Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100288801 |
| ensemblid | ENSG00000172969.8 |
| hgncid | 33626 |
| symbol | FRG2C |
| name | FSHD region gene 2 family member C |
| refseq_nuc | NM_001124759.5 |
| refseq_prot | NP_001118231.1 |
| ensembl_nuc | ENST00000308062.8 |
| ensembl_prot | ENSP00000312299.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 75664328 |
| end | 75667173 |
| strand | + |
| ver | v1.2 |
| region | chr3:75664328-75667173 |
| region5000 | chr3:75659328-75672173 |
| regionname0 | FRG2C_chr3_75664328_75667173 |
| regionname5000 | FRG2C_chr3_75659328_75672173 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 282 | 299 | 85 | 64 | 106 | 8 | 34 | 82 | FRG2C_chr3_75659328_75672173 | FRG2C | MGKGN others(277): Show |
chr3 | 75659328 | 75672173 |
| a0002 | 0/0 | 282 | 83 | 4 | 16 | 42 | 10 | 11 | 34 | FRG2C_chr3_75659328_75672173 | FRG2C | MGKGN others(277): Show |
chr3 | 75659328 | 75672173 |
| a0003 | 0/0 | 282 | 19 | 0 | 0 | 18 | 0 | 1 | 17 | FRG2C_chr3_75659328_75672173 | FRG2C | MGKGN others(277): Show |
chr3 | 75659328 | 75672173 |
| a0004 | 0/0 | 282 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FRG2C_chr3_75659328_75672173 | FRG2C | MGKGN others(277): Show |
chr3 | 75659328 | 75672173 |
| a0005 | 0/0 | 282 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | MGKGN others(277): Show |
chr3 | 75659328 | 75672173 |
| a0006 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | MGKGN others(277): Show |
chr3 | 75659328 | 75672173 |
| a0007 | 0/0 | 282 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | MGKGN others(277): Show |
chr3 | 75659328 | 75672173 |
| a0008 | 0/0 | 282 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | MGKGN others(277): Show |
chr3 | 75659328 | 75672173 |
| a0009 | 0/0 | 282 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | MGKGN others(277): Show |
chr3 | 75659328 | 75672173 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 846 | 239 | 69 | 49 | 85 | 7 | 27 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0001c0003 | 0/0 | 846 | 55 | 15 | 12 | 20 | 1 | 7 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0001c0005 | 0/0 | 846 | 4 | 1 | 3 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0001c0010 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0002c0002 | 0/0 | 846 | 83 | 4 | 16 | 42 | 10 | 11 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0003c0004 | 0/0 | 846 | 19 | 0 | 0 | 18 | 0 | 1 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0004c0006 | 0/0 | 846 | 3 | 0 | 0 | 3 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0005c0007 | 0/0 | 846 | 2 | 2 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0006c0011 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0007c0009 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0008c0012 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 | ||
| a0009c0008 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ATGGG others(841): Show |
chr3 | 75659328 | 75672173 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2033 | 197 | 45 | 38 | 83 | 5 | 24 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0001c0001t0003 | 0/0 | 2034 | 13 | 6 | 3 | 0 | 2 | 2 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0001c0001t0004 | 0/0 | 2033 | 18 | 18 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0001c0001t0005 | 0/0 | 2033 | 9 | 0 | 8 | 0 | 0 | 1 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0001c0001t0009 | 0/0 | 2033 | 2 | 0 | 0 | 2 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0001c0003t0003 | 0/0 | 2034 | 48 | 10 | 12 | 19 | 1 | 6 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0001c0003t0006 | 0/0 | 2031 | 3 | 3 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2026): Show |
chr3 | 75659328 | 75672173 |
| a0001c0003t0010 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0001c0003t0012 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0001c0003t0013 | 0/0 | 2034 | 1 | 0 | 0 | 0 | 0 | 1 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0001c0003t0015 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0001c0005t0001 | 0/0 | 2033 | 4 | 1 | 3 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0001c0010t0001 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0002c0002t0002 | 0/0 | 2034 | 73 | 0 | 16 | 37 | 9 | 11 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0002c0002t0003 | 0/0 | 2034 | 4 | 4 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0002c0002t0007 | 0/0 | 2033 | 3 | 0 | 0 | 3 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0002c0002t0008 | 0/0 | 2034 | 2 | 0 | 0 | 1 | 1 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0002c0002t0011 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0003c0004t0001 | 0/0 | 2033 | 19 | 0 | 0 | 18 | 0 | 1 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0004c0006t0001 | 0/0 | 2033 | 3 | 0 | 0 | 3 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0005c0007t0001 | 0/0 | 2033 | 2 | 2 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0006c0011t0003 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0007c0009t0014 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2029): Show |
chr3 | 75659328 | 75672173 |
| a0008c0012t0001 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| a0009c0008t0016 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | ACACT others(2028): Show |
