Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 174 |
| ensemblid | ENSG00000081051.8 |
| hgncid | 317 |
| symbol | AFP |
| name | alpha fetoprotein |
| refseq_nuc | NM_001134.3 |
| refseq_prot | NP_001125.1 |
| ensembl_nuc | ENST00000395792.7 |
| ensembl_prot | ENSP00000379138.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 73436221 |
| end | 73456174 |
| strand | + |
| ver | v1.2 |
| region | chr4:73436221-73456174 |
| region5000 | chr4:73431221-73461174 |
| regionname0 | AFP_chr4_73436221_73456174 |
| regionname5000 | AFP_chr4_73431221_73461174 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 609 | 353 | 68 | 68 | 161 | 17 | 37 | 121 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| a0002 | 0/0 | 609 | 23 | 21 | 1 | 0 | 0 | 1 | 0 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| a0003 | 0/0 | 609 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| a0004 | 0/0 | 609 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| a0005 | 0/0 | 284 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(279): Show |
chr4 | 73431221 | 73461174 |
| a0006 | 0/0 | 609 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| a0007 | 0/0 | 609 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| a0008 | 0/0 | 609 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| a0009 | 0/0 | 609 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| a0010 | 0/0 | 609 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| a0011 | 0/0 | 609 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | MKWVE others(604): Show |
chr4 | 73431221 | 73461174 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1827 | 329 | 50 | 66 | 161 | 16 | 35 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0001c0003 | 0/0 | 1827 | 15 | 14 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0001c0004 | 1/0 | 1827 | 4 | 3 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0001c0005 | 0/0 | 1827 | 3 | 1 | 1 | 0 | 1 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0001c0013 | 0/0 | 1827 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0001c0014 | 0/0 | 1827 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0002c0002 | 0/0 | 1827 | 23 | 21 | 1 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0003c0006 | 0/0 | 1827 | 3 | 0 | 1 | 0 | 0 | 2 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0004c0009 | 0/0 | 1827 | 2 | 0 | 1 | 0 | 1 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0005c0008 | 0/0 | 1612 | 2 | 0 | 1 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1607): Show |
chr4 | 73431221 | 73461174 | ||
| a0006c0007 | 0/0 | 1827 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0007c0010 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0008c0012 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0009c0016 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0010c0015 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 | ||
| a0011c0011 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATGAA others(1822): Show |
chr4 | 73431221 | 73461174 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2426 | 172 | 29 | 24 | 94 | 10 | 15 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0001t0002 | 0/1 | 2426 | 146 | 19 | 41 | 60 | 6 | 19 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0001t0003 | 0/0 | 2426 | 7 | 0 | 0 | 6 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0001t0004 | 0/0 | 2426 | 2 | 1 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0001t0005 | 0/0 | 2426 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0001t0006 | 0/0 | 2426 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0003t0001 | 0/0 | 2426 | 15 | 14 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0004t0002 | 1/0 | 2426 | 4 | 3 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0005t0002 | 0/0 | 2426 | 3 | 1 | 1 | 0 | 1 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0013t0001 | 0/0 | 2426 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0001c0014t0001 | 0/0 | 2426 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0002c0002t0002 | 0/0 | 2426 | 23 | 21 | 1 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0003c0006t0002 | 0/0 | 2426 | 3 | 0 | 1 | 0 | 0 | 2 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0004c0009t0002 | 0/0 | 2426 | 2 | 0 | 1 | 0 | 1 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0005c0008t0002 | 0/0 | 2211 | 2 | 0 | 1 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2206): Show |
chr4 | 73431221 | 73461174 |
| a0006c0007t0002 | 0/0 | 2426 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0007c0010t0001 | 0/0 | 2426 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0008c0012t0002 | 0/0 | 2426 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0009c0016t0001 | 0/0 | 2426 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0010c0015t0002 | 0/0 | 2426 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| a0011c0011t0002 | 0/0 | 2426 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | ATTGT others(2421): Show |
chr4 | 73431221 | 73461174 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 69 | 14 | 9 | 34 | 6 | 6 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0003 | 0/0 | 22 | 0 | 7 | 13 | 1 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0005 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0008 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0015 | 0/0 | 6 | 0 | 3 | 0 | 1 | 2 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0016 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0002 | 0/0 | 25 | 0 | 9 | 12 | 2 | 2 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0004 | 0/0 | 15 | 5 | 3 | 0 | 1 | 6 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0006 | 0/0 | 14 | 0 | 12 | 2 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0007 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0009 | 0/0 | 8 | 3 | 0 | 2 | 1 | 2 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0011 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0012 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0014 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0021 