Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55363 |
| ensemblid | ENSG00000136929.13 |
| hgncid | 17509 |
| symbol | HEMGN |
| name | hemogen |
| refseq_nuc | NM_197978.3 |
| refseq_prot | NP_932095.1 |
| ensembl_nuc | ENST00000616898.2 |
| ensembl_prot | ENSP00000480020.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 97926791 |
| end | 97938172 |
| strand | - |
| ver | v1.2 |
| region | chr9:97926791-97938172 |
| region5000 | chr9:97921791-97943172 |
| regionname0 | HEMGN_chr9_97926791_97938172 |
| regionname5000 | HEMGN_chr9_97921791_97943172 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 484 | 312 | 64 | 62 | 127 | 16 | 41 | 93 | HEMGN_chr9_97921791_97943172 | HEMGN | MDLGK others(479): Show |
chr9 | 97921791 | 97943172 |
| a0002 | 0/0 | 484 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | MDLGK others(479): Show |
chr9 | 97921791 | 97943172 |
| a0003 | 0/0 | 484 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | MDLGK others(479): Show |
chr9 | 97921791 | 97943172 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1452 | 282 | 62 | 48 | 123 | 15 | 32 | HEMGN_chr9_97921791_97943172 | HEMGN | ATGGA others(1447): Show |
chr9 | 97921791 | 97943172 | ||
| a0001c0002 | 0/0 | 1452 | 27 | 2 | 14 | 2 | 0 | 9 | HEMGN_chr9_97921791_97943172 | HEMGN | ATGGA others(1447): Show |
chr9 | 97921791 | 97943172 | ||
| a0001c0003 | 0/0 | 1452 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | ATGGA others(1447): Show |
chr9 | 97921791 | 97943172 | ||
| a0001c0005 | 0/0 | 1452 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | ATGGA others(1447): Show |
chr9 | 97921791 | 97943172 | ||
| a0002c0006 | 0/0 | 1452 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | ATGGA others(1447): Show |
chr9 | 97921791 | 97943172 | ||
| a0003c0004 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | ATGGA others(1447): Show |
chr9 | 97921791 | 97943172 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2082 | 130 | 30 | 15 | 66 | 4 | 15 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2077): Show |
chr9 | 97921791 | 97943172 |
| a0001c0001t0002 | 1/1 | 2084 | 93 | 18 | 19 | 36 | 6 | 12 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2079): Show |
chr9 | 97921791 | 97943172 |
| a0001c0001t0003 | 0/0 | 2076 | 46 | 3 | 13 | 20 | 5 | 5 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2071): Show |
chr9 | 97921791 | 97943172 |
| a0001c0001t0004 | 0/0 | 2078 | 4 | 3 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2073): Show |
chr9 | 97921791 | 97943172 |
| a0001c0001t0005 | 0/0 | 2076 | 4 | 3 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2071): Show |
chr9 | 97921791 | 97943172 |
| a0001c0001t0006 | 0/0 | 2084 | 4 | 4 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2079): Show |
chr9 | 97921791 | 97943172 |
| a0001c0001t0007 | 0/0 | 2084 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2079): Show |
chr9 | 97921791 | 97943172 |
| a0001c0002t0003 | 0/0 | 2076 | 26 | 1 | 14 | 2 | 0 | 9 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2071): Show |
chr9 | 97921791 | 97943172 |
| a0001c0002t0004 | 0/0 | 2078 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2073): Show |
chr9 | 97921791 | 97943172 |
| a0001c0003t0001 | 0/0 | 2082 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2077): Show |
chr9 | 97921791 | 97943172 |
| a0001c0005t0002 | 0/0 | 2084 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2079): Show |
chr9 | 97921791 | 97943172 |
| a0002c0006t0001 | 0/0 | 2082 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2077): Show |
chr9 | 97921791 | 97943172 |
| a0003c0004t0001 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | AGTCA others(2077): Show |
chr9 | 97921791 | 97943172 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 98 | 22 | 14 | 50 | 3 | 9 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0002 | 1/1 | 58 | 12 | 14 | 21 | 3 | 6 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0003 | 0/0 | 23 | 0 | 7 | 13 | 1 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0005 | 0/0 | 10 | 0 | 4 | 0 | 4 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0005g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0002t0003g0004 | 0/0 | 16 | 1 | 7 | 1 | 0 | 7 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0002t0003g0007 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0001c0005t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0002c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| a0003c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | FIN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00323 | hp1 | a0001 | c0005 | t0002 | g0048 | EUR | FIN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0067 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01975 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CDX | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0069 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0071 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03942 | hp2 | a0002 | c0006 | t0001 | g0045 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0068 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | LWK | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | LWK | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19089 | hp2 | a0003 | c0004 | t0001 | g0052 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ASW | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | TSI | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | TSI | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | GIH | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | USA | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | LWK | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0002 | REF | REF | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97930754 | T | C | 1 | a0003 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.641A>G | p.His214Arg | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/4 | 677/2084 | 641/1455 | 214/484 | chr9 | 97930754 | |||
| chr9:97930800 | C | A | 1 | a0002 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.595G>T | p.Asp199Tyr | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/4 | 631/2084 | 595/1455 | 199/484 | chr9 | 97930800 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97927411 | A | G | 1 | a0001c0002 | 27 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(24): Show |
synonymous_variant | LOW | c.1428T>C | p.Asn476Asn | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 1464/2084 | 1428/1455 | 476/484 | chr9 | 97927411 | |||
| chr9:97930366 | G | T | 1 | a0001c0005 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.1029C>A | p.Ile343Ile | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/4 | 1065/2084 | 1029/1455 | 343/484 | chr9 | 97930366 | |||