chr3 | 75659328 | 75672173 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/1 | 196 | 45 | 37 | 83 | 5 | 24 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0001t0003g0006 | 0/0 | 10 | 3 | 3 | 0 | 2 | 2 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0001t0004g0005 | 0/0 | 15 | 15 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0001t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0001t0005g0001 | 0/0 | 9 | 0 | 8 | 0 | 0 | 1 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0003t0003g0003 | 0/0 | 47 | 9 | 12 | 19 | 1 | 6 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0003t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0003t0006g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0003t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0003t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0003t0013g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0003t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0005t0001g0008 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0001c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0002c0002t0002g0002 | 0/0 | 72 | 0 | 16 | 36 | 9 | 11 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0002c0002t0003g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0002c0002t0007g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0002c0002t0008g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0002c0002t0011g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0003c0004t0001g0004 | 0/0 | 19 | 0 | 0 | 18 | 0 | 1 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0004c0006t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0005c0007t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0006c0011t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0007c0009t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0008c0012t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| a0009c0008t0016g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00323 | hp2 | a0002 | c0002 | t0008 | g0002 | EUR | FIN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00558 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00597 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00609 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00621 | hp1 | a0002 | c0002 | t0011 | g0013 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00735 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01099 | hp1 | a0001 | c0005 | t0001 | g0008 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01099 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01106 | hp1 | a0001 | c0005 | t0001 | g0008 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0008 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01255 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01256 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01261 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01433 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01975 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02056 | hp1 | a0006 | c0011 | t0003 | g0003 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02155 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | CDX | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02257 | hp1 | a0001 | c0003 | t0012 | g0003 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02258 | hp2 | a0005 | c0007 | t0001 | g0002 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02280 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02280 | hp2 | a0007 | c0009 | t0014 | g0007 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02293 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02683 | hp2 | a0001 | c0003 | t0003 | g0003 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02970 | hp1 | a0001 | c0003 | t0006 | g0009 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02976 | hp1 | a0001 | c0003 | t0006 | g0009 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03195 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03209 | hp1 | a0005 | c0007 | t0001 | g0002 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03225 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03486 | hp1 | a0008 | c0012 | t0001 | g0001 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03491 | hp2 | a0001 | c0003 | t0003 | g0003 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0003 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03516 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | ESN | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03688 | hp1 | a0001 | c0003 | t0003 | g0003 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03710 | hp1 | a0001 | c0003 | t0003 | g0003 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | BEB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04184 | hp1 | a0003 | c0004 | t0001 | g0004 | SAS | BEB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04199 | hp2 | a0001 | c0003 | t0003 | g0003 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04228 | hp1 | a0001 | c0003 | t0013 | g0003 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | YRI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18522 | hp2 | a0009 | c0008 | t0016 | g0017 | AFR | YRI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18612 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | CHB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | YRI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18940 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18943 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18946 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18946 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18947 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18948 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18951 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18956 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18960 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18961 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18963 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18965 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18966 | hp1 | a0004 | c0006 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18973 | hp2 | a0004 | c0006 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18974 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18975 