007c0007t0001g0148 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.843+1333C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73490092 | |||||||
| chr4:73490147 | ATAATC | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.843+1389_843+1393d others(7): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73490147 | |||||||
| chr4:73490187 | C | CA | 17 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0141 others(14): Show |
20 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.843+1444dupA | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 73490187 | ||||||
| chr4:73490187 | CA | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0055 others(15): Show |
22 | HG01243.hp1 HG01884.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.843+1444delA | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 73490187 | ||||||
| chr4:73490214 | A | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0110 a0012c0013t0001g0030 |
3 | HG00408.hp2 NA18981.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.843+1455A>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73490214 | |||||||
| chr4:73490323 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.844-1549T>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73490323 | |||||||
| chr4:73490421 | TG | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.844-1450delG | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73490421 | |||||||
| chr4:73490458 | G | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.844-1414G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73490458 | |||||||
| chr4:73490883 | C | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0056 others(6): Show |
16 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.844-989C>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73490883 | |||||||
| chr4:73491338 | G | A | 1 | a0002c0002t0001g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.844-534G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73491338 | |||||||
| chr4:73491370 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.844-502A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73491370 | |||||||
| chr4:73491406 | C | G | 1 | a0002c0002t0001g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.844-466C>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73491406 | |||||||
| chr4:73491424 | A | G | 1 | a0002c0002t0001g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.844-448A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73491424 | |||||||
| chr4:73491491 | T | C | 1 | a0007c0007t0001g0148 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.844-381T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73491491 | |||||||
| chr4:73491586 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(69): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.844-286G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73491586 | |||||||
| chr4:73491780 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.844-92T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73491780 | |||||||
| chr4:73491801 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.844-71A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73491801 | |||||||
| chr4:73491804 | C | T | 1 | a0007c0007t0001g0148 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.844-68C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 7/14 | chr4 | 73491804 | |||||||
| chr4:73492134 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1058+48A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492134 | |||||||
| chr4:73492141 | T | A | 1 | a0001c0001t0001g0130 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1058+55T>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492141 | |||||||
| chr4:73492150 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0116 |
3 | HG00558.hp2 HG02080.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1058+64G>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492150 | |||||||
| chr4:73492560 | T | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1058+474T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492560 | |||||||
| chr4:73492596 | G | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0194 a0001c0001t0001g0204 |
3 | HG06807.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1058+510G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492596 | |||||||
| chr4:73492624 | C | CT | 30 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0067 others(27): Show |
37 | HG00140.hp2 HG00733.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1058+549dupT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73492624 | ||||||
| chr4:73492624 | CT | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(14): Show |
23 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1058+549delT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73492624 | ||||||
| chr4:73492656 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1058+570A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492656 | |||||||
| chr4:73492773 | C | A | 1 | a0007c0007t0001g0148 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1058+687C>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492773 | |||||||
| chr4:73492792 | C | CA | 6 | a0001c0001t0001g0054 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
7 | HG02071.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.1058+724dupA | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73492792 | ||||||
| chr4:73492792 | CA | C | 45 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0028 others(42): Show |
57 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1058+724delA | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73492792 | ||||||
| chr4:73492867 | G | GT | 12 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(9): Show |
15 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+792dupT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73492867 | ||||||
| chr4:73492874 | T | G | 16 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0041 others(13): Show |
23 | HG01358.hp2 HG01496.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.1058+788T>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492874 | |||||||
| chr4:73492876 | T | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0218 |
3 | HG00609.hp1 NA18949.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1058+790T>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492876 | |||||||
| chr4:73492896 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0098 |
2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1058+810T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492896 | |||||||
| chr4:73492994 | C | T | 9 | a0002c0002t0001g0016 a0002c0002t0001g0061 a0002c0002t0001g0062 others(6): Show |