| chr9:97931145 | A | G | 2 | a0001c0003 a0003c0004 |
3 | NA18947.hp2 NA18981.hp1 NA19089.hp2 |
synonymous_variant | LOW | c.250T>C | p.Leu84Leu | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/4 | 286/2084 | 250/1455 | 84/484 | chr9 | 97931145 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97927093 | A | T | 1 | a0001c0001t0005 | 4 | HG01243.hp1 HG01891.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*291T>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 291 | chr9 | 97927093 | ||||||
| chr9:97927168 | TAC | T | 4 | a0001c0001t0001 a0001c0003t0001 a0002c0006t0001 others(1): Show |
134 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*214_*215delGT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 214 | chr9 | 97927168 | ||||||
| chr9:97927168 | TACACAC | T | 2 | a0001c0001t0004 a0001c0002t0004 |
5 | HG02818.hp2 HG02886.hp1 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*210_*215delGTGTGT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 210 | chr9 | 97927168 | ||||||
| chr9:97927168 | TACACACA others(1): Show |
T | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0002t0003 |
76 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*208_*215delGTGTGT others(2): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 208 | chr9 | 97927168 | ||||||
| chr9:97927250 | T | G | 1 | a0001c0001t0007 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134A>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 134 | chr9 | 97927250 | ||||||
| chr9:97927260 | G | A | 2 | a0001c0001t0006 a0001c0001t0007 |
5 | HG02451.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*124C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 124 | chr9 | 97927260 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97927585 | C | T | 1 | a0001c0001t0004g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1361-107G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97927585 | |||||||
| chr9:97927635 | G | C | 2 | a0001c0001t0002g0056 a0001c0001t0002g0058 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1361-157C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97927635 | |||||||
| chr9:97927902 | T | G | 1 | a0001c0001t0004g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1361-424A>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97927902 | |||||||
| chr9:97928025 | A | AT | 13 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0002g0013 others(10): Show |
20 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1361-548dupA | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928025 | |||||||
| chr9:97928025 | A | ATT | 5 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0037 others(2): Show |
15 | HG00597.hp1 HG00642.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-549_1361-548d others(4): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928025 | |||||||
| chr9:97928025 | A | T | 1 | a0001c0001t0006g0025 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1361-547T>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928025 | |||||||
| chr9:97928025 | AT | A | 8 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0015 others(5): Show |
42 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-548delA | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928025 | |||||||
| chr9:97928079 | T | G | 1 | a0001c0001t0006g0065 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1361-601A>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928079 | |||||||
| chr9:97928125 | C | G | 1 | a0001c0001t0002g0017 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1361-647G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928125 | |||||||
| chr9:97928239 | A | G | 1 | a0001c0001t0001g0009 | 4 | NA18944.hp2 NA18955.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1361-761T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928239 | |||||||
| chr9:97928242 | G | T | 2 | a0001c0001t0004g0029 a0001c0001t0004g0072 |
2 | HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1361-764C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928242 | |||||||
| chr9:97928273 | A | G | 26 | a0001c0001t0002g0039 a0001c0001t0002g0055 a0001c0001t0003g0003 others(23): Show |
82 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1361-795T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928273 | |||||||
| chr9:97928342 | T | C | 1 | a0001c0001t0003g0016 | 2 | NA18961.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1361-864A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928342 | |||||||
| chr9:97928699 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1361-1221A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928699 | |||||||
| chr9:97928736 | G | T | 1 | a0001c0001t0002g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1361-1258C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928736 | |||||||
| chr9:97928816 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1360+1219T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928816 | |||||||
| chr9:97928857 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1360+1178A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928857 | |||||||
| chr9:97928886 | G | A | 26 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(23): Show |
82 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1360+1149C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928886 | |||||||
| chr9:97928916 | A | G | 1 | a0002c0006t0001g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1360+1119T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928916 | |||||||
| chr9:97929115 | C | T | 25 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(22): Show |
80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1360+920G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929115 | |||||||
| chr9:97929138 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1360+897T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929138 | |||||||
| chr9:97929482 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1360+553C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929482 | |||||||
| chr9:97929618 | T | TG | 25 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(22): Show |
80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1360+416_1360+417i others(3): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929618 | |||||||
| chr9:97929620 | A | G | 1 | a0001c0001t0003g0034 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1360+415T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929620 | |||||||
| chr9:97929648 | T | G | 1 | a0001c0001t0006g0063 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1360+387A>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929648 | |||||||