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0003g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0003t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0003t0001g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0003t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0004t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0004t0002g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0005t0002g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0005t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0013t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0001c0014t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0003c0006t0002g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0004c0009t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0005c0008t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0005c0008t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0006c0007t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0006c0007t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0007c0010t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0008c0012t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0009c0016t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0010c0015t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| a0011c0011t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00099 | hp2 | a0001 | c0005 | t0002 | g0093 | EUR | GBR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00140 | hp1 | a0004 | c0009 | t0002 | g0004 | EUR | GBR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | FIN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00642 | hp1 | a0005 | c0008 | t0002 | g0083 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01192 | hp2 | a0001 | c0005 | t0002 | g0002 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01256 | hp1 | a0003 | c0006 | t0002 | g0012 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01433 | hp1 | a0004 | c0009 | t0002 | g0004 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | IBS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | IBS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0084 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02055 | hp1 | a0001 | c0005 | t0002 | g0002 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CDX | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CDX | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02258 | hp2 | a0001 | c0004 | t0002 | g0025 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0018 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02622 | hp1 | a0001 | c0004 | t0002 | g0025 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02738 | hp2 | a0003 | c0006 | t0002 | g0012 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0065 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02965 | hp1 | a0007 | c0010 | t0001 | g0063 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0018 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03098 | hp1 | a0006 | c0007 | t0002 | g0103 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03098 | hp2 | a0006 | c0007 | t0002 | g0012 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03195 | hp2 | a0008 | c0012 | t0002 | g0108 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0039 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0036 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03579 | hp2 | a0001 | c0004 | t0002 | g0025 | AFR | MSL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03688 | hp1 | a0003 | c0006 | t0002 | g0012 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03710 | hp2 | a0001 | c0014 | t0001 | g0001 | SAS | PJL | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03834 | hp2 | a0001 | c0013 | t0001 | g0016 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0064 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | YRI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18984 | hp2 | a0009 | c0016 | t0001 | g0008 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19030 | hp1 | a0010 | c0015 | t0002 | g0079 | AFR | LWK | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | LWK | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19086 | hp1 | a0011 | c0011 | t0002 | g0020 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | YRI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0106 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0113 | AFR | ACB | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | USA | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | USA | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA18955 | hp2 | a0005 | c0008 | t0002 | g0076 | EAS | JPT | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | LWK | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | LWK | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0082 | REF | REF | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0002 | g0114 | REF | REF | AFP_chr4_73431221_73461174 | AFP | chr4 | 73431221 | 73461174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73440656 | G | C | 1 | a0007 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.325G>C | p.Gly109Arg | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/15 | 367/2426 | 325/1830 | 109/609 | chr4 | 73440656 | |||
| chr4:73442372 | A | C | 1 | a0004 | 2 | HG00140.hp1 HG01433.hp1 |
missense_variant | MODERATE | c.559A>C | p.Lys187Gln | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 5/15 | 601/2426 | 559/1830 | 187/609 | chr4 | 73442372 | |||
| chr4:73443395 | C | A | 1 | a0011 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.664C>A | p.His222Asn | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/15 | 706/2426 | 664/1830 | 222/609 | chr4 | 73443395 | |||
| chr4:73445051 | C | G | 1 | a0003 | 3 | HG01256.hp1 HG02738.hp2 HG03688.hp1 |
missense_variant | MODERATE | c.772C>G | p.Leu258Val | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/15 | 814/2426 | 772/1830 | 258/609 | chr4 | 73445051 | |||
| chr4:73445057 | C | G | 1 | a0009 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.778C>G | p.Leu260Val | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/15 | 820/2426 | 778/1830 | 260/609 | chr4 | 73445057 | |||
| chr4:73447055 | CGGACACT others(1268): Show |
C | 1 | a0005 | 2 | HG00642.hp1 NA18955.hp2 |
exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.844-272_1058+788de others(1): Show |
AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 73447055 | ||||||