11 | HG02027.hp2 HG02056.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1058+908C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73492994 | |||||||
| chr4:73493046 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1058+960G>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493046 | |||||||
| chr4:73493212 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0129 |
3 | NA18983.hp1 NA18988.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1058+1126T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493212 | |||||||
| chr4:73493267 | A | G | 14 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(11): Show |
17 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.1058+1181A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493267 | |||||||
| chr4:73493299 | T | G | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1058+1213T>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493299 | |||||||
| chr4:73493307 | A | G | 1 | a0001c0001t0003g0147 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1058+1221A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493307 | |||||||
| chr4:73493395 | A | G | 3 | a0001c0001t0001g0197 a0001c0001t0001g0202 a0001c0001t0001g0223 |
3 | HG00597.hp1 NA18960.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1058+1309A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493395 | |||||||
| chr4:73493424 | G | A | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1058+1338G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493424 | |||||||
| chr4:73493516 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0091 a0001c0001t0001g0115 |
4 | HG02451.hp2 HG02723.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+1430C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493516 | |||||||
| chr4:73493573 | C | G | 13 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(10): Show |
16 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1058+1487C>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493573 | |||||||
| chr4:73493759 | C | T | 1 | a0001c0001t0003g0147 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1059-1541C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493759 | |||||||
| chr4:73493809 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1059-1491T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493809 | |||||||
| chr4:73493839 | A | G | 13 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
19 | HG01109.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1059-1461A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493839 | |||||||
| chr4:73493865 | T | C | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1059-1435T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73493865 | |||||||
| chr4:73494060 | G | GGT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
177 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.1059-1213_1059-121 others(6): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73494060 | ||||||
| chr4:73494060 | G | GGTGT | 3 | a0001c0001t0001g0076 a0001c0001t0001g0093 a0001c0001t0001g0107 |
3 | HG00099.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1059-1215_1059-121 others(8): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73494060 | ||||||
| chr4:73494060 | GGT | G | 34 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0022 others(31): Show |
48 | HG00597.hp1 HG01070.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1059-1213_1059-121 others(6): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73494060 | ||||||
| chr4:73494060 | GGTGT | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(64): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1059-1215_1059-121 others(8): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73494060 | ||||||
| chr4:73494060 | GGTGTGT | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(13): Show |
30 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.1059-1217_1059-121 others(10): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73494060 | ||||||
| chr4:73494067 | G | A | 3 | a0004c0004t0001g0047 a0004c0004t0001g0159 a0004c0004t0001g0166 |
4 | HG02258.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-1233G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73494067 | |||||||
| chr4:73494081 | G | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0217 |
2 | HG00323.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1059-1219G>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73494081 | |||||||
| chr4:73494397 | CT | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0035 others(6): Show |
13 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1059-895delT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 73494397 | ||||||
| chr4:73494836 | G | T | 1 | a0001c0001t0003g0147 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1059-464G>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73494836 | |||||||
| chr4:73494903 | G | A | 1 | a0001c0001t0003g0147 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1059-397G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73494903 | |||||||
| chr4:73494925 | C | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1059-375C>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73494925 | |||||||
| chr4:73495105 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1059-195G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73495105 | |||||||
| chr4:73495274 | A | C | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1059-26A>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 8/14 | chr4 | 73495274 | |||||||
| chr4:73495446 | T | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(10): Show |
16 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1191+14T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73495446 | |||||||
| chr4:73495510 | G | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0194 a0001c0001t0001g0204 |
3 | HG06807.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1191+78G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73495510 | |||||||
| chr4:73495537 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1191+105T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73495537 | |||||||
| chr4:73495553 | C | T | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1191+121C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73495553 | |||||||
| chr4:73495650 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1191+218A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73495650 | |||||||
| chr4:73495747 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1191+315A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73495747 | |||||||