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18979 | hp1 | a0002 | c0002 | t0007 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18979 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18987 | hp1 | a0002 | c0002 | t0007 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18988 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18989 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18990 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18994 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18995 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19002 | hp1 | a0002 | c0002 | t0008 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19007 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19009 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19009 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19012 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | LWK | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19058 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19063 | hp2 | a0004 | c0006 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19064 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19067 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19070 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19074 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19078 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19081 | hp1 | a0002 | c0002 | t0007 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19086 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19091 | hp2 | a0001 | c0010 | t0001 | g0001 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19240 | hp1 | a0001 | c0003 | t0006 | g0009 | AFR | YRI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ASW | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20752 | hp2 | a0001 | c0003 | t0003 | g0003 | EUR | TSI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | TSI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | GIH | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02109 | hp1 | a0001 | c0003 | t0003 | g0015 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | USA | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18955 | hp1 | a0001 | c0003 | t0015 | g0003 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | USA | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA21309 | hp1 | a0001 | c0003 | t0010 | g0016 | AFR | LWK | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| NA21309 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | LWK | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | FRG2C_chr3_75659328_75672173 | FRG2C | chr3 | 75659328 | 75672173 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:75664401 | C | A | 1 | a0003 | 19 | HG00597.hp1 HG04184.hp1 NA18940.hp1 others(16): Show |
missense_variant | MODERATE | c.22C>A | p.Pro8Thr | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/4 | 74/2033 | 22/849 | 8/282 | chr3 | 75664401 | |||
| chr3:75664404 | G | A | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.25G>A | p.Asp9Asn | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/4 | 77/2033 | 25/849 | 9/282 | chr3 | 75664404 | |||
| chr3:75664413 | T | C | 2 | a0002 a0005 |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
missense_variant | MODERATE | c.34T>C | p.Cys12Arg | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/4 | 86/2033 | 34/849 | 12/282 | chr3 | 75664413 | |||
| chr3:75664829 | T | G | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.189T>G | p.Asp63Glu | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/4 | 241/2033 | 189/849 | 63/282 | chr3 | 75664829 | |||
| chr3:75664890 | G | A | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.250G>A | p.Gly84Arg | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/4 | 302/2033 | 250/849 | 84/282 | chr3 | 75664890 | |||
| chr3:75665147 | A | G | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.278A>G | p.Gln93Arg | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/4 | 330/2033 | 278/849 | 93/282 | chr3 | 75665147 | |||
| chr3:75665174 | G | T | 1 | a0008 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.305G>T | p.Ser102Ile | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/4 | 357/2033 | 305/849 | 102/282 | chr3 | 75665174 | |||
| chr3:75665186 | T | G | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.317T>G | p.Ile106Ser | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/4 | 369/2033 | 317/849 | 106/282 | chr3 | 75665186 | |||
| chr3:75665193 | A | C | 1 | a0004 | 3 | NA18966.hp1 NA18973.hp2 NA19063.hp2 |
missense_variant | MODERATE | c.324A>C | p.Gln108His | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/4 | 376/2033 | 324/849 | 108/282 | chr3 | 75665193 | |||
| chr3:75665551 | A | G | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.359A>G | p.Asn120Ser | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 411/2033 | 359/849 | 120/282 | chr3 | 75665551 | |||
| chr3:75665620 | A | G | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.428A>G | p.Asp143Gly | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 480/2033 | 428/849 | 143/282 | chr3 | 75665620 | |||
| chr3:75665637 | A | C | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.445A>C | p.Ser149Arg | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 497/2033 | 445/849 | 149/282 | chr3 | 75665637 | |||
| chr3:75665658 | C | T | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.466C>T | p.Arg156Cys | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 518/2033 | 466/849 | 156/282 | chr3 | 75665658 | |||
| chr3:75665668 | G | A | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.476G>A | p.Arg159Gln | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 528/2033 | 476/849 | 159/282 | chr3 | 75665668 | |||