| chr4:73449423 | A | C | 1 | a0010 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.1147A>C | p.Lys383Gln | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 9/15 | 1189/2426 | 1147/1830 | 383/609 | chr4 | 73449423 | |||
| chr4:73450677 | C | T | 1 | a0006 | 2 | HG03098.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.1352C>T | p.Thr451Ile | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/15 | 1394/2426 | 1352/1830 | 451/609 | chr4 | 73450677 | |||
| chr4:73452612 | C | T | 1 | a0008 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1640C>T | p.Thr547Ile | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/15 | 1682/2426 | 1640/1830 | 547/609 | chr4 | 73452612 | |||
| chr4:73453821 | C | G | 2 | a0002 a0010 |
24 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
missense_variant | MODERATE | c.1709C>G | p.Ala570Gly | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 13/15 | 1751/2426 | 1709/1830 | 570/609 | chr4 | 73453821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73447476 | C | T | 1 | a0001c0001 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.858C>T | p.Ser286Ser | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/15 | 900/2426 | 858/1830 | 286/609 | chr4 | 73447476 | |||
| chr4:73450660 | G | A | 1 | a0001c0003 | 15 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(12): Show |
synonymous_variant | LOW | c.1335G>A | p.Ser445Ser | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/15 | 1377/2426 | 1335/1830 | 445/609 | chr4 | 73450660 | |||
| chr4:73450678 | C | T | 1 | a0001c0014 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1353C>T | p.Thr451Thr | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/15 | 1395/2426 | 1353/1830 | 451/609 | chr4 | 73450678 | |||
| chr4:73450711 | C | T | 1 | a0001c0013 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1386C>T | p.Cys462Cys | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/15 | 1428/2426 | 1386/1830 | 462/609 | chr4 | 73450711 | |||
| chr4:73452460 | T | C | 1 | a0001c0005 | 3 | HG00099.hp2 HG01192.hp2 HG02055.hp1 |
synonymous_variant | LOW | c.1488T>C | p.Gly496Gly | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/15 | 1530/2426 | 1488/1830 | 496/609 | chr4 | 73452460 | |||
| chr4:73452613 | A | G | 15 | a0001c0001 a0001c0003 a0001c0005 others(12): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
synonymous_variant | LOW | c.1641A>G | p.Thr547Thr | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/15 | 1683/2426 | 1641/1830 | 547/609 | chr4 | 73452613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73455648 | C | T | 1 | a0001c0001t0004 | 2 | HG01175.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*28C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 15/15 | 368 | chr4 | 73455648 | ||||||
| chr4:73455840 | T | C | 1 | a0001c0001t0005 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*220T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 15/15 | 560 | chr4 | 73455840 | ||||||
| chr4:73455883 | A | G | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(5): Show |
200 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*263A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 15/15 | 603 | chr4 | 73455883 | ||||||
| chr4:73456063 | T | C | 1 | a0001c0001t0003 | 7 | HG00438.hp2 HG02083.hp1 HG02155.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*443T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 15/15 | 783 | chr4 | 73456063 | ||||||
| chr4:73456120 | A | C | 1 | a0001c0001t0006 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*500A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 15/15 | 840 | chr4 | 73456120 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73436354 | T | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(49): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
splice_region_variant&intron_variant | LOW | c.85+7T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 1/14 | chr4 | 73436354 | |||||||
| chr4:73436434 | A | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(49): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.85+87A>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 1/14 | chr4 | 73436434 | |||||||
| chr4:73436498 | T | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0101 others(67): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.85+151T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 1/14 | chr4 | 73436498 | |||||||
| chr4:73436573 | T | G | 1 | a0002c0002t0002g0026 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.85+226T>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 1/14 | chr4 | 73436573 | |||||||
| chr4:73436824 | T | C | 70 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0101 others(67): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.86-336T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 1/14 | chr4 | 73436824 | |||||||
| chr4:73437083 | A | C | 6 | a0001c0001t0002g0004 a0001c0001t0002g0021 a0001c0001t0002g0024 others(3): Show |
27 | HG00140.hp1 HG00639.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.86-77A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 1/14 | chr4 | 73437083 | |||||||
| chr4:73437153 | T | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0101 others(57): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
splice_region_variant&intron_variant | LOW | c.86-7T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 1/14 | chr4 | 73437153 | |||||||
| chr4:73437483 | G | A | 42 | a0001c0001t0001g0077 a0001c0001t0002g0002 a0001c0001t0002g0006 others(39): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.137+272G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 2/14 | chr4 | 73437483 | |||||||
| chr4:73437535 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.137+324T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 2/14 | chr4 | 73437535 | |||||||
| chr4:73437658 | T | A | 1 | a0001c0001t0004g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.137+447T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 2/14 | chr4 | 73437658 | |||||||
| chr4:73437686 | A | T | 3 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | HG01070.hp2 HG01071.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.137+475A>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 2/14 | chr4 | 73437686 | |||||||