| chr9:97929827 | G | A | 5 | a0001c0001t0002g0039 a0001c0001t0006g0025 a0001c0001t0006g0063 others(2): Show |
6 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1360+208C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929827 | |||||||
| chr9:97929955 | T | TA | 25 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(22): Show |
80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1360+79dupT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929955 | |||||||
| chr9:97931298 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.174-77G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931298 | |||||||
| chr9:97931427 | A | G | 1 | a0001c0001t0004g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.174-206T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931427 | |||||||
| chr9:97931435 | G | C | 7 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0067 others(4): Show |
27 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.174-214C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931435 | |||||||
| chr9:97931574 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.174-353C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931574 | |||||||
| chr9:97931783 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.174-562T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931783 | |||||||
| chr9:97932365 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.174-1144A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932365 | |||||||
| chr9:97932676 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.174-1455G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932676 | |||||||
| chr9:97932677 | G | A | 1 | a0001c0002t0003g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.174-1456C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932677 | |||||||
| chr9:97932727 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0074 |
11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.174-1506G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932727 | |||||||
| chr9:97932739 | G | T | 1 | a0001c0002t0003g0070 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.174-1518C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932739 | |||||||
| chr9:97932803 | C | CAAAA | 14 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(11): Show |
48 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.174-1586_174-1583d others(6): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932803 | |||||||
| chr9:97932803 | C | CAAAAA | 8 | a0001c0001t0003g0015 a0001c0001t0003g0038 a0001c0001t0004g0072 others(5): Show |
29 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.174-1587_174-1583d others(7): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932803 | |||||||
| chr9:97932803 | CA | C | 6 | a0001c0001t0001g0049 a0001c0001t0002g0020 a0001c0001t0002g0073 others(3): Show |
8 | HG00323.hp1 HG01517.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.174-1583delT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932803 | |||||||
| chr9:97932930 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.174-1709T>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932930 | |||||||
| chr9:97932973 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.174-1752A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932973 | |||||||
| chr9:97933007 | T | C | 1 | a0001c0001t0006g0025 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.174-1786A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933007 | |||||||
| chr9:97933114 | T | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0074 |
11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.174-1893A>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933114 | |||||||
| chr9:97933494 | T | C | 25 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(22): Show |
80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.174-2273A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933494 | |||||||
| chr9:97933502 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0074 |
11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.174-2281G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933502 | |||||||
| chr9:97933511 | A | T | 1 | a0001c0001t0002g0046 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.174-2290T>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933511 | |||||||
| chr9:97933618 | C | T | 2 | a0001c0001t0001g0044 a0002c0006t0001g0045 |
2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.174-2397G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933618 | |||||||
| chr9:97933619 | G | A | 33 | a0001c0001t0001g0035 a0001c0001t0002g0006 a0001c0001t0002g0037 others(30): Show |
97 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.174-2398C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933619 | |||||||
| chr9:97933726 | C | T | 1 | a0001c0002t0003g0067 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.173+2445G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933726 | |||||||
| chr9:97933921 | T | C | 25 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(22): Show |
80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.173+2250A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933921 | |||||||
| chr9:97933986 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.173+2185C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933986 | |||||||
| chr9:97934117 | T | C | 1 | a0001c0001t0004g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.173+2054A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934117 | |||||||
| chr9:97934354 | G | A | 25 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(22): Show |
80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.173+1817C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934354 | |||||||
| chr9:97934384 | A | G | 1 | a0001c0001t0002g0012 | 3 | HG00642.hp2 HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.173+1787T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934384 | |||||||
| chr9:97934392 | A | AAGGAGAG others(3): Show |
11 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(8): Show |
43 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.173+1769_173+1778d others(12): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934392 | |||||||
| chr9:97934404 | G | C | 3 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0074 |
11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.173+1767C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934404 | |||||||
| chr9:97934435 | AGGGGGAG others(10): Show |
A | 1 | a0001c0001t0001g0024 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.173+1719_173+1735d others(19): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934435 | |||||||