| chr3:75665680 | G | A | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.488G>A | p.Arg163Gln | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 540/2033 | 488/849 | 163/282 | chr3 | 75665680 | |||
| chr3:75665686 | T | C | 1 | a0007 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.494T>C | p.Leu165Pro | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 546/2033 | 494/849 | 165/282 | chr3 | 75665686 | |||
| chr3:75665689 | A | G | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.497A>G | p.Glu166Gly | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 549/2033 | 497/849 | 166/282 | chr3 | 75665689 | |||
| chr3:75665743 | C | T | 1 | a0006 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.551C>T | p.Ser184Leu | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 603/2033 | 551/849 | 184/282 | chr3 | 75665743 | |||
| chr3:75665820 | C | A | 1 | a0002 | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
missense_variant | MODERATE | c.628C>A | p.Leu210Met | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 680/2033 | 628/849 | 210/282 | chr3 | 75665820 | |||
| chr3:75665948 | T | A | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.756T>A | p.Asp252Glu | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 808/2033 | 756/849 | 252/282 | chr3 | 75665948 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:75664415 | T | C | 1 | a0009c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.36T>C | p.Cys12Cys | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/4 | 88/2033 | 36/849 | 12/282 | chr3 | 75664415 | |||
| chr3:75664826 | A | G | 1 | a0009c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.186A>G | p.Ser62Ser | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/4 | 238/2033 | 186/849 | 62/282 | chr3 | 75664826 | |||
| chr3:75664859 | A | G | 1 | a0009c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.219A>G | p.Glu73Glu | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/4 | 271/2033 | 219/849 | 73/282 | chr3 | 75664859 | |||
| chr3:75665160 | G | A | 1 | a0009c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.291G>A | p.Arg97Arg | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/4 | 343/2033 | 291/849 | 97/282 | chr3 | 75665160 | |||
| chr3:75665558 | G | T | 1 | a0009c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.366G>T | p.Thr122Thr | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 418/2033 | 366/849 | 122/282 | chr3 | 75665558 | |||
| chr3:75665606 | C | T | 1 | a0005c0007 | 2 | HG02258.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.414C>T | p.Ile138Ile | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 466/2033 | 414/849 | 138/282 | chr3 | 75665606 | |||
| chr3:75665684 | C | T | 1 | a0009c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.492C>T | p.Ala164Ala | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 544/2033 | 492/849 | 164/282 | chr3 | 75665684 | |||
| chr3:75665726 | C | T | 1 | a0003c0004 | 19 | HG00597.hp1 HG04184.hp1 NA18940.hp1 others(16): Show |
synonymous_variant | LOW | c.534C>T | p.Thr178Thr | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 586/2033 | 534/849 | 178/282 | chr3 | 75665726 | |||
| chr3:75665747 | G | A | 1 | a0009c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.555G>A | p.Glu185Glu | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 607/2033 | 555/849 | 185/282 | chr3 | 75665747 | |||
| chr3:75665763 | C | T | 1 | a0001c0010 | 1 | NA19091.hp2 | synonymous_variant | LOW | c.571C>T | p.Leu191Leu | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 623/2033 | 571/849 | 191/282 | chr3 | 75665763 | |||
| chr3:75665825 | C | T | 1 | a0009c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.633C>T | p.Leu211Leu | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 685/2033 | 633/849 | 211/282 | chr3 | 75665825 | |||
| chr3:75665865 | T | C | 3 | a0001c0003 a0003c0004 a0006c0011 |
75 | HG00597.hp1 HG00609.hp1 HG00735.hp1 others(72): Show |
synonymous_variant | LOW | c.673T>C | p.Leu225Leu | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 725/2033 | 673/849 | 225/282 | chr3 | 75665865 | |||
| chr3:75665921 | C | A | 1 | a0001c0005 | 4 | HG01099.hp1 HG01106.hp1 HG01243.hp1 others(1): Show |
synonymous_variant | LOW | c.729C>A | p.Val243Val | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 781/2033 | 729/849 | 243/282 | chr3 | 75665921 | |||
| chr3:75665936 | T | A | 1 | a0009c0008 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.744T>A | p.Pro248Pro | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 796/2033 | 744/849 | 248/282 | chr3 | 75665936 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:75664345 | A | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-35A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/4 | 35 | chr3 | 75664345 | ||||||
| chr3:75664356 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/4 | 24 | chr3 | 75664356 | ||||||
| chr3:75666048 | T | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7T>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 7 | chr3 | 75666048 | ||||||
| chr3:75666051 | G | C | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10G>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 10 | chr3 | 75666051 | ||||||
| chr3:75666069 | G | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 28 | chr3 | 75666069 | ||||||
| chr3:75666071 | A | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 30 | chr3 | 75666071 | ||||||
| chr3:75666087 | GCTT | G | 1 | a0001c0003t0006 | 3 | HG02970.hp1 HG02976.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*52_*54delTCT | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 52 | INFO_REALIGN_3_PRIME | chr3 | 75666087 | |||||
| chr3:75666105 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 64 | chr3 | 75666105 | ||||||
| chr3:75666110 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*69C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 69 | chr3 | 75666110 | ||||||