| chr4:73437757 | T | C | 1 | a0001c0001t0002g0040 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-417T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 2/14 | chr4 | 73437757 | |||||||
| chr4:73437872 | T | C | 2 | a0001c0001t0002g0073 a0001c0001t0002g0074 |
2 | HG00408.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.138-302T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 2/14 | chr4 | 73437872 | |||||||
| chr4:73437953 | T | C | 1 | a0002c0002t0002g0018 | 4 | HG01109.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-221T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 2/14 | chr4 | 73437953 | |||||||
| chr4:73438006 | T | A | 1 | a0001c0001t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.138-168T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 2/14 | chr4 | 73438006 | |||||||
| chr4:73438401 | T | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.270+95T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73438401 | |||||||
| chr4:73438661 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(49): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.270+355G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73438661 | |||||||
| chr4:73438664 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.270+358A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73438664 | |||||||
| chr4:73438927 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.270+621G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73438927 | |||||||
| chr4:73438971 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.270+665A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73438971 | |||||||
| chr4:73439320 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.270+1014A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439320 | |||||||
| chr4:73439334 | C | T | 1 | a0001c0003t0001g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.270+1028C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439334 | |||||||
| chr4:73439473 | T | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0099 |
3 | HG06807.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.271-1129T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439473 | |||||||
| chr4:73439485 | A | G | 1 | a0008c0012t0002g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.271-1117A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439485 | |||||||
| chr4:73439576 | A | C | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.271-1026A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439576 | |||||||
| chr4:73439584 | G | A | 1 | a0001c0001t0004g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.271-1018G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439584 | |||||||
| chr4:73439678 | T | C | 1 | a0001c0001t0002g0038 | 2 | HG02004.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.271-924T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439678 | |||||||
| chr4:73439802 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.271-800T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439802 | |||||||
| chr4:73439808 | A | C | 1 | a0001c0001t0003g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.271-794A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439808 | |||||||
| chr4:73439943 | GTA | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.271-651_271-650del others(2): Show |
AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 73439943 | ||||||
| chr4:73439952 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0002g0007 a0001c0001t0002g0073 others(3): Show |
17 | HG00408.hp1 HG00558.hp1 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.271-650T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73439952 | |||||||
| chr4:73440012 | T | G | 1 | a0001c0001t0002g0031 | 2 | NA18954.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.271-590T>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73440012 | |||||||
| chr4:73440014 | A | T | 1 | a0001c0001t0002g0031 | 2 | NA18954.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.271-588A>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73440014 | |||||||
| chr4:73440085 | C | T | 2 | a0001c0001t0002g0020 a0011c0011t0002g0020 |
4 | NA18983.hp2 NA19056.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-517C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73440085 | |||||||
| chr4:73440163 | G | T | 1 | a0001c0001t0002g0038 | 2 | HG02004.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.271-439G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73440163 | |||||||
| chr4:73440196 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.271-406T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73440196 | |||||||
| chr4:73440219 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.271-383C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73440219 | |||||||
| chr4:73440231 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.271-371G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73440231 | |||||||
| chr4:73440451 | T | C | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.271-151T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 3/14 | chr4 | 73440451 | |||||||
| chr4:73440954 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.482+141A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73440954 | |||||||
| chr4:73441354 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.482+541C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441354 | |||||||
| chr4:73441359 | G | T | 4 | a0001c0001t0002g0038 a0001c0001t0002g0107 a0001c0001t0004g0104 others(1): Show |
5 | HG01884.hp2 HG02004.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.482+546G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441359 | |||||||
| chr4:73441391 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.482+578C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441391 | |||||||
| chr4:73441429 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG02486.hp2 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.482+616G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441429 | |||||||
| chr4:73441436 | T | A | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.482+623T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441436 | |||||||
| chr4:73441538 | C | A | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.482+725C>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441538 | |||||||