| chr9:97934451 | A | AG | 15 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0002g0002 others(12): Show |
28 | HG00597.hp1 HG00639.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.173+1719dupC | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934451 | |||||||
| chr9:97934453 | G | T | 1 | a0001c0001t0002g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.173+1718C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934453 | |||||||
| chr9:97934458 | A | G | 1 | a0001c0001t0003g0033 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.173+1713T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934458 | |||||||
| chr9:97934518 | A | G | 5 | a0001c0001t0002g0039 a0001c0001t0006g0025 a0001c0001t0006g0063 others(2): Show |
6 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.173+1653T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934518 | |||||||
| chr9:97934989 | G | C | 1 | a0001c0001t0001g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.173+1182C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934989 | |||||||
| chr9:97935005 | A | G | 25 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(22): Show |
80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.173+1166T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935005 | |||||||
| chr9:97935048 | C | G | 1 | a0001c0001t0002g0012 | 3 | HG00642.hp2 HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.173+1123G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935048 | |||||||
| chr9:97935101 | C | A | 1 | a0001c0001t0004g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.173+1070G>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935101 | |||||||
| chr9:97935111 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.173+1060C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935111 | |||||||
| chr9:97935192 | A | G | 1 | a0001c0001t0003g0033 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.173+979T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935192 | |||||||
| chr9:97935366 | T | A | 34 | a0001c0001t0001g0035 a0001c0001t0002g0006 a0001c0001t0002g0017 others(31): Show |
99 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.173+805A>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935366 | |||||||
| chr9:97935730 | C | T | 1 | a0001c0001t0003g0032 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.173+441G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935730 | |||||||
| chr9:97935865 | A | G | 7 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0067 others(4): Show |
27 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.173+306T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935865 | |||||||
| chr9:97936079 | T | C | 3 | a0001c0001t0004g0029 a0001c0001t0005g0010 a0001c0001t0005g0031 |
5 | HG01243.hp1 HG01891.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.173+92A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97936079 | |||||||
| chr9:97936091 | T | C | 1 | a0001c0001t0004g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.173+80A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97936091 | |||||||
| chr9:97936142 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.173+29C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97936142 | |||||||
| chr9:97936353 | C | G | 1 | a0001c0001t0001g0019 | 2 | NA18951.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.80-89G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936353 | |||||||
| chr9:97936401 | T | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0074 |
11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-137A>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936401 | |||||||
| chr9:97936895 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0041 |
3 | HG01891.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.80-631G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936895 | |||||||
| chr9:97936956 | C | A | 11 | a0001c0001t0001g0035 a0001c0001t0002g0037 a0001c0001t0003g0003 others(8): Show |
43 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.80-692G>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936956 | |||||||
| chr9:97936960 | T | C | 28 | a0001c0001t0001g0035 a0001c0001t0002g0006 a0001c0001t0002g0037 others(25): Show |
91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.80-696A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936960 | |||||||
| chr9:97937061 | C | G | 1 | a0001c0001t0001g0040 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.80-797G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937061 | |||||||
| chr9:97937074 | G | C | 1 | a0001c0001t0002g0017 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.80-810C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937074 | |||||||
| chr9:97937081 | C | T | 1 | a0001c0001t0002g0017 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.80-817G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937081 | |||||||
| chr9:97937328 | A | G | 1 | a0001c0001t0002g0011 | 3 | HG03704.hp2 HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.79+730T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937328 | |||||||
| chr9:97937479 | G | T | 1 | a0001c0001t0002g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+579C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937479 | |||||||
| chr9:97937488 | C | T | 1 | a0001c0001t0004g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79+570G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937488 | |||||||
| chr9:97937548 | A | C | 28 | a0001c0001t0001g0035 a0001c0001t0002g0006 a0001c0001t0002g0037 others(25): Show |
91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.79+510T>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937548 | |||||||
| chr9:97937670 | C | T | 1 | a0001c0001t0004g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+388G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937670 | |||||||
| chr9:97937698 | TA | T | 2 | a0001c0001t0003g0005 a0001c0001t0003g0028 |
11 | HG00280.hp1 HG00735.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+359delT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937698 | |||||||
| chr9:97937875 | T | C | 28 | a0001c0001t0001g0035 a0001c0001t0002g0006 a0001c0001t0002g0037 others(25): Show |
91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.79+183A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937875 | |||||||
| chr9:97937960 | C | CT | 20 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0002g0014 others(17): Show |
61 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.79+97dupA | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937960 |