| chr4:73496182 | T | C | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1191+750T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496182 | |||||||
| chr4:73496213 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0093 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1191+781T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496213 | |||||||
| chr4:73496246 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1191+814A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496246 | |||||||
| chr4:73496267 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0218 |
2 | HG00609.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1191+835A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496267 | |||||||
| chr4:73496275 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0175 |
2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1191+843T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496275 | |||||||
| chr4:73496374 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1191+942G>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496374 | |||||||
| chr4:73496446 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1191+1014A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496446 | |||||||
| chr4:73496503 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1191+1071C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496503 | |||||||
| chr4:73496600 | C | T | 13 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
19 | HG01109.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1192-1052C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496600 | |||||||
| chr4:73496635 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1192-1017A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496635 | |||||||
| chr4:73496642 | T | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0172 others(8): Show |
14 | HG00733.hp1 HG00738.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192-1010T>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496642 | |||||||
| chr4:73496665 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1192-987T>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496665 | |||||||
| chr4:73496670 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1192-982G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496670 | |||||||
| chr4:73496787 | T | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1192-865T>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496787 | |||||||
| chr4:73496900 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1192-752C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496900 | |||||||
| chr4:73496926 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1192-726A>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73496926 | |||||||
| chr4:73497017 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1192-635A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73497017 | |||||||
| chr4:73497386 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1192-266G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73497386 | |||||||
| chr4:73497535 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1192-117A>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73497535 | |||||||
| chr4:73497565 | T | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1192-87T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73497565 | |||||||
| chr4:73497635 | A | T | 3 | a0004c0004t0001g0047 a0004c0004t0001g0159 a0004c0004t0001g0166 |
4 | HG02258.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1192-17A>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 9/14 | chr4 | 73497635 | |||||||
| chr4:73497968 | A | T | 17 | a0001c0001t0001g0067 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1289+219A>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/14 | chr4 | 73497968 | |||||||
| chr4:73497995 | T | C | 1 | a0001c0001t0003g0147 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1289+246T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/14 | chr4 | 73497995 | |||||||
| chr4:73498101 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1289+352T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/14 | chr4 | 73498101 | |||||||
| chr4:73498106 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0219 a0001c0001t0001g0226 |
3 | NA18956.hp1 NA18991.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1289+357T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/14 | chr4 | 73498106 | |||||||
| chr4:73498194 | C | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0214 |
2 | HG02071.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1289+445C>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/14 | chr4 | 73498194 | |||||||
| chr4:73498283 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1289+534T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/14 | chr4 | 73498283 | |||||||
| chr4:73498478 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1290-636C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/14 | chr4 | 73498478 | |||||||
| chr4:73498741 | T | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1290-373T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/14 | chr4 | 73498741 | |||||||
| chr4:73498867 | G | A | 1 | a0007c0007t0001g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1290-247G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 10/14 | chr4 | 73498867 | |||||||
| chr4:73499275 | CT | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(116): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1422+44delT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr4 | 73499275 | ||||||
| chr4:73499275 | CTT | C | 7 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0001g0167 others(4): Show |
7 | HG01070.hp1 HG01167.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1422+43_1422+44del others(2): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr4 | 73499275 | ||||||
| chr4:73499279 | T | C | 1 | a0007c0007t0001g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1422+33T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/14 | chr4 | 73499279 | |||||||
| chr4:73499289 | T | A | 17 | a0001c0001t0001g0204 a0002c0002t0001g0016 a0002c0002t0001g0025 others(14): Show |
21 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1422+43T>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/14 | chr4 | 73499289 | |||||||
| chr4:73499290 | T | A | 39 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(36): Show |
57 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1422+44T>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/14 | chr4 | 73499290 | |||||||
| chr4:73499290 | TA | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0141 a0001c0001t0001g0158 others(4): Show |