| chr4:73441542 | G | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.482+729G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441542 | |||||||
| chr4:73441547 | C | G | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.482+734C>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441547 | |||||||
| chr4:73441567 | C | CA | 4 | a0001c0001t0001g0010 a0001c0003t0001g0010 a0001c0003t0001g0065 others(1): Show |
10 | HG01884.hp1 HG02074.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-710dupA | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 73441567 | ||||||
| chr4:73441567 | C | CAA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.483-711_483-710dup others(2): Show |
AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 73441567 | ||||||
| chr4:73441567 | C | CAAA | 42 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0047 others(39): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.483-712_483-710dup others(3): Show |
AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 73441567 | ||||||
| chr4:73441567 | C | CAAAA | 10 | a0001c0001t0002g0006 a0001c0001t0002g0032 a0001c0001t0002g0033 others(7): Show |
25 | HG00639.hp1 HG01071.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.483-713_483-710dup others(4): Show |
AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 73441567 | ||||||
| chr4:73441675 | ATTC | A | 1 | a0001c0004t0002g0025 | 3 | HG02258.hp2 HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.483-612_483-610del others(3): Show |
AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 73441675 | ||||||
| chr4:73441952 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0078 |
5 | HG02083.hp2 NA18948.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.483-344G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441952 | |||||||
| chr4:73441961 | C | T | 2 | a0001c0001t0002g0033 a0001c0001t0002g0094 |
3 | NA18959.hp2 NA18992.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.483-335C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73441961 | |||||||
| chr4:73442004 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
178 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.483-292G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73442004 | |||||||
| chr4:73442005 | G | T | 1 | a0001c0001t0002g0038 | 2 | HG02004.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.483-291G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73442005 | |||||||
| chr4:73442270 | T | A | 1 | a0001c0001t0001g0102 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.483-26T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 4/14 | chr4 | 73442270 | |||||||
| chr4:73442526 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.615+98T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 5/14 | chr4 | 73442526 | |||||||
| chr4:73442552 | T | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0047 |
7 | NA18964.hp1 NA18971.hp1 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.615+124T>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 5/14 | chr4 | 73442552 | |||||||
| chr4:73442770 | TGAA | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0101 others(66): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.615+346_615+348del others(3): Show |
AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr4 | 73442770 | ||||||
| chr4:73442837 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.615+409G>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 5/14 | chr4 | 73442837 | |||||||
| chr4:73442930 | T | A | 1 | a0001c0001t0002g0098 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.616-417T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 5/14 | chr4 | 73442930 | |||||||
| chr4:73443002 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.616-345G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 5/14 | chr4 | 73443002 | |||||||
| chr4:73443091 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.616-256T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 5/14 | chr4 | 73443091 | |||||||
| chr4:73443092 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.616-255C>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 5/14 | chr4 | 73443092 | |||||||
| chr4:73443462 | C | G | 1 | a0007c0010t0001g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.713+18C>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73443462 | |||||||
| chr4:73443725 | C | G | 1 | a0008c0012t0002g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.713+281C>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73443725 | |||||||
| chr4:73443755 | C | G | 44 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0110 others(41): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.713+311C>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73443755 | |||||||
| chr4:73443796 | C | A | 3 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | HG01070.hp2 HG01071.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.713+352C>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73443796 | |||||||
| chr4:73443856 | A | G | 2 | a0001c0001t0002g0037 a0001c0001t0002g0099 |
3 | HG06807.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.713+412A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73443856 | |||||||
| chr4:73443864 | A | G | 1 | a0001c0005t0002g0093 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.713+420A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73443864 | |||||||
| chr4:73444339 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.714-654A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73444339 | |||||||
| chr4:73444393 | A | C | 2 | a0001c0001t0001g0008 a0009c0016t0001g0008 |
10 | HG00438.hp1 HG00621.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.714-600A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73444393 | |||||||
| chr4:73444540 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714-453C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73444540 | |||||||
| chr4:73444598 | A | G | 1 | a0002c0002t0002g0036 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.714-395A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73444598 | |||||||