| chr3:75666113 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 72 | chr3 | 75666113 | ||||||
| chr3:75666114 | C | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*73C>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 73 | chr3 | 75666114 | ||||||
| chr3:75666160 | T | C | 1 | a0001c0003t0010 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*119T>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 119 | chr3 | 75666160 | ||||||
| chr3:75666168 | T | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*127T>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 127 | chr3 | 75666168 | ||||||
| chr3:75666189 | G | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*148G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 148 | chr3 | 75666189 | ||||||
| chr3:75666264 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*223C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 223 | chr3 | 75666264 | ||||||
| chr3:75666272 | A | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*231A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 231 | chr3 | 75666272 | ||||||
| chr3:75666304 | T | A | 4 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0008 others(1): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*263T>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 263 | chr3 | 75666304 | ||||||
| chr3:75666328 | G | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*287G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 287 | chr3 | 75666328 | ||||||
| chr3:75666332 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*291C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 291 | chr3 | 75666332 | ||||||
| chr3:75666345 | T | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*304T>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 304 | chr3 | 75666345 | ||||||
| chr3:75666356 | A | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 315 | chr3 | 75666356 | ||||||
| chr3:75666388 | C | CT | 13 | a0001c0001t0003 a0001c0003t0003 a0001c0003t0006 others(10): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*358dupT | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 359 | INFO_REALIGN_3_PRIME | chr3 | 75666388 | |||||
| chr3:75666391 | T | C | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*350T>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 350 | chr3 | 75666391 | ||||||
| chr3:75666394 | T | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353T>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 353 | chr3 | 75666394 | ||||||
| chr3:75666414 | A | G | 1 | a0001c0003t0015 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 373 | chr3 | 75666414 | ||||||
| chr3:75666429 | G | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*388G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 388 | chr3 | 75666429 | ||||||
| chr3:75666439 | G | T | 1 | a0007c0009t0014 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398G>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 398 | chr3 | 75666439 | ||||||
| chr3:75666489 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*448C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 448 | chr3 | 75666489 | ||||||
| chr3:75666531 | C | T | 1 | a0001c0003t0013 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 490 | chr3 | 75666531 | ||||||
| chr3:75666545 | A | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504A>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 504 | chr3 | 75666545 | ||||||
| chr3:75666546 | A | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*505A>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 505 | chr3 | 75666546 | ||||||
| chr3:75666548 | G | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507G>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 507 | chr3 | 75666548 | ||||||
| chr3:75666573 | G | C | 1 | a0002c0002t0008 | 2 | HG00323.hp2 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*532G>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 532 | chr3 | 75666573 | ||||||
| chr3:75666602 | G | C | 1 | a0001c0001t0005 | 9 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*561G>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 561 | chr3 | 75666602 | ||||||
| chr3:75666626 | A | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*585A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 585 | chr3 | 75666626 | ||||||
| chr3:75666630 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*589C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 589 | chr3 | 75666630 | ||||||
| chr3:75666633 | G | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*592G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 592 | chr3 | 75666633 | ||||||
| chr3:75666639 | G | C | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*598G>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 598 | chr3 | 75666639 | ||||||
| chr3:75666648 | C | T | 1 | a0001c0001t0004 | 18 | HG02145.hp1 HG02257.hp2 HG02486.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*607C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 607 | chr3 | 75666648 | ||||||
| chr3:75666659 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*618C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 618 | chr3 | 75666659 | ||||||
| chr3:75666732 | A | G | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*691A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 691 | chr3 | 75666732 | ||||||
| chr3:75666737 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*696C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 696 | chr3 | 75666737 | ||||||
| chr3:75666743 | C | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*702C>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 702 | chr3 | 75666743 | ||||||