9 | HG02258.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1422+52delA | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr4 | 73499290 | ||||||
| chr4:73499291 | A | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0040 others(1): Show |
7 | HG01261.hp1 HG01261.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1422+45A>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/14 | chr4 | 73499291 | |||||||
| chr4:73499349 | C | T | 1 | a0007c0007t0001g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1422+103C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 11/14 | chr4 | 73499349 | |||||||
| chr4:73500235 | T | C | 1 | a0001c0001t0001g0054 | 2 | HG03491.hp2 HG03492.hp2 |
splice_region_variant&intron_variant | LOW | c.1646+8T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73500235 | |||||||
| chr4:73500313 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1646+86C>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73500313 | |||||||
| chr4:73500366 | A | G | 6 | a0001c0001t0001g0140 a0001c0001t0001g0187 a0001c0001t0001g0189 others(3): Show |
6 | NA18945.hp2 NA18977.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1646+139A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73500366 | |||||||
| chr4:73500386 | A | AT | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1646+169dupT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 73500386 | ||||||
| chr4:73500386 | A | ATT | 17 | a0001c0001t0001g0067 a0001c0001t0001g0165 a0001c0001t0001g0183 others(14): Show |
20 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1646+168_1646+169d others(4): Show |
AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 73500386 | ||||||
| chr4:73500386 | AT | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
15 | HG01496.hp2 HG01934.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.1646+169delT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 73500386 | ||||||
| chr4:73500488 | CA | C | 14 | a0001c0001t0001g0067 a0001c0001t0001g0165 a0002c0002t0001g0016 others(11): Show |
17 | HG00140.hp2 HG01123.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1646+266delA | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 73500488 | ||||||
| chr4:73500574 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1646+347G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73500574 | |||||||
| chr4:73500826 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1646+599A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73500826 | |||||||
| chr4:73500870 | A | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0121 |
2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1646+643A>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73500870 | |||||||
| chr4:73500929 | T | C | 13 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
19 | HG01109.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1646+702T>C | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73500929 | |||||||
| chr4:73501206 | CT | C | 36 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(33): Show |
47 | HG00140.hp2 HG01109.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1647-579delT | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 73501206 | ||||||
| chr4:73501249 | A | G | 2 | a0001c0001t0001g0044 a0007c0007t0001g0148 |
3 | HG02895.hp1 HG02896.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1647-538A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73501249 | |||||||
| chr4:73501383 | C | T | 125 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(122): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1647-404C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73501383 | |||||||
| chr4:73501683 | C | T | 3 | a0005c0005t0001g0168 a0005c0005t0001g0169 a0005c0005t0001g0170 |
3 | HG01070.hp1 HG01071.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1647-104C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73501683 | |||||||
| chr4:73501697 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1647-90C>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73501697 | |||||||
| chr4:73501762 | T | G | 4 | a0001c0001t0001g0158 a0004c0004t0001g0047 a0004c0004t0001g0159 others(1): Show |
5 | HG02258.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1647-25T>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 12/14 | chr4 | 73501762 | |||||||
| chr4:73501989 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1779+70C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 13/14 | chr4 | 73501989 | |||||||
| chr4:73502117 | C | T | 4 | a0001c0001t0001g0158 a0004c0004t0001g0047 a0004c0004t0001g0159 others(1): Show |
5 | HG02258.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1779+198C>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 13/14 | chr4 | 73502117 | |||||||
| chr4:73502303 | A | T | 1 | a0002c0002t0001g0016 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1779+384A>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 13/14 | chr4 | 73502303 | |||||||
| chr4:73502439 | T | TC | 23 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(20): Show |
31 | HG01109.hp2 HG01167.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1779+521dupC | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 73502439 | ||||||
| chr4:73502482 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1779+563A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 13/14 | chr4 | 73502482 | |||||||
| chr4:73502591 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1780-459A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 13/14 | chr4 | 73502591 | |||||||
| chr4:73502774 | C | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0037 others(2): Show |
8 | HG00621.hp1 HG01175.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1780-276C>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 13/14 | chr4 | 73502774 | |||||||
| chr4:73503301 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.*40+191A>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 14/14 | chr4 | 73503301 | |||||||
| chr4:73503555 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.*41-321A>T | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 14/14 | chr4 | 73503555 | |||||||
| chr4:73503581 | G | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(94): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.*41-295G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 14/14 | chr4 | 73503581 | |||||||
| chr4:73503689 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.*41-187G>A | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 14/14 | chr4 | 73503689 | |||||||
| chr4:73503823 | C | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.*41-53C>G | AFM | ENSG00000079557.5 | transcript | ENST00000226355.5 | protein_coding | 14/14 | chr4 | 73503823 |