| chr4:73444819 | C | T | 1 | a0001c0001t0004g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.714-174C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73444819 | |||||||
| chr4:73444844 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.714-149C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73444844 | |||||||
| chr4:73444854 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.714-139T>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | chr4 | 73444854 | |||||||
| chr4:73444978 | C | CT | 4 | a0001c0001t0002g0011 a0001c0001t0002g0032 a0001c0001t0002g0096 others(1): Show |
12 | HG02040.hp2 HG02080.hp2 HG02135.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.714-7dupT | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 73444978 | ||||||
| chr4:73445127 | A | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(48): Show |
195 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
splice_region_variant&intron_variant | LOW | c.843+5A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445127 | |||||||
| chr4:73445364 | A | T | 1 | a0001c0001t0001g0017 | 5 | HG00408.hp2 HG02015.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.843+242A>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445364 | |||||||
| chr4:73445368 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.843+246C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445368 | |||||||
| chr4:73445411 | C | T | 4 | a0001c0001t0002g0006 a0001c0001t0002g0080 a0001c0001t0002g0081 others(1): Show |
17 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.843+289C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445411 | |||||||
| chr4:73445590 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.843+468T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445590 | |||||||
| chr4:73445611 | G | C | 1 | a0006c0007t0002g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.843+489G>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445611 | |||||||
| chr4:73445623 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.843+501C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445623 | |||||||
| chr4:73445646 | A | T | 1 | a0001c0001t0002g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.843+524A>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445646 | |||||||
| chr4:73445711 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.843+589C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445711 | |||||||
| chr4:73445716 | C | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
193 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.843+594C>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445716 | |||||||
| chr4:73445941 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.843+819T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73445941 | |||||||
| chr4:73446080 | A | G | 1 | a0001c0003t0001g0065 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.843+958A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446080 | |||||||
| chr4:73446113 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.843+991A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446113 | |||||||
| chr4:73446219 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.843+1097A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446219 | |||||||
| chr4:73446250 | A | C | 1 | a0001c0001t0002g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.843+1128A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446250 | |||||||
| chr4:73446291 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.843+1169C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446291 | |||||||
| chr4:73446312 | G | T | 1 | a0001c0001t0001g0029 | 2 | NA18747.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.844-1150G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446312 | |||||||
| chr4:73446397 | A | G | 3 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | HG01070.hp2 HG01071.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.844-1065A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446397 | |||||||
| chr4:73446482 | A | G | 1 | a0001c0001t0004g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.844-980A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446482 | |||||||
| chr4:73446587 | CTGATAAA others(57): Show |
C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.844-805_844-742del others(64): Show |
AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 73446587 | ||||||
| chr4:73446690 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0004g0104 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.844-772G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446690 | |||||||
| chr4:73446765 | A | C | 1 | a0001c0003t0001g0022 | 3 | HG01243.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.844-697A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446765 | |||||||
| chr4:73446835 | A | G | 65 | a0001c0001t0001g0077 a0001c0001t0001g0105 a0001c0001t0001g0109 others(62): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.844-627A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446835 | |||||||
| chr4:73446906 | G | C | 1 | a0001c0001t0001g0054 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.844-556G>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446906 | |||||||
| chr4:73446938 | C | T | 1 | a0002c0002t0002g0039 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.844-524C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446938 | |||||||
| chr4:73446983 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.844-479C>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446983 | |||||||
| chr4:73446993 | G | T | 5 | a0001c0001t0001g0105 a0002c0002t0002g0023 a0002c0002t0002g0039 others(2): Show |
8 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.844-469G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73446993 | |||||||
| chr4:73447025 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.844-437T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73447025 | |||||||
| chr4:73447055 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.844-407C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73447055 | |||||||
| chr4:73447120 | C | T | 9 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0021 others(6): Show |
37 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.844-342C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73447120 | |||||||