| chr3:75666756 | G | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 715 | chr3 | 75666756 | ||||||
| chr3:75666777 | T | C | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*736T>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 736 | chr3 | 75666777 | ||||||
| chr3:75666791 | A | C | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*750A>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 750 | chr3 | 75666791 | ||||||
| chr3:75666859 | A | G | 1 | a0001c0003t0006 | 3 | HG02970.hp1 HG02976.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*818A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 818 | chr3 | 75666859 | ||||||
| chr3:75666906 | G | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*865G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 865 | chr3 | 75666906 | ||||||
| chr3:75666930 | G | A | 1 | a0001c0003t0012 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*889G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 889 | chr3 | 75666930 | ||||||
| chr3:75667009 | C | T | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*968C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 968 | chr3 | 75667009 | ||||||
| chr3:75667036 | C | A | 1 | a0001c0001t0009 | 2 | HG00558.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*995C>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 995 | chr3 | 75667036 | ||||||
| chr3:75667037 | G | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*996G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 996 | chr3 | 75667037 | ||||||
| chr3:75667073 | A | G | 1 | a0002c0002t0011 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1032A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 1032 | chr3 | 75667073 | ||||||
| chr3:75667152 | T | A | 1 | a0009c0008t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1111T>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 4/4 | 1111 | chr3 | 75667152 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:75664563 | G | A | 1 | a0001c0001t0004g0011 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.178+6G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664563 | |||||||
| chr3:75664569 | G | C | 5 | a0001c0003t0003g0003 a0001c0003t0012g0003 a0001c0003t0013g0003 others(2): Show |
51 | HG00609.hp1 HG00735.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.178+12G>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664569 | |||||||
| chr3:75664574 | C | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178+17C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664574 | |||||||
| chr3:75664587 | T | G | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178+30T>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664587 | |||||||
| chr3:75664593 | G | A | 3 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0007c0009t0014g0007 |
14 | HG01109.hp1 HG01192.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+36G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664593 | |||||||
| chr3:75664611 | T | C | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178+54T>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664611 | |||||||
| chr3:75664617 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.178+60G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664617 | |||||||
| chr3:75664631 | G | A | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178+74G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664631 | |||||||
| chr3:75664643 | T | C | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178+86T>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664643 | |||||||
| chr3:75664675 | C | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178+118C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664675 | |||||||
| chr3:75664679 | T | C | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178+122T>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664679 | |||||||
| chr3:75664707 | A | G | 20 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0003t0003g0003 others(17): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.179-112A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664707 | |||||||
| chr3:75664716 | G | C | 1 | a0001c0001t0003g0006 | 10 | HG01109.hp1 HG01192.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.179-103G>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664716 | |||||||
| chr3:75664728 | C | A | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.179-91C>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664728 | |||||||
| chr3:75664746 | T | G | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.179-73T>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664746 | |||||||
| chr3:75664752 | A | G | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.179-67A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664752 | |||||||
| chr3:75664753 | T | A | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.179-66T>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664753 | |||||||
| chr3:75664758 | G | C | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.179-61G>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664758 | |||||||
| chr3:75664797 | C | T | 10 | a0001c0003t0003g0003 a0001c0003t0003g0015 a0001c0003t0006g0009 others(7): Show |
76 | HG00597.hp1 HG00609.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.179-22C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664797 | |||||||
| chr3:75664804 | A | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.179-15A>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664804 | |||||||
| chr3:75664807 | C | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.179-12C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664807 | |||||||
| chr3:75664812 | C | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.179-7C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 1/3 | chr3 | 75664812 | |||||||
| chr3:75664988 | A | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.256+92A>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/3 | chr3 | 75664988 | |||||||
| chr3:75664995 | A | G | 7 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0003g0002 others(4): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.256+99A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/3 | chr3 | 75664995 | |||||||
| chr3:75665034 | C | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.257-92C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/3 | chr3 | 75665034 | |||||||
| chr3:75665035 | G | A | 1 | a0001c0003t0006g0009 | 3 | HG02970.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.257-91G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/3 | chr3 | 75665035 | |||||||
| chr3:75665051 | G | A | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.257-75G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/3 | chr3 | 75665051 | |||||||
| chr3:75665089 | T | C | 2 | a0001c0001t0004g0010 a0001c0005t0001g0008 |
6 | HG01099.hp1 HG01106.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.257-37T>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/3 | chr3 | 75665089 | |||||||
| chr3:75665112 | C | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.257-14C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/3 | chr3 | 75665112 | |||||||
| chr3:75665113 | A | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.257-13A>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 2/3 | chr3 | 75665113 | |||||||
| chr3:75665228 | T | G | 8 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0003t0003g0003 others(5): Show |
65 | HG00609.hp1 HG00735.hp1 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.334+25T>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665228 | |||||||
| chr3:75665231 | G | T | 1 | a0003c0004t0001g0004 | 19 | HG00597.hp1 HG04184.hp1 NA18940.hp1 others(16): Show |
intron_variant | MODIFIER | c.334+28G>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665231 | |||||||
| chr3:75665234 | G | T | 1 | a0003c0004t0001g0004 | 19 | HG00597.hp1 HG04184.hp1 NA18940.hp1 others(16): Show |
intron_variant | MODIFIER | c.334+31G>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665234 | |||||||
| chr3:75665240 | G | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334+37G>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665240 | |||||||
| chr3:75665243 | G | T | 2 | a0002c0002t0002g0014 a0009c0008t0016g0017 |
2 | NA18522.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.334+40G>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665243 | |||||||
| chr3:75665272 | G | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334+69G>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665272 | |||||||
| chr3:75665295 | A | G | 3 | a0001c0001t0004g0005 a0001c0001t0004g0010 a0001c0001t0004g0011 |
18 | HG02145.hp1 HG02257.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.334+92A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665295 | |||||||
| chr3:75665296 | C | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334+93C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665296 | |||||||
| chr3:75665307 | C | A | 1 | a0003c0004t0001g0004 | 19 | HG00597.hp1 HG04184.hp1 NA18940.hp1 others(16): Show |
intron_variant | MODIFIER | c.334+104C>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665307 | |||||||
| chr3:75665307 | C | T | 1 | a0001c0003t0010g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.334+104C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665307 | |||||||
| chr3:75665314 | G | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334+111G>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665314 | |||||||
| chr3:75665317 | A | G | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334+114A>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665317 | |||||||
| chr3:75665335 | A | C | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334+132A>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665335 | |||||||
| chr3:75665346 | T | C | 1 | a0002c0002t0011g0013 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.334+143T>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665346 | |||||||
| chr3:75665381 | T | G | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.335-146T>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665381 | |||||||
| chr3:75665397 | C | G | 8 | a0001c0003t0003g0003 a0001c0003t0003g0015 a0001c0003t0010g0016 others(5): Show |
72 | HG00597.hp1 HG00609.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.335-130C>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665397 | |||||||
| chr3:75665406 | C | G | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.335-121C>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665406 | |||||||
| chr3:75665415 | G | A | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.335-112G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665415 | |||||||
| chr3:75665429 | G | A | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.335-98G>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665429 | |||||||
| chr3:75665457 | C | T | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.335-70C>T | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665457 | |||||||
| chr3:75665491 | C | A | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.335-36C>A | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665491 | |||||||
| chr3:75665497 | T | G | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.335-30T>G | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665497 | |||||||
| chr3:75665512 | A | C | 1 | a0009c0008t0016g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.335-15A>C | FRG2C | ENSG00000172969.8 | transcript | ENST00000308062.8 | protein_coding | 3/3 | chr3 | 75665512 |