| chr4:73447147 | A | T | 1 | a0001c0001t0002g0006 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.844-315A>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73447147 | |||||||
| chr4:73447190 | G | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(118): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.844-272G>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73447190 | |||||||
| chr4:73447205 | C | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(50): Show |
198 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.844-257C>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73447205 | |||||||
| chr4:73447293 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(118): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.844-169T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73447293 | |||||||
| chr4:73447336 | C | T | 5 | a0001c0001t0002g0004 a0001c0001t0002g0021 a0001c0001t0002g0024 others(2): Show |
20 | HG00140.hp1 HG00639.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.844-126C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73447336 | |||||||
| chr4:73447452 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.844-10T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 7/14 | chr4 | 73447452 | |||||||
| chr4:73447751 | G | A | 1 | a0002c0002t0002g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1058+75G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73447751 | |||||||
| chr4:73447756 | G | A | 1 | a0002c0002t0002g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1058+80G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73447756 | |||||||
| chr4:73447839 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1058+163A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73447839 | |||||||
| chr4:73447911 | A | C | 1 | a0001c0001t0002g0004 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1058+235A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73447911 | |||||||
| chr4:73447919 | G | T | 1 | a0001c0001t0002g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1058+243G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73447919 | |||||||
| chr4:73448009 | T | C | 1 | a0001c0005t0002g0093 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1058+333T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448009 | |||||||
| chr4:73448011 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1058+335G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448011 | |||||||
| chr4:73448013 | A | T | 1 | a0001c0001t0004g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1058+337A>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448013 | |||||||
| chr4:73448241 | C | T | 1 | a0001c0001t0002g0038 | 2 | HG02004.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1058+565C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448241 | |||||||
| chr4:73448424 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0024 |
7 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+748G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448424 | |||||||
| chr4:73448439 | A | T | 1 | a0001c0001t0001g0061 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1058+763A>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448439 | |||||||
| chr4:73448448 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1058+772T>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448448 | |||||||
| chr4:73448549 | T | C | 9 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0021 others(6): Show |
37 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1059-786T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448549 | |||||||
| chr4:73448932 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(50): Show |
198 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1059-403C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448932 | |||||||
| chr4:73448985 | C | A | 2 | a0001c0001t0002g0107 a0001c0001t0004g0104 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1059-350C>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73448985 | |||||||
| chr4:73449006 | A | G | 1 | a0001c0001t0001g0005 | 14 | HG02071.hp2 NA18948.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.1059-329A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73449006 | |||||||
| chr4:73449059 | T | C | 1 | a0001c0001t0002g0024 | 3 | HG00639.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1059-276T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73449059 | |||||||
| chr4:73449088 | G | A | 1 | a0008c0012t0002g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1059-247G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73449088 | |||||||
| chr4:73449142 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0027 |
8 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059-193G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73449142 | |||||||
| chr4:73449302 | A | G | 2 | a0001c0001t0002g0037 a0001c0001t0002g0099 |
3 | HG06807.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1059-33A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 8/14 | chr4 | 73449302 | |||||||
| chr4:73449693 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1191+226A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 9/14 | chr4 | 73449693 | |||||||
| chr4:73449834 | A | G | 1 | a0001c0001t0002g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1192-202A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 9/14 | chr4 | 73449834 | |||||||
| chr4:73449959 | A | G | 1 | a0001c0001t0003g0060 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1192-77A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 9/14 | chr4 | 73449959 | |||||||
| chr4:73449975 | A | C | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1192-61A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 9/14 | chr4 | 73449975 | |||||||
| chr4:73450181 | G | C | 1 | a0001c0001t0001g0027 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1289+48G>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 10/14 | chr4 | 73450181 | |||||||
| chr4:73450259 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1289+126A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 10/14 | chr4 | 73450259 | |||||||
| chr4:73450417 | T | A | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1290-198T>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 10/14 | chr4 | 73450417 | |||||||
| chr4:73451012 | G | A | 63 | a0001c0001t0001g0077 a0001c0001t0002g0002 a0001c0001t0002g0004 others(60): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1428+259G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/14 | chr4 | 73451012 | |||||||
| chr4:73451176 | A | G | 1 | a0008c0012t0002g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1428+423A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/14 | chr4 | 73451176 | |||||||
| chr4:73451218 | G | T | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1428+465G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/14 | chr4 | 73451218 | |||||||
| chr4:73451237 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1428+484G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/14 | chr4 | 73451237 | |||||||
| chr4:73451486 | A | G | 1 | a0001c0001t0006g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1428+733A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/14 | chr4 | 73451486 | |||||||
| chr4:73451909 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1429-492C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/14 | chr4 | 73451909 | |||||||
| chr4:73452096 | G | A | 1 | a0002c0002t0002g0084 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1429-305G>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/14 | chr4 | 73452096 | |||||||
| chr4:73452306 | C | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1429-95C>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/14 | chr4 | 73452306 | |||||||
| chr4:73452332 | T | G | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1429-69T>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 11/14 | chr4 | 73452332 | |||||||
| chr4:73452683 | A | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0059 |
2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1652+59A>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73452683 | |||||||
| chr4:73452684 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1652+60C>A | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73452684 | |||||||
| chr4:73452713 | G | C | 1 | a0008c0012t0002g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1652+89G>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73452713 | |||||||
| chr4:73452783 | A | G | 1 | a0001c0001t0004g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1652+159A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73452783 | |||||||
| chr4:73452816 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1652+192T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73452816 | |||||||
| chr4:73452819 | C | T | 1 | a0002c0002t0002g0106 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1652+195C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73452819 | |||||||
| chr4:73453002 | T | C | 1 | a0001c0001t0002g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1652+378T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73453002 | |||||||
| chr4:73453420 | G | GAGA | 3 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | HG01070.hp2 HG01071.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1653-344_1653-342d others(5): Show |
AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 73453420 | ||||||
| chr4:73453464 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1653-301C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73453464 | |||||||
| chr4:73453565 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1653-200C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73453565 | |||||||
| chr4:73453566 | T | G | 67 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0002g0002 others(64): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1653-199T>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73453566 | |||||||
| chr4:73453592 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1653-173C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 12/14 | chr4 | 73453592 | |||||||
| chr4:73453966 | G | T | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1785+69G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 13/14 | chr4 | 73453966 | |||||||
| chr4:73454016 | A | T | 1 | a0001c0001t0002g0038 | 2 | HG02004.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1785+119A>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 13/14 | chr4 | 73454016 | |||||||
| chr4:73454094 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1785+197A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 13/14 | chr4 | 73454094 | |||||||
| chr4:73454177 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(51): Show |
199 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1785+280C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 13/14 | chr4 | 73454177 | |||||||
| chr4:73454398 | T | C | 1 | a0001c0001t0002g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1785+501T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 13/14 | chr4 | 73454398 | |||||||
| chr4:73454400 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1785+503A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 13/14 | chr4 | 73454400 | |||||||
| chr4:73454591 | A | G | 9 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0021 others(6): Show |
37 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1786-645A>G | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 13/14 | chr4 | 73454591 | |||||||
| chr4:73455186 | G | T | 1 | a0001c0001t0002g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1786-50G>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 13/14 | chr4 | 73455186 | |||||||
| chr4:73455292 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA20752.hp1 | splice_donor_variant&intron_variant | HIGH | c.*10+2T>C | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 14/14 | chr4 | 73455292 | |||||||
| chr4:73455534 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0047 |
7 | NA18964.hp1 NA18971.hp1 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.*11-97C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 14/14 | chr4 | 73455534 | |||||||
| chr4:73455621 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.*11-10C>T | AFP | ENSG00000081051.8 | transcript | ENST00000395792.7 | protein_coding | 14/14 | chr4 | 73455